EP3168856A2 - Sources de rayons x utilisant l'accumulation linéaire - Google Patents
Sources de rayons x utilisant l'accumulation linéaire Download PDFInfo
- Publication number
- EP3168856A2 EP3168856A2 EP16200793.4A EP16200793A EP3168856A2 EP 3168856 A2 EP3168856 A2 EP 3168856A2 EP 16200793 A EP16200793 A EP 16200793A EP 3168856 A2 EP3168856 A2 EP 3168856A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- ray
- target
- rays
- source
- electron
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000009825 accumulation Methods 0.000 title abstract description 17
- 239000000463 material Substances 0.000 claims abstract description 213
- 239000000758 substrate Substances 0.000 claims abstract description 140
- 238000010894 electron beam technology Methods 0.000 claims abstract description 123
- 230000003287 optical effect Effects 0.000 claims description 33
- 238000000576 coating method Methods 0.000 claims description 25
- 229910052721 tungsten Inorganic materials 0.000 claims description 24
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 23
- 230000005540 biological transmission Effects 0.000 claims description 22
- 239000011133 lead Substances 0.000 claims description 22
- 239000010937 tungsten Substances 0.000 claims description 22
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 21
- 229910003460 diamond Inorganic materials 0.000 claims description 20
- 239000010432 diamond Substances 0.000 claims description 20
- 239000010949 copper Substances 0.000 claims description 19
- 238000001228 spectrum Methods 0.000 claims description 18
- 239000010936 titanium Substances 0.000 claims description 16
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 15
- 229910052802 copper Inorganic materials 0.000 claims description 15
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 14
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 13
- 229910052750 molybdenum Inorganic materials 0.000 claims description 13
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 12
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 12
- 229910052790 beryllium Inorganic materials 0.000 claims description 12
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 claims description 12
- 239000011733 molybdenum Substances 0.000 claims description 12
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 12
- 229910052799 carbon Inorganic materials 0.000 claims description 10
- 239000010948 rhodium Substances 0.000 claims description 10
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims description 9
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 9
- 229910052733 gallium Inorganic materials 0.000 claims description 9
- 229910052594 sapphire Inorganic materials 0.000 claims description 9
- 239000010980 sapphire Substances 0.000 claims description 9
- 229910052710 silicon Inorganic materials 0.000 claims description 9
- 239000010703 silicon Substances 0.000 claims description 9
- 229910052719 titanium Inorganic materials 0.000 claims description 9
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 8
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 8
- 239000000956 alloy Substances 0.000 claims description 8
- 229910045601 alloy Inorganic materials 0.000 claims description 8
- 239000011651 chromium Substances 0.000 claims description 8
- 239000011248 coating agent Substances 0.000 claims description 8
- 239000010931 gold Substances 0.000 claims description 8
- 229910002804 graphite Inorganic materials 0.000 claims description 8
- 239000010439 graphite Substances 0.000 claims description 8
- 229910052703 rhodium Inorganic materials 0.000 claims description 8
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 8
- 229910052709 silver Inorganic materials 0.000 claims description 8
- 239000004332 silver Substances 0.000 claims description 8
- 239000011135 tin Substances 0.000 claims description 8
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 7
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 7
- 229910052782 aluminium Inorganic materials 0.000 claims description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 7
- 229910052792 caesium Inorganic materials 0.000 claims description 7
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 claims description 7
- 229910052804 chromium Inorganic materials 0.000 claims description 7
- 229910017052 cobalt Inorganic materials 0.000 claims description 7
- 239000010941 cobalt Substances 0.000 claims description 7
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 7
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 7
- 229910052737 gold Inorganic materials 0.000 claims description 7
- 229910052738 indium Inorganic materials 0.000 claims description 7
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims description 7
- 229910052763 palladium Inorganic materials 0.000 claims description 7
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 7
- 229910052718 tin Inorganic materials 0.000 claims description 7
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 6
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 6
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 6
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 6
- 229910052788 barium Inorganic materials 0.000 claims description 6
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 6
- 229910052741 iridium Inorganic materials 0.000 claims description 6
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims description 6
- 229910052742 iron Inorganic materials 0.000 claims description 6
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 6
- 229910052759 nickel Inorganic materials 0.000 claims description 6
- 229910052758 niobium Inorganic materials 0.000 claims description 6
- 239000010955 niobium Substances 0.000 claims description 6
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims description 6
- 229910052697 platinum Inorganic materials 0.000 claims description 6
- 229910052707 ruthenium Inorganic materials 0.000 claims description 6
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 6
- 229910052715 tantalum Inorganic materials 0.000 claims description 6
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims description 6
- 239000010409 thin film Substances 0.000 claims description 6
- 229910052720 vanadium Inorganic materials 0.000 claims description 6
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims description 6
- 229910052727 yttrium Inorganic materials 0.000 claims description 6
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 claims description 6
- 229910052725 zinc Inorganic materials 0.000 claims description 6
- 239000011701 zinc Substances 0.000 claims description 6
- 229910052726 zirconium Inorganic materials 0.000 claims description 6
- 229910052582 BN Inorganic materials 0.000 claims description 5
- 238000009304 pastoral farming Methods 0.000 claims description 5
- 238000000295 emission spectrum Methods 0.000 claims description 3
- 238000004846 x-ray emission Methods 0.000 abstract description 24
- 230000035515 penetration Effects 0.000 description 27
- 239000013077 target material Substances 0.000 description 24
- 230000001965 increasing effect Effects 0.000 description 20
- 230000003993 interaction Effects 0.000 description 17
- 238000004519 manufacturing process Methods 0.000 description 12
- 238000012546 transfer Methods 0.000 description 11
- 230000005461 Bremsstrahlung Effects 0.000 description 10
- 238000013461 design Methods 0.000 description 10
- 238000001816 cooling Methods 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 230000005855 radiation Effects 0.000 description 9
- 239000010410 layer Substances 0.000 description 8
- 230000007246 mechanism Effects 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 238000010521 absorption reaction Methods 0.000 description 7
- 230000009102 absorption Effects 0.000 description 6
- 230000002238 attenuated effect Effects 0.000 description 6
- 230000008901 benefit Effects 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 238000003384 imaging method Methods 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 238000012876 topography Methods 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 5
- 238000003491 array Methods 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 230000009103 reabsorption Effects 0.000 description 5
- 230000008021 deposition Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 238000005086 pumping Methods 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 238000002083 X-ray spectrum Methods 0.000 description 3
- 230000003466 anti-cipated effect Effects 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 239000012809 cooling fluid Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 230000004907 flux Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- 239000011343 solid material Substances 0.000 description 3
- 238000011144 upstream manufacturing Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 239000002041 carbon nanotube Substances 0.000 description 2
- 229910021393 carbon nanotube Inorganic materials 0.000 description 2
- 239000002826 coolant Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000002050 diffraction method Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000010408 film Substances 0.000 description 2
- 238000009501 film coating Methods 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000007689 inspection Methods 0.000 description 2
- 230000000670 limiting effect Effects 0.000 description 2
- 229910001338 liquidmetal Inorganic materials 0.000 description 2
- 230000000116 mitigating effect Effects 0.000 description 2
- 239000002086 nanomaterial Substances 0.000 description 2
- 239000002071 nanotube Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000001902 propagating effect Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 229910052702 rhenium Inorganic materials 0.000 description 2
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 2
- 230000003595 spectral effect Effects 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- 229910000952 Be alloy Inorganic materials 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 230000010748 Photoabsorption Effects 0.000 description 1
- 235000014443 Pyrus communis Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 238000010420 art technique Methods 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000013590 bulk material Substances 0.000 description 1
- 229910052729 chemical element Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 239000011258 core-shell material Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000007435 diagnostic evaluation Methods 0.000 description 1
- 238000002059 diagnostic imaging Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000004453 electron probe microanalysis Methods 0.000 description 1
- 238000000609 electron-beam lithography Methods 0.000 description 1
- 238000001352 electron-beam projection lithography Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 238000012921 fluorescence analysis Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000003574 free electron Substances 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 238000009428 plumbing Methods 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000010408 sweeping Methods 0.000 description 1
- 230000001360 synchronised effect Effects 0.000 description 1
- 230000003685 thermal hair damage Effects 0.000 description 1
- 238000003325 tomography Methods 0.000 description 1
- 235000012431 wafers Nutrition 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 238000004876 x-ray fluorescence Methods 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J35/00—X-ray tubes
- H01J35/02—Details
- H01J35/04—Electrodes ; Mutual position thereof; Constructional adaptations therefor
- H01J35/08—Anodes; Anti cathodes
- H01J35/10—Rotary anodes; Arrangements for rotating anodes; Cooling rotary anodes
- H01J35/105—Cooling of rotating anodes, e.g. heat emitting layers or structures
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J2235/00—X-ray tubes
- H01J2235/08—Targets (anodes) and X-ray converters
- H01J2235/083—Bonding or fixing with the support or substrate
- H01J2235/084—Target-substrate interlayers or structures, e.g. to control or prevent diffusion or improve adhesion
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J2235/00—X-ray tubes
- H01J2235/08—Targets (anodes) and X-ray converters
- H01J2235/086—Target geometry
Definitions
- the embodiments disclosed herein relate to high-brightness sources of x-rays. Such high brightness sources may be useful for a variety of applications in which x-rays are employed, including manufacturing inspection, metrology, crystallography, structure and composition analysis and medical imaging and diagnostic systems.
- the laboratory x-ray source was later improved by Coolidge in the early 20 th century [see, for example, William D. Coolidge, U.S. Patents 1,211,092, issued Jan. 2, 1917 , 1,917,099, issued Jul. 4, 1933 , and 1,946,312, issued Feb. 6, 1934 ], and, later in the 20 th century, systems generating very intense beams of x-rays using synchrotrons or free electron lasers (FELs) have been developed. These synchrotron or FEL systems, however, are physically very large systems, requiring large buildings and acres of land for their implementation. For compact, practical lab-based systems and instruments, most x-ray sources today still use the fundamental mechanism of the Coolidge tube.
- FIG. 1 An example of the simplest x-ray source, a transmission x-ray source 08, is illustrated in FIG. 1
- the source comprises a vacuum environment (typically 10 -6 torr or better) commonly provided by a sealed vacuum tube 02 or active pumping, manufactured with sealed electrical leads 21 and 22 that pass from the negative and positive terminals of a high voltage source 10 outside the tube to the various elements inside the vacuum tube 02.
- the source 08 will typically comprise mounts 03 which secure the vacuum tube 02 in a housing 05, and the housing 05 may additionally comprise shielding material, such as lead, to prevent x-rays from being radiated by the source 08 in unwanted directions.
- an emitter 11 connected through the lead 21 to the high voltage source 10 serves as a cathode and generates a beam of electrons 111, often by running a current through a filament.
- the target 01 is electrically connected to the opposite high voltage lead 22 to be at low voltage, thus serving as an anode.
- the emitted electrons 111 accelerate towards the target 01 and collide with it at high energy, with the energy of the electrons determined by the magnitude of the accelerating voltage.
- the collision of the electrons 111 into the solid target 01 induces several effects, including the emission of x-rays 888, some of which exit the vacuum tube 02 through a window 04 designed to transmit x-rays.
- the target 01 is deposited or mounted directly on the window 04 and the window 04 forms a portion of the wall of the vacuum chamber.
- the target may be formed as an integral part of the window 04 itself.
- the source 80 comprises a vacuum environment (typically 10 -6 torr or better) commonly maintained by a sealed vacuum tube 20 or active pumping, and manufactured with sealed electrical leads 21 and 22 that pass from the negative and positive terminals of a high voltage source 10 outside the tube to the various elements inside the vacuum tube 20.
- the source 80 will typically comprise mounts 30 which secure the vacuum tube 20 in a housing 50, and the housing 50 may additionally comprise shielding material, such as lead, to prevent x-rays from being radiated by the source 80 in unwanted directions.
- an emitter 11 connected through the lead 21 to the high voltage source 10 serves as a cathode and generates a beam of electrons 111, often by running a current through a filament.
- a target 100 supported by a target substrate 110 is electrically connected to the opposite high voltage lead 22 and target support 32 to be at low voltage, thus serving as an anode.
- the electrons 111 accelerate towards the target 100 and collide with it at high energy, with the energy of the electrons determined by the magnitude of the accelerating voltage.
- the collision of the electrons 111 into the target 100 induces several effects, including the emission of x-rays, some of which exit the vacuum tube 20 and are transmitted through a window 40 that is transparent to x-rays.
- the target 100 and substrate 110 may be integrated or comprise a solid block of the same material, such as copper (Cu).
- electron optics electrostatic or electromagnetic lenses
- electron sources comprising multiple emitters may be provided to provide a larger, distributed source of electrons.
- the electrons in the electron beam 111 collide with the target 100 at its surface 102, and the electrons that pass through the surface transfer their energy into the target 100 in an interaction volume 200, generally defined by the incident electron beam footprint (area) times the electron penetration depth.
- the interaction volume 200 is typically "pear” or “teardrop” shaped in three dimensions, and symmetric around the electron propagation direction.
- the interaction volume will be represented by the convolution of this "teardrop" shape with the lateral beam intensity profile.
- the penetration depth is much larger than for a material with greater density, such as most elements used for x-ray generation.
- electron energy may simply be converted into heat. Some absorbed energy may excite the generation of secondary electrons, typically detected from a region 221 located near the surface, while some electrons may also be backscattered, which, due to their higher energy, can be detected from a somewhat larger region 231.
- x-rays 888 are generated and radiated outward in all directions.
- the x-ray emission can have a complex energy spectrum. As the electrons penetrate the material, they decelerate and lose energy, and therefore different parts of the interaction volume 200 produce x-rays with different properties.
- a typical x-ray radiation spectrum for emission from the collision of 100 keV electrons with a tungsten target is illustrated in FIG. 4 .
- the broad spectrum x-ray emission 388 arises from electrons that were diverted from their initial trajectory, depending on how close they pass to various nuclei and other electrons.
- the reduction in electron energy and the change momentum associated with the change in direction generate the radiation of x-rays.
- the change in energy is a continuum, and therefore, the energy of the generated x-rays also is a continuum.
- Greater emission occurs at the low end of the energy spectrum, with far less occurring at higher energy, and reaching an absolute limit of no x-rays with energy larger than the original electron energy (in this example, 100 keV). Due to their origin in deceleration of electrons, this kind of continuum x-ray emission 388 is commonly called bremsstrahlung, after the German word "bremsen” for "braking".
- bremsstrahlung x-rays 888 are typically emitted isotropically, i.e. with little variation in intensity with emission direction [see, for example, D. Gonzales, B. Cavness, and S. Williams, "Angular distribution of thick-target bremsstrahlung produced by electrons with initial energies ranging from 10 to 20 keV incident on Ag", Phys. Rev. A, vol. 84, 052726 (2011 )], higher energy excitation can have increased emission normal to the electron beam, i.e.
- the x-ray source 08 or 80 will typically have a window 04 or 40.
- This window 04 or 40 may additionally comprise a filter, such as a sheet or layer of aluminum, that attenuates the low energy x-rays, producing the modified energy spectrum 488 shown in FIG. 4 .
- the emission is generally called “characteristic lines", since they are a characteristic of the particular material.
- the sharp lines 988 in the example of an x-ray emission spectrum shown in FIG. 4 are “characteristic lines” for tungsten.
- Individual characteristic lines can be quite bright, and may be monochromatized with an appropriate filter or crystal monochromator where a monochromatic source is desired.
- the relative x-ray intensity (flux) ratio of the characteristic line(s) to the bremsstrahlung radiation depends on the element and the incident electron energy, and can vary substantially. In general, a maximum ratio for a given target material is obtained when the incident electron energy is 3 to 5 times the ionization energy of the inner shell electrons.
- these characteristic x-rays 388 are primarily generated in a fraction of the electron penetration depth, shown as the second largest shaded portion 248 of the interaction volume 200.
- the relative depth is influenced in part by the energy of the electrons 111, which typically falls off with increasing depth. If the electron energy does not exceed the binding energy for electrons within the target, no characteristic x-rays will be emitted at all. The greatest emission of characteristic lines may occur under bombardment with electrons having three to five times the energy of the emitted characteristic x-ray photons. Because these characteristic x-rays result from atomic emission between electron shells, the emission will generally be entirely isotropic.
- the actual dimensions of this interaction volume 200 may vary, depending on the energy and angle of incidence of the electrons, the surface topography and other properties (including local charge density), and the density and atomic composition of the target material.
- the composition of the target material is selected to provide x-ray spectra with ideal characteristics for a specific application, such as strong characteristic lines at particular wavelengths of interest, or bremsstrahlung radiation over a desired bandwidth.
- Control of the x-ray emission properties of a source may be governed by the selection of an electron energy (typically changed by varying the accelerating voltage), x-ray target material selection, and by the geometry of x-ray collection from the target.
- the x-ray brightness (also called “brilliance” by some), defined as the number of x-ray photons per second per solid angle in mrad 2 per area of the x-ray source in mm 2 (some measures may also include a bandwidth window of 0.1% in the definition), is an important figure-of-merit for a source, as it relates to obtaining good signal-to-noise ratios for downstream applications.
- the brightness can be increased by adjusting the geometric factors to maximize the collected x-rays.
- the surface of the target 100 in a reflection x-ray source is generally mounted at an angle ⁇ (as was also shown in FIG. 2 ) and bombarded by a distributed electron beam 111.
- the five spots are more spread out and brightness is reduced, while for low angle ⁇ , the five source spots appear to be closer together, thus emitting more x-rays into the same solid angle and resulting in an increased brightness.
- emission at 0° occurs parallel to the surface of a solid metal target for conventional sources, and since the x-rays must propagate along a long length of the target material before emission, most of the produced x-rays will be attenuated (reabsorbed) by the target material, reducing brightness.
- a source with take-off angle of around 6° to 15° (depending on the source configuration, target material, and electron energy) will often provide the greatest practical brightness, concentrating the apparent size of the source while reducing re-absorption within the target material and is therefore commonly used in commercial x-ray sources.
- the effective source area is the projected area viewed along the direction along which x-ray are collected for use, i.e. along the axis of the x-ray beam. Because of the limited electron penetration depth, the effective source area for an incident electron beam with a size comparable or larger than the electron penetration depth is dependent on the angle between the axis of the x-ray beam and the surface of the target, referred to as the "take-off angle". When the electron beam size is much larger than the electron penetration depth, the effective source area decreases with decreasing take-off angle. This effect has been used to increase x-ray source brightness.
- Another way to increase the brightness of the x-ray source for bremsstrahlung radiation is to use a target material with a higher atomic number Z, as efficiency of x-ray production for bremsstrahlung radiation scales with increasingly higher atomic number materials.
- the x-ray emitting material should ideally have good thermal properties, such as a high melting point and high thermal conductivity, in order to allow higher electron power loading on the source to increase x-ray production.
- FIG. 6A a cross-section is shown for a rotating anode x-ray source 580 comprising a target anode 500 that typically rotates between 3,300 and 10,000 rpm.
- the target anode 500 is connected by a shaft 530 to a rotor 520 supported by conducting bearings 524 that connect, through its mount 522, to the lead 22 and the positive terminal of the high voltage supply 10.
- the rotation of the rotor 520, shaft 530 and anode 500, all within the vacuum chamber 20, is typically driven inductively by stator windings 525 mounted outside the vacuum.
- the surface of the target anode 500 is shown in more detail in FIG. 6B .
- the edge 510 of the rotating target anode 500 is sometimes beveled at an angle, and the source of the electron beam 511 is in a position to direct the electron beam onto the beveled edge 510 of the target anode 500, generating x-rays 888 from a target spot 501.
- the target spot 501 generates x-rays, it heats up, but as the target anode 500 rotates, the heated spot moves away from the target spot 501, and the electron beam 511 now irradiates a cooler portion of the target anode 500.
- the hot spot has the time of one rotation to cool before becoming heated again when it passes through the hot spot 501.
- Another approach to mitigating heat is to use a target with a thin layer of target x-ray material deposited onto a substrate with high heat conduction. Because the interaction volume is thin, for electrons with energies up to 100 keV the target material itself need not be thicker than a few microns, and can be deposited onto a substrate, such as diamond, sapphire or graphite that conducts the heat away quickly. However, as noted in Table I, diamond is a very poor electrical conductor, so the design of any anode fabricated on a diamond substrate must still provide an electrical connection between the target material of the anode and the positive terminal of the high voltage. [Diamond mounted anodes for x-ray sources have been described by, for example, K. Upadhya et al. US Patent 4,972,449 ; B. Spitsyn et. al. US Patent 5,148,462 ; and M. Fryda et al., US Patent 6,850,598 ].
- the substrate may also comprise channels for a coolant, for example liquids such as water or ethylene glycol, or a gas such as hydrogen or helium, that remove heat from the substrate [see, for example, Paul E. Larson, US Patent 5,602,899 ]
- a coolant for example liquids such as water or ethylene glycol, or a gas such as hydrogen or helium, that remove heat from the substrate
- a gas such as hydrogen or helium
- the substrate may in turn be mounted to a heat sink comprising copper or some other material chosen for its thermally conducting properties.
- the heat sink may also comprise channels for a coolant, to transport the heat away [See, for example, Edward J. Morton, US Patent 8,094,784 ].
- thermoelectric coolers or cryogenic systems have been used to provide further cooling to an x-ray target mounted onto a heat sink, again, all with the goal of achieving higher x-ray brightness without melting or damaging the target material through excessive heating.
- Jets of liquid metal require an elaborate plumbing system and consumables, are limited in the materials (and thus values of Z and their associated spectra) that may be used, and are difficult to scale to larger output powers.
- In the case of thin film targets of uniform solid material coated onto diamond substrates there is still a limitation in the amount of heat that can be tolerated before damage to the film may occur, even if used in a rotating anode configuration. Conduction of heat only occurs through the bottom of the film. In a lateral dimension, the same conduction problem exists as exists in the bulk material.
- an x-ray source that may be used to achieve higher x-ray brightness through the use of a higher electron current density, but that is still compact enough to fit in a laboratory or table-top environment, or even be useful in portable devices.
- Such brighter sources would enable x-ray based tools that offer better signal to noise ratios for imaging and other scientific and diagnostic applications.
- the x-ray target configurations may comprise a number of microstructures of one or more selected x-ray generating materials fabricated in close thermal contact with (such as embedded in or buried in) a substrate with high thermal conductivity, such that the heat is more efficiently drawn out of the x-ray generating material. This in turn allows bombardment of the x-ray generating material with higher electron density and/or higher energy electrons, which leads to greater x-ray brightness.
- a significant advantage to some embodiments is that the orientation of the microstructures allows the use of an on-axis collection angle, allowing the accumulation of x-rays from several microstructures to be aligned to appear to originate at a single origin, and can be used for alignments at "zero-angle" x-ray emission.
- the linear accumulation of x-rays from the multiple origins leads to greater x-ray brightness.
- Some embodiments of the invention additionally comprise x-ray optical elements that collect the x-rays emitted from one structure and re-focus them to overlap with the x-rays from a second structure. This relaying of x-rays can also lead to greater x-ray brightness.
- Some embodiments of the invention comprise an additional cooling system to transport the away from the anode or anodes. Some embodiments of the invention additionally comprise rotating the anode or anodes comprising targets with microstructured patterns in order to further dissipate heat and increase the accumulated x-ray brightness.
- FIG. 7 illustrates an embodiment of a reflective x-ray system 80-A according to the invention.
- the source comprises a vacuum environment (typically 10 -6 torr or better) commonly maintained by a sealed vacuum chamber 20 or active pumping, and manufactured with sealed electrical leads 21 and 22 that pass from the negative and positive terminals of a high voltage source 10 outside the tube to the various elements inside the vacuum chamber 20.
- the source 80-A will typically comprise mounts 30 which secure the vacuum chamber 20 in a housing 50, and the housing 50 may additionally comprise shielding material, such as lead, to prevent x-rays from being radiated by the source 80-A in unwanted directions.
- an emitter 11 connected through the lead 21 to the high voltage source 10 serves as a cathode and generates a beam of electrons 111, often by running a current through a filament.
- Any number of prior art techniques for electron beam generation may be used for the embodiments of the invention disclosed herein. Additional known techniques used for electron beam generation include heating for thermionic emission, Schottky emission (a combination of heating and field emission), emitters comprising nanostructures such as carbon nanotubes), and by use of ferroelectric materials.
- a target 1100 comprising a target substrate 1000 and regions 700 of x-ray generating material is electrically connected to the opposite high voltage lead 22 and target support 32 to be at low voltage, thus serving as an anode.
- the electrons 111 accelerate towards the target 1100 and collide with it at high energy, with the energy of the electrons determined by the magnitude of the accelerating voltage.
- the collision of the electrons 111 into the target 1100 induces several effects, including the emission of x-rays, some of which exit the vacuum tube 20 and are transmitted through a window 40 that is transparent to x-rays.
- an electron control mechanism 70 such as an electrostatic lens system or other system of electron optics that is controlled and coordinated with the electron dose and voltage provided by the emitter 11 by a controller 10-1 through a lead 27.
- the electron beam 111 may therefore be scanned, focused, defocused, or otherwise directed onto a target 1100 comprising one or more microstructures 700 fabricated to be in close thermal contact with a substrate 1000.
- the alignment of the microstructures 700 may be arranged such that the bombardment of several of the microstructures 700 by the electron beam or beams 111 will excite emission in a direction orthogonal to the surface normal of the target in such a manner that the intensity in the direction of view will add or accumulate.
- the direction may also be selected by means of an aperture 840 in a screen 84 for the system to form the directional beam 888 that exits the system through a window 40.
- the aperture 840 may be positioned outside the vacuum chamber, or, more commonly, the window 40 itself may serve as the aperture.
- the aperture may be inside the vacuum chamber.
- Targets such as those to be used in x-ray sources according to the invention disclosed herein have been described in detail in the co-pending US Patent Application entitled STRUCTURED TARGETS FOR X-RAY GENERATION ( US Patent Application 14/465,816, filed Aug. 21, 2014 ), which is hereby incorporated by reference in its entirety and included as Appendix A. Any of the target designs and configurations disclosed in the above referenced co-pending Application may be considered for use as a component in any or all of the x-ray sources disclosed herein.
- FIG. 8 illustrates a target as may be used in some embodiments of the invention.
- a substrate 1000 has a region 1001 that comprises an array of microstructures 700 comprising x-ray generating material (typically a metallic material) that are arranged in a regular array of right rectangular prisms.
- x-ray generating material typically a metallic material
- electrons 111 bombard the target from above, and generate heat and x-rays in the microstructures 700.
- the material in the substrate 1000 is selected such that it has relatively low energy deposition rate for electrons in comparison to the x-ray generating microstructure material (typically by selecting a low Z material for the substrate), and therefore will not generate a significant amounts of heat and x-rays.
- the substrate 1000 material may also be chosen to have a high thermal conductivity, typically larger than 100 W/(m °C), and the microstructures are typically embedded within the substrate, i.e. if the microstructures are shaped as rectangular prisms, it is preferred that at least five of the six sides are in close thermal contact with the substrate 1000, so that heat generated in the microstructures 700 is effectively conducted away into the substrate 1000.
- targets used in other embodiments may have fewer direct contact surfaces.
- the term "embedded” is used in this disclosure, at least half of the surface area of the microstructure will be in close thermal contact with the substrate.
- a target 1100 according to the invention may be inserted as a replacement for the target 01 for the transmission x-ray source 08 illustrated in FIG. 1 , or for the target 100 illustrated in the reflecting x-ray source 80 of FIG. 2 , or adapted for use as the target 500 used in the rotating anode x-ray source 580 of FIG. 6 .
- microstructure when the word "microstructure” is used herein, it is specifically referring to microstructures comprising x-ray generating material.
- Other structures such as the cavities used to form the x-ray microstructures, have dimensions of the same order of magnitude, and might also be considered “microstructures".
- structures such as “structures”, “cavities”, “holes”, “apertures”, etc. may be used for these structures when they are formed in materials, such as the substrate, that are not selected for their x-ray generating properties.
- the word “microstructure” will be reserved for structures comprising materials selected for their x-ray generating properties.
- microstructure x-ray generating structures with dimensions smaller than 1 micron, or even as small as nanoscale dimensions (i.e. greater than 10 nm) may also be described by the word “microstructures” as used herein.
- FIG. 9 illustrates another target as may be used in some embodiments of the invention in which the electron beam 111-F is directed by electrostatic lenses to form a more concentrated, focused spot.
- the target 1100-F will still comprise a region 1001-F comprising an array of microstructures 700-F comprising x-ray material, but the size and dimensions of this region 1001-F can be matched to regions where electron exposure will occur.
- the "tuning" of the source geometry and the x-ray generating material can be controlled such that the designs mostly limit the amount of heat generated to the microstructured region 1001-F, while also reducing the design and manufacturing complexity. This may be especially useful when used with electron beams focused to form a micro-spot, or by more intricate systems that form a more complex electron exposure pattern.
- FIG. 10 illustrates another target as may be used in some embodiments of the invention, in which the target 1100-E still has a region 1001-E with an array of microstructures 700-E comprising x-ray material that emit x-rays when exposed to electrons 111, but the region 1001-E is positioned flush with or near the edge of the substrate 1000-E.
- This configuration may be useful in targets where the substrate comprises a material that absorbs x-rays, and so emission at near-zero angles would be significantly attenuated in a configuration, as was shown in FIG. 8 .
- a disadvantage of the target of FIG. 10 is that a significant portion of the substrate on one side of the microstructures 700-E is gone. Heat therefore is not carried away from the microstructures symmetrically, and the local heating may increase, impairing heat flow.
- the target 1100-R comprises a substrate 1000-R with a recessed shelf 1002-R. This allows the region 1001-R comprising an array of microstructures 700-R to be positioned flush with, or close to, a recessed edge 1003-R of the substrate, and emit x-rays at or near zero angle without being reabsorbed by the substrate 1000-R, yet provides a more symmetric heat sink for the heat generated when exposed to electrons 111.
- FIG. 12 illustrates the relative interaction between a beam of electrons 111 and a target comprising a substrate 1000 and microstructures 700 of x-ray material. As illustrated, only three electron paths are shown, with two representative of electrons bombarding the two shown microstructures 700, and one interacting with the substrate.
- Table II illustrates some of the estimated penetration depths for some common x-ray target materials. Table II: Estimates of penetration depth for 60 keV electrons into some materials. Material Z Density (g/cm 3 ) Penetration Depth ( ⁇ m) Diamond 6 3.5 13.28 Copper 29 8.96 5.19 Molybdenum 42 10.28 4.52 Tungsten 74 19.25 2.41
- the dimension marked as R to the left side of FIG. 12 corresponds to a reference dimension of 10 microns, and the depth D in the x-ray generating material, which, when set to be 2/3 (66%) of the electron penetration depth for copper, becomes D ⁇ 3.5 ⁇ m.
- the majority of characteristic Cu K x-rays are generated within depth D .
- the electron interactions below that depth typically generate few characteristic K-line x-rays but will contribute to the heat generation, thus resulting in a low thermal gradient along the depth direction.
- One embodiment of the invention limits the depth of the microstructured x-ray generating material in the target to between one third and two thirds of the electron penetration depth at the incident electron energy.
- the lower mass density of the substrate leads to a lower energy deposition rate in the substrate material immediately below the x-ray generating material, which in turn leads to a lower temperature in the substrate material below. This results in a higher thermal gradient between the x-ray generating material and the substrate, enhancing heat transfer.
- the thermal gradient is further enhanced by the high thermal conductivity of the substrate material.
- selecting the depth D to be less than the electron penetration depth is also generally preferred for efficient generation of bremsstrahlung radiation, because the electrons below that depth have lower energy and thus lower x-ray production efficiency.
- the depth of the x-ray material may be selected to be 50% of the electron penetration depth. In other embodiments, the depth of the x-ray material may be selected to be 33% of the electron penetration depth. In other embodiments, the depth D for the microstructures may be selected related to the "continuous slowing down approximation" (CSDA) range for electrons in the material. Other depths may be specified depending on the x-ray spectrum desired and the properties of the selected x-ray material.
- CSDA continuous slowing down approximation
- a particular ratio between the depth and the lateral dimensions (such as width W and length L ) of the x-ray generating material may also be specified. For example, if the depth is selected to be a particular dimension D, then the lateral dimensions W and/or L may be selected to be no more than 5x D , giving a maximum ratio of 5. In other targets as may be used in some embodiments of the invention, the lateral dimensions W and/or L may be selected to be no more than 2x D .
- the depth D and lateral dimensions W and L may be defined relative to the axis of electron propagation, or defined with respect to the orientation of the surface of the x-ray generating material. For normal incidence electrons, these will be the same dimensions. For electrons incident at an angle, care must be taken to make sure the appropriate projections are used.
- FIG. 13 illustrates the relative x-ray generation from the various regions shown in FIG. 12 .
- X-rays 888 comprise characteristic x-rays emitted from the region 248 where they are generated in the x-ray generating material, while the regions 1280 and 1080 where the electrons interact with the substrate generate characteristic x-rays of the substrate element(s), (but not characteristic x-rays of the element(s) of the x-ray generating material in the x-ray generating region 248).
- bremsstrahlung radiation x-rays emitted from the region 248 of the x-ray generating material are typically much stronger than in the regions 1280 and 1080 where electrons encounter only the low Z substrate, which emit weak continuum x-rays 1088 and 1228.
- FIG. 13 shows x-rays emitted only to the right, this is in anticipation of a window or collector being placed to the right, when this target is used in the low-angle high-brightness configuration discussed in FIG. 5 .
- X-rays are in fact typically emitted in all directions from these regions.
- FIG. 13 illustrates an arrangement that allows the linear accumulation of characteristic x-rays along the microstructures and therefore can produce a relatively strong characteristic x-ray signal.
- many lower energy x-rays will be attenuated by the target materials, which will effectively act as an x-ray filter.
- Other selections of materials and geometric parameters may be chosen (e.g. a non-linear scheme) if non-characteristic, continuum x-rays are desired, such as applications in which a bandpass of low energy x-rays are desired (e.g. for imaging or fluorescence analysis of low Z materials).
- a target with a surface with additional properties in three dimensions (3-D) may be desired.
- the apparent x-ray source size and area is at minimum (and brightness maximized) when viewed parallel to surface, i.e. at a zero degree (0°) take-off angle.
- the apparent brightest of x-ray emission occurs when viewed at 0° take-off angle.
- the emission from within the x-ray generating material will accumulate as it propagates at 0° through the material.
- the attenuation of x-rays between their points of origin inside the target as they propagate through the material to the surface increases with decreasing take-off angle, due to the longer distance traveled within the material, and often becomes largest at or near 0° take-off angle. Reabsorption may therefore counterbalance any increased brightness that viewing at near 0° achieves.
- the distance through which an x-ray beam will be reduced in intensity by 1/e is called the x-ray attenuation length, and therefore, a configuration in which the emitted x-rays pass through as little additional material as possible, with the distance selected to be related to the x-ray attenuation length, may be desired.
- FIG. 14 An illustration of a target as may be used in some embodiments of the invention is presented in FIG. 14 .
- an x-ray generating region comprising a single microstructure 2700 is configured at or near a recessed edge 2003 of the substrate on a shelf 2002, similar to the situation illustrated in FIG. 11 .
- the x-ray generating microstructure 2700 is in the shape of a rectangular bar of x-ray generating material, is embedded in a substrate 2000, and emits x-rays 2888 when bombarded with electrons 111.
- the thickness of the bar D (along the surface normal of the target) is selected to be between one third and two thirds of the electron penetration depth of the x-ray generating material at the incident electron energy for optimal thermal performance. It may also be selected to obtain a desired x-ray source size in the vertical direction.
- the width of the bar W is selected to obtain a desired source size in the corresponding direction. As illustrated, W ⁇ 1.5 D , but could be substantially smaller or larger, depending on the size of the source spot desired.
- the length of the bar L as illustrated is L ⁇ 4D , but may be any dimension, and may typically be determined to be between 1 ⁇ 4 to 3 times the x-ray attenuation length for the selected x-ray generating material.
- FIG. 15 An illustration of an alternative target as may be used in some embodiments of the invention is presented in FIG. 15 .
- an x-ray generating region with six microstructures 2701, 2702, 2703, 2704, 2705, 2706 is configured at or near a recessed edge 2003 of the substrate on a shelf 2002, similar to the situation illustrated in FIG. 11 and FIG. 14 .
- the x-ray generating microstructures 2701, 2702, 2703, 2704, 2705, 2706 are arranged in a linear array of x-ray generating right rectangular prisms embedded in a substrate 2000, and emit x-rays 2888-D when bombarded with electrons 111.
- the total volume of x-ray generating material is the same as in the previous illustration of FIG. 14 .
- the thickness of the bar D (along the surface normal of the target) is selected to be between one third and two thirds of the electron penetration depth of the x-ray generating material at the incident electron energy for optimal thermal performance, as in the case shown in FIG. 14 .
- the width of the bar W is selected to obtain a desired source size in the corresponding direction and as illustrated, W ⁇ 1.5 D, as in the case shown in FIG. 14 . As discussed previously, it could also be substantially smaller or larger, depending on the size of the source spot desired.
- each sub-bar now has five faces transferring heat into the substrate, increasing the heat transfer away from the x-ray generating sub-bars 2701-2706 and into the substrate.
- the separation between the sub-bars is a distance d ⁇ 1, although larger or smaller dimensions may also be used, depending on the amount of x-rays absorbed by the substrate and the relative thermal gradients that may be achieved between the specific materials of the x-ray generating microstructures 2701-2706 and the substrate 2000.
- the total length of the x-ray generating sub-bars will commonly be about twice the linear attenuation length for x-rays in the x-ray generating material, but can be selected from half to more than 3 times that distance.
- the thickness of the bar (along the surface normal of the target) D was selected to be equal to one third to two thirds of the electron penetration depth of the x-ray generating material at the incident electron energy for optimal thermal performance, but it can be substantially larger. It may also be selected to obtain a desired x-ray source size in that direction which is approximately equal.
- the bars as shown may be embedded in the substrate (as shown), but if the thermal load generated in the x-ray generating material is not too large, they may also be placed on top of the substrate.
- FIG. 16 illustrates a region 1001 of a target as may be used in some embodiments of the invention that comprises an array of microstructures 700 in the form of right rectangular prisms comprising x-ray generating material arranged in a regular array.
- FIG. 16A presents a perspective view of the sixteen microstructures 700 for this target, while FIG. 16B illustrates a top down view of the same region, and FIG. 16C presents a side/cross-section view of the same region.
- side/cross-section view in this disclosure, the view meant is one as if a cross-section of the object had been made, and then viewed from the side towards the cross-sectioned surface. This shows both detail at the point of the cross-section as well as material deeper inside that might be seen from the side, assuming the substrate itself were transparent [which, in the case of diamond, is generally true for visible light].
- the microstructures have been fabricated such that they are in close thermal contact on five of six sides with the substrate. As illustrated, the top of the microstructures 700 are flush with the surface of the substrate, but other targets in which the microstructure is recessed may be fabricated, and still other targets in which the microstructures present a topographical "bump" relative to the surface of the substrate may also be fabricated.
- An alternative target as may be used in some embodiments of the invention may have several microstructures of right rectangular prisms simply deposited upon the surface of the substrate. In this case, only the bottom base of the prism would be in thermal contact with the substrate.
- the heat transfer is illustrated with representative arrows in FIG. 17 , in which the heat generated in microstructures 700 embedded in a substrate 1000 is conducted out of the microstructures 700 through the bottom and sides (arrows for transfer through the sides out of the plane of the drawing are not shown).
- FIG. 18 illustrates a region 1013 of a target according to an embodiment of invention that comprises a checkerboard array of microstructures 700 and 701 in the form of right rectangular prisms comprising x-ray generating material.
- the array as shown is arranged as an embedded array in the surface of the substrate.
- FIG. 18A presents a perspective view of the twenty-five embedded microstructures 700 and 701
- FIG. 18B illustrates a top down view of the same region
- FIG. 18C presents a side/cross-section view of the same region with recessed regions shown with dotted lines.
- FIG. 19 An illustration of another target as may be used in some embodiments of the invention is presented in FIG. 19 , which shows a region 2001 of a target according to an embodiment of invention with an array of microstructures 2790 and 2791 comprising x-ray generating material having a thickness D .
- the array as shown is a modified checkerboard pattern of right rectangular prisms, but other configurations and arrays of microstructures may be used as well.
- these microstructures 2790 and 2791 are embedded in the surface of the substrate.
- the surface of the substrate comprises a predetermined non-planar topography, and in this particular case, a plurality of steps along the surface normal of the substrate 2000.
- the height of each step is h ⁇ D, but the step height may be selected to be between 1x and 3x the thickness of the microstructures.
- the total height of all the steps may be selected to be equal or less than the desired x-ray source size along the vertical (thickness) direction.
- the total width of the microstructured region may be equal to the desired x-ray source size in the corresponding direction.
- the overall appearance resembles a staircase of x-ray sources.
- FIG. 19A presents a perspective view of the eighteen embedded microstructures 2790 and 2791, while FIG. 19B illustrates a top down view of the same region, and FIG. 19C presents a side/cross-section view of the same region.
- An electrically conductive layer may be coated on the top of the staircase structures when the substrate is beryllium, diamond, sapphire, silicon, or silicon carbide.
- FIG. 20 illustrates the x-ray emission 888-S from the staircase target of FIG. 19C when bombarded by electrons 111.
- the prisms of x-ray generating material heat up when electrons collide with them, and because each of the prisms of x-ray generating material has five sides in thermal contact with the substrate 2000, conduction of heat away from the x-ray material is still larger than a configuration in which the x-ray material is deposited on the surface.
- the emission is of x-rays unattenuated by absorption from other neighboring prisms and negligibly attenuated by neighboring substrate material.
- each prism will therefore be increased, especially when compared to the x-ray emission from the target of FIG. 18 , which also illustrates a number of prisms 700 and 701 of x-ray generating material arranged in a checkerboard pattern.
- each prism is embedded in the substrate, therefore having five surfaces in thermal contact with the substrate 1000, but the emission to the side at 0° will be attenuated by both the prisms of the neighboring columns and the substrate material.
- Such an embodiment comprising a target with topography may be manufactured by first preparing a substrate with topography, and then embedding the prisms of x-ray material following the fabrication processes for the previously described planar substrates.
- the initial steps that create cavities to be filled with x-ray material may be enhanced to create the staircase topography structure in an initially flat substrate.
- additional alignment steps such as those known to those skilled in the art of planar processing, may be employed if overlay of the embedded prisms with a particular feature of topography is desired.
- Microstrutures may be embedded with some distance to the edges of the staircase, as illustrated in FIGs. 19 and 20 , or flush with as edge (as was shown in FIG. 10 ).
- a determination of which configuration is appropriate for a specific application may depend on the exact properties of the x-ray generation material and substrate material, so that, for example, the additional brightness achieved with increased electron current enabled by the thermal transfer through five vs. four surfaces may be compared with the additional brightness achieved with free space emission vs. reabsorption through a section of substrate material.
- the additional costs associated with the alignment and overlay steps, as well as the multiple processing steps that may be needed to pattern multiple prisms on multiple layers, may need to be considered in comparison to the increased brightness achievable.
- microstructures comprising multiple x-ray generating materials, microstructures comprising alloys of x-ray generating materials, microstructures deposited with an anti-diffusion layer or an adhesion layer, microstructures with a thermally conducting overcoat, microstructures with a thermally conducting and electrically conducting overcoat, microstructured buried within a substrate and the like.
- microstructures that may comprise any number of conventional x-ray target materials (such as copper (Cu), and molybdenum (Mo) and tungsten (W)) that are patterned as features of micron scale dimensions on (or embedded in) a thermally conducting substrate, such as diamond or sapphire.
- the microstructures may alternatively comprise unconventional x-ray target materials, such as tin (Sn), sulfur (S), titanium (Ti), antimony (Sb), etc. that have thus far been limited in their use due to poor thermal properties.
- target configurations that may be used in embodiments of the invention, as has been described in the above cited US Patent Application Ser. No. 14/465,816 , are arrays of microstructures that take any number of geometric shapes, such as cubes, rectangular blocks, regular prisms, right rectangular prisms, trapezoidal prisms, spheres, ovoids, barrel shaped objects, cylinders, triangular prisms, pyramids, tetrahedra, or other particularly designed shapes, including those with surface textures or structures that enhance surface area, to best generate x-rays of high brightness and that also efficiently disperse heat.
- geometric shapes such as cubes, rectangular blocks, regular prisms, right rectangular prisms, trapezoidal prisms, spheres, ovoids, barrel shaped objects, cylinders, triangular prisms, pyramids, tetrahedra, or other particularly designed shapes, including those with surface textures or structures that enhance surface area, to best generate x-rays of high brightness and that also efficiently dispers
- microstructures comprising various materials as the x-ray generating materials, including aluminum, titanium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, gallium, zinc, yttrium, zirconium, molybdenum, niobium, ruthenium, rhenium, rhodium, palladium, silver, tin, iridium, tantalum, tungsten, indium, cesium, barium, gold, platinum, lead and combinations and alloys thereof.
- materials as the x-ray generating materials including aluminum, titanium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, gallium, zinc, yttrium, zirconium, molybdenum, niobium, ruthenium, rhenium, rhodium, palladium, silver, tin, iridium, tantalum, tungsten, indium, cesium, barium, gold, platinum, lead
- the embodiments described so far include a variety of x-ray target configurations that comprise a plurality of microstructures comprising x-ray material that can be used as targets in x-ray sources to generate x-rays with increased brightness.
- These target configurations have been described as being bombarded with electrons and emitting x-rays, but may be used as the static x-ray target in an otherwise conventional source, replacing either the target 01 from the transmission x-ray source 08 of FIG. 1 , or the target 100 from the reflective x-ray source 80 of FIG. 2 with a microstructured target to form an x-ray source in accord with some embodiments of the invention.
- the targets described above may be embodied in a moving x-ray target, replacing, for example, the target 500 from the rotating anode x-ray source 80 of FIG. 6 with a microstructured target as described above to create a source with a moving microstrucutred target in accord with other embodiments of the invention.
- FIG. 21 illustrates a collection of x-ray emitters arranged in a linear array.
- the long axis of the linear array runs from left to right in the figure, while the short axis would run in and out of the plane of the figure.
- Several x-ray generating elements 801, 802, 803, 804... etc. comprising one or more x-ray generating materials are bombarded by beams electrons 1111, 1112, 1113, 1114, ... etc. at high voltage (anywhere from 1 to 250 keV), and form sub-sources that emit x-rays 818, 828, 838, 848, ... etc.
- the analysis here is for a view along the axis down the center of the linear array of sub-sources, where a screen 84 with an aperture 840 has been positioned.
- the aperture allows the accumulated zero-angle x-rays to emerge from the source, but in practice, an aperture which allows several degrees of emitted x-rays emitted at ⁇ 3° or even at ⁇ 6° to the surface normal may be designed for use in some applications. It is generally preferred that the window be at normal or near normal incidence to the long axis of the linear array, but in some embodiments, a window tilted to an angle as large as 85° may be useful.
- the emission for the right-most emitter as illustrated simply propagates to the right through free space.
- the x-rays from the other emitters are attenuated through absorption, scattering, or other loss mechanisms encountered while passing through whatever material lies between emitters, and also by divergence from the propagation axis and by losses encountered by passage through the neighboring emitter(s) as well.
- T a T l , a > 0
- T a T l , a > 0
- the x-ray attenuation may be different for x-rays of different energies, and that the product of T 1 and T 2,1 may vary considerably for a given material over a range of wavelengths.
- FIG. 22 illustrates the 1/e attenuation length for x-rays having energies ranging from 1 keV to 400 keV for three x-ray generating materials: Molybdenum (Mo), Copper (Cu), Tungsten (W); and from 10 keV to 400 keV for three substrate materials: Graphite (C), Beryllium (Be) and water (H 2 O).
- a larger L 1 / e means a larger T i .
- Embodiments of the invention may allow the control and adjustment of some, all, or none of these variables.
- the beam or beams of electrons 111 or 1111, 1112, 1113, etc. bombarding the x-ray generating elements 801, 802, 803... etc. may be shaped and directed using one or more electron control mechanisms 70 such as electron optics, electrostatic lenses or magnetic focusing elements.
- electron control mechanisms 70 such as electron optics, electrostatic lenses or magnetic focusing elements.
- electrostatic lenses are placed within the vacuum environment of the x-ray source, while the magnetic focusing elements can be placed outside the vacuum.
- Various other electron imaging techniques such as the reflective electron beam control system disclosed in the prior art REBL (Reflective Electron Beam Lithography system) as described in US Patent 6,870,172 "Maskless reflection electron beam projection lithography" may also be used to create a complex pattern of electron exposure.
- Electrons may bombard the elements at normal incidence, as illustrated in FIG. 21 and again illustrated in FIG. 23A ; with electron beams 1121, 1122, 1123 etc. at an angle ⁇ , as illustrated in FIG. 23B ; with electron beams 1131, 1132, 1133 etc. at multiple angles (such as a focused electron beam), as illustrated in FIG. 23C ; with electron beams 1141, 1142, 1143 etc. bombarding the microstructures 700 from opposite sides and at an angle ⁇ , as illustrated in FIG. 23D ; with electron beams 1151, 1152, 1153 etc. at with varying intensity or electron density, as illustrated in FIG. 23E ; with a uniform large area beam of electrons 111 as illustrated in FIG. 23F , or any combination of the many arrangements of electron beams that may be devised by those skilled in the art.
- the actual design of the pattern for electron exposure may depend in part on the material properties of the x-ray generating material and/or the material filling the regions between the x-ray generating elements. If the x-ray generating material is highly absorbing, greater electron density may be used to bombard the regions that emit x-rays that have to travel the greatest distance through other x-ray generating elements, as illustrated in FIG. 23E . Likewise, if the electron penetration depth is large, the x-ray generating material may be bombarded with electrons at an angle, as illustrated in FIG. 23B . If the electron penetration depth is larger than desired, thinner regions of x-ray generating material may be used, creating a source of smaller vertical dimension.
- the area of electron exposure can be adjusted so that the electron beam or beams primarily bombard the x-ray generating elements 1001, 1002, 1003, etc. and do not bombard the regions in between the elements.
- the space between x-ray generating elements can be filled not with vacuum but with a solid material that facilitates heat transfer away from the x-ray generating elements.
- Such source targets comprising arrays of multiple x-ray generating elements embedded or buried in a thermally conducting substrate such as diamond were disclosed in the co-pending U.S. Patent Application Ser. No. 14/465,816 as discussed above, which has been incorporated by reference in its entirety.
- the area between the x-ray generating elements comprises solid material and is also bombarded with electrons, it too will tend to heat up under electron exposure, which will reduce the thermal gradient with the x-ray generating elements and therefore reduce the heat flow out of the x-ray generating element.
- a source having multiple electron beams that are used to bombard distinct x-ray generating elements independently may also be configured to allow a different accelerating voltage to be used with the different electron beam sources.
- a source 80-B is illustrated in FIG. 24 .
- the previous high voltage source 10 is again connected through a lead 21-A to an electron emitter 11-A that emits electrons 111-A towards a target 1100-B.
- two additional "boosters" for voltage 10-B and 10-C are also provided, and these higher voltage potentials are connected through leads 21-B and 21-C to additional electron emitters 11-B and 11-C which emit electrons 111-B and 111-C of different energies.
- the target 1100-B comprising the x-ray generating elements 801, 802, 803, ...etc. will usually be uniformly set to the ground potential
- the individual electron beam sources used to target the different x-ray generating elements may be set to different potentials, and electrons of varying energy may therefore be used to bombard the different x-ray generating elements 801, 802, 803,
- This may offer advantages for x-ray emission management, in that electrons of different energies may generate different x-ray emission spectra, depending on the materials used in the individual x-ray generating elements.
- the heat load generated may also be managed through the use of different electron energies.
- the design of the electron optics for such a multiple beam configuration to keep the various multiple beams from interfering with each other and providing electrons of the wrong energy to the wrong target element may be complex.
- the different x-ray generating elements may comprise different x-ray emitting materials, so that the on-axis view presents a diverse spectrum of characteristic x-rays from the different materials.
- Materials that are relatively transparent to x-rays may be used in the position closest to the output window 840 (e.g. the element furthest to the right in FIG. 21 ), while those that are more strongly absorbing may be used for elements on the other side of the array, so that they attenuate the other sources less.
- the distance between the x-ray generating elements may be varied, depending on the expected thermal load for different materials. For example, a larger space between elements may be used for elements that are expected to generate more heat under electron bombardment, while smaller gaps may be used if less heat is expected.
- the x-ray generating elements 1801, 1802, 1803, ... etc. may have varying sizes and geometric shapes. This may be especially useful for situations where different materials are used, and the electron deceleration processes and x-ray absorption are different for the different materials.
- a useful figure of merit that may be considered in the design of the x-ray generating elements for linear accumulation x-ray sources is the ratio of the 1/e attenuation length for the x-rays within the material to one half of the "continuous slowing down approximation" (CSDA) range for the electrons.
- the CSDA range for the electrons is typically larger than the penetration depth, since an electron can lose energy through several collisions as it slows down.
- FIG. 26A illustrates a plot of these two functions for tungsten
- FIG. 26B illustrates a plot of the ratio.
- the x-ray data is from the previously cited source by Henke et al., while the CSDA range data is from the Physical Measurement Laboratory of NIST ⁇ http://physics.nist.gov/PhysRefData/Star/Text/ESTAR.html>.
- This ratio may be considered a figure-of-merit for the generation of x-rays for a material when used for the linear accumulation of x-rays, since its value is large when the x-ray transparency of the material is large (increasing T i for that microstructure) but its value is also large when the CDSA range is small, (which means the electrons are absorbed quickly, and the x-rays appear to be emitted from a spot of smaller depth).
- FIG. 27 plots this ratio for a large range of x-ray energies for three materials (Cu, Mo and W). Once an x-ray material has been selected for the characteristic lines desired, this ratio may be used to suggest a particular energy range (such as ⁇ 55 keV for tungsten) so that the system may be configured to operate in so that this figure-of-merit is relatively large.
- a particular energy range such as ⁇ 55 keV for tungsten
- the thickness of the microstructures may be set to be 1 ⁇ 2 or less of CSDA as measured in the direction of e-beam propagation.
- a thin foil coating of material may be sufficient to provide the x-ray emission needed, and more complex embedded or buried microstructures may not be required.
- the x-ray generating elements 801, 802, 803, 804, ... etc. need not be continuously bombarded by electrons, but the electron beams 1211, 1212, 1213, 1214, etc.... may be switched on and off to distribute the heat load over time. This may be particularly effective when viewed on-axis, since all x-rays appear to be coming from the same origin.
- FIG. 28 A time-multiplexed embodiment is illustrated in FIG. 28 .
- the electron beams 1211 and 1214 for elements 801 and 804 respectively are on, while the others are off.
- the system may be switched between these configurations simply by blanking the various electron beams, or by blocking the beams with mechanical shutters or by repositioning the electron beams.
- electron beams may simply scan over target comprising the x-ray generating materials. In some embodiments, this may be a regular raster scan, while in other embodiments, the scan may be non-uniform, "dwelling" on or scanning over the x-ray generating region more slowly, while moving rapidly from one x-ray generating region to another. In other embodiments, an electron beam may be designed to bombard all x-ray generating regions simultaneously or multiple electron beams impinging the x-ray generating regions near simultaneously, but having the electron beam(s) turn on and off rapidly, creating a "pulsed" x-ray source. This may have some advantages for certain specific applications.
- Sources with variable timing for electron exposures may also be especially useful for embodiments that use different types of embedded microstructures bombarded with electrons at different potentials, as mentioned above, to excite a diverse spectrum of x-ray energies.
- a slightly off-axis configuration may be preferred. Examples of such configurations are illustrated in FIG. 29 .
- FIG. 29A the x-ray emission through an off-axis window 841 or aperture in a screen 84 or wall is illustrated. Because the x-ray emission is generally isotropic, emission from all microstructures bombarded with electrons will emit in this direction as well. However, the various rays of this emission 878 that pass through the aperture 841 will not propagate in the same direction and will diverge, giving the appearance of an extended source. If the appearance of an extended source is desired, however, using such an off-axis, small -angle collection configuration for the x-rays may be suitable.
- FIG. 29B illustrates the emission from multiple microstructures, this time in a direction away from the incident electron beams 1111, 1112, 1113, etc.
- the spacing of the microstructures 801, 802, 803... is much larger relative to their size, so the off-axis angle that x-rays can be detected by a detector without attenuation from neighboring x-ray emitting elements is much smaller than for the situation illustrated in FIG. 29A .
- FIG. 30 and FIG. 31 Illustrated in FIG. 30 and FIG. 31 (which shows more detail for the target) is a more general x-ray system 80-C, incorporating some of the above-discussed elements.
- the system comprises an electron system controller 10-V that directs various voltages through a number of leads 21-A, 21-B, and 21-C to a number of electron emitters 11-A, 11-B, and 11-C that produce electron beams 111-A, 111-B, 111-C etc.
- Each of these electron beams 111-A, 111-B, 111-C may be controlled by signals from the system controller 10-V through leads 27-A, 27-B, and 27-C that govern electron optics 70-A, 70-B, and 70-C.
- the system additionally comprises a cooling system, comprising a reservoir 90 filled with a cooling fluid 93, typically water, that is moved by means of a mechanism 1209 such as a pump through cooling channels 1200, including a cooling channel that passes through the substrate 1000 of the target 1100-C.
- a cooling fluid 93 typically water
- FIG. 31 illustrates the target 1100-C under bombardment by electrons in an extended version of this system in which two additional electron beams 111-D and 111-E have been added.
- both of the beams 111-D and 111-E have a higher current than the three electron beams to the right 111-A, 111-B, and 111-C
- the leftmost electron beam 111-E has a highest current density of all the beams, illustrating that the beams need not be of equal density.
- the leftmost x-ray generating elements 804 and 805 receiving the higher current are also illustrated as having larger gaps between them and their neighboring microstructures than is provided between the rightmost elements 801, 802, and 803, which receive lower electron current.
- 804 and 805 may be comprised of materials that are higher in atomic number than 801, 802, and 803.
- a conducting overcoat 770 that is both thermally conducting (to remove heat) and electrically conducting, providing a return path to ground 722 for the electrons. Also provided is a screen 84 with an aperture 840 to allow x-rays that are on-axis to radiate away from the target.
- FIG. 32 One embodiment of a source 80-D using a target with multiple x-ray generating elements arranged for linear accumulation is illustrated in FIG. 32 , with the target 2200 shown in more detail in FIG. 33 .
- a controller 10-2 provides high voltage to two emitters 11-D and 11-E that emit electron beams 1221 and 1222 towards opposite sides of a target 2200.
- the properties of the electron beams 1221 and 1222, such as the position, direction, focusing etc. are controlled by electron optics 70-D and 70-E, respectively through leads 27-D and 27-E that coordinate the properties of the beam with the beam current and high voltage settings, all governed by the controller 10-2.
- the target 2200 comprises a substrate 2200 and two thin coatings 2221 and 2222 of x-ray generating material, one on each side of the substrate 2200.
- the electron beams 1221 and 1222 are directed by the electron optics 70-D and 70-E to bombard the thin coatings 2221 and 2222 on opposite sides of the target 2200 at locations such that the x-rays 821 and 822 that are generated from each location are aligned with an aperture 840 in a screen 84 that allows a beam of x-rays 2888 to by emitted from the source 80-D.
- the electron optics 70-D and 70-E may be used to focus the electron beams 1221 and 1222 to spots as small as 25 ⁇ m or even smaller.
- the alignment of the two electron bombardment spots to produce superimposed x-ray emission patterns will be carried out by placing an x-ray detector beyond the aperture 840 and measuring the intensity of the x-ray beam 2888 as the position and focus of the electron beams 1221 and 1222 are changed using electron optics 70-D and 70-E.
- the two spots can be considered aligned when the simultaneous intensity from both spots is maximized on the detector.
- the target 2200 may be rigidly mounted to structures within the vacuum chamber, or may be mounted such that its position may be varied. In some embodiments, the target may be mounted as a rotating anode, to further dissipate heating.
- the thickness of the coatings 2221 and 2222 can be selected based on the anticipated electron energy and the penetration depth or the CSDA estimate for the material. If the bombardment occurs at an angle to the surface normal, as illustrated, the angle of incidence can also affect the selection of the coating thickness.
- the tilt of the target 2200 relative to the electron beams 1221 and 1222 is shown as ⁇ 45°, any angle from 0° to 90° that allows x-rays to be emitted may be used.
- FIG. 34 A system 580-R comprising these features is illustrated in FIG. 34 .
- a controller 10-3 provides high voltage through leads 21-G and 21-F to two emitters 11-F and 11-G that emit electron beams 2511-F and 2511-G respectively.
- a source 80-D as described above is not limited to a single target with two sides. Shown in FIG. 35 is a pair of targets 2203, 2204, each with two coatings 2231 and 2232, and 2241 and 2242 respectively of x-ray generating material on a substrate 2230 and 2240, respectively.
- the source will have a similar configuration to that illustrated in FIG. 32 , except that there are now four electron beams 1231, 1232, 1241, 1242 that are controlled to bombard the respective coatings on two targets 2203, 2204 and generate x-rays 831 and 832, and 841 and 842 respectively.
- the four x-ray generating spots are aligned with an aperture 840 in a screen 84 to appear to originate from a single point of origin.
- An alignment procedure as discussed above for the case of a two-sided target, except that now the four electron beams 1231, 1232, 1241, and 1242 are adjusted to maximize the total x-ray intensity at a detector placed beyond the aperture 840.
- the targets 2203 and 2204 may be rigidly mounted to structures within the vacuum chamber, or may be mounted such that their position may be varied. In some embodiments, the targets 2203 and 2204 may be mounted as rotating anodes, to further dissipate heating. The rotation of the targets 2203 and 2204 may be synchronized or independently controlled.
- the thickness of the coatings 2231, 2232 and 2241, 2242 can be selected based on the anticipated electron energy and the penetration depth or the CSDA estimate for the material. If the bombardment occurs at an angle to the surface normal, as illustrated, the angle of incidence can also affect the selection of the coating thickness.
- the tilt of the targets 2203 and 2204 relative to the electron beams 1231, 1232 and 1222 is shown as ⁇ 45°, any angle from 0° to 90° that allows x-rays to be emitted may be used.
- the coatings for the various targets may be selected to be different x-ray materials.
- the upstream coatings 2241 and 2242 may be selected to be a material such as silver (Ag) or palladium (Pd) while the downstream coatings 2231 and 2232 may be selected to be rhodium (Rh), which has a higher transmission for the characteristic x-rays generated by the upstream targets.
- This may provide a blended x-ray spectrum, comprising multiple characteristic lines from multiple elements.
- a tunable blend of x-rays may be achieved.
- the coatings themselves need not be uniform materials, but may be alloys of various x-ray generating substances, designed to produce a blend of characteristic x-rays.
- FIG. 36 illustrates another embodiment in which the target comprises microstructures of x-ray generating material embedded in the substrate instead of thin coatings.
- Two targets 2301 and 2302 are shown (although a single target, such as illustrated in FIGs. 32 and 33 , may also be configured in this manner as well), each with four microstructures of x-ray generating material 2311, 2312, 2313, 2314, and 2321, 2322, 2323, 2324, respectively embedded to on each side of a substrate 2310, 2320 respectively. Electron beams 1281, 1282, 1283, and 1284 are directed onto the targets 2301, 2302, and produce x-rays that form a beam 882 that appears to originate from the same source when aligned with an aperture 840-B in a screen 84-B.
- the embedded microstructures for this embodiment may comprise different x-ray generating materials, or an alloy or blend of x-ray generating materials to achieve a desired spectral output.
- FIG. 37 Another embodiment in which the target 2400 is aligned with a distributed electron beam 2411 is illustrated in FIG. 37 .
- the electron beam 2411 is focused to several spots onto a coating 2408 of x-ray generating material formed on a substrate 2410.
- the electron beam 2411 may be adjusted so that the multiple spots are formed in an aligned row, and their x-ray emission 2488 along the row (at zero-angle) will appear to originate from a single point of origin.
- FIG. 38 A variation of this embodiment is illustrated in FIG. 38 .
- microstructures 2481, 2482, 2483 of x-ray generating material are embedded in the substrate 2410.
- the distributed electron beam 2411 bombards these microstructures, again generating x-rays 2488 that appear to originate from a single point of origin.
- multiple x-ray emissions from several points of origin are simply aligned such that they appear to be overlapped, and hence appear to simply be a single brighter x-ray source when viewed from a particular angle.
- x-ray emission is generally isotropic, and therefore most of the x-ray energy is lost if an aperture with only a small viewing angle is used.
- x-ray optical elements such as grazing angle mirrors, mirrors with multilayer coatings, or more complex Wolter optics or capillary optics may be used.
- the relation between the targets and the optics will be established at the time of fabrication.
- the optics may be secured in place, either with a particular mount or an epoxy designed for use in a vacuum, using an alignment procedure such as those well known by those skilled in the art of optical fabrication.
- the final alignment may be accomplished as described previously, by placing an x-ray detector at the output aperture and adjusting the focus and position for the various electron beams to achieve maximum x-ray intensity. Final adjustments may also be made for the alignment of the optical elements using x-rays.
- the detector may also be used to provide feedback to the electron beam controllers, providing, for example, a measure of spectral output, which may in turn be used to direct an electron beam generating a particular characteristic line to increase or decrease its power.
- targets need to be illuminated with electrons with the same angle of incidence.
- some materials may have different penetration depths, and therefore bombarding with electrons at a different angle of incidence may be more efficient at producing x-rays for that particular target.
- different electron densities, energies, angles, focus conditions, etc. may be used for different targets.
- emission occurs isotropically from all the targets, and that the collection and focusing x-ray optics lenses operate on x-rays propagating in both directions. Therefore a detector placed on the opposite end of the chain of targets may serve as a monitor for the calibration, overall power of the x-ray system. 2 nd beam, too.
- FIG. 39 illustrates an embodiment using three aligned targets 2801, 2802, 2803 each comprising a microstructure 2881, 2882, 2883 of x-ray generating material embedded in a substrate 2811, 2812, 2813.
- Each of the targets is bombarded by an electron beam 1181, 1182, 1183 respectively to generate x-rays 2818, 2828, 2838 respectively.
- x-ray imaging mirror optics 2821, 2822, 2831, 2832 are positioned to collect x-rays emitted at wider angles and redirect them to a focus at a position corresponding to the x-ray generating spot another x-ray.target.
- the focus is set to be the x-ray generating spot in the adjacent target, but in some embodiments, all the x-ray mirrors may be designed to focus x-rays to the same point, for example, at the final x-ray generating spot in the final (rightmost) x-ray target.
- imaging mirror optics 2821, 2822, 2831, 2832 may be any conventional x-ray imaging optical element, such as an ellipsoidal mirror with a reflecting surface typically fabricated from glass, or surface coated with a high mass density material, or an x-ray multilayer coated reflector (typically fabricated using layers of molybdenum (Mo) and silicon (Si)) or a crystal optic, or a combination thereof.
- x-ray imaging optical element such as an ellipsoidal mirror with a reflecting surface typically fabricated from glass, or surface coated with a high mass density material, or an x-ray multilayer coated reflector (typically fabricated using layers of molybdenum (Mo) and silicon (Si)) or a crystal optic, or a combination thereof.
- Mo molybdenum
- Si silicon
- the first (upstream) x-ray target 2830 now comprises a substrate 2833 in which microstructures 2883 of x-ray generating material have been embedded, as has been described elsewhere.
- the intensity of the x-rays 2838-A emitted from this target 2830 will be increased due to the linear accumulation of the x-rays emitted from these several microstructures 2883, and may contribute to a brighter overall x-ray source in this embodiment, just as they do in the previously described embodiments.
- the electron beam 1183-A may be adjusted to have a different incidence angle (as illustrated), size, shape and focus from the embodiment of FIG. 39 in order to bombard the microstructures 2883 more effectively.
- FIG. 41 Another variation of this embodiment is illustrated in FIG. 41 .
- the second x-ray beam 2988-L propagating to the left is also illustrated.
- This second x-ray beam propagates through a second aperture 840-L in a plate 84-L, and can be used as a second x-ray exposure source, or can be used in conjunction with a detector 4444 to serve as a monitor for x-ray beam properties such as brightness, brilliance, total intensity, flux, energy spectrum, beam profile, and divergence or convergence.
- FIG. 42 Another embodiment of the invention is illustrated in FIG. 42 .
- the optical elements 2921 and 2931 collecting x-rays emitted from one target and focusing them downstream are now optical elements known as Wolter optics.
- Wolter optics are a well known system of nested mirrors to collect and focus x-rays, typically having parabolic and/or hyperbolic reflecting surfaces with each element typically used at grazing angle.
- the reflecting surface is a glass.
- the glass surface may be coated with a high mass density material or an x-ray multilayer (typically fabricated using layers of molybdenum (Mo) and silicon (Si)).
- FIG. 43A and FIG. 43B illustrate a prior art embodiments of Wolter optics used for x-rays comprising a variety of cylindrical lenses oriented both horizontally and vertically.
- the material selection and coatings used for these optical elements may be selected to match the spectrum of x-rays anticipated to be emitted from the various x-ray origins.
- FIG. 44 Another embodiment of the invention is illustrated in FIG. 44 .
- the optical elements 2941 and 2951 collecting x-rays emitted from one target and focusing them downstream are now optical elements known as polycapillary optics.
- Polycapillary optics are similar to fiber optics, in that x-rays are guided through a thin fiber to emerge at the other end in a desired position.
- fiber optics which comprise a solid fiber of glass that reflects using total internal reflection
- polycapillary optics comprise a number of hollow tubes, and the x-rays are guided down the tubes by an external reflection from the material at grazing angles.
- Polycapillary optics are a well known means of collecting and redirecting x-rays, and any of a number of conventional polycapillary optical elements may be used in the embodiments of the invention disclosed here. It is generally considered, however, that a polycapillary optic comprising multiple capillary fibers be used so that x-rays emitted at many angles can be collected and directed to a point of desired focus.
- FIGs. 39 through 42 and 44 may be interchangeable, with for example, the Wolter optics 2931 replacing the mirrors 2821, 2822 in FIG. 41 .
- targets comprising microstructures are used in these illustrations, targets comprising thin films such as were illustrated in FIGs. 33 and 35 may be used in conjunction with these focusing x-ray optics as well.
- the orientation of the microstructures allows the use of an on-axis collection angle, allowing accumulation of x-rays from several microstructures to be aligned, appearing to have a single origin, also known as "zero-angle" x-ray emission.
Landscapes
- X-Ray Techniques (AREA)
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361880151P | 2013-09-19 | 2013-09-19 | |
US201361894073P | 2013-10-22 | 2013-10-22 | |
US201461931519P | 2014-01-24 | 2014-01-24 | |
US201462008856P | 2014-06-06 | 2014-06-06 | |
US14/465,816 US20150092924A1 (en) | 2013-09-04 | 2014-08-21 | Structured targets for x-ray generation |
PCT/US2014/056688 WO2015084466A2 (fr) | 2013-09-19 | 2014-09-19 | Sources de rayons x utilisant l'accumulation linéaire |
EP14868433.5A EP3047501A4 (fr) | 2013-09-19 | 2014-09-19 | Sources de rayons x utilisant l'accumulation linéaire |
Related Parent Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP14868433.5A Division EP3047501A4 (fr) | 2013-09-19 | 2014-09-19 | Sources de rayons x utilisant l'accumulation linéaire |
EP14868433.5A Division-Into EP3047501A4 (fr) | 2013-09-19 | 2014-09-19 | Sources de rayons x utilisant l'accumulation linéaire |
Publications (3)
Publication Number | Publication Date |
---|---|
EP3168856A2 true EP3168856A2 (fr) | 2017-05-17 |
EP3168856A3 EP3168856A3 (fr) | 2017-08-23 |
EP3168856B1 EP3168856B1 (fr) | 2019-07-03 |
Family
ID=53274258
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP16200793.4A Active EP3168856B1 (fr) | 2013-09-19 | 2014-09-19 | Sources de rayons x utilisant l'accumulation linéaire |
EP14868433.5A Withdrawn EP3047501A4 (fr) | 2013-09-19 | 2014-09-19 | Sources de rayons x utilisant l'accumulation linéaire |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP14868433.5A Withdrawn EP3047501A4 (fr) | 2013-09-19 | 2014-09-19 | Sources de rayons x utilisant l'accumulation linéaire |
Country Status (4)
Country | Link |
---|---|
EP (2) | EP3168856B1 (fr) |
JP (2) | JP2016537797A (fr) |
CN (1) | CN105556637B (fr) |
WO (1) | WO2015084466A2 (fr) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107887243A (zh) * | 2017-09-19 | 2018-04-06 | 中国电子科技集团公司第三十八研究所 | 一种用于电子束扫描ct的x射线源的阵列靶及制作方法 |
WO2022126071A1 (fr) * | 2020-12-07 | 2022-06-16 | Sigray, Inc. | Système d'imagerie radiographique 3d à haut débit utilisant une source de rayons x de transmission |
WO2022180401A1 (fr) * | 2021-02-25 | 2022-09-01 | Modular Energy Technologies Ltd. | Appareil d'expérimentation et de génération d'électricité |
US11885755B2 (en) | 2022-05-02 | 2024-01-30 | Sigray, Inc. | X-ray sequential array wavelength dispersive spectrometer |
US11992350B2 (en) | 2022-03-15 | 2024-05-28 | Sigray, Inc. | System and method for compact laminography utilizing microfocus transmission x-ray source and variable magnification x-ray detector |
Families Citing this family (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20150117599A1 (en) | 2013-10-31 | 2015-04-30 | Sigray, Inc. | X-ray interferometric imaging system |
US10297359B2 (en) | 2013-09-19 | 2019-05-21 | Sigray, Inc. | X-ray illumination system with multiple target microstructures |
US10269528B2 (en) | 2013-09-19 | 2019-04-23 | Sigray, Inc. | Diverging X-ray sources using linear accumulation |
US10295485B2 (en) | 2013-12-05 | 2019-05-21 | Sigray, Inc. | X-ray transmission spectrometer system |
US10304580B2 (en) | 2013-10-31 | 2019-05-28 | Sigray, Inc. | Talbot X-ray microscope |
USRE48612E1 (en) | 2013-10-31 | 2021-06-29 | Sigray, Inc. | X-ray interferometric imaging system |
US10401309B2 (en) | 2014-05-15 | 2019-09-03 | Sigray, Inc. | X-ray techniques using structured illumination |
US10352880B2 (en) | 2015-04-29 | 2019-07-16 | Sigray, Inc. | Method and apparatus for x-ray microscopy |
US10295486B2 (en) | 2015-08-18 | 2019-05-21 | Sigray, Inc. | Detector for X-rays with high spatial and high spectral resolution |
KR101724213B1 (ko) * | 2015-12-04 | 2017-04-18 | 전남대학교산학협력단 | 엑스선 하베스팅 장치 |
US10247683B2 (en) | 2016-12-03 | 2019-04-02 | Sigray, Inc. | Material measurement techniques using multiple X-ray micro-beams |
WO2018175570A1 (fr) | 2017-03-22 | 2018-09-27 | Sigray, Inc. | Procédé de réalisation d'une spectroscopie des rayons x et système de spectromètre d'absorption de rayons x |
GB2565138A (en) * | 2017-08-04 | 2019-02-06 | Adaptix Ltd | X-ray generator |
US10847336B2 (en) * | 2017-08-17 | 2020-11-24 | Bruker AXS, GmbH | Analytical X-ray tube with high thermal performance |
US10624195B2 (en) * | 2017-10-26 | 2020-04-14 | Moxtek, Inc. | Tri-axis x-ray tube |
CN108269725A (zh) * | 2018-01-24 | 2018-07-10 | 宁波英飞迈材料科技有限公司 | 一种脉冲式x射线发生装置及产生方法 |
JP6857400B2 (ja) | 2018-03-01 | 2021-04-14 | 株式会社リガク | X線発生装置、及びx線分析装置 |
US10578566B2 (en) | 2018-04-03 | 2020-03-03 | Sigray, Inc. | X-ray emission spectrometer system |
US10845491B2 (en) | 2018-06-04 | 2020-11-24 | Sigray, Inc. | Energy-resolving x-ray detection system |
GB2591630B (en) | 2018-07-26 | 2023-05-24 | Sigray Inc | High brightness x-ray reflection source |
US10656105B2 (en) * | 2018-08-06 | 2020-05-19 | Sigray, Inc. | Talbot-lau x-ray source and interferometric system |
CN112638261A (zh) | 2018-09-04 | 2021-04-09 | 斯格瑞公司 | 利用滤波的x射线荧光的系统和方法 |
US11056308B2 (en) | 2018-09-07 | 2021-07-06 | Sigray, Inc. | System and method for depth-selectable x-ray analysis |
WO2021011209A1 (fr) | 2019-07-15 | 2021-01-21 | Sigray, Inc. | Source de rayons x avec anode tournante à pression atmosphérique |
CN114729907B (zh) * | 2019-09-03 | 2023-05-23 | 斯格瑞公司 | 用于计算机层析x射线荧光成像的系统和方法 |
CN111479377A (zh) * | 2020-04-22 | 2020-07-31 | 吉林大学 | 一种d-d中子管靶膜保护层 |
CN115667896B (zh) * | 2020-05-18 | 2024-06-21 | 斯格瑞公司 | 使用晶体分析器和多个检测元件的x射线吸收光谱的系统和方法 |
JP7525409B2 (ja) | 2021-01-05 | 2024-07-30 | 浜松ホトニクス株式会社 | X線発生装置及びx線撮像システム |
JP2022105846A (ja) | 2021-01-05 | 2022-07-15 | 浜松ホトニクス株式会社 | X線発生用ターゲット、x線発生装置及びx線撮像システム |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1211092A (en) | 1915-06-05 | 1917-01-02 | Gen Electric | X-ray tube. |
US1917099A (en) | 1929-10-18 | 1933-07-04 | Gen Electric | x-ray tube |
US1946312A (en) | 1927-10-18 | 1934-02-06 | Gen Electric | X-ray tube |
US4972449A (en) | 1990-03-19 | 1990-11-20 | General Electric Company | X-ray tube target |
US5148462A (en) | 1991-04-08 | 1992-09-15 | Moltech Corporation | High efficiency X-ray anode sources |
US5602899A (en) | 1996-01-31 | 1997-02-11 | Physical Electronics Inc. | Anode assembly for generating x-rays and instrument with such anode assembly |
US6850598B1 (en) | 1999-07-26 | 2005-02-01 | Fraunhofer Gesellschaft zur Förderung der angewandten Forschung e.V. | X-ray anode and process for its manufacture |
US6870172B1 (en) | 2004-05-21 | 2005-03-22 | Kla-Tencor Technologies Corporation | Maskless reflection electron beam projection lithography |
US8094784B2 (en) | 2003-04-25 | 2012-01-10 | Rapiscan Systems, Inc. | X-ray sources |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2548447B1 (fr) * | 1983-06-28 | 1986-02-21 | Thomson Csf | Tube a rayons x a foyer de forte intensite |
JPH11304728A (ja) * | 1998-04-23 | 1999-11-05 | Hitachi Ltd | X線計測装置 |
US6125167A (en) * | 1998-11-25 | 2000-09-26 | Picker International, Inc. | Rotating anode x-ray tube with multiple simultaneously emitting focal spots |
JP2003149392A (ja) * | 2001-11-09 | 2003-05-21 | Tohken Co Ltd | X線増強反射板及びx線検査装置 |
US7003077B2 (en) * | 2003-10-03 | 2006-02-21 | General Electric Company | Method and apparatus for x-ray anode with increased coverage |
US7551722B2 (en) * | 2004-04-08 | 2009-06-23 | Japan Science And Technology Agency | X-ray target and apparatuses using the same |
DE102005034687B3 (de) * | 2005-07-25 | 2007-01-04 | Siemens Ag | Drehkolbenstrahler |
JP4878311B2 (ja) * | 2006-03-03 | 2012-02-15 | キヤノン株式会社 | マルチx線発生装置 |
JP4912743B2 (ja) * | 2006-05-18 | 2012-04-11 | 浜松ホトニクス株式会社 | X線管及びそれを用いたx線照射装置 |
JP5647607B2 (ja) * | 2008-08-14 | 2015-01-07 | コーニンクレッカ フィリップス エヌ ヴェ | マルチセグメント陽極ターゲットを備えた回転陽極を有するx線管、及びそれを有するx線スキャナシステム |
US8644451B2 (en) * | 2009-03-27 | 2014-02-04 | Shozo Aoki | X-ray generating apparatus and inspection apparatus using the same therein |
CN102422364B (zh) * | 2009-05-12 | 2015-08-05 | 皇家飞利浦电子股份有限公司 | 具有多个电子发射器的x射线源 |
JP2011029072A (ja) * | 2009-07-28 | 2011-02-10 | Canon Inc | X線発生装置及びそれを備えたx線撮像装置。 |
CN101644689A (zh) * | 2009-08-21 | 2010-02-10 | 江苏天瑞仪器股份有限公司 | 一种多靶材x光管 |
JP5984403B2 (ja) * | 2012-01-31 | 2016-09-06 | キヤノン株式会社 | ターゲット構造体及びそれを備える放射線発生装置 |
-
2014
- 2014-09-19 CN CN201480051973.6A patent/CN105556637B/zh active Active
- 2014-09-19 WO PCT/US2014/056688 patent/WO2015084466A2/fr active Application Filing
- 2014-09-19 EP EP16200793.4A patent/EP3168856B1/fr active Active
- 2014-09-19 EP EP14868433.5A patent/EP3047501A4/fr not_active Withdrawn
- 2014-09-19 JP JP2016544039A patent/JP2016537797A/ja active Pending
-
2018
- 2018-09-26 JP JP2018179789A patent/JP6659025B2/ja active Active
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1211092A (en) | 1915-06-05 | 1917-01-02 | Gen Electric | X-ray tube. |
US1946312A (en) | 1927-10-18 | 1934-02-06 | Gen Electric | X-ray tube |
US1917099A (en) | 1929-10-18 | 1933-07-04 | Gen Electric | x-ray tube |
US4972449A (en) | 1990-03-19 | 1990-11-20 | General Electric Company | X-ray tube target |
US5148462A (en) | 1991-04-08 | 1992-09-15 | Moltech Corporation | High efficiency X-ray anode sources |
US5602899A (en) | 1996-01-31 | 1997-02-11 | Physical Electronics Inc. | Anode assembly for generating x-rays and instrument with such anode assembly |
US6850598B1 (en) | 1999-07-26 | 2005-02-01 | Fraunhofer Gesellschaft zur Förderung der angewandten Forschung e.V. | X-ray anode and process for its manufacture |
US8094784B2 (en) | 2003-04-25 | 2012-01-10 | Rapiscan Systems, Inc. | X-ray sources |
US6870172B1 (en) | 2004-05-21 | 2005-03-22 | Kla-Tencor Technologies Corporation | Maskless reflection electron beam projection lithography |
Non-Patent Citations (17)
Title |
---|
"CRC Handbook of Chemistry and Physics", 2009, CRC PRESS |
"On a New Kind of Rays", NATURE, vol. 53, 23 January 1896 (1896-01-23), pages 274 - 276 |
ALIREZA NOJEH: "Carbon Nanotube Electron Sources: From Electron Beams to Energy Conversion and Optophononics", ISRN NANOMATERIALS, vol. 2014, pages 23 |
B.L. HENKE; E.M. GULLIKSON; J.C. DAVIS: "X-ray interactions: photoabsorption, scattering, transmission, and reflection at E=50-30000 eV, Z=1-92", ATOMIC DATA AND NUCLEAR DATA TABLES, vol. 54, no. 2, July 1993 (1993-07-01), pages 181 - 342 |
D. GONZALES; B. CAVNESS; S. WILLIAMS: "Angular distribution of thick-target bremsstrahlung produced by electrons with initial energies ranging from 10 to 20 keV incident on Ag", PHYS. REV. A, vol. 84, 2011, pages 052726 |
D.S. HWANG; T. SAITO; N. FUJIMORI: "New etching process for device fabrication using diamond", DIAMOND & RELATED MATERIALS, vol. 13, 2004, pages 2207 - 2210, XP004614859, DOI: doi:10.1016/j.diamond.2004.07.020 |
E.R. DOBROVINSKAYA ET AL.: "Sapphire: Material, Manufacturing, Applications,", 2009, SPRINGER SCIENCE + BUSINESS MEDIA, article "Thermal Properties" |
H. MASUDA ET AL.: "Fabrication of Through-Hole Diamond Membranes by Plasma Etching Using Anodic Porous Alumina Mask", ELECTROCHEMICAL AND SOLID-STATE LETTERS, vol. 4, no. 11, 2001, pages G101 - G103 |
H. RIEGE: "Electron Emission from Ferroelectrics - A Review", CERN REPORT CERN AT/93-18, July 1993 (1993-07-01) |
J. TANIGUCHI ET AL.: "Diamond Nanoimprint Lithography", NANOTECHNOLOGY, vol. 13, 2002, pages 592 - 596, XP020066978, DOI: doi:10.1088/0957-4484/13/5/309 |
J.G. CHERVENAK; A. LIUZZI: "Experimental thick-target bremsstrahlung spectra from electrons in the range 10 to 30 kev", PHYS. REV. A, vol. 12, no. 1, July 1975 (1975-07-01), pages 26 - 33 |
M. OTENDAL ET AL.: "A 9 keV electron-impact liquid-gallium-jet x-ray source", REV. SCI. INSTRUM., vol. 79, 2008, pages 016102 |
P.J. POTTS: "A Handbook of Silicate Rock Analysis", 1987, SPRINGER NETHERLANDS, article "Electron Probe Microanalysis", pages: 336 |
SHIGEHIKO YAMAMOTO: "Fundamental physics of vacuum electron sources", REPORTS ON PROGRESS IN PHYSICS, vol. 69, 2006, pages 181 - 232, XP020096275, DOI: doi:10.1088/0034-4885/69/1/R04 |
W.C. RONTGEN: "Eine Neue Art von Strahlen", 1895, WURZBURG VERLAG |
X.D. WANG ET AL.: "Precise patterning of diamond films for MEMS application", J. MATERIAL PROCESSING TECHNOLOGY, vol. 127, 2002, pages 230 - 233, XP002527670, DOI: doi:10.1016/S0924-0136(02)00147-4 |
Y. ANDO ET AL.: "Smooth and high-rate reactive ion etching of diamond", DIAMOND AND RELATED MATERIALS, vol. 11, 2002, pages 824 - 827, XP004357027, DOI: doi:10.1016/S0925-9635(01)00617-3 |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107887243A (zh) * | 2017-09-19 | 2018-04-06 | 中国电子科技集团公司第三十八研究所 | 一种用于电子束扫描ct的x射线源的阵列靶及制作方法 |
WO2022126071A1 (fr) * | 2020-12-07 | 2022-06-16 | Sigray, Inc. | Système d'imagerie radiographique 3d à haut débit utilisant une source de rayons x de transmission |
US11686692B2 (en) | 2020-12-07 | 2023-06-27 | Sigray, Inc. | High throughput 3D x-ray imaging system using a transmission x-ray source |
WO2022180401A1 (fr) * | 2021-02-25 | 2022-09-01 | Modular Energy Technologies Ltd. | Appareil d'expérimentation et de génération d'électricité |
US11992350B2 (en) | 2022-03-15 | 2024-05-28 | Sigray, Inc. | System and method for compact laminography utilizing microfocus transmission x-ray source and variable magnification x-ray detector |
US11885755B2 (en) | 2022-05-02 | 2024-01-30 | Sigray, Inc. | X-ray sequential array wavelength dispersive spectrometer |
Also Published As
Publication number | Publication date |
---|---|
EP3047501A2 (fr) | 2016-07-27 |
EP3168856A3 (fr) | 2017-08-23 |
WO2015084466A3 (fr) | 2015-07-30 |
JP6659025B2 (ja) | 2020-03-04 |
CN105556637B (zh) | 2019-12-10 |
JP2019012695A (ja) | 2019-01-24 |
EP3047501A4 (fr) | 2017-06-21 |
WO2015084466A2 (fr) | 2015-06-11 |
EP3168856B1 (fr) | 2019-07-03 |
CN105556637A (zh) | 2016-05-04 |
JP2016537797A (ja) | 2016-12-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP3168856B1 (fr) | Sources de rayons x utilisant l'accumulation linéaire | |
US9543109B2 (en) | X-ray sources using linear accumulation | |
US9390881B2 (en) | X-ray sources using linear accumulation | |
US10269528B2 (en) | Diverging X-ray sources using linear accumulation | |
US10297359B2 (en) | X-ray illumination system with multiple target microstructures | |
US9570265B1 (en) | X-ray fluorescence system with high flux and high flux density | |
US9449781B2 (en) | X-ray illuminators with high flux and high flux density | |
US20170162288A1 (en) | X-ray illuminators with high flux and high flux density | |
US10416099B2 (en) | Method of performing X-ray spectroscopy and X-ray absorption spectrometer system | |
US20150092924A1 (en) | Structured targets for x-ray generation | |
US9448190B2 (en) | High brightness X-ray absorption spectroscopy system | |
Hemberg et al. | Liquid-metal-jet anode electron-impact x-ray source | |
WO2017204850A1 (fr) | Sources de rayons x divergents utilisant une accumulation linéaire | |
US11056308B2 (en) | System and method for depth-selectable x-ray analysis | |
CN110530907B (zh) | X射线吸收测量系统 | |
US8121258B2 (en) | Device for providing a high energy X-ray beam | |
WO2015187219A1 (fr) | Système de mesure d'absorption des rayons x | |
US7436931B2 (en) | X-ray source for generating monochromatic x-rays | |
JP7117452B2 (ja) | 高輝度反射型x線源 | |
EP3602020B1 (fr) | Procédé de réalisation d'une spectroscopie des rayons x et système de spectromètre d'absorption de rayons x | |
JP6973816B2 (ja) | 半導体x線ターゲット | |
WO2019074548A1 (fr) | Système d'éclairage à rayons x à multiples microstructures cibles | |
US20230218247A1 (en) | Microfocus x-ray source for generating high flux low energy x-rays |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION HAS BEEN PUBLISHED |
|
AC | Divisional application: reference to earlier application |
Ref document number: 3047501 Country of ref document: EP Kind code of ref document: P |
|
AK | Designated contracting states |
Kind code of ref document: A2 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
|
AK | Designated contracting states |
Kind code of ref document: A3 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: H01J 35/08 20060101AFI20170719BHEP |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE |
|
17P | Request for examination filed |
Effective date: 20180222 |
|
RBV | Designated contracting states (corrected) |
Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: GRANT OF PATENT IS INTENDED |
|
INTG | Intention to grant announced |
Effective date: 20190107 |
|
GRAJ | Information related to disapproval of communication of intention to grant by the applicant or resumption of examination proceedings by the epo deleted |
Free format text: ORIGINAL CODE: EPIDOSDIGR1 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE |
|
GRAR | Information related to intention to grant a patent recorded |
Free format text: ORIGINAL CODE: EPIDOSNIGR71 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: GRANT OF PATENT IS INTENDED |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE PATENT HAS BEEN GRANTED |
|
INTC | Intention to grant announced (deleted) | ||
AC | Divisional application: reference to earlier application |
Ref document number: 3047501 Country of ref document: EP Kind code of ref document: P |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
INTG | Intention to grant announced |
Effective date: 20190527 |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP Ref country code: AT Ref legal event code: REF Ref document number: 1151989 Country of ref document: AT Kind code of ref document: T Effective date: 20190715 |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R096 Ref document number: 602014049716 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: MP Effective date: 20190703 |
|
REG | Reference to a national code |
Ref country code: LT Ref legal event code: MG4D |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: MK05 Ref document number: 1151989 Country of ref document: AT Kind code of ref document: T Effective date: 20190703 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: AT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 Ref country code: SE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 Ref country code: HR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 Ref country code: NO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20191003 Ref country code: FI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 Ref country code: LT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 Ref country code: BG Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20191003 Ref country code: PT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20191104 Ref country code: NL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 Ref country code: CZ Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LV Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 Ref country code: RS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 Ref country code: ES Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20191004 Ref country code: AL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 Ref country code: IS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20191103 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: TR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: PL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 Ref country code: RO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 Ref country code: EE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 Ref country code: IT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 Ref country code: DK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SM Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 Ref country code: IS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200224 Ref country code: MC Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 Ref country code: SK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R097 Ref document number: 602014049716 Country of ref document: DE |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
PG2D | Information on lapse in contracting state deleted |
Ref country code: IS |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190919 Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190919 Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190930 Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190930 |
|
26N | No opposition filed |
Effective date: 20200603 |
|
REG | Reference to a national code |
Ref country code: BE Ref legal event code: MM Effective date: 20190930 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190930 Ref country code: SI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20191003 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20191003 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: CY Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190930 Ref country code: HU Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO Effective date: 20140919 Ref country code: MT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190703 |
|
P01 | Opt-out of the competence of the unified patent court (upc) registered |
Effective date: 20230802 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20240812 Year of fee payment: 11 |