CA1075813A - Inversion et regeneration dans les dispositifs a transfert de charge - Google Patents

Info

Publication number

CA1075813A

CA1075813A CA121,990A CA121990A CA1075813A CA 1075813 A CA1075813 A CA 1075813A CA 121990 A CA121990 A CA 121990A CA 1075813 A CA1075813 A CA 1075813A

Authority

CA

Canada

Prior art keywords

field plate

zone

charge

adjacent

type

Prior art date

1970-10-22

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.)

Expired

Links

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• CIPO
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• 230000008929 regeneration Effects 0.000 title claims abstract description 19
• 239000002800 charge carrier Substances 0.000 claims description 33
• 238000001514 detection method Methods 0.000 claims description 15
• 239000004065 semiconductor Substances 0.000 claims description 14
• 230000006872 improvement Effects 0.000 claims description 12
• 238000005381 potential energy Methods 0.000 claims description 12
• 239000000463 material Substances 0.000 claims description 11
• 238000002347 injection Methods 0.000 claims description 7
• 239000007924 injection Substances 0.000 claims description 7
• 230000004044 response Effects 0.000 claims description 5
• 230000035945 sensitivity Effects 0.000 claims description 4
• 239000000758 substrate Substances 0.000 claims 6
• 238000005513 bias potential Methods 0.000 claims 3
• 230000005669 field effect Effects 0.000 claims 2
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• 150000002500 ions Chemical class 0.000 description 10
• 239000004020 conductor Substances 0.000 description 3
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
• 241000272168 Laridae Species 0.000 description 2
• 230000008878 coupling Effects 0.000 description 2
• 238000010168 coupling process Methods 0.000 description 2
• 238000005859 coupling reaction Methods 0.000 description 2
• 239000012212 insulator Substances 0.000 description 2
• WTEVQBCEXWBHNA-YFHOEESVSA-N neral Chemical compound CC(C)=CCC\C(C)=C/C=O WTEVQBCEXWBHNA-YFHOEESVSA-N 0.000 description 2
• ODPOAESBSUKMHD-UHFFFAOYSA-L 6,7-dihydrodipyrido[1,2-b:1',2'-e]pyrazine-5,8-diium;dibromide Chemical compound [Br-].[Br-].C1=CC=[N+]2CC[N+]3=CC=CC=C3C2=C1 ODPOAESBSUKMHD-UHFFFAOYSA-L 0.000 description 1
• 244000201986 Cassia tora Species 0.000 description 1
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• 101150039033 Eci2 gene Proteins 0.000 description 1
• AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 description 1
• 101100490488 Mus musculus Add3 gene Proteins 0.000 description 1
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• 244000269722 Thea sinensis Species 0.000 description 1
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• XPAOKCSHUNYPBS-XSBNNCSWSA-N [(2r,3s,5r)-5-(6-aminopurin-9-yl)-3-hydroxyoxolan-2-yl]methyl [(2r,3r,5s)-3-(hydroxymethyl)-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl] hydrogen phosphate Chemical compound O=C1NC(=O)C(C)=CN1[C@H]1O[C@H](OP(O)(=O)OC[C@@H]2[C@H](C[C@@H](O2)N2C3=NC=NC(N)=C3N=C2)O)[C@@H](CO)C1 XPAOKCSHUNYPBS-XSBNNCSWSA-N 0.000 description 1
• 230000003321 amplification Effects 0.000 description 1
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• WTEVQBCEXWBHNA-JXMROGBWSA-N citral A Natural products CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 1
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• NCAIGTHBQTXTLR-UHFFFAOYSA-N phentermine hydrochloride Chemical compound [Cl-].CC(C)([NH3+])CC1=CC=CC=C1 NCAIGTHBQTXTLR-UHFFFAOYSA-N 0.000 description 1
• 241000894007 species Species 0.000 description 1
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