CN108067631A - 一种在溶液中稳定的贵金属孤原子材料 - Google Patents
一种在溶液中稳定的贵金属孤原子材料 Download PDFInfo
- Publication number
- CN108067631A CN108067631A CN201611004958.3A CN201611004958A CN108067631A CN 108067631 A CN108067631 A CN 108067631A CN 201611004958 A CN201611004958 A CN 201611004958A CN 108067631 A CN108067631 A CN 108067631A
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- Prior art keywords
- atom
- noble metal
- orphan
- platinum
- solution
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- 229910000510 noble metal Inorganic materials 0.000 title claims abstract description 48
- 239000000463 material Substances 0.000 title claims abstract description 42
- 229920001400 block copolymer Polymers 0.000 claims abstract description 15
- 238000002360 preparation method Methods 0.000 claims abstract description 15
- 239000003223 protective agent Substances 0.000 claims abstract description 12
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 10
- 239000004721 Polyphenylene oxide Chemical group 0.000 claims abstract description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229920000570 polyether Chemical group 0.000 claims abstract description 7
- -1 medical synthesis Substances 0.000 claims abstract description 6
- 229910052751 metal Inorganic materials 0.000 claims abstract description 4
- 239000002184 metal Substances 0.000 claims abstract description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 75
- 229910052697 platinum Inorganic materials 0.000 claims description 31
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 19
- 239000000126 substance Substances 0.000 claims description 18
- 235000019441 ethanol Nutrition 0.000 claims description 14
- 239000010970 precious metal Substances 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 229920001223 polyethylene glycol Polymers 0.000 claims description 9
- 239000002202 Polyethylene glycol Substances 0.000 claims description 8
- CLSUSRZJUQMOHH-UHFFFAOYSA-L platinum dichloride Chemical compound Cl[Pt]Cl CLSUSRZJUQMOHH-UHFFFAOYSA-L 0.000 claims description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 6
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 5
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 4
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 claims description 4
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 229910052700 potassium Inorganic materials 0.000 claims description 4
- 239000011591 potassium Substances 0.000 claims description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 4
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 claims description 4
- 229910052741 iridium Inorganic materials 0.000 claims description 3
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052763 palladium Inorganic materials 0.000 claims description 3
- 229920000151 polyglycol Polymers 0.000 claims description 3
- 239000010695 polyglycol Substances 0.000 claims description 3
- 229910052703 rhodium Inorganic materials 0.000 claims description 3
- 239000010948 rhodium Substances 0.000 claims description 3
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 3
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 claims description 2
- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 claims description 2
- 239000004912 1,5-cyclooctadiene Substances 0.000 claims description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 2
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 2
- 235000010323 ascorbic acid Nutrition 0.000 claims description 2
- 229960005070 ascorbic acid Drugs 0.000 claims description 2
- 239000011668 ascorbic acid Substances 0.000 claims description 2
- FOSZYDNAURUMOT-UHFFFAOYSA-J azane;platinum(4+);tetrachloride Chemical compound N.N.N.N.[Cl-].[Cl-].[Cl-].[Cl-].[Pt+4] FOSZYDNAURUMOT-UHFFFAOYSA-J 0.000 claims description 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 235000015165 citric acid Nutrition 0.000 claims description 2
- 235000019253 formic acid Nutrition 0.000 claims description 2
- 239000008103 glucose Substances 0.000 claims description 2
- 235000001727 glucose Nutrition 0.000 claims description 2
- 235000011187 glycerol Nutrition 0.000 claims description 2
- 239000010931 gold Substances 0.000 claims description 2
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 claims description 2
- 229910052762 osmium Inorganic materials 0.000 claims description 2
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 claims description 2
- NWAHZABTSDUXMJ-UHFFFAOYSA-N platinum(2+);dinitrate Chemical compound [Pt+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O NWAHZABTSDUXMJ-UHFFFAOYSA-N 0.000 claims description 2
- 229910052707 ruthenium Inorganic materials 0.000 claims description 2
- 229910052709 silver Inorganic materials 0.000 claims description 2
- 239000004332 silver Substances 0.000 claims description 2
- 239000011780 sodium chloride Substances 0.000 claims description 2
- 239000011975 tartaric acid Substances 0.000 claims description 2
- 235000002906 tartaric acid Nutrition 0.000 claims description 2
- DWQQQVOLSPRXJV-UHFFFAOYSA-N C(C)NCC.[Cl] Chemical compound C(C)NCC.[Cl] DWQQQVOLSPRXJV-UHFFFAOYSA-N 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 claims 1
- 229910010277 boron hydride Inorganic materials 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims 1
- 229910052737 gold Inorganic materials 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 abstract description 12
- 238000003786 synthesis reaction Methods 0.000 abstract description 11
- 239000002105 nanoparticle Substances 0.000 abstract description 4
- 238000000034 method Methods 0.000 abstract description 3
- 239000012567 medical material Substances 0.000 abstract description 2
- 239000002082 metal nanoparticle Substances 0.000 abstract description 2
- 239000002994 raw material Substances 0.000 abstract description 2
- 239000000243 solution Substances 0.000 abstract 2
- 238000009825 accumulation Methods 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000002086 nanomaterial Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 238000004294 195Pt NMR spectroscopy Methods 0.000 description 13
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 6
- 229920001296 polysiloxane Polymers 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 238000010992 reflux Methods 0.000 description 5
- 238000001514 detection method Methods 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000001467 acupuncture Methods 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 229910000497 Amalgam Inorganic materials 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 241000416536 Euproctis pseudoconspersa Species 0.000 description 1
- 229910002621 H2PtCl6 Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910020437 K2PtCl6 Inorganic materials 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 229910019029 PtCl4 Inorganic materials 0.000 description 1
- QYSYEILYXGRUOM-UHFFFAOYSA-N [Cl].[Pt] Chemical compound [Cl].[Pt] QYSYEILYXGRUOM-UHFFFAOYSA-N 0.000 description 1
- SFCAFDBIINGSIO-UHFFFAOYSA-L [Pt](Cl)Cl.C(C)NCC Chemical compound [Pt](Cl)Cl.C(C)NCC SFCAFDBIINGSIO-UHFFFAOYSA-L 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- QNILTEGFHQSKFF-UHFFFAOYSA-N n-propan-2-ylprop-2-enamide Chemical compound CC(C)NC(=O)C=C QNILTEGFHQSKFF-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920002627 poly(phosphazenes) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229910000923 precious metal alloy Inorganic materials 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- FBEIPJNQGITEBL-UHFFFAOYSA-J tetrachloroplatinum Chemical compound Cl[Pt](Cl)(Cl)Cl FBEIPJNQGITEBL-UHFFFAOYSA-J 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Classifications
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- B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
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- B22F9/16—Making metallic powder or suspensions thereof using chemical processes
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- B22F1/10—Metallic powder containing lubricating or binding agents; Metallic powder containing organic material
- B22F1/107—Metallic powder containing lubricating or binding agents; Metallic powder containing organic material containing organic material comprising solvents, e.g. for slip casting
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Abstract
本发明提供了一种溶液中稳定贵金属孤原子的材料,由贵金属孤原子和保护剂组成。以含有硅氧基团以及聚醚基团的嵌段共聚物为保护剂,使还原态贵金属孤原子稳定存在。该材料制备的过程中可用含还原剂的水溶液为溶剂。其中贵金属可占保护剂重量的任意比例。本发明系首次在溶液中制得贵金属孤原子材料,通过采用特殊的保护剂,避免了合成过程中初级孤原子的聚积导致纳米粒子的产生。该材料的还原态孤原子区别于已知金属纳米粒子,可用于能源材料、医药合成、医疗材料、催化剂制备等领域。也为数目可控的同种或异种金属团簇、纳米材料的合成提了基础孤原子原料。
Description
技术领域
本发明属于新材料发明领域,具体材料为一种在溶液中稳定的贵金属孤原子材料。
背景技术
贵金属及其合金因其优良的性能成为现代工业中广泛应用的材料。由于其高温抗腐蚀性、高可靠性、高精度和长的使用寿命等特点,贵金属被广泛应用于航空航天、航海工业和军工用精密仪器制作中,如弹簧片、膜盒、导电游丝、轴尖等原件。同时,由于其材料生理上的无毒性、良好的延展性及生物相容性,贵金属被广泛应用于医学材料的制备中。比如在牙科领域中的汞齐合金和铸造合金两大主要牙用贵金属合金,医疗用金针、银针和硬针,医用电子器材电极材料等。再有,贵金属拥有独特的催化性能和稳定性,尤其是铂族金属(铱、铑、钯和铂),其被广泛应用于石油化工,氢燃料电池等领域。然而贵金属资源的稀缺性以及制造工艺技术的落后使得贵金属的价格居高不下,严重制约了其在各个领域的充分利用。
贵金属孤原子为贵金属的利用提供了广阔的空间。Maria Flytzani-Stephanopoulos等(Acc.Chem.Res,2014,47,783.)报道了在各种不同的载体上Au单原子材料的合成,并将其成功的应用于水煤气变换反应。张涛等(Nature Chem.,2011,3,634.)报道了在氧化铁的表面Pt单原子材料的合成,并将其成功应用于一氧化碳的氧化反应,反应的转化频率提高了2-3倍。然而采用固体表面分散的方法得到的单原子材料不仅存在着载量低,不稳定等诸多问题,同时,由于固体表面与贵金属单原子的相互作用,贵金属单原子并不是以孤立状态存在的,其存在状态绑定于固体表面,不易于从固体表面剥离,因而不能作为原料用于生成和制备更为广泛的物质。还原态的贵金属原子在溶液中运动的自由度大,极易聚集导致纳米粒子的产生,所以以溶液为介质分散还原态贵金属原子得到孤立状态的贵金属孤原子材料一直是科学技术领域的巨大挑战。乙烯基吡咯烷酮聚合物和异丙基丙烯酰胺聚合物等(J.Phys.Chem.B,1999,103,3818.;Langmuir 1997,13,6465.)高分子聚合物被广泛应用于溶液中贵金属材料的合成,然而这些高分子聚合物无法阻止初始还原态的贵金属孤原子聚集长大成为纳米粒子,所以溶液中还原态贵金属孤原子的成功合成至今仍无人报道。
基于以上的研究现状可知,如何既能克服依靠固体表面分散制备孤原子材料载量低,不稳定等缺点,又能消除溶液中初始还原态贵金属孤原子聚集长大的趋势,从而得到一种有效的制备贵金属孤原子材料的方法具有重要的意义。
发明内容
本发明的目的在于提供一种在溶液中稳定的贵金属孤原子材料。
本发明提供的一种在溶液中稳定的贵金属孤原子材料由贵金属孤原子和保护剂组成。
所述的贵金属孤原子为铂系元素或后铂系元素;所述铂系元素为钯、铑、铱、钌、锇或铂;所述后铂系元素为银或金。
所述的的贵金属孤原子为铂;以铂元素原子质量为195的同位素的核磁信号在-2600和-2800ppm之间为主要特征。
所述的保护剂是含有硅氧基团以及聚醚基团的嵌段共聚物。
所述的含有硅氧基团以及聚醚基团的嵌段共聚物中优选聚硅氧烷-聚二醇类化合物。
所述的聚硅氧烷-聚二醇类化合物中优选聚硅氧烷-聚乙二醇嵌段共聚物,其结构式如下:
所述的贵金属孤原子可占保护剂重量的任意比例。
所述的贵金属孤原子占保护剂的质量比优选0.001%-50%.
一种溶液中稳定的贵金属孤原子材料的制备方法,其特征在于按照以下步骤进行:将含有硅氧基团以及聚醚基团的嵌段共聚物,贵金属化合物前驱体,和还原剂、水按照一定比例充分混合;在-30-200℃下,反应0.5–200h后溶液中的还原剂将贵金属化合物前驱体还原为零价的贵金属单原子,从而得到能够稳定存在的贵金属单原子溶液;
所述的还原剂和贵金属化合物前驱体的物质的量比例变化范围为:1.0-107倍。
所述的还原剂和水的物质的量比例变化范围为:1:105-30:1。
所述的贵金属化合物前驱体占保护剂重量任意比。
所述贵金属化合物前驱体包括:氯铂酸、氯铂酸钠、氯铂酸钾、氯化亚铂、氯化铂、二乙胺氯化铂、硝酸铂、1,5-环辛二烯二氯化铂、三氯·(乙烯)合铂酸钾、二氯四氨合铂、二腈苯基二氯合铂、二(亚磷酸三苯酯)二氯化铂或四氯铂酸铵中的一种。
所述还原剂为醇类化合物、葡萄糖、甲酸、柠檬酸、酒石酸、抗坏血酸、水合肼或硼氢化物中的一种。
所述醇类化合物为甲醇、乙醇、丙醇、异丙醇、正丁醇,异丁醇,仲丁醇,叔丁醇、乙二醇,丙三醇中的一种或几种混合物。
本发明首次实现了在溶液相中还原态贵金属孤原子的制备。相对于传统的溶液相中金属材料的合成而言,避免了金属纳米粒子的形成,得到以孤个金属原子形式存在的还原态孤原子溶液。相对于固体表面负载的孤原子材料而言,其具有载量高,稳定性好的特点。
附图说明
图1,实施例1,2,3,4,5,6的紫外可见图谱。
图2为实施例1,2,3,4,5,6的195PtNMR谱图。
具体实施方式
下面以在溶液中稳定的铂孤原子材料为例对本发明做进一步的详细说明。本专利的保护内容并不以具体实施方式为限,而是由权利要求限制。
实施例1
溶液中铂孤原子的制备:将0.6465g聚乙二醇-聚硅氧烷嵌段共聚物,135ml乙醇,10.2ml水以及4.8ml浓度为0.018404mol/L氯铂酸溶液充分混合,然后升温,在105℃下冷凝回流3小时使氯铂酸完全还原。经紫外和195Pt NMR检测可知合成得到了铂孤原子材料。紫外可见吸收光谱图(图1)表明:氯铂酸被完全还原。(说明:在265nm处的紫外吸收峰代表PtCl6 2-离子的吸收峰,而该紫外吸收峰的消失说明氯铂酸被完全还原。)195Pt NMR谱图(图2)表明:还原态的铂孤原子形成。(说明:K2PtCl6的195Pt NMR在0ppm处,PtCl4 2-的峰在-1617ppm处,而Pt孤原子的195Pt NMR峰在-2680ppm处,同时并没有检测到铂纳米粒子的纳特位移大宽峰:-35000ppm到10000ppm,这说明H2PtCl6完全还原且Pt孤原子生成,同时没有Pt纳米粒子产生。)
实施例2
溶液中铂孤原子的制备:将0.6465g聚乙二醇-聚硅氧烷嵌段共聚物,4.05mg乙醇(乙醇与氯铂酸物质的量之比为1:1),145ml水以及4.8ml浓度为0.018404mol/L氯铂酸溶液充分混合(乙醇与水的物质的量比例为1:105),然后升温,在105℃下冷凝回流3小时使氯铂酸完全还原。经紫外和195Pt NMR检测可知合成得到了铂孤原子材料。紫外可见图谱如图1所示,195PtNMR谱图如图2所示。
实施例3
溶液中铂孤原子的制备:将0.6465g聚乙二醇-聚硅氧烷嵌段共聚物,148.5ml乙醇,1.02ml水以及0.48ml浓度为0.18404mol/L氯铂酸溶液充分混合(乙醇与水的物质的量比例为30:1),然后升温,在105℃下冷凝回流3小时使氯铂酸完全还原。经紫外和195Pt NMR检测可知合成得到了铂孤原子材料。紫外可见图谱如图1所示,195PtNMR谱图如图2所示。
实施例4
溶液中铂孤原子的制备:将0.6465g聚乙二醇-聚硅氧烷嵌段共聚物,882g乙醇(1.14L,乙醇加入量为氯铂酸物质的量的107倍),100.2ml水以及4.8ml浓度为0.018404mol/L氯铂酸溶液充分混合,然后升温,在105℃下冷凝回流3小时使氯铂酸完全还原。经紫外和195Pt NMR检测可知合成得到了铂孤原子材料。紫外可见图谱如图1所示,195PtNMR谱图如图2所示。
实施例5
溶液中铂孤原子的制备:将1719.92g聚乙二醇-聚硅氧烷嵌段共聚物,1000ml乙醇,100ml水以及4.8ml浓度为0.018404mol/L氯铂酸溶液充分混合(铂孤原子占保护剂质量的0.001%),然后升温,在105℃下冷凝回流3小时使氯铂酸完全还原。紫外可见图谱如图1所示,195PtNMR谱图如图2所示。
实施例6
溶液中铂孤原子的制备:将0.0344g聚乙二醇-聚硅氧烷嵌段共聚物,135ml乙醇,10.2ml水以及4.8ml浓度为0.018404mol/L氯铂酸溶液充分混合(铂孤原子占保护剂质量的50%),然后升温,在105℃下冷凝回流3小时使氯铂酸完全还原。紫外可见图谱如图1所示,195PtNMR谱图如图2所示。
Claims (11)
1.一种溶液中稳定的贵金属孤原子材料,其特征在于该材料由贵金属孤原子和保护剂组成。
2.按照权利要求1所述的一种溶液中稳定的贵金属孤原子材料,其特征在于所述的贵金属孤原子为铂系元素或后铂系元素;所述铂系元素为钯、铑、铱、钌、锇或铂;所述后铂系元素为银或金。
3.按照权利要求1所述的一种溶液中稳定的贵金属孤原子材料,其特征在于所述的的贵金属孤原子为铂;以铂元素原子质量为195的同位素的核磁信号在-2600和-2800ppm之间为主要特征。
4.按照权利要求1所述的一种溶液中稳定的贵金属孤原子材料,其特征在于所述的保护剂是含有硅氧基团以及聚醚基团的嵌段共聚物。
5.按照权利要求4所述的一种溶液中稳定的贵金属孤原子材料,其特征在于所述的含有硅氧基团以及聚醚基团的嵌段共聚物中优选聚硅氧烷-聚二醇类化合物。
6.按照权利要求5所述的一种溶液中稳定的贵金属孤原子材料,其特征在于所述的聚硅氧烷-聚二醇类化合物中优选聚硅氧烷-聚乙二醇嵌段共聚物,其结构式如下:
。
7.按照权利要求1所述的一种溶液中稳定的贵金属孤原子材料,其特征在于所述的贵金属孤原子可占保护剂质量的任意比。
8.一种溶液中稳定的贵金属孤原子材料的制备方法,其特征在于按照以下步骤进行:将含有硅氧基团以及聚醚基团的嵌段共聚物,贵金属化合物前驱体,和还原剂、水按照一定比例充分混合;在-30-200℃下,反应0.5-200h得到贵金属孤原子,从而得到能够稳定存在的贵金属单原子溶液;
所述的还原剂和贵金属化合物前驱体的物质的量比例变化范围为:1-107倍。
所述的还原剂和水的物质的量比例变化范围为:1:105-30:1。
9.按照权利要求8所述一种溶液中稳定的贵金属孤原子材料的制备方法,其特征在于所述贵金属化合物前驱体包括:氯铂酸、氯铂酸钠、氯铂酸钾、氯化亚铂、氯化铂、二乙胺氯化铂、硝酸铂、1,5-环辛二烯二氯化铂、三氯·(乙烯)合铂酸钾、二氯四氨合铂、二腈苯基二氯合铂、二(亚磷酸三苯酯)二氯化铂或四氯铂酸铵中的一种。
10.按照权利要求8所述的一种溶液中稳定的贵金属孤原子材料的制备方法,其特征在于所述还原剂为醇类化合物、葡萄糖、甲酸、柠檬酸、酒石酸、抗坏血酸、水合肼或硼氢化物中的一种。
11.按照权利要求10所述的一种溶液中稳定的贵金属孤原子材料的制备方法,其特征在于所述醇类化合物为甲醇、乙醇、丙醇、异丙醇、正丁醇,异丁醇,仲丁醇,叔丁醇、乙二醇,丙三醇中的一种或几种混合物。
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CN111250725A (zh) * | 2018-11-30 | 2020-06-09 | 中国科学院大连化学物理研究所 | 一种溶液中稳定的异核双金属原子材料的制备方法 |
CN111250692A (zh) * | 2018-11-30 | 2020-06-09 | 中国科学院大连化学物理研究所 | 一种溶液中稳定的异核双金属原子材料 |
WO2020155672A1 (zh) * | 2019-01-31 | 2020-08-06 | 中国科学院大连化学物理研究所 | 一种在溶液中稳定的还原态贵金属孤原子材料和制备方法 |
CN114522681A (zh) * | 2020-11-23 | 2022-05-24 | 中国科学院大连化学物理研究所 | 一种提高贵金属孤原子在氢气气氛中稳定性的方法 |
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Cited By (9)
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CN110465313A (zh) * | 2018-05-10 | 2019-11-19 | 中国科学院大连化学物理研究所 | 含氯零价铂化合物及其制备方法与其在硅氢加成中的应用 |
CN111250725A (zh) * | 2018-11-30 | 2020-06-09 | 中国科学院大连化学物理研究所 | 一种溶液中稳定的异核双金属原子材料的制备方法 |
CN111250692A (zh) * | 2018-11-30 | 2020-06-09 | 中国科学院大连化学物理研究所 | 一种溶液中稳定的异核双金属原子材料 |
CN111250692B (zh) * | 2018-11-30 | 2021-11-09 | 中国科学院大连化学物理研究所 | 一种溶液中稳定的异核双金属原子材料 |
CN111250725B (zh) * | 2018-11-30 | 2022-09-16 | 中国科学院大连化学物理研究所 | 一种溶液中稳定的异核双金属原子材料的制备方法 |
WO2020155672A1 (zh) * | 2019-01-31 | 2020-08-06 | 中国科学院大连化学物理研究所 | 一种在溶液中稳定的还原态贵金属孤原子材料和制备方法 |
CN111496265A (zh) * | 2019-01-31 | 2020-08-07 | 中国科学院大连化学物理研究所 | 一种在溶液中稳定的还原态贵金属孤原子材料和制备方法 |
CN114522681A (zh) * | 2020-11-23 | 2022-05-24 | 中国科学院大连化学物理研究所 | 一种提高贵金属孤原子在氢气气氛中稳定性的方法 |
CN114522681B (zh) * | 2020-11-23 | 2023-10-13 | 中国科学院大连化学物理研究所 | 一种提高贵金属孤原子在氢气气氛中稳定性的方法 |
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EP3539656A4 (en) | 2020-05-20 |
US20190329225A1 (en) | 2019-10-31 |
CN108067631B (zh) | 2019-11-08 |
KR20190091280A (ko) | 2019-08-05 |
CA3045346A1 (en) | 2018-05-17 |
EP3539656A1 (en) | 2019-09-18 |
JP2020506285A (ja) | 2020-02-27 |
JP6928214B2 (ja) | 2021-09-01 |
WO2018085958A1 (zh) | 2018-05-17 |
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