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Chalcogenide and pnictide nanocrystals from the silylative deoxygenation of metal oxides

机译:来自金属氧化物甲硅烷基化脱氧的硫属化物和对丙烯纳米晶体

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摘要

Transition metal chalcogenide and pnictide nanocrystals are of interest for optoelectronic and catalytic applications. Here, we present a generalized route to the synthesis of these materials from the silylative deoxygenation of metal oxides with trimethylsilyl reagents. Specific nanophases produced in this way include Ni3S2, Ni5Se5, Ni2P, Co9S8, Co3Se4, CoP, Co2P, and heterobimetallic (Ni/Co)(9)S-8. The resulting chalcogenide nanocrystals are hollow, likely due to differential rates of ion diffusion during the interfacial phase transformation reaction (Kirkendall-type effect). In contrast, the phosphide nanocrystals are solid, likely because they form at higher reaction temperatures. In all cases, simultaneous partial decomposition of the deoxygenating silyl reagent produces a coating of amorphous silica around the newly formed nanocrystals, which could impact their stability and recyclability.
机译:过渡金属硫属化物和对丙烯纳米晶体对光电和催化应用感兴趣。 这里,我们向三甲基甲硅烷基拉甲硅烷基的金属氧化物的甲硅烷基脱氧合成这些材料的一般途径。 以这种方式产生的特定纳米碱基包括Ni3 S2,Ni5 Se 5,Ni2P,CO9S8,CO 3 SE,COP,CO 2P和杂二种(Ni / CO)(9)S-8。 所得的硫属化物纳米晶体是中空的,可能是由于在界面相变反应(Kirkendall型效果)期间离子扩散的差分速率。 相反,磷化物纳米晶体是固体,可能是因为它们在更高的反应温度下形成。 在所有情况下,脱氧甲硅烷基试剂的同时分解在新形成的纳米晶体周围产生一包非晶二氧化硅,这可能影响其稳定性和可回收性。

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