摘要
Here it is shown that polyoxometalate (POM) clusters (H3PW12O40·xH2O, PW12) can be introduced to interact with Au nanoclusters to form the “A-B-A-B” type building block (“A” represents Au nanoclusters and “B” stands for PW12 clusters), which continue to grow into copolymer-analogue Au−PW12 sub-1 nm nanowires. Due to the synergetic effect of Au nanoclusters and POMs, the obtained Au−PW12 sub-1 nm nanowires efficiently perform catalytic activity in the photo-electrochemical converting CO2 into CO. Under light, the catalyst maintains remarkable faradic efficiency (FE) of ≈99% from −0.7 to −0.9V (RHE), which is better than that in dark (FE of 66.4–90.64% from −0.7 to −0.9 V (RHE)). Density functional theory calculations and cryo-electron microscope images support the “A-B-A-B” type of structure and mechanistic studies also reveal the higher reactivity toward COOH* formation and CO adsorption on the catalyst, which lead to the superior catalytic activity in CO2 reduction reaction.
| 源语言 | 英语 |
|---|---|
| 文章编号 | 2006260 |
| 期刊 | Small |
| 卷 | 17 |
| 期 | 4 |
| DOI | |
| 出版状态 | 已出版 - 27 1月 2021 |
| 已对外发布 | 是 |
指纹
探究 'Au-Polyoxometalates A-B-A-B Type Copolymer-Analogue Sub-1 nm Nanowires' 的科研主题。它们共同构成独一无二的指纹。引用此
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