Authors: Junli Liu, Shibin Wang, Nan Liu, Deren Yang, Hongwei Wang, Hanshi Hu, Jing Zhuang, Xun Wang
Published: 2020-12-30
Source: Full article
AbstractHere 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.