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用于将光催化CO高效选择性还原为C1产物的VO修饰层状双氢氧化物纳米片

VO -Modified Layered Double Hydroxides Nanosheets for Highly Selective Photocatalytic CO Reduction to C1 Products.

作者信息

Bai Sha, Ning Chenjun, Wang Huijuan, Liu Guihao, Zheng Lirong, Song Yu-Fei

机构信息

State Key Laboratory of Chemical Resource Engineering, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.

Institute of High Energy Physics, The Chinese Academy of Sciences, Beijing, 100049, P. R. China.

出版信息

Small. 2022 Oct;18(40):e2203787. doi: 10.1002/smll.202203787. Epub 2022 Sep 4.

Abstract

The conversion of CO into high-value added chemicals driven by solar energy is an effective way to solve environmental problems, which is, however, largely restricted by the competition reaction of the hydrogen evolution reaction (HER) and easy electron-hole recombination, etc. Herein, VO -supported ultrathin NiMgV-layered double hydroxide (V/NiMgV-LDH) nanosheets are successfully fabricated, and the extended X-ray absorption fine structure (EXAFS) and density function theory (DFT) calculations reveal that VO species are located on the top of V atoms in the NiMgV-LDH laminate. The V/NiMgV-LDH is proved to be highly efficient for the photocatalytic CO reduction reaction (CO PR) with high selectivity of 99% for C1 products and nearly no HER (<1%) takes place under visible light. Contrast experiments using NiMgV-LDH as the catalyst for CO PR show a CO selectivity of 71.40% and a H selectivity of 28.11%. Such excellent performance of V/NiMgV-LDH can be attributed to the following reasons: 1) the V/NiMgV-LDH modulates the band structure and promotes the separation of electrons and holes; 2) strong bonding between V/NiMgV-LDH and CO* and H* facilitates the hydrogenation to form CH and inhibits the formation of by-product H at the same time.

摘要

由太阳能驱动将一氧化碳转化为高附加值化学品是解决环境问题的有效途径,然而,这在很大程度上受到析氢反应(HER)的竞争反应以及容易的电子-空穴复合等因素的限制。在此,成功制备了负载VO的超薄NiMgV层状双氢氧化物(V/NiMgV-LDH)纳米片,扩展X射线吸收精细结构(EXAFS)和密度泛函理论(DFT)计算表明VO物种位于NiMgV-LDH层状结构中V原子的顶部。V/NiMgV-LDH被证明对光催化CO还原反应(CO PR)具有高效性,对C1产物的选择性高达99%,并且在可见光下几乎不发生HER(<1%)。使用NiMgV-LDH作为CO PR催化剂的对比实验显示CO选择性为71.40%,H选择性为28.11%。V/NiMgV-LDH的这种优异性能可归因于以下原因:1)V/NiMgV-LDH调节能带结构并促进电子和空穴的分离;2)V/NiMgV-LDH与CO和H之间的强键合促进氢化形成CH,同时抑制副产物H的形成。

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