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基于面的碘氧化铋重构用于(BiO)₂CO边缘面的选择性生长以最大化CO转化效率

Face-Dependent Reconstruction of Bi-Oxyiodides toward Selective Growth of (BiO) CO Edge Side to Maximize CO Conversion Efficiency.

作者信息

Lim Taewaen, Seo Junhyeok

机构信息

Department of Chemistry, Gwangju Institute of Science and Technology, Gwangju, 61005, Republic of Korea.

Research Center for Innovative Energy and Carbon Optimized Synthesis for Chemicals (Inn-ECOSysChem), Gwangju Institute of Science and Technology, Gwangju, 61005, Republic of Korea.

出版信息

ChemSusChem. 2023 Oct 6;16(19):e202300869. doi: 10.1002/cssc.202300869. Epub 2023 Jul 31.

Abstract

Chemical reconstruction of bismuth oxyiodides using bicarbonates is tried to selectively grow (BiO) CO edge side. Orthorhombic o-Bi O I undergoes a total reconstruction process by its phase transformation into tetragonal (BiO) CO (BOC-o) to form a well-aligned nanosheet array with maximally exposing CO moiety at the edge side. The post-reconstruction BOC-o catalyst achieved 100 % Faradaic efficiency at -0.86 V vs. RHE for CO -to-formate conversion. However, another conservative reconstruction of tetragonal t-BiOI into tetragonal (BiO) CO (BOC-t) exposed majorly a less reactive [BiO] layer. At low overpotential regions, the catalytic cycle of BOC-o begins with the initial conversion of the CO moiety into formate at the [-OBi-(CO )-BiO-] site, but at high overpotential regions, the [BiO] layer undergoes reduction to metallic Bi and multi-catalytic species proceed with CO reduction. Otherwise, the deactivation of Bi site by an organic molecule switched on another catalysis of proton reduction, preventing CO reduction.

摘要

尝试使用碳酸氢盐对碘氧化铋进行化学重构,以选择性地生长(BiO)CO边缘侧。正交晶系的o-BiOI通过相转变为四方晶系的(BiO)CO(BOC-o)经历完全重构过程,形成排列良好的纳米片阵列,在边缘侧最大程度地暴露CO部分。重构后的BOC-o催化剂在相对于可逆氢电极(RHE)为-0.86 V时,将CO转化为甲酸盐的法拉第效率达到100%。然而,将四方晶系的t-BiOI另一种保守重构为四方晶系的(BiO)CO(BOC-t)主要暴露了活性较低的[BiO]层。在低过电位区域,BOC-o的催化循环始于CO部分在[-OBi-(CO)-BiO-]位点最初转化为甲酸盐,但在高过电位区域,[BiO]层还原为金属Bi,多种催化物种进行CO还原。否则,有机分子使Bi位点失活会开启另一种质子还原催化,从而阻止CO还原。

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