Lim Taewaen, Seo Junhyeok
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.
ChemSusChem. 2023 Oct 6;16(19):e202300869. doi: 10.1002/cssc.202300869. Epub 2023 Jul 31.
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.
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。