等结构
化学
光催化
二氧化碳电化学还原
催化作用
选择性
还原(数学)
吸收(声学)
产量(工程)
化学工程
碳纤维
表征(材料科学)
溶剂热合成
无机化学
可见光谱
载流子
纳米技术
光化学
二氧化碳
电子波段
吸收光谱法
二氧化钛
多相催化
作者
Haili Guo,Yao-Mei Fu,Shuangxue Wu,Li Liu,Xinlong Wang,Chao Qin,Zhong‐Min Su
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2025-09-19
卷期号:64 (39): 19764-19770
被引量:1
标识
DOI:10.1021/acs.inorgchem.5c03269
摘要
Photocatalytic reduction technology offers a promising pathway for the sustainable transformation of carbon dioxide into value-added chemicals. In this study, two isostructural three-dimensional pillared [W10O32]4--based metal-organic frameworks (POMOFs), [M2(4,4'-bipy)6(DMA)2W10O32] (M = Co 1, Ni 2), have been synthesized under solvothermal conditions. Structural characterization verifies their effective light absorption and photogenerated charge separation capability. As photocatalysts for CO2 reduction, compound 1 achieves an effective gaseous product (CO + H2) yield of 3149.4 μmol g-1 h-1, while compound 2 exhibits moderate yields of 1171.1 μmol g-1 h-1 with a CO selectivity of 79%. Mechanistic investigations suggest that the electronic band structures of 1 and 2 facilitate the catalytic reduction of CO2 to CO. This research advances the development of tailored [W10O32]4--based POMOFs for enhanced photocatalytic CO2 conversion.
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