光催化
化学
光电流
X射线光电子能谱
二氧化碳电化学还原
无机化学
氢氧化物
异质结
光化学
一氧化碳
材料科学
化学工程
催化作用
有机化学
光电子学
工程类
作者
Jingwen Wei,Shiming Zhang,Jiangli Sun,Ting Liang,Zuji Li,Zhihong Li,Xiaoling Yi,Ruting Xiong,Jie‐Ying Deng,Zebin Yu,Shuangfei Wang,Yanping Hou
标识
DOI:10.1016/j.jcis.2022.08.148
摘要
Development of efficient photocatalysts is essential for carbon dioxide (CO2) photocatalytic reduction. In this study, Z-scheme CoAl-layered double hydroxide (LDH)/indium vanadate (InVO4) heterojunction photocatalysts were synthesized using hydrothermal method, and their performance toward CO2 reduction and mechanism were determined. Results of characterizations showed that the CoAl-LDH/InVO4-30 exhibited desired morphology, the most efficient photogenerated carriers separation and charge transfer, and the highest photocurrent response. X-ray photoelectron spectroscopy (XPS) and electron spin resonance (ESR) manifested that charge transfer of the CoAl-LDH/InVO4 conformed to Z-scheme mechanism. The CoAl-LDH/InVO4-30 exhibited the highest carbon monoxide (CO) yield of 174.4 μmol g-1 within 2 h of reaction, which was 2.46 and 9.79 times of pure CoAl-LDH and InVO4, respectively. The CO selectivity was up to nearly 100%. Moreover, in-situ fourier transform infrared spectroscopy (ISFT-IR) demonstrated that bicarbonate (HCO3*) and carboxylate (COOH*) were the main intermediates during the CO2 reduction process, and possible CO2 reduction pathways were proposed. This work provides a reference for construction of Z-scheme LDH-based heterojunctions for efficient CO2 photoreduction.
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