异质结
纳米棒
煤
材料科学
产量(工程)
三乙醇胺
电子
光催化
激发态
光电子学
化学工程
纳米技术
化学
分析化学(期刊)
有机化学
催化作用
物理
复合材料
原子物理学
工程类
量子力学
作者
Jinghao Hua,Changchang Ma,Dayu Wu,Haitao Huang,Xiaojun Dai,Kaidi Wu,Haihong Wang,Zhaowei Bian,Sheng Feng
标识
DOI:10.1016/j.jallcom.2023.172516
摘要
In this study, a novel Z-scheme Bi19S27Br3/CoAl-LDH heterojunction was prepared. An interface charge transfer channel was established between Bi19S27Br3 and CoAl-LDH, accelerating the transition efficiency of interface electrons from CoAl-LDH to Bi19S27Br3. Thereby ensuring more excited electrons to participate in CO2 photoreduction reactions. The reduction products were tested under artificial light conditions, and triethanolamine was selected as a sacrificial agent. After 5 h of illumination, the CO yield of Bi19S27Br3/CoAl-LDH Z-scheme heterojunction was 86.41 μmol·g−1 is 4 times and 7 times higher than Bi19S27Br3 and CoAl-LDH, respectively. The yield of CH4 in Bi19S27Br3/CoAl-LDH is 3.97 μmol·g−1 is 4 times higher than CoAl-LDH. Also Bi19S27Br3 itself does not produce CH4. The results indicate that the Z-scheme heterojunction effectively enhances the photoreduction ability of CO2, providing a new approach for accurately controlling the direction of photo generated charge separation to prepare high-performance photocatalysts.
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