光催化
异质结
三元运算
纳米颗粒
材料科学
重组
可见光谱
热液循环
电场
纳米技术
光电子学
化学工程
化学
物理
催化作用
生物化学
量子力学
计算机科学
工程类
基因
程序设计语言
作者
Yan Liu,Lizhi Feng,Chaoyue Zheng
标识
DOI:10.1021/acsanm.4c03584
摘要
Cd 0.8 Mn 0.2 S is a ternary particulate chemical substance that faces significant challenges with carrier recombination in the field of photocatalysis. To address this issue, we formed an internal electric field and constructed S-scheme heterojunctions using Cu 2 O and Cd 0.8 Mn 0.2 S nanoparticles, thereby reducing the recombination rate of photogenerated carriers. We synthesized Cd 0.8 Mn 0.2 S using a hydrothermal method, followed by employing ultrasonic self-assembly to closely couple Cd 0.8 Mn 0.2 S with Cu 2 O. In this configuration, Cd 0.8 Mn 0.2 S acts as the electron acceptor and Cu 2 O acts as the electron donor. The Cd 0.8 Mn 0.2 S/Cu 2 O structure forms a tight interface, providing the shortest transfer distance for electron migration. The S-scheme heterojunction strategy effectively lowers the chemical reaction barriers and facilitates vectorial separation of photogenerated carriers. Under 10 W white light illumination, the Cd 0.8 Mn 0.2 S/Cu 2 O composite photocatalyst demonstrates remarkable hydrogen evolution activity, achieving a hydrogen production rate of 40.06 mmol·g –1 ·h –1 . This S-scheme interface strategy paves the way for the structural design and large-scale application of highly active visible light photocatalysts.
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