化学
电子转移
分解水
光催化
氧化还原
电子
产量(工程)
化学物理
法拉第效率
静电学
量子产额
涂层
铬
光化学
电子供体
量子效率
金属
半导体
化学工程
水处理
电子受体
可见光谱
钴
光催化分解水
次级电子
光诱导电子转移
原子物理学
电子空穴
作者
Ren Itagaki,Akinobu Nakada,Hajime Suzuki,Osamu Tomita,Ryu Abe
摘要
Z-scheme water splitting with a redox mediator, which transports electrons from an H2- to an O2-evolving photocatalyst, has been widely studied to achieve efficient overall water splitting. However, backward electron transfer with the redox mediator is an intrinsic drawback of Z-scheme water splitting, because it interrupts the desired H2 and O2 evolution. Although a CrOx shell coating on metal cocatalysts on an H2-evolving photocatalyst is widely used to block backward electron transfer, this strategy relies on potentially toxic chromium species of which elution is possible under the photocatalytic operation. Herein, we demonstrate a chromium-free approach that suppresses backward electron transfer by manipulating electrostatic interactions at the photocatalyst–mediator interface. The designed charge-switchable cobalt complex serves as a superior mediator that selectively suppresses backward electron transfer from a positively charged H2-evolving photocatalyst without using a CrOx shell, leading to efficient Z-scheme water splitting with an apparent quantum yield of 7.2%.
科研通智能强力驱动
Strongly Powered by AbleSci AI