材料科学
异质结
Atom(片上系统)
调解人
人工光合作用
光合作用
电子
纳米技术
化学物理
光电子学
物理
生物
量子力学
植物
光催化
计算机科学
催化作用
生物化学
嵌入式系统
内分泌学
作者
Xiaowen Ruan,Minghua Xu,Chunsheng Ding,Jing Leng,Guozhen Fang,Depeng Meng,Wei Zhang,Zhifeng Jiang,Sai Kishore Ravi,Xiaoqiang Cui,Jiaguo Yu
标识
DOI:10.1002/aenm.202405478
摘要
Abstract Developing conductor‐mediated S‐scheme heterojunction photocatalysts imitating natural photosynthetic systems emerges as a promising approach to hydrogen peroxide (H 2 O 2 ) production. However, achieving precise coupling between two semiconductors with a charge shuttle and modulating the interfacial interactions still remain a significant bottleneck. Herein, we propose a catalyst architecture with a Cd single atom mediated S‐scheme heterojunction formed by interfacing CdS and TiO 2 nanoparticles. This catalyst exhibits an H 2 O 2 production rate as high as 60.33 µmol g −1 min −1 under UV–vis light irradiation, which is attributed to the efficient charge transport at the interface of CdS and TiO 2 thanks to the Cd single atom mediated S‐scheme. In‐situ X‐ray photoelectron spectroscopy (XPS) and electron spin resonance (ESR) spin‐trapping tests confirm the S‐scheme charge transfer route. Femtosecond transient absorption (fs‐TA) spectroscopy and other ex‐situ characterizations further corroborate the efficient charge transport across the catalyst interface. This work offers a new perspective on constructing single atoms mediated heterojunctions to enhance photocatalytic performance.
科研通智能强力驱动
Strongly Powered by AbleSci AI