光催化
异质结
材料科学
贵金属
化学工程
晶体结构
纳米技术
Crystal(编程语言)
制氢
电子转移
催化作用
金属
光化学
光电子学
化学
结晶学
冶金
计算机科学
程序设计语言
工程类
生物化学
作者
Yanlin Jia,Zizhao Wang,Xiu-Qing Qiao,Lei Huang,Shenglong Gan,Dongfang Hou,Jun Zhao,Chenghua Sun,Dongsheng Li
标识
DOI:10.1016/j.cej.2021.130368
摘要
Assembling the composition synergism and structure adjustment to efficiently accelerate the charge transfer and separation, is emerging as a promising strategy for advanced photocatalytic H2 evolution. Herein, an efficient ZnO/CdS/MoS2 photocatalyst with similar componments crystal structures and integrated S-scheme heterojunction and cocatalyst effects, was constructed to synergistically promote the photocatalytic H2 evolution of CdS. The optimized ZnO/CdS/MoS2 heterojunction with an MoS2 mass ratio of 6 wt% (ZCM-3) revealed the highest H2 evolution rate of 10247.4 μmol g−1h−1, 30.7-fold and 3.0-fold higher than that of bare CdS (323.5 μmol g−1h−1) and optimized ZnO/CdS (3400.8 μmol g−1h−1), respectively. Moreover, the slight change in H2 production activities and retained crystal structures after five consecutive cycles indicate the stability of the photocatalyst. Detailed experimental results and DFT calculation elucidated that the substantially boosted photocatalytic performance was originated not only from the fast electron transfer and separation through the intimate contact, but also the synergistic effect between the S-scheme and cocatalyst. A possible mechanism was speculated based on the results, which can enriche the research for S-scheme heterojunction photocatalytic system and provide new insights for the design of efficient H2 production photocatalyst.
科研通智能强力驱动
Strongly Powered by AbleSci AI