光催化
制氢
三元运算
氧化还原
材料科学
分解水
瓶颈
复合数
化学工程
环境污染
纳米技术
耐久性
氢
化学
催化作用
冶金
计算机科学
复合材料
环境科学
有机化学
工程类
生物化学
环境保护
嵌入式系统
程序设计语言
作者
Chao Wu,Weixin Huang,Huanmin Liu,Kangle Lv,Qin Li
标识
DOI:10.1016/j.apcatb.2023.122653
摘要
Facing the increasingly serious issues of energy crisis and environmental pollution, it is vital to develop efficient and durable photocatalysis systems for hydrogen (H2) production from water splitting. However, for the famous CdS-based systems, the bottleneck of poor efficiency and low stability arisen from photocorrosion has not been broken through yet. In this study, a ternary composite of CdS, MoS2 and Ti3C2 MXene with intimately contact interfaces was successfully constructed via an in situ growth method, which exhibited reinforced photocatalytic H2-production activity and increased photocorrosion resistant capability. Both of experimental characterizations and density functional theory (DFT) calculations well proved that the photogenerated holes and electrons of CdS timely migrated to Ti3C2 and MoS2, respectively. As a consequence, the optimal sample displayed a high H2 production rate of 14.88 mmol·h−1·g−1 with a lifetime of up to 78 h, and the component and structure of the composite were kept intact during the photocatalysis reaction. This work highlights the synergistic effect of the Ti3C2 MXene and MoS2 as redox dual cocatalysts on the promoted photocatalytic performance and durability of CdS, which can be anticipated to significantly enhance the commercial availability of CdS and even boost its incorporation into industrial applications.
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