材料科学
黑磷
石墨氮化碳
量子点
异质结
氮化物
纳米材料
化学工程
载流子
光催化
纳米技术
碳纤维
石墨烯
氮化碳
带隙
光电子学
催化作用
复合材料
复合数
图层(电子)
工程类
化学
生物化学
作者
Wanying Lei,Yang Mi,Rongjuan Feng,Ping Liu,Song Hu,Jiaguo Yu,Xinfeng Liu,José A. Rodríguez,Jiaou Wang,Lei Zheng,Kun Tang,Sixu Zhu,Gang Liu,Minghua Liu
出处
期刊:Nano Energy
[Elsevier]
日期:2018-06-02
卷期号:50: 552-561
被引量:163
标识
DOI:10.1016/j.nanoen.2018.06.001
摘要
Abstract As an emerging post-graphene two-dimensional (2D) nanomaterial, black phosphorus (BP) is attracting a great deal of current attention for the direct conversion of solar energy into solar fuels on account of its unique tunable direct-bandgap and high charge-carrier mobility. Herein, for the first time, we immobilize BP quantum dots (BPQDs) onto graphitic carbon nitride (g-C3N4) nanosheets to create a 0D-2D inorganic-organic hybrid via a conventional and cost–effective sonication approach. The as-prepared BPQDs/g-C3N4 hybrids display BPQD content-dependent performance in visible-light-driven hydrogen generation. 5 wt% BPQDs/g-C3N4 with cyclability exhibits the greatest hydrogen evolution rate of 271 μmol h−1 g−1 that is 5.6 and 4.2 times greater than that of pristine g-C3N4 and BPQDs, respectively. We demonstrate that the type-II band alignment, the formation of phosphorus–carbon bonds and the efficient interfacial charge separation between well-dispersed BPQDs and g-C3N4 synergetically enhance the photoactivity and photostability. This study opens possibilities to create viable BP-based heterostructures for energy conversion and storage.
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