Hybrid 0D-2D black phosphorus quantum dots-graphitic carbon nitride nanosheets for efficient hydrogen evolution

被引:160
作者
Lei, Wanying [1 ,2 ,3 ]
Mi, Yang [1 ]
Feng, Rongjuan [1 ]
Liu, Ping [4 ]
Hu, Song [1 ]
Yu, Jiaguo [5 ]
Liu, Xinfeng [1 ]
Rodriguez, Jose A. [4 ]
Wang, Jia-ou [6 ]
Zheng, Lei [6 ]
Tang, Kun [6 ]
Zhu, Sixu [6 ]
Liu, Gang [1 ]
Liu, Minghua [1 ,3 ]
机构
[1] Natl Ctr Nanosci & Technol, CAS Ctr Excellence Nanosci, CAS Key Lab Standardizat & Measurement Nanotechno, Beijing 100190, Peoples R China
[2] Peking Univ, Acad Adv Interdisciplinary Studies, Beijing 100871, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Brookhaven Natl Lab, Chem Dept, Upton, NY 11973 USA
[5] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Hubei, Peoples R China
[6] Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China
关键词
Black phosphorus; Graphitic carbon nitride; Quantum dots; 0D-2D hybrid; Water splitting; 2-DIMENSIONAL MATERIALS; ENERGY-CONVERSION; H-2; EVOLUTION; PHOTOCATALYST; REDUCTION; STORAGE; FUNCTIONALIZATION; PERFORMANCE; COMPOSITES; CHALLENGES;
D O I
10.1016/j.nanoen.2018.06.001
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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 mu mol 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.
引用
收藏
页码:552 / 561
页数:10
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