Constructing Co3O4/g-C3N4 Ultra-Thin Nanosheets with Z-Scheme Charge Transfer Pathway for Efficient Photocatalytic Water Splitting

被引:9
作者
Guo, Yuan [1 ]
Liu, Wanqing [1 ]
Duan, Wei [1 ]
Wang, Siyu [1 ]
Jia, Liqun [1 ]
Zhang, Guoqing [1 ]
Zhu, Baolin [1 ]
Huang, Weiping [1 ]
Zhang, Shoumin [1 ]
机构
[1] Nankai Univ, TKL Met & Mol Based Mat Chem, Dept Chem, Key Lab Adv Energy Mat Chem MOE, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
Co3O4; g-C3N4 ultra-thin nanosheets; Z-scheme charge transfer pathway; photocatalytic; water splitting; H-2; evolution; GRAPHITIC CARBON NITRIDE; HETEROJUNCTION; G-C3N4; DEGRADATION; EVOLUTION; SURFACE; PERFORMANCE; COCATALYST; STABILITY; ENERGY;
D O I
10.3390/nano11123341
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Photocatalytic water splitting for hydrogen generation is a significant pathway for sustainable energy conversion and production. The photocatalysts with a Z-scheme water splitting charge transfer pathway is superior due to the good separation and migration ability of photoexcited charge carriers. Herein, Co3O4/g-C3N4 photocatalysts with Z-scheme charge transfer pathway were successfully constructed by an electrostatic interaction-annealing method. The as-prepared Co3O4/g-C3N4 ultra-thin nanosheets were tested and analyzed by XRD, EA, ICP, SEM, TEM, AFM, XPS, UV-Vis DRS, PL and photoelectrochemical measurements. Moreover, the influences of fabrication parameters on performance of Co3O4/g-C3N4 catalysts were investigated, and 0.5% Co3O4/g-C3N4 exhibited the optimal activity. Based on the characterization and catalytic performance, the Z-scheme charge transfer pathway of Co3O4/g-C3N4 was established and put forward. To further improve the catalytic performance of Co3O4/g-C3N4, 0.5% Pt was added as a co-catalyst. The obtained Pt/0.5% Co3O4/g-C3N4 was recyclable and remained the original catalytic water splitting performance within 20 h. The modification of Co3O4 and Pt improved the separation and migration of e(-) and h(+), and induced the increased hydrogen evolution rate of g-C3N4.
引用
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页数:14
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