Fe2O3/C-C3N4-Based Tight Heterojunction for Boosting Visible Light-Driven Photocatalytic Water Oxidation

被引:64
|
作者
Kong, Lingqiao [1 ,2 ]
Yan, Junqing [1 ,2 ]
Li, Ping [1 ,2 ]
Liu, Shengzhong Frank [1 ,2 ,3 ]
机构
[1] Shaanxi Normal Univ, Sch Mat Sci & Engn, Minist Educ, Key Lab Appl Surface & Colloid Chem, 620 West Changan Ave, Xian 710119, Shaanxi, Peoples R China
[2] Shaanxi Normal Univ, Sch Mat Sci & Engn, Shaanxi Engn Lab Adv Energy Technol, 620 West Changan Ave, Xian 710119, Shaanxi, Peoples R China
[3] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, iChEM, 457 Zhongshan Rd Dalian, Dalian 116023, Peoples R China
来源
关键词
alpha-Fe2O3; g-C3N4; Heterojunction; Water oxidation; Photocatalysis; GRAPHITIC CARBON NITRIDE; OXYGEN REDUCTION REACTION; Z-SCHEME; HYDROGEN-PRODUCTION; IN-SITU; EVOLUTION REACTION; AMORPHOUS-CARBON; SOLAR HYDROGEN; G-C3N4; PERFORMANCE;
D O I
10.1021/acssuschemeng.8b01799
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recently, photocatalytic water splitting for clean hydrogen (H-2) energy through the use of solar energy has been considered to be a promising means of renewable energy conversion. Because of the high activation barriers of oxygen (O-2) generation, the half reaction, i.e., water oxidation, is the rate-limiting steps of the overall water splitting efficiency. Photocatalysts with high activity and nonmetal usage are needed. Herein, we report one new thin-layered heterojunction sample of Fe2O3/C-C3N4, containing layered alpha-Fe2O3 and carbon-coated g-C3N4, obtained through one simple repeatable solid-state synthesis strategy. The layered FeOOH and g-C3N4 are first synthesized working as the precursors. Under N-2 atmosphere and 580 degrees C, the dehydration of FeOOH happens, and it transfers into layered alpha-Fe2O3; the water vapor destroys the van der Waals force of g-C3N4 and induces the parts of edge carbonization. Under the synergistic effect of vapor and heating, the thin-layered Fe2O3/C-C3N4 heterojunction is obtained. Without cocatalyst addition, the obtained sample shows efficient visible-light-driven photocatalytic water oxidation performance, i.e., a 22.3 mu mol/h oxygen evolution rate under the LED lamp of lambda = 420 nm illumination, 3, 16, and 30 times higher than reference Fe2O3/C3N4, bare alpha-Fe2O3, and g-C3N4, respectively. The key parameters for the enhanced photocatalytic activity can be attributable to the carbon layer and the tight contact structure, which can work as the carrier (electrons from g-C3N4 and holes from alpha-Fe2O3) collection center and provide the small migration resistance. Moreover, the carbon shows a different migration rate for electrons and holes and then facilitates the separation of carriers to some extent. To our knowledge, no other papers on Fe2O3/C-C3N4-based photocatalytic water oxidation have been reported. This work can provide a new insight for synthesis of g-C3N4-based photocatalysts, and also help us understand the water oxidation reaction.
引用
收藏
页码:10436 / 10444
页数:17
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