Enhanced photocatalytic activity of g-C3N4/MnO composites for hydrogen evolution under visible light

被引:23
作者
Mao, Na [1 ,2 ]
Gao, Xiaomin [1 ]
Zhang, Chong [1 ]
Shu, Chang [1 ]
Ma, Wenyan [1 ]
Wang, Feng [3 ,4 ]
Jiang, Jia-Xing [1 ]
机构
[1] Shaanxi Normal Univ, Sch Mat Sci & Engn, Shaanxi Key Lab Adv Energy Devices, Key Lab Macro Mol Sci Shaanxi Prov, Xian 710062, Shaanxi, Peoples R China
[2] Weinan Normal Univ, Coll Chem & Mat, Weinan 714099, Peoples R China
[3] Wuhan Inst Technol, Sch Chem Engn & Pharm, Key Lab Green Chem Proc, Minist Educ, Wuhan 430073, Hubei, Peoples R China
[4] Zhengzhou Univ, Sch Mat Sci & Engn, Zhengzhou 450001, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
GRAPHITIC CARBON NITRIDE; CONJUGATED MICROPOROUS POLYMERS; H-2; EVOLUTION; PERFORMANCE; NANOCOMPOSITES; FABRICATION; CONVERSION; NANOSHEETS; OXIDATION; EFFICIENT;
D O I
10.1039/c9dt02748c
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In this work, a range of g-C3N4/MnO composites were constructed using g-C3N4 nanosheets modified with MnO, and the photocatalytic performance for hydrogen evolution was evaluated by using these as-prepared g-C3N4/MnO composites as photocatalysts. It was found that the photocatalytic activity of the g-C3N4/MnO composites for hydrogen evolution is significantly enhanced compared with that of pristine g-C3N4 since the formation of heterojunctions between the MnO nanoparticles and g-C3N4 nanosheets through coordination covalent bonds promotes the charge carrier transfer and separation abilities of the composites. The loading mass of MnO also has a large influence on the photocatalytic activity of the g-C3N4/MnO composites. Particularly, the g-C3N4/MnO-5 composite with 5 wt% MnO shows superior photocatalytic activity with a hydrogen evolution rate of 559 mu mol h(-1) g(-1) under visible light, which is about 9 times that of the bulky g-C3N4. These findings demonstrate that the combination of metal oxides and g-C3N4 to construct composite photocatalysts is an effective method to improve the photocatalytic performance.
引用
收藏
页码:14864 / 14872
页数:9
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