Constructing oxygen-doped g-C3N4 nanosheets with an enlarged conductive band edge for enhanced visible-light-driven hydrogen evolution

被引:77
作者
Sun, Shaodong [1 ]
Li, Jia [1 ]
Cui, Jie [1 ]
Gou, Xufeng [1 ]
Yang, Qing [1 ]
Liang, Shuhua [1 ]
Yang, Zhimao [2 ]
Zhang, Jianmin [3 ]
机构
[1] Xian Univ Technol, Sch Mat Sci & Engn, Shaanxi Prov Key Lab Elect Mat & Infiltrat Techno, Xian 710048, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, State Key Lab Mech Behav Mat, MOE Key Lab Nonequilibrium Synth & Modulat Conden, Ctr Suzhou Nano Sci & Technol,Sch Sci, Xian 710049, Shaanxi, Peoples R China
[3] Shaanxi Normal Univ, Coll Phys & Informat Technol, Xian 710062, Shaanxi, Peoples R China
基金
美国国家科学基金会; 国家高技术研究发展计划(863计划);
关键词
GRAPHITIC CARBON NITRIDE; PHOTOCATALYTIC NO OXIDATION; C3N4; PHOTOREACTIVITY; PERFORMANCE; ACTIVATION; CONVERSION; PRECURSOR; CLUSTERS;
D O I
10.1039/c8qi00242h
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Doping protocols have been widely investigated due to their effectiveness in tuning the energy band gaps of photocatalysts for improved photocatalytic activity. Here, we demonstrated the efficient and facile hydrogen peroxide-assisted hydrothermal reforming of melamine to synthesize a new oxygen (O)-doped precursor that was then transferred to O-doped g-C3N4 nanosheets, with an increased conductive band edge compared to bulk g-C3N4, via direct thermal polymerization. Owing to synergistic interaction between the 2D ultrathin nanosheet structure with large surface area and the enhanced conductive band edge caused by appropriate oxygen doping, the as-synthesized O-doped g-C3N4 nanosheets showed highly enhanced photocatalytic hydrogen evolution activity, about 10.7 times higher than pristine C3N4 under visible light irradiation, achieving an apparent quantum yield of 13.04% at 420 nm. Significantly, this precursor pre-doping strategy might provide a promising pathway for preparing heteroatom-doped g-C3N4.
引用
收藏
页码:1721 / 1727
页数:7
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