Nickel nanoparticles coated with graphene layers as efficient co-catalyst for photocatalytic hydrogen evolution

被引:82
作者
Fang, Li Jun [1 ,2 ]
Wang, Xue Lu [1 ]
Li, Yu Hang [1 ]
Liu, Peng Fei [1 ]
Wang, Yu Lei [1 ]
Zeng, Hui Dan [2 ]
Yang, Hua Gui [1 ]
机构
[1] East China Univ Sci & Technol, Sch Mat Sci & Engn, Dept Key Lab Ultrafine Mat, Minist Educ, 130 Meilong Rd, Shanghai 200237, Peoples R China
[2] East China Univ Sci & Technol, Dept Sch Mat Sci & Engn, 130 Meilong Rd, Shanghai 200237, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Photocatalysis; Co-catalyst; Hydrogen; Ni@C; Graphene layers; CARBON NITRIDE NANOSHEETS; HIGHLY EFFICIENT; CHARGE SEPARATION; WATER; G-C3N4; NANOCOMPOSITE; ABSORPTION; FRAMEWORKS; COMPOSITE; STORAGE;
D O I
10.1016/j.apcatb.2016.07.033
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
Metallic nickel nanoparticles well dispersed in graphitized carbon matrix (Ni@C) by pyrolysis of metal organic frameworks and leaching treatment of hydrochloric acid could greatly enhance the photocatalytic activity of g-C3N4 under visible light irradiation. For 2.0 wt% Ni@Cig-C3N4, the average hydrogen evolution rate is 2.15 mmol h(-1) g(-1), which is around 88 times higher than that of pure g-C3N4, and even better than that of platinum-loaded g-C3N4. The remarkably improved photocatalytic activities through loading Ni@C can be attributed to the cooperative work of Ni nanoparticles and graphene layers, which facilitate the separation of photo-generated carriers and suppress the recombination of the electron-hole pairs. In addition, the hollow onion-like structure can restrain the formation of Ni-hydrogen bonds which modulates desorption of hydrogen. Our studies may open up a promising strategy to design economical noble-metal-free co-catalysts for efficient solar energy conversion. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:578 / 584
页数:7
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