共 47 条
Pt nanoparticles embedded spine-like g-C3N4 nanostructures with superior photocatalytic activity for H2 generation and CO2 reduction
被引:45
作者:

Zhang, Xiao
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机构:
Curtin Univ, Fuels & Energy Technol Inst, Perth, WA 6845, Australia
Curtin Univ, Dept Chem Engn, Perth, WA 6845, Australia Curtin Univ, Fuels & Energy Technol Inst, Perth, WA 6845, Australia

Yang, Ping
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Univ Jinan, Sch Mat Sci & Engn, Jinan 250022, Peoples R China Curtin Univ, Fuels & Energy Technol Inst, Perth, WA 6845, Australia

Jiang, San Ping
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h-index: 0
机构:
Curtin Univ, Fuels & Energy Technol Inst, Perth, WA 6845, Australia
Curtin Univ, Dept Chem Engn, Perth, WA 6845, Australia Curtin Univ, Fuels & Energy Technol Inst, Perth, WA 6845, Australia
机构:
[1] Curtin Univ, Fuels & Energy Technol Inst, Perth, WA 6845, Australia
[2] Curtin Univ, Dept Chem Engn, Perth, WA 6845, Australia
[3] Univ Jinan, Sch Mat Sci & Engn, Jinan 250022, Peoples R China
基金:
澳大利亚研究理事会;
关键词:
g-C3N4;
spine-like cages;
photocatalysis;
CO2;
reduction;
H-2;
generation;
D O I:
10.1088/1361-6528/abdcee
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Conventional two-dimensional (2D) graphitic carbon nitride, 2D g-C3N4 with its layered structures and flat and smooth 2D surface possesses certain disadvantages that is affecting their photocatalytic performances. In this paper, new nanostructured spine-like three-dimensional (3D) g-C3N4 nanostructures are created for the first time via a new three-step synthesis method. In this method, self-assembly of layered precursors and H+ intercalation introduced by acid treatment play an important role for the unique nanostructure formation of 3D g-C3N4 nanostructures. The spine-like 3D g-C3N4 nanostructures show a superior photocatalytic performance for H-2 generation, achieving 4500 mu molg(-1)h(-1), 8.2 times higher than that on conventional 2D g-C3N4. Remarkably spine-like 3D g-C3N4 nanostructures demonstrate a clear photocatalytic activity toward CO2 reduction to CH4 (0.71 mu molg(-1)h(-1)) in contrast to the negligible photocatalytic performance of conventional 2D g-C3N4 for the reaction. Adding Pt clusters as co-catalysts substantially enhance the CH4 generation rate of the 3D g-C3N4 nanostructures by 4 times (2.7 mu molg(-1)h(-1)). Spine-like 3D g-C3N4 caged nanostructure leads to the significantly increased active sites and negatively shifted conduction band position in comparison with conventional 2D g-C3N4, favorable for the photocatalytic reduction reaction. This study demonstrates a new platform for the development of efficient photocatalysts based on nanostructured 3D g-C3N4 for H-2 generation and conversion of CO2 to useful fuels such as CH4.
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