Amino modulation on the surface of graphitic carbon nitride for enhanced photocatalytic hydrogen production

被引:39
作者
Yang, Heng [1 ]
Zhang, Awang [1 ]
Ding, Jianjun [2 ,3 ]
Hu, Rui [2 ]
Gong, Yi [2 ]
Li, Xiangyang [2 ]
Chen, Lin [2 ,3 ]
Chen, Peng [1 ]
Tian, Xingyou [2 ]
机构
[1] Anhui Univ, Sch Chem & Chem Engn, Hefei 230601, Peoples R China
[2] Chinese Acad Sci, Inst Solid State Phys, Hefei Inst Phys Sci, Key Lab Photovolta & Energy Conservat Mat, Hefei 230031, Anhui, Peoples R China
[3] Anhui Inst Innovat Ind Technol, Hefei 230088, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalytic hydrogen production; Carbon nitride; Urea; Amino groups; Solvothermal; G-C3N4; NANOSHEETS; BORON-NITRIDE; LIGHT; NITROGEN; WATER; DEGRADATION; OXIDATION;
D O I
10.1016/j.carbon.2024.118841
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
Bulk graphitic carbon nitride suffers from the disadvantages of a small specific surface area, high recombination of photogenerated charge carriers, and low surface catalytic activity, which greatly limits its application in catalytic reactions. In this study, amino groups were incorporated into the structure of bulk carbon nitride by solvothermal treatment facilitated by an optimal content of urea. The experimental data suggested that the introduced amino groups modified the morphology and structure of bulk carbon nitride, and improved the charge separation. More importantly, the enriched amino groups promoted the formation of nitrogen -rich carbon nitride, which was conducive to the deposition and reduction of ultrafine Pt nanoparticles. The resulting Pt/gC3N4 composite exhibited excellent visible -light -driven activity for hydrogen evolution. A high rate of 410.51 mu mol h-1 with an apparent quantum efficiency of 17 % was achieved, which is 85.5 times higher than that of bulk carbon nitride. The effective approach developed in this work could provide new insights into the design of bulk carbon nitride with enhanced performance.
引用
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页数:10
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