Facile synthesis of mesoporous polymeric carbon nitride nanosheets anchored by Pt with ultralow loading for high-efficiency photocatalytic H2 evolution

被引:2
|
作者
Ye, Siyuan [1 ]
Su, Changsheng [2 ]
He, Lili [3 ]
Li, Mengli [1 ]
Yan, Zheng [1 ]
Wu, Jun [4 ]
Shen, Hongxia [1 ]
Cao, Xuebo [1 ]
机构
[1] Jiaxing Univ, Coll Biol Chem Sci & Engn, 118 Jiahang Rd, Jiaxing 314001, Peoples R China
[2] Univ Notre Dame, Dept Chem & Biomol Engn, Notre Dame, IN 46556 USA
[3] St Paul Univ Philippines, Grad Sch, St Paul, Philippines
[4] Jiaxing Nanhu Univ, Jiaxing 314001, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
CHEMICAL EXFOLIATION; G-C3N4; NANOSHEETS; GRAPHITIC C3N4; REDUCTION; CATALYSTS; GRAPHENE; FRAMEWORKS;
D O I
10.1039/d1dt03554a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The facile fabrication of low-cost photocatalysts with enhanced activity and high atomic utilization is becoming increasingly necessary for solar energy usage and/or conversion. In this work, a series of mesoporous carbon nitride nanosheets with an enlarged specific surface area was synthesized via an inorganic acid-assisted exfoliation method without any soft or hard templates. An ultralow loading of downsized noble metal Pt was anchored on these porous nanosheets, exhibiting enhanced photocatalytic activity. The formation of mesoporous nanosheets in carbon nitride was expected to boost the mass transfer and shorten the charge carrier transfer route during the photocatalytic reaction. The characterization of samples revealed that the enhanced conductivity and photocurrent of the carbon nitride nanosheets also contributed to the enhanced H-2 evolution activity. The maximum H-2 production rates of 172.92 mu mol h(-1) and 321 mu mol h(-1) were achieved over the nanosheets derived from melamine and urea under visible light irradiation, which are 10.92- and 2.22-fold that of the corresponding bulk carbon nitride, respectively. This exfoliation method was demonstrated to be an efficient and universal method for the preparation of carbon nitride nanosheets with a mesoporous structure and high atom utilization of the co-catalyst for H-2 evolution from water.
引用
收藏
页码:241 / 249
页数:9
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