Synergistic regulation of g-C3N4 band structure by phosphorus and sodium doping to enhance photocatalytic hydrogen peroxide production efficiency

被引:3
作者
Wang, Yuting [1 ]
Wang, Mengxiang [1 ]
Zhang, Xuya [1 ]
Pan, Xinru [1 ]
Cui, Yongpeng [1 ]
Liu, Daoqing [1 ]
Wang, Yajun [1 ]
Yao, Wenqing [2 ]
机构
[1] China Univ Petr, Coll New Energy & Mat, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
[2] Tsinghua Univ, Dept Chem, Beijing Key Lab Analyt Methods & Instrumentat, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalysis; H2O2; production; P; Na-codoping; Carbon nitride; GRAPHITIC CARBON NITRIDE; DOPED G-C3N4; DEGRADATION; OXIDATION; WATER; POLLUTANTS; NANOSHEETS; EVOLUTION;
D O I
10.1016/j.jcat.2024.115807
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
In addressing the industrial need for a simple, equipment-minimal, and non-toxic method of in-situ hydrogen peroxide (H2O2) production, this paper presents a cost-effective, environmentally friendly photocatalyst. Our design strategy focuses on the dual-element doping of phosphorus and sodium into graphitic carbon nitride (gC(3)N(4)), chosen to synergistically enhance photocatalytic performance. This approach yields a notable H2O2 production concentration of 3001.64 mu mol center dot g(-1) center dot L-1 within 100 min, using isopropanol as a sacrificial agent, which was 61-fold increase compared to bulk g-C3N4. Density Functional Theory (DFT) calculations were performed to elucidate the alterations in the band structure of the catalyst induced by dual-element doping, which consequentially engendered an asymmetric intrinsic electric field. Additionally, oxygen's transition state affinity due to phosphorus doping was also investigated to reveal the mechanisms of synergistic catalysis. This development contributes to meeting industrial demands for pollutant degradation via Fenton processes and presents a sustainable alternative to traditional H2O2 production methods.
引用
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页数:11
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