Binary heteroatom dopants enable carbon-based heterostructures for efficient photoelectrocatalytic H2O2 synthesis in a wide pH range

被引:4
作者
Zhu, Qiong [2 ,3 ]
Shi, Yuxin [2 ,3 ]
Tao, Ying [2 ,3 ]
Fu, Lanlan [2 ,3 ]
Zhang, Chi [2 ,3 ]
Shang, Huan [1 ,2 ,4 ]
Zhang, Dieqing [2 ,4 ]
Li, Guisheng [1 ,2 ,3 ,4 ]
机构
[1] Univ Shanghai Sci & Technol, Sch Mat & Chem, Shanghai 200093, Peoples R China
[2] Shanghai Normal Univ, Shanghai Frontiers Sci Ctr Biomimet Catalysis, Shanghai Key Lab Rare Earth Funct Mat, Educ Minist,Key Lab Resource Chem, Shanghai 200234, Peoples R China
[3] Shanghai Normal Univ, Sch Environm & Geog Sci, Shanghai 200234, Peoples R China
[4] Univ Shanghai Sci & Technol, Shanghai 200093, Peoples R China
关键词
Photoelectrocatalysis; Binary heteroatom doping; Carbon nitride; Wide pH environment; SELECTIVE OXYGEN REDUCTION; HYDROGEN-PEROXIDE; VISIBLE-LIGHT; NITRIDE; OXIDATION;
D O I
10.1016/j.cej.2024.149066
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Photoelectrocatalytic (PEC) H2O2 synthesis from water and oxygen is a prospective approach for the manufacture of solar fuels and value-added versatile chemicals. However, the development of the efficient photocathode remains a formidable challenge because of the inferior selectivity and yield of H2O2 derived from the multiple electron transfers affected by pH conditions. Herein, we report a metal -free carbon -based heterostructure material with N, S co -doping, where binary heteroatom-doped carbon sphere (N,S-CS) is loaded on carbon nitride (C3N4) polymer, achieving an efficient synthesis of H2O2 in a wide pH range. DFT calculations and experimental results uncover that S- and N -site can suppress the O -O cleavage and facilitate the *OOH formation through their subtle microenvironment, mediating the superior 2e- oxygen reduction selectivity to H2O2 in acids and alkalis, respectively. This work provides a cost-effective strategy for designing an efficient photocathode for H2O2 production in a wide pH environment.
引用
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页数:9
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