Engineering defects in graphitic carbon nitride photocatalysts

被引:12
作者
Li, Qi [1 ]
Zhao, Siyu [1 ,2 ]
Jiang, Baojiang [2 ]
Jaroniec, Mietek [3 ]
Zhang, Liping [1 ]
机构
[1] Shenzhen MSU BIT Univ, Fac Mat Sci, Shenzhen 518172, Peoples R China
[2] Heilongjiang Univ, Key Lab Funct Inorgan Mat Chem, Minist Educ Peoples Republ China, Harbin 150080, Peoples R China
[3] Kent State Univ, Dept Chem & Biochem, Kent, OH 44242 USA
基金
中国国家自然科学基金;
关键词
Graphitic carbon nitride; Photocatalysis; Defect engineering; Doping; Vacancies; Functional groups; Struc- tural disorder; HYDROGEN EVOLUTION; DOPED G-C3N4; POLYMER PHOTOCATALYST; HIGHLY EFFICIENT; H2O2; PRODUCTION; WATER; NANOSHEETS; SEMICONDUCTORS; PERFORMANCE; ACTIVATION;
D O I
10.1016/j.mattod.2024.09.019
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Graphitic carbon nitride (g-C3N4) has emerged as a promising metal-free photocatalyst. However, it continues to face significant challenges in achieving competitive activities both in laboratories and practical applications. Defect engineering is a versatile strategy to refine the intrinsic properties of semiconductor photocatalysts, modulating their electronic structure, charge dynamics and active surface sites. Given rapid advancements in this field, there is an urgent need to overview the progress in engineering of defects in g-C3N4, which is essential for a deeper understanding of the activity of this photocatalyst. This review focuses on the synthesis, characterization, and physiochemical properties of defect-engineered g-C3N4, including g-C3N4 with substitutional dopants, interstitial dopants, vacancies, functional groups and/or structural disorder. It also explores various applications of g-C3N4 materials with introduced defects for photocatalytic H2 evolution, CO2 reduction, N2 fixation and organic transformations, along with the mechanisms underlying their performance at the molecular level. Finally, this review article presents a perspective on the design, synthesis and properties of defect- modified g-C3N4 photocatalysts.
引用
收藏
页码:886 / 904
页数:19
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