TY - JOUR
T1 - Synthesis of Leaf-Vein-Like g-C3N4 with Tunable Band Structures and Charge Transfer Properties for Selective Photocatalytic H2O2 Evolution
AU - Feng, Chengyang
AU - Tang, Lin
AU - Deng, Yaocheng
AU - Wang, Jiajia
AU - Luo, Jun
AU - Liu, Yani
AU - Ouyang, Xilian
AU - Yang, Haoran
AU - Yu, Jiangfang
AU - Wang, Jingjing
N1 - Generated from Scopus record by KAUST IRTS on 2023-09-23
PY - 2020/9/1
Y1 - 2020/9/1
N2 - Photocatalytic H2O2 evolution through two-electron oxygen reduction has attracted wide attention as an environmentally friendly strategy compared with the traditional anthraquinone or electrocatalytic method. Herein, a biomimetic leaf-vein-like g-C3N4 as an efficient photocatalyst for H2O2 evolution is reported, which owns tenable band structure, optimized charge transfer, and selective two-electron O2 reduction. The mechanism for the regulation of band structure and charge transfer is well studied by combining experiments and theoretical calculations. The H2O2 yield of CN4 (287 µmol h−1) is about 3.3 times higher than that of pristine CN (87 µmol h−1), and the apparent quantum yield for H2O2 evolution over CN4 reaches 27.8% at 420 nm, which is much higher than that for many other current photocatalysts. This work not only provides a novel strategy for the design of photocatalyst with excellent H2O2 evolution efficiency, but also promotes deep understanding for the role of defect and doping sites on photocatalytic activity.
AB - Photocatalytic H2O2 evolution through two-electron oxygen reduction has attracted wide attention as an environmentally friendly strategy compared with the traditional anthraquinone or electrocatalytic method. Herein, a biomimetic leaf-vein-like g-C3N4 as an efficient photocatalyst for H2O2 evolution is reported, which owns tenable band structure, optimized charge transfer, and selective two-electron O2 reduction. The mechanism for the regulation of band structure and charge transfer is well studied by combining experiments and theoretical calculations. The H2O2 yield of CN4 (287 µmol h−1) is about 3.3 times higher than that of pristine CN (87 µmol h−1), and the apparent quantum yield for H2O2 evolution over CN4 reaches 27.8% at 420 nm, which is much higher than that for many other current photocatalysts. This work not only provides a novel strategy for the design of photocatalyst with excellent H2O2 evolution efficiency, but also promotes deep understanding for the role of defect and doping sites on photocatalytic activity.
UR - https://onlinelibrary.wiley.com/doi/10.1002/adfm.202001922
UR - http://www.scopus.com/inward/record.url?scp=85089312850&partnerID=8YFLogxK
U2 - 10.1002/adfm.202001922
DO - 10.1002/adfm.202001922
M3 - Article
SN - 1057-9257
VL - 30
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 39
ER -