TY - JOUR
T1 - Carbon dots modified metallated graphdiyne with enhanced electron transfer and O2 adsorption capacity for efficient H2O2 photoproduction
AU - Si, Honglin
AU - Zhu, Mude
AU - Li, Zenan
AU - Wang, Jiaxuan
AU - Li, Jiacheng
AU - Xu, Linli
AU - Huang, Hui
AU - Liu, Yang
AU - Wong, Wai Yeung
AU - Kang, Zhenhui
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/7/15
Y1 - 2025/7/15
N2 - Hydrogen peroxide (H2O2), a promising liquid fuel and environmentally friendly oxidant, can be produced efficiently through photocatalysis, one of the most green and effective methods. Herein, we demonstrate the use of carbon dots (CDs) modified nickel (II) graphdiyne (CDs/Ni-GDY) as a photocatalyst to achieve efficient production of H2O2 under visible light irradiation without sacrificial agents. The optimum CDs/Ni-GDY photocatalyst exhibits high efficiency for photocatalytic H2O2 production, with a production rate of 1755.18 μmol·h−1·g−1 under visible-light irradiation (λ ≥ 420 nm) in pure water, through simultaneously occurring two-electron oxygen reduction reaction and four-electron water oxidation reaction. In this system, the nickel atoms serve as the active sites, while CDs enhance light absorption and O2 adsorption and increase the interfacial electron transfer process. This work elucidates the structure–activity relationship between the active sites and the promoter of CDs, achieving an improvement in their efficient catalytic performance and providing a new perspective for photocatalytic material design.
AB - Hydrogen peroxide (H2O2), a promising liquid fuel and environmentally friendly oxidant, can be produced efficiently through photocatalysis, one of the most green and effective methods. Herein, we demonstrate the use of carbon dots (CDs) modified nickel (II) graphdiyne (CDs/Ni-GDY) as a photocatalyst to achieve efficient production of H2O2 under visible light irradiation without sacrificial agents. The optimum CDs/Ni-GDY photocatalyst exhibits high efficiency for photocatalytic H2O2 production, with a production rate of 1755.18 μmol·h−1·g−1 under visible-light irradiation (λ ≥ 420 nm) in pure water, through simultaneously occurring two-electron oxygen reduction reaction and four-electron water oxidation reaction. In this system, the nickel atoms serve as the active sites, while CDs enhance light absorption and O2 adsorption and increase the interfacial electron transfer process. This work elucidates the structure–activity relationship between the active sites and the promoter of CDs, achieving an improvement in their efficient catalytic performance and providing a new perspective for photocatalytic material design.
KW - Carbon dots
KW - HO photoproduction
KW - Interfacial electron transfer
KW - Metallated graphdiyne
KW - O adsorption
UR - http://www.scopus.com/inward/record.url?scp=105005955189&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2025.163963
DO - 10.1016/j.cej.2025.163963
M3 - Journal article
AN - SCOPUS:105005955189
SN - 1385-8947
VL - 516
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 163963
ER -