TY - JOUR
T1 - Enhanced photocatalytic H2 evolution and anti-photocorrosion of sulfide photocatalyst by improving surface reaction
T2 - A review
AU - Xie, Xiang
AU - Ge, Peng
AU - Xue, Ruiting
AU - Lv, Hongfei
AU - Xue, Wenhua
AU - Liu, Enzhou
N1 - This work was supported by the National Natural Science Foundation of China (11974276 and 22078261), the Natural Science Basic Research Program of Shaanxi (No. 2020JM-422), Key Science and Technology Innovation Team of Shaanxi Province (2022TD-33).
Publisher Copyright:
© 2023 Hydrogen Energy Publications LLC
PY - 2023/7/26
Y1 - 2023/7/26
N2 - The photocatalytic evolution of hydrogen is a potential method for acquiring green hydrogen from nature. Unfortunately, this technique has limitations owing to a lack of knowledge of the reaction processes, despite the fact that in recent decades significant scientific adva`nces have been achieved regarding catalyst design and efficiency. Often neglected in favor of heterojunction engineering or band engineering, the chemical environment of catalysts has long been the subject of research. This article offers insight into the photocatalytic H2 evolution from the surface reaction. It was underlined that reactant adsorption and surface charge extraction have a significant impact on the enhancement of photocatalytic H2 evolution and anti-photocorrosion properties of the catalyst, which are also strongly connected to the catalyst's chemical environment. Specifically, this study emphasizes the significance of surface/interface condition, type and concentration of electrolytes, reaction solvents, and temperature, etc., during photocatalytic H2 development, all of which play a crucial role in surface charge extraction of catalyst. In addition, the surface kinetics, adsorption and diffusion of reactants, the selectivity of intermediates, etc., are emphasized for designing highly efficient reaction systems in future applications of photocatalysis. It was shown that more comprehensive methodologies are urgently required for constructing efficient and stable photocatalytic reaction systems by merging catalyst design and reaction environment manipulation. This review may provide fresh ideas for the use of photocatalytic solar energy conversion.
AB - The photocatalytic evolution of hydrogen is a potential method for acquiring green hydrogen from nature. Unfortunately, this technique has limitations owing to a lack of knowledge of the reaction processes, despite the fact that in recent decades significant scientific adva`nces have been achieved regarding catalyst design and efficiency. Often neglected in favor of heterojunction engineering or band engineering, the chemical environment of catalysts has long been the subject of research. This article offers insight into the photocatalytic H2 evolution from the surface reaction. It was underlined that reactant adsorption and surface charge extraction have a significant impact on the enhancement of photocatalytic H2 evolution and anti-photocorrosion properties of the catalyst, which are also strongly connected to the catalyst's chemical environment. Specifically, this study emphasizes the significance of surface/interface condition, type and concentration of electrolytes, reaction solvents, and temperature, etc., during photocatalytic H2 development, all of which play a crucial role in surface charge extraction of catalyst. In addition, the surface kinetics, adsorption and diffusion of reactants, the selectivity of intermediates, etc., are emphasized for designing highly efficient reaction systems in future applications of photocatalysis. It was shown that more comprehensive methodologies are urgently required for constructing efficient and stable photocatalytic reaction systems by merging catalyst design and reaction environment manipulation. This review may provide fresh ideas for the use of photocatalytic solar energy conversion.
KW - Kinetics
KW - Photocatalyst
KW - Photocorrosion
KW - Surface reaction
UR - http://www.scopus.com/inward/record.url?scp=85151548214&partnerID=8YFLogxK
U2 - 10.1016/j.ijhydene.2023.03.193
DO - 10.1016/j.ijhydene.2023.03.193
M3 - Journal article
AN - SCOPUS:85151548214
SN - 0360-3199
VL - 48
SP - 24264
EP - 24284
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
IS - 63
ER -