中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
AAl2Se4/XSe2 (A= Cd, Hg; X= Ti, Zr, Hf) heterostructures for photocatalytic overall water splitting with Z-scheme: Insight from nonadiabatic dynamics simulation and Gibbs free energy

文献类型:期刊论文

作者Sun, Hao1; Yang, Chuan-Lu1,2; Li, Xiaohu2,3; Liu, Yuliang1; Zhao, Wenkai1
刊名INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
出版日期2024-11-26
卷号92页码:124-135
关键词Solar-to-hydrogen Photocatalytic Direct Z -scheme Gibbs free energy Nonadiabatic dynamics
ISSN号0360-3199
DOI10.1016/j.ijhydene.2024.10.224
产权排序2
英文摘要To identify optimal monolayers for photocatalytic water splitting, we screened the lowest-energy structures of CdAl2Se4 and HgAl2Se4 monolayers with the P-3m1 space group from two pools of 675 allotropes. Unfortunately, the valence band maximum of these newfound monolayers did not meet the potential requirement for the oxygen evolution reaction. This led us to explore AAl2Se4/XSe2 (A = Cd, Hg; X = Ti, Zr, Hf) heterostructures. Among these, we constructed several Z-schemes for overall water splitting, achieving a maximum solar-to-hydrogen efficiency (eta ' STH) of 38.28%. Non-adiabatic molecular dynamics simulations revealed that the electron transfer for hydrogen evolution reaction (HER) and hole transfer for oxygen evolution reaction (OER) in HgAl2Se4/ZrSe2 and CdAl2Se4/HfSe2 heterostructures are slower compared to the other five heterostructures, suggesting that their reduction and oxidation activities are well-protected. Notably, CdAl2Se4/TiSe2 demonstrated the shortest electron-hole recombination time, indicating superior photocatalytic efficiency for the Z-scheme. Additionally, the Gibbs free energies for HERs and OERs in CdAl2Se4/TiSe2, CdAl2Se4/ZrSe2, and CdAl2Se4/HfSe2 are lower than the energies provided by the overpotential, implying spontaneous HER and OER processes. Therefore, AAl2Se4/XSe2 (A = Cd, Hg; X = Ti, Zr, Hf) heterostructures, particularly CdAl2Se4/TiSe2, show great promise as candidates for efficient photocatalytic water splitting to produce hydrogen.
WOS关键词CHARGE SEPARATION ; HETEROJUNCTION ; TRANSITION ; EVOLUTION
资助项目National Natural Science Foundation of China[12374232]
WOS研究方向Chemistry ; Electrochemistry ; Energy & Fuels
语种英语
WOS记录号WOS:001343785200001
出版者PERGAMON-ELSEVIER SCIENCE LTD
资助机构National Natural Science Foundation of China
源URL[http://ir.xao.ac.cn/handle/45760611-7/7089]  
专题天体化学研究团组
通讯作者Yang, Chuan-Lu
作者单位1.Ludong Univ, Sch Phys & Optoelect Engn, Yantai 264025, Peoples R China
2.Chinese Acad Sci, Xinjiang Astron Observ, Urumqi 830011, Peoples R China
3.Chinese Acad Sci, Key Lab Radio Astron, Urumqi 830011, Peoples R China
推荐引用方式
GB/T 7714
Sun, Hao,Yang, Chuan-Lu,Li, Xiaohu,et al. AAl2Se4/XSe2 (A= Cd, Hg; X= Ti, Zr, Hf) heterostructures for photocatalytic overall water splitting with Z-scheme: Insight from nonadiabatic dynamics simulation and Gibbs free energy[J]. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY,2024,92:124-135.
APA Sun, Hao,Yang, Chuan-Lu,Li, Xiaohu,Liu, Yuliang,&Zhao, Wenkai.(2024).AAl2Se4/XSe2 (A= Cd, Hg; X= Ti, Zr, Hf) heterostructures for photocatalytic overall water splitting with Z-scheme: Insight from nonadiabatic dynamics simulation and Gibbs free energy.INTERNATIONAL JOURNAL OF HYDROGEN ENERGY,92,124-135.
MLA Sun, Hao,et al."AAl2Se4/XSe2 (A= Cd, Hg; X= Ti, Zr, Hf) heterostructures for photocatalytic overall water splitting with Z-scheme: Insight from nonadiabatic dynamics simulation and Gibbs free energy".INTERNATIONAL JOURNAL OF HYDROGEN ENERGY 92(2024):124-135.

入库方式: OAI收割

来源:新疆天文台

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