期刊
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 24, 期 29, 页码 17623-17631出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2cp02387c
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资金
- National Key R&D Program of China [2017YFA0303600]
- National Natural Science Foundation of China [11974253]
- Science Specialty Program of Sichuan University [2020SCUNL210]
Understanding the microscopic mechanisms of electronic excitation in water clusters is crucial for solar energy applications. This study investigates the photodissociation process of water clusters and photoinduced charge transfer. The research reveals the difficulty of dissociating the plane tetramer (H2O)(4) under laser irradiation and identifies the Cu-6 chain as the most cost-effective plasmon catalyst for water splitting.
Understanding the microscopic mechanisms of electronic excitation in water clusters is a very important and challenging problem in a series of solar energy applications, such as solar water evaporation, photolysis, etc. Here we employ real time-time-dependent density functional theory (RT-TDDFT) and Ehrenfest dynamics to investigate the photodissociation dynamic process of (H2O)(N=1-10) clusters and photoinduced charge transfer in them. The research presented here confirms that the plane tetramer, (H2O)(4), is the most difficult one to be dissociated under laser irradiation in the ten clusters for its high (S-4) symmetry; the overall order of the ease of decomposition is as follows: (H2O)(6-p) > (H2O)(8) > (H2O)(6-c) > (H2O)(7) > (H2O)(10) > (H2O)(1) > (H2O)(3) > (H2O)(2) > (H2O)(9) > (H2O)(5) > (H2O)(4). Plasmon catalyst-induced water splitting is a promising and feasible way to efficiently convert solar to chemical energy via reducing the laser amplitude threshold significantly; and among the Ag-6, Au-6, Cu-6, Al-6 chains and several Cu-6 clusters with O-h symmetry, the Cu-6 chain seems to be the most cost-effective one. This article aims at unraveling the fundamental mechanisms and providing valuable physical insights into the behavior of water splitting to pave the way for the theoretical and experimental design of the photolysis process.
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