The interfacial structure of super-concentration LiNO3 aqueous electrolyte studied by second harmonic generation

被引:3
作者
Bai, Ruipeng [1 ,2 ]
Lin, Yuan [2 ,3 ]
Guo, Yuan [1 ,2 ]
Zhang, Zhen [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Chem, CAS Res, Educ Ctr Excellence Mol Sci,Beijing Natl Lab Mol S, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Inst Chem, Chinese Acad Sci, CAS Res, Educ Ctr Excellence Mol Sci,Beijing Natl Lab Mol S, Beijing 100190, Peoples R China
关键词
MOLECULAR-DYNAMICS SIMULATIONS; 2ND HARMONIC-GENERATION; IN-SALT ELECTROLYTE; AIR/WATER INTERFACE; HYDROGEN EVOLUTION; SURFACE; POLYCRYSTALLINE; OXIDATION; ORDER; IONS;
D O I
10.1063/5.0093428
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The interfacial structure of a super-concentration LiNO3 aqueous electrolyte was studied using non-resonant second harmonic generation (SHG) and heterodyne-detected SHG spectra. First, we investigated the electric double layer structure at the air/LiNO3 interface. As the concentration of LiNO3 increased, the SHG intensity first increased and then remained unchanged, while the SHG phase changed by about 5 & DEG;. These results reveal that there was only a small amount of NO3- at the interface. The increase of the SHG intensity resulted from the thickening of the interfacial water molecular layer. In addition, we studied the broadening mechanism of the electrochemical stability window (ESW) for the super-concentrated LiNO3 aqueous electrolyte. During cyclic voltammetry scanning, the potential-dependent SHG curves of the Pt/LiNO3 interface verify that at the cathodic end of the ESW, as the concentration of LiNO3 increased, the orientation angle theta of Pt-H changed less and the number density N-s of Pt-H gradually decreased, which indicates the decrease of the number of adsorbed H atoms on the Pt electrode surface. Therefore, the decrease of the number of free water molecules on the Pt electrode surface resulted in an expanded ESW. Published under an exclusive license by AIP Publishing.
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页数:9
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