Moment-Tensor-Based Constant-Potential Modeling of Electrical Double Layers
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| Main Authors: | , , , , , , , , , |
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| Format: | Preprint |
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2024
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| _version_ | 1866910311429177344 |
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| author | Wang, Zhenxiang Chen, Ming Wu, Jiedu Ji, Xiangyu Zeng, Liang Peng, Jiaxing Yan, Jiawei Kornyshev, Alexei A. Mao, Bingwei Feng, Guang |
| author_facet | Wang, Zhenxiang Chen, Ming Wu, Jiedu Ji, Xiangyu Zeng, Liang Peng, Jiaxing Yan, Jiawei Kornyshev, Alexei A. Mao, Bingwei Feng, Guang |
| contents | Constant-potential molecular dynamics (MD) simulations are indispensable for understanding the capacitance, structure, and dynamics of electrical double layers (EDLs) at the atomistic level. However, the classical constant-potential method, relying on the so-called 'floating charges' to keep electrode equipotential, overlooks quantum effects on the electrode and always underestimates EDL capacitance for typical electrochemical systems featuring metal electrodes in aqueous electrolytes. Here, we propose a universal theoretical framework as moment-tensor-based constant potential method (mCPM) to capture electronic structure variations with electric moments. For EDLs at Au(111) electrodes, mCPM-based MD reveals bell-shaped capacitance curves in magnitude and shape both quantitatively consistent with experiments. It further unveils the potential-dependent local electric fields, agreeing with experimental observations of redshift vibration of interfacial water under negative polarization and predicting a blueshift under positive polarization, and identifies geometry dependence of two time scales during EDL formation. |
| format | Preprint |
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arxiv_https___arxiv_org_abs_2401_17145 |
| institution | arXiv |
| publishDate | 2024 |
| record_format | arxiv |
| spellingShingle | Moment-Tensor-Based Constant-Potential Modeling of Electrical Double Layers Wang, Zhenxiang Chen, Ming Wu, Jiedu Ji, Xiangyu Zeng, Liang Peng, Jiaxing Yan, Jiawei Kornyshev, Alexei A. Mao, Bingwei Feng, Guang Chemical Physics Mesoscale and Nanoscale Physics Constant-potential molecular dynamics (MD) simulations are indispensable for understanding the capacitance, structure, and dynamics of electrical double layers (EDLs) at the atomistic level. However, the classical constant-potential method, relying on the so-called 'floating charges' to keep electrode equipotential, overlooks quantum effects on the electrode and always underestimates EDL capacitance for typical electrochemical systems featuring metal electrodes in aqueous electrolytes. Here, we propose a universal theoretical framework as moment-tensor-based constant potential method (mCPM) to capture electronic structure variations with electric moments. For EDLs at Au(111) electrodes, mCPM-based MD reveals bell-shaped capacitance curves in magnitude and shape both quantitatively consistent with experiments. It further unveils the potential-dependent local electric fields, agreeing with experimental observations of redshift vibration of interfacial water under negative polarization and predicting a blueshift under positive polarization, and identifies geometry dependence of two time scales during EDL formation. |
| title | Moment-Tensor-Based Constant-Potential Modeling of Electrical Double Layers |
| topic | Chemical Physics Mesoscale and Nanoscale Physics |
| url | https://arxiv.org/abs/2401.17145 |