Roy Tribeni, Goel Saurav, Costa Luciano T, Titirici Maria-Magdalena, Offer Gregory J, Marinescu Monica, Wang Huizhi
Department of Mechanical Engineering, Imperial College London, London SW7 2AZ, United Kingdom.
Department of Mechanical Engineering, Birla Institute of Technology and Science Pilani, Pilani Campus, Pilani 333031, India.
J Chem Phys. 2023 Dec 28;159(24). doi: 10.1063/5.0166976.
Electrochemical Double Layer Capacitors (EDLCs) with ionic liquid electrolytes outperform conventional ones using aqueous and organic electrolytes in energy density and safety. However, understanding the electrochemical behaviors of ionic liquid electrolytes under compressive/tensile strain is essential for the design of flexible EDLCs as well as normal EDLCs, which are subject to external forces during assembly. Despite many experimental studies, the compression/stretching effects on the performance of ionic liquid EDLCs remain inconclusive and controversial. In addition, there is hardly any evidence of prior theoretical work done in this area, which makes the literature on this topic scarce. Herein, for the first time, we developed an atomistic model to study the processes underlying the electrochemical behaviors of ionic liquids in an EDLC under strain. Constant potential non-equilibrium molecular dynamics simulations are conducted for EMIM BF4 placed between two graphene walls as electrodes. Compared to zero strain, low compression of the EDLC resulted in compromised performance as the electrode charge density dropped by 29%, and the performance reduction deteriorated significantly with a further increase in compression. In contrast, stretching is found to enhance the performance by increasing the charge storage in the electrodes by 7%. The performance changes with compression and stretching are due to changes in the double-layer structure. In addition, an increase in the value of the applied potential during the application of strain leads to capacity retention with compression revealed by the newly performed simulations.
具有离子液体电解质的电化学双层电容器(EDLCs)在能量密度和安全性方面优于使用水性和有机电解质的传统电容器。然而,了解离子液体电解质在压缩/拉伸应变下的电化学行为对于柔性EDLC以及普通EDLC的设计至关重要,因为它们在组装过程中会受到外力作用。尽管有许多实验研究,但离子液体EDLC性能的压缩/拉伸效应仍未定论且存在争议。此外,几乎没有证据表明该领域之前有过理论研究,这使得关于该主题的文献稀缺。在此,我们首次开发了一个原子模型来研究应变下EDLC中离子液体电化学行为的潜在过程。对置于两个石墨烯壁作为电极之间的EMIM BF4进行了恒电位非平衡分子动力学模拟。与零应变相比,EDLC的低压缩导致性能下降,因为电极电荷密度下降了29%,并且随着压缩的进一步增加,性能下降显著恶化。相反,发现拉伸通过使电极中的电荷存储增加7%来提高性能。性能随压缩和拉伸的变化是由于双层结构的变化。此外,新进行的模拟表明,在施加应变期间施加电位值的增加会导致压缩时容量保持。