铱-石墨烯:钠离子电池的新型二维电极材料

IF 8.9 2区 工程技术 Q1 ENERGY & FUELS
Manpreet Kaur, Nidhi Duhan, T.J. Dhilip Kumar
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引用次数: 0

摘要

利用密度泛函理论评估了铱-石墨烯单层在钠离子电池(SIB)中存储离子的有效性。该纳米层具有稳定的动态和热结构,以及可靠的机械性能。态密度和带状结构计算证实了单层的优异导电性。经评估,瑙离子电池的存储容量和能量密度分别为 1116.7 mAhg-1 和 2854.9 mWhg-1。此外,Na 离子的能垒(0.079 eV)较小,扩散速率(2.83 x 10-4 cm2s-1)较高,这表明它们在整个循环过程中很容易在纳米层表面迁移。此外,SIB 的开路电压为 0.15 V,符合商业设计要求。根据理论研究,铱石墨烯显然具有作为下一代 SIB 优异电极的巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Irida-graphene: A new two-dimensional electrode material for sodium-ion batteries

Irida-graphene: A new two-dimensional electrode material for sodium-ion batteries
The effectiveness of the irida-graphene monolayer for ion storage in sodium-ion batteries (SIBs) is evaluated using density functional theory. The nanolayer possesses a stable structure both dynamically and thermally, along with dependable mechanical properties. The density of states and band structure computations confirmed the excellent conductivity of the monolayer. The storage capacity and energy density have been assessed at 1116.7 mAhg−1, and 2854.9 mWhg−1 respectively, for Na-ion batteries. Additionally, the small energy barrier of 0.079 eV and heightened diffusion rate of 2.83 x 10−4 cm2s−1 for Na ions indicate their easy migration across the surface of the nanolayer during the complete cycle. Furthermore, the open circuit voltage obtained 0.15 V for SIBs, is consistent with the commercial design requirements. Based on the theoretical investigation, irida-graphene clearly demonstrates excellent potential as a superior electrode for next-generation SIBs.
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来源期刊
Journal of energy storage
Journal of energy storage Energy-Renewable Energy, Sustainability and the Environment
CiteScore
11.80
自引率
24.50%
发文量
2262
审稿时长
69 days
期刊介绍: Journal of energy storage focusses on all aspects of energy storage, in particular systems integration, electric grid integration, modelling and analysis, novel energy storage technologies, sizing and management strategies, business models for operation of storage systems and energy storage developments worldwide.
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