Suppr超能文献

使用基于氢化物的电解质和硫化铜电极的长循环寿命钙金属电池。

Calcium Metal Batteries with Long Cycle Life Using a Hydride-Based Electrolyte and Copper Sulfide Electrode.

作者信息

Kisu Kazuaki, Mohtadi Rana, Orimo Shin-Ichi

机构信息

Institute for Materials Research (IMR), Tohoku University, Katahira 2-1-1, Aoba-ku, Sendai, 980-8577, Japan.

Materials Research Department, Toyota Research Institute of North America, Ann Arbor, MI, 48105, USA.

出版信息

Adv Sci (Weinh). 2023 Aug;10(22):e2301178. doi: 10.1002/advs.202301178. Epub 2023 May 19.

Abstract

As potential alternatives to Li-ion batteries, rechargeable Ca metal batteries offer advantageous features such as high energy density, cost-effectiveness, and natural elemental abundance. However, challenges, such as Ca metal passivation by electrolytes and a lack of cathode materials with efficient Ca storage capabilities, impede the development of practical Ca metal batteries. To overcome these limitations, the applicability of a CuS cathode in Ca metal batteries and its electrochemical properties are verified herein. Ex situ spectroscopy and electron microscopy results show that a CuS cathode comprising nanoparticles that are well dispersed in a high-surface-area carbon matrix can serve as an effective cathode for Ca storage via the conversion reaction. This optimally functioning cathode is coupled with a tailored, weakly coordinating monocarborane-anion electrolyte, namely, Ca(CB H ) in 1,2-dimethoxyethane/tetrahydrofuran, which enables reversible Ca plating/stripping at room temperature. The combination affords a Ca metal battery with a long cycle life of over 500 cycles and capacity retention of 92% based on the capacity of the 10th cycle. This study confirms the feasibility of the long-term operation of Ca metal anodes and can expedite the development of Ca metal batteries.

摘要

作为锂离子电池的潜在替代品,可充电钙金属电池具有高能量密度、成本效益和天然元素丰度高等优势特性。然而,诸如电解质导致钙金属钝化以及缺乏具有高效钙存储能力的阴极材料等挑战,阻碍了实用钙金属电池的发展。为克服这些限制,本文验证了硫化铜阴极在钙金属电池中的适用性及其电化学性能。非原位光谱和电子显微镜结果表明,由纳米颗粒组成且均匀分散在高比表面积碳基质中的硫化铜阴极,可通过转化反应作为有效的钙存储阴极。这种功能最佳的阴极与一种经过定制的、弱配位的单碳硼烷阴离子电解质(即1,2 - 二甲氧基乙烷/四氢呋喃中的Ca(CB₁₁H₁₂))相结合,能够在室温下实现可逆的钙电镀/脱镀。这种组合提供了一种钙金属电池,其循环寿命超过500次,基于第10次循环的容量,容量保持率为92%。这项研究证实了钙金属阳极长期运行的可行性,并可加快钙金属电池的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0846/10401151/09e933345a5d/ADVS-10-2301178-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验