Ultrahigh Capacity from Complexation‐Enabled Aluminum‐Ion Batteries with C70 as the Cathode

Author:

Huang Chenli1,Yang Ying2,Li Mengyang3,Qi Xiaoqun1,Pan Changwang1,Guo Kun1,Bao Lipiao1,Lu Xing14ORCID

Affiliation:

1. State Key Laboratory of Materials Processing and Die & Mould Technology School of Materials Science and Engineering Huazhong University of Science and Technology 1037, Luoyu Road Wuhan 430074 P. R. China

2. Institute of New Energy for Vehicles School of Materials Science and Engineering Tongji University Shanghai 201804 P. R. China

3. School of Physics Xidian University Xi'an 710071 P. R. China

4. School of Chemistry and Chemical Engineering Hainan University No. 58, Renmin Avenue Haikou 570228 P.R.China

Abstract

AbstractRestricted by the available energy storage modes, currently rechargeable aluminum‐ion batteries (RABs) can only provide a very limited experimental capacity, regardless of the very high gravimetric capacity of Al (2980 mAh g−1). Here, a novel complexation mechanism is reported for energy storage in RABs by utilizing 0D fullerene C70 as the cathode. This mechanism enables remarkable discharge voltage (≈1.65 V) and especially a record‐high reversible specific capacity (750 mAh g−1 at 200 mA g−1) of RABs. By means of in situ Raman monitoring, mass spectrometry, and density functional theory (DFT) calculations, it is found that this elevated capacity is attributed to the direct complexation of one C70 molecule with 23.5 (super)halogen moieties (superhalogen AlCl4 and/or halogen Cl) in average, forming (super)halogenated C70·(AlCl4)mCln‐m complexes. Upon discharging, decomplexation of C70·(AlCl4)mCln‐m releases AlCl4/Cl ions while preserving the intact fullerene cage. This work provides a new route to realize high‐capacity and long‐life batteries following the complexation mechanism.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hubei Province

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials,General Materials Science

Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3