Interface Preconstruction Enables Robust Passivation of the Ah-Level Aqueous Li-ion Batteries

化学 钝化 水溶液 接口(物质) 离子 水介质 化学工程 物理化学 有机化学 图层(电子) 吉布斯等温线 工程类
作者
Anxing Zhou,Jinkai Zhang,Ming Chen,Xinyan Li,Shuwei Li,Jintao Ma,Tianshi Lv,Xiangzhen Zhu,Guang Feng,Liumin Suo
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:147 (14): 11811-11820 被引量:31
标识
DOI:10.1021/jacs.4c15852
摘要

The solid electrolyte interphase (SEI) offers effective passivation on the anode for aqueous lithium-ion batteries (ALIBs). Conventional passivation in ALIBs mainly relies on the LiF-contained SEI originating from anion reduction in the electrolyte. However, such SEI formation is a competitive reaction negatively impacted by the parasitic hydrogen evolution reaction (HER), resulting in high Li + irreversible consumption and imperfect bare flaws. To address this issue, we propose preconstructing an artificial interphase by introducing a multifunctional interface additive CsF to build superior passivation on the anode in ALIBs. CsF first undergoes a displacement reaction with LiTFSI from the fresh electrolyte to form the LiF in situ on the interface of the anode before the cycles, avoiding the extra Li + irreversible consumption. Meanwhile, we uncover that the dissolving Cs + in the electrolyte can destroy the hydrogen bond network of the water to lower water activity on the anode interface and strongly interact with TFSI – to form the cation–anion complex, facilitating the anion proximity to the anode interface. The anion reduction based on the artificial interphase can finally help achieve the robust SEI in ALIBs. Such passivation stabilizes the aqueous electrolyte, significantly suppressing the side reaction of the HER that allows ALIBs to obtain a superior long life above 2000 cycles. The ampere-hour-level (Ah-level) pouch cell achieves an energy density of 57 Wh/kg and 176 Wh/L with high energy efficiency (∼94%).
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
温柔的斩发布了新的文献求助10
1秒前
1秒前
1秒前
hayley完成签到,获得积分10
1秒前
科研通AI6.3应助一只眠羊采纳,获得10
1秒前
1秒前
李健的小迷弟应助Lc20020320采纳,获得10
1秒前
orixero应助SamYang采纳,获得10
1秒前
2秒前
2秒前
新煜完成签到,获得积分10
3秒前
华仔应助愚者先生采纳,获得10
3秒前
4秒前
4秒前
真王一博发布了新的文献求助30
5秒前
汉堡包应助穆雨采纳,获得10
6秒前
6秒前
pblack发布了新的文献求助10
6秒前
7秒前
7秒前
8秒前
李健的小迷弟应助孙大伟采纳,获得10
8秒前
9秒前
9秒前
99411发布了新的文献求助10
10秒前
awa606发布了新的文献求助10
10秒前
11秒前
StudentYu发布了新的文献求助10
11秒前
xushanqi发布了新的文献求助10
11秒前
123发布了新的文献求助10
11秒前
Angela发布了新的文献求助10
11秒前
12秒前
12秒前
yhzbmw发布了新的文献求助10
12秒前
13秒前
14秒前
jsinm-thyroid完成签到 ,获得积分10
14秒前
抽抽完成签到,获得积分10
14秒前
科研通AI6.4应助xiaoluo采纳,获得10
14秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
48V Low-voltage Power Distribution Network (PDN) Architecture Industry Report, 2024 800
ズームレンズの光学設計に関する研究 800
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 700
Matrix Methods in Data Mining and Pattern Recognition Second Edition 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7294839
求助须知:如何正确求助?哪些是违规求助? 8913385
关于积分的说明 18872341
捐赠科研通 6961264
什么是DOI,文献DOI怎么找? 3210127
关于科研通互助平台的介绍 2379484
邀请新用户注册赠送积分活动 2186400