材料科学
阳极
锂(药物)
金属锂
金属
纳米技术
电化学
Crystal(编程语言)
化学工程
冶金
电极
计算机科学
物理化学
医学
化学
工程类
内分泌学
程序设计语言
作者
Jian Tan,Longli Ma,Pengshu Yi,Yuan Wang,Zhiheng Li,Zhan Fang,Xuanyang Li,Shan He,Xuefeng Wang,Mingxin Ye,Jianfeng Shen
标识
DOI:10.1002/adma.202403570
摘要
Abstract A formidable challenge to achieve the practical applications of rechargeable lithium (Li) metal batteries (RLMBs) is to suppress the uncontrollable growth of Li dendrites. One of the most effective solutions is to fabricate Li metal anodes with specific crystal plane, but still lack of a simple and high‐efficient approach. Herein, to overcome this key challenge, we report a facile and controllable way for the scalable customization of polished Li metal anodes with highly preferred (110) and (200) crystallographic orientation (donating as polished Li(110) and polished Li(200), respectively) by regulating the times of accumulative roll bonding at room temperature. In light of the inherent characteristics of polished Li(110) and polished Li(200), the influence of Li atomic structure on the electrochemical performance of RLMBs is deeply elucidated by combining theoretical calculations with relative experimental proofs. In particular, polished Li(110) crystal plane is demonstrated to induce Li + uniform deposition, promoting the formation of flat and dense Li deposits. Impressively, the polished Li(110)||LiFePO 4 full cells exhibit unprecedented cycling stability with 10000 cycles at 10 C almost without capacity degradation, indicating the great potential application prospect of such textured Li metal. More valuably, this work provides an important reference for low‐cost, continued, and large‐scale production of Li metal anodes with highly preferred crystal orientation through roll‐to‐roll manufacturability. This article is protected by copyright. All rights reserved
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