A Novel Kinetically-Driven Approach to Forming Columnar {110}-textured Lithium Metal Anodes with Extended Cycle Life

IF 26 1区 材料科学 Q1 CHEMISTRY, PHYSICAL
Zhiqiang Zheng, Guang Xia, Jiajia Ye, Zhanghua Fu, Tian Qiu, Chuang Chen, Mark J. Biggs, Cheng Hu
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Abstract

Constructing {110}-textured lithium (Li) metal anodes is a promising strategy to extend battery life. While preparation of such anodes has been the subject of a few studies, their focus has been exclusively on thermodynamically-driven (equilibrium) strategies. Through a systematic screening of bath conditions, the study reported here identifies a novel kinetically-driven protocol that enhances the volume fraction of {110} texture by more than fivefold compared to equilibrium approaches. The protocol involves Li deposition at high current densities or low temperatures in a commonly used LiNO3-containing ether-based electrolyte. Columnar {110}-oriented grains are formed through a growth rate selection process arising from the stronger electronic coupling and faster electron transfer rate between Li(110) and Li+ cations compared to other lattice planes. LiNO3 plays a crucial role by inhibiting the deposition on the Li(110) plane less than the other planes. Simple bath condition adjustments yield optimized {110}-textured Li anodes with improved plating/stripping homogeneity that suppresses dendrite formation and electrolyte consumption, resulting in extended cycle life in lean-electrolyte full cells. This kinetically-driven approach offers mechanistic insight into Li texture formation and a promising route to high-performance Li metal anodes.

Abstract Image

Abstract Image

一种新的动力学驱动方法形成具有延长循环寿命的柱状{110}织构锂金属阳极
构造{110}结构的锂(Li)金属阳极是一种很有前途的延长电池寿命的策略。虽然这种阳极的制备一直是少数研究的主题,但他们的重点是热力学驱动(平衡)策略。通过对浴槽条件的系统筛选,本文报道的研究确定了一种新的动力学驱动方案,与平衡方法相比,该方案将{110}织构的体积分数提高了五倍以上。该方案涉及在高电流密度或低温下在常用的含lino3的醚基电解质中沉积Li。与其他晶格面相比,由于Li(110)和Li+阳离子之间的电子耦合更强,电子转移速率更快,从而通过生长速率选择过程形成柱状{110}取向晶粒。LiNO3对Li(110)平面沉积的抑制作用小于其他平面。简单的镀液条件调整可以产生优化的{110}结构的锂阳极,改善了镀/剥离的均匀性,抑制了枝晶的形成和电解质的消耗,从而延长了贫电解质充满电池的循环寿命。这种动力学驱动的方法提供了对锂织构形成的机理洞察,并为高性能锂金属阳极提供了一条有前途的途径。
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来源期刊
Advanced Energy Materials
Advanced Energy Materials CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
41.90
自引率
4.00%
发文量
889
审稿时长
1.4 months
期刊介绍: Established in 2011, Advanced Energy Materials is an international, interdisciplinary, English-language journal that focuses on materials used in energy harvesting, conversion, and storage. It is regarded as a top-quality journal alongside Advanced Materials, Advanced Functional Materials, and Small. With a 2022 Impact Factor of 27.8, Advanced Energy Materials is considered a prime source for the best energy-related research. The journal covers a wide range of topics in energy-related research, including organic and inorganic photovoltaics, batteries and supercapacitors, fuel cells, hydrogen generation and storage, thermoelectrics, water splitting and photocatalysis, solar fuels and thermosolar power, magnetocalorics, and piezoelectronics. The readership of Advanced Energy Materials includes materials scientists, chemists, physicists, and engineers in both academia and industry. The journal is indexed in various databases and collections, such as Advanced Technologies & Aerospace Database, FIZ Karlsruhe, INSPEC (IET), Science Citation Index Expanded, Technology Collection, and Web of Science, among others.
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