Surface-to-bulk synergistic modification enables stable interface of Ni-rich oxide cathode for all-solid-state lithium batteries

IF 5.5 3区 材料科学 Q1 ELECTROCHEMISTRY
Xinxin Li , Yujia Chen , Kai Lv , Jingshun Liu , Aruuhan Bayaguud , Xuelei Li
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Abstract

All-solid-state lithium batteries (ASSLBs) are supposed to a highly forward-looking battery technology by reason of their conspicuous energy density and excellent safety. Ni-rich layered oxide cathodes have been extensively studied in ASSLB systems with sulfide electrolytes owing to their high voltage and preeminent specific capacity. However, the electrochemical performance of ASSLBs is severely degraded due to the interfacial physical contact failure, space charge layer effect, and chemical/electrochemical side reactions between sulfide electrolytes and Ni-rich oxide cathodes. In this work, the surface of LiNi0.92Co0.04Mn0.04O2 (NCM92) is coated with a nano-level CeO2 buffer layer and is simultaneously doped with Ce element (NCM92–1%Ce) by one-step wet chemical method. Ce doping is beneficial for maintaining structural stability and suppressing irreversible phase transition. The CeO2 buffer layer can efficaciously avoid the oxidation and decomposition phenomenon at the interface between NCM92 and sulfide electrolyte. As expected, NCM92–1%Ce cathode shows the discharge specific capacity of 141.46 mAh g−1 after 80 cycles at 0.2C with 79.32% capacity retention rate, which is much higher than that of the unmodified NCM92 cathode. The results indicate that the surface-to-bulk synergistic modification strategy can successfully improve the structure toughness and interface stability of Ni-rich oxide cathode for ASSLBs with sulfide electrolytes.

Abstract Image

表层与内层协同改性实现了全固态锂电池富镍氧化物正极的稳定界面
全固态锂电池(ASSLB)因其显著的能量密度和出色的安全性而被认为是一种极具前瞻性的电池技术。由于富镍层状氧化物正极具有高电压和出色的比容量,在硫化物电解质的全固态锂电池系统中得到了广泛的研究。然而,由于界面物理接触失效、空间电荷层效应以及硫化物电解质与富镍氧化物阴极之间的化学/电化学副反应,ASSLB 的电化学性能严重下降。在这项研究中,采用一步湿化学法在 LiNi0.92Co0.04Mn0.04O2 (NCM92) 表面涂覆了一层纳米级 CeO2 缓冲层,并同时掺杂了 Ce 元素(NCM92-1%Ce)。掺杂 Ce 有利于保持结构稳定性和抑制不可逆相变。CeO2 缓冲层可有效避免 NCM92 与硫化物电解质界面的氧化和分解现象。正如预期的那样,NCM92-1%Ce 阴极在 0.2C 下循环 80 次后,放电比容量为 141.46 mAh g-1,容量保持率为 79.32%,远高于未改性的 NCM92 阴极。结果表明,面-体协同改性策略可成功提高硫化物电解质 ASSLBs 富氧化镍阴极的结构韧性和界面稳定性。
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来源期刊
Electrochimica Acta
Electrochimica Acta 工程技术-电化学
CiteScore
11.30
自引率
6.10%
发文量
1634
审稿时长
41 days
期刊介绍: Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.
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