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集成结构调制在水系锌离子电池中诱导快速电荷转移

Integrated Structural Modulation Inducing Fast Charge Transfer in Aqueous Zinc-Ion Batteries.

作者信息

Naresh Nibagani, Park Youngtae, Jeong Su Hwan, Lee Sang Jun, Lee Dong Park, Lee So Hyun, Ryu Gyeong Hee, Jung Young Hwa, Kim Joo-Hyung

机构信息

Department of Materials Engineering and Convergence Technology, Gyeongsang National University, Jinju, 52828, Republic of Korea.

Hydrogen Research Department, Korea Institute of Energy Research (KIER), 152 Gajeong-ro Yuseong-gu, Daejeon, 34129, Republic of Korea.

出版信息

Small. 2024 Nov;20(48):e2406249. doi: 10.1002/smll.202406249. Epub 2024 Sep 2.

Abstract

Aqueous Zn-ion batteries (AZIBs) are promising energy-storage devices owing to their exceptional safety, long cycle life, simple production, and high storage capacity. Manganese oxides are considered potential cathode materials for AZIBs, primarily because of their safety, low cost, simple synthesis, and high storage capacity. However, MnO-based cathodes tend to deteriorate structurally during long-term cycling, which reduces their reversible capacity. In this study, an advanced α-MnO@SnO nanocomposite via facile hydrothermal synthesis is developed. The synergistic effects of lattice disorder and increased electron conductivity in the α-MnO@SnO nanocomposite mitigate structural degradation and enhance the overall electrochemical performance. The nanocomposite exhibits a high reversible capacity of 347 mAh g at a current density of 100 mA g after 50 cycles. Furthermore, it exhibits excellent rate performance and stable capacity even after 1000 cycles, maintaining a capacity of 78 mAh g at a high current density of 5 A g. This excellent electrochemical performance is attributed to the reversible Zn intercalation in α-MnO@SnO nanocomposites due to the increased structural stability and fast ion/electron exchange caused by the distortion of the tunnel structure, on the basis of various ex situ experiments, density functional theory calculations, and electrochemical characterizations.

摘要

水系锌离子电池(AZIBs)因其卓越的安全性、长循环寿命、生产简单和高存储容量而成为很有前景的储能装置。锰氧化物被认为是水系锌离子电池的潜在阴极材料,主要是因为其安全性、低成本、合成简单和高存储容量。然而,基于MnO的阴极在长期循环过程中往往会发生结构退化,这降低了它们的可逆容量。在本研究中,通过简便的水热合成法制备了一种先进的α-MnO@SnO纳米复合材料。α-MnO@SnO纳米复合材料中晶格无序和电子电导率增加的协同效应减轻了结构退化并增强了整体电化学性能。该纳米复合材料在50次循环后,在100 mA g的电流密度下表现出347 mAh g的高可逆容量。此外,即使在1000次循环后,它仍表现出优异的倍率性能和稳定的容量,在5 A g的高电流密度下保持78 mAh g的容量。基于各种非原位实验、密度泛函理论计算和电化学表征,这种优异的电化学性能归因于α-MnO@SnO纳米复合材料中可逆的锌嵌入,这是由于隧道结构的畸变导致结构稳定性增加和离子/电子快速交换。

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