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具有双机制的富氧空位BiSeO纳米片用于铵离子电池

Oxygen Vacancy-Enriched BiSeO Nanosheets with Dual Mechanism for Ammonium-Ion Batteries.

作者信息

Ling Dandan, Wang Qi, Tian Guofu, Yu Hao, Zhang Daohong, Wang Qiufan

机构信息

Key Laboratory of Catalysis and Energy Materials Chemistry of Ministry of Education & Hubei Key Laboratory of Catalysis and Materials Science, Hubei R&D Center of Hyperbranched Polymers Synthesis and Applications, South-Central Minzu University, Wuhan 430074, China.

Guangdong Provincial Laboratory of Chemistry and Fine Chemical Engineering Jieyang Center, Jieyang 515200, China.

出版信息

ACS Nano. 2023 Dec 26;17(24):25222-25233. doi: 10.1021/acsnano.3c08460. Epub 2023 Dec 7.

Abstract

Ammonium ions feature a light molar mass and small hydrated radius, and the interesting interaction between NH and host materials has attracted widespread attention in aqueous energy storage, while few studies focus on high-performance NH storage anodes. Herein, we present a high-performance inset-type anode for aqueous ammonium-ion batteries (AIBs) based on BiSeO nanosheets. A reversible NH/H co-intercalation/deintercalation accompanied by hydrogen bond formation/breaking and a conversion reaction mechanism in layered BiSeO is proposed according to characterizations. Accordingly, the optimized BiSeO anode has a high reversible capacity of 341.03 mAh g at 0.3 A g in 1 M NHCl electrolyte and an impressive capacity retention of 86.7% after 7000 cycles at 3 A g, which is related to the existence of oxygen vacancies that enhance ion/electron transfer and promote the formation of hydrogen bonds between NH and the host material. When the rocking-chair ammonium-ion battery is assembled using a MnO cathode, the device delivers an ultrahigh capacity of 140.73 mAh g at 0.15 A g and energy density of 207.13 Wh kg at the power density of 2985.07 W kg. This work provides a promising strategy for designing high-performance anodes for next-generation AIBs.

摘要

铵离子具有轻的摩尔质量和小的水合半径,并且NH与主体材料之间有趣的相互作用在水系储能中引起了广泛关注,而很少有研究聚焦于高性能的NH存储负极。在此,我们展示了一种基于BiSeO纳米片的用于水系铵离子电池(AIBs)的高性能嵌入型负极。根据表征结果,提出了在层状BiSeO中伴随氢键形成/断裂的可逆NH⁺/H⁺共嵌入/脱嵌以及一种转化反应机制。相应地,优化后的BiSeO负极在1 M NH₄Cl电解液中0.3 A g电流密度下具有341.03 mAh g的高可逆容量,并且在3 A g电流密度下循环7000次后容量保持率高达86.7%,这与氧空位的存在有关,氧空位增强了离子/电子传输并促进了NH⁺与主体材料之间氢键的形成。当使用MnO₂正极组装摇椅式铵离子电池时,该器件在0.15 A g电流密度下具有140.73 mAh g的超高容量,在2985.07 W kg的功率密度下能量密度为207.13 Wh kg。这项工作为设计下一代AIBs的高性能负极提供了一种有前景的策略。

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