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由硫酸镉水溶液电解质驱动的可充电镉金属电池。

Rechargeable Cadmium Metal Batteries Enabled by an Aqueous CdSO Electrolyte.

作者信息

Song Haobin, Cui Yang-Feng, Zhao Nan, Li Wenjing, Huang Shaozhuan, Yang Hui Ying

机构信息

Pillar of Engineering Product Development, Singapore University of Technology and Design, 8 Somapah Road, Singapore 487372, Singapore.

Key Laboratory of Catalysis and Energy Materials Chemistry of Ministry of Education & Hubei Key Laboratory of Catalysis and Materials Science, South-Central Minzu University, Wuhan, Hubei 430074, China.

出版信息

ACS Nano. 2025 Apr 1;19(12):12170-12181. doi: 10.1021/acsnano.5c00124. Epub 2025 Mar 19.

Abstract

Rechargeable aqueous cadmium (Cd) metal batteries enabled by the Cd plating and stripping behaviors of anode show great promise for next-generation energy storage applications due to the superior corrosion resistance, high specific capacity (476.5 mAh g), suitable redox potential (-0.4 V vs standard hydrogen electrode), and cost-effectiveness of Cd anode. However, this field is still in its infancy, with limited scientific exploration and numerous unresolved challenges. Therefore, to bridge the existing research gap in the field of Cd metal batteries, this study conducted a comprehensive investigation into the electrochemical performance of the Cd metal, utilizing a stable and low-cost aqueous CdSO solution as an electrolyte. It is revealed that the solvation structure of Cd transitions from [Cd(HO)] to [Cd(HO)(SO)] as the CdSO concentration increases from 0.5 to 3 M. This transition reduces the activity of HO around Cd, promotes charge transfer, and enhances desolvation/solvation kinetics during Cd plating/stripping processes. Consequently, when the concentration of CdSO reached nearly saturated 3 M, the Cd anode presents optimal corrosion-resistant and dendrite-free capabilities, reflecting in durable Cd plating/stripping performance for over 2000 h with a high Coulombic efficiency of 99.7%. Furthermore, the Cd//VO full cell achieves an ultralong cycle life, maintaining stable performance for 30,000 cycles with minimal capacity degradation. The high reversibility of the Cd anode and the exceptional performance of the full cell affirm the potential of aqueous CdSO electrolyte as a foundation for the future development of Cd metal batteries, offering profound insights and guidance for advancing aqueous energy storage technology.

摘要

基于阳极镉的电镀和剥离行为的可充电水系镉金属电池,因其阳极具有优异的耐腐蚀性、高比容量(476.5 mAh g)、合适的氧化还原电位(相对于标准氢电极-0.4 V)以及成本效益,在下一代储能应用中展现出巨大潜力。然而,该领域仍处于起步阶段,科学探索有限,存在诸多未解决的挑战。因此,为弥合镉金属电池领域现有的研究差距,本研究以稳定且低成本的硫酸镉水溶液为电解质,对镉金属的电化学性能进行了全面研究。结果表明,随着硫酸镉浓度从0.5 M增加到3 M,镉的溶剂化结构从[Cd(HO)]转变为[Cd(HO)(SO)]。这种转变降低了镉周围氢氧根离子的活性,促进了电荷转移,并增强了镉电镀/剥离过程中的去溶剂化/溶剂化动力学。因此,当硫酸镉浓度达到近饱和的3 M时,镉阳极表现出最佳的耐腐蚀和无枝晶能力,在超过2000小时的时间内具有持久的镉电镀/剥离性能,库仑效率高达99.7%。此外,镉//钒全电池实现了超长循环寿命,在30000次循环中保持稳定性能,容量衰减极小。镉阳极的高可逆性和全电池的优异性能证实了硫酸镉水系电解质作为镉金属电池未来发展基础的潜力,为推进水系储能技术提供了深刻的见解和指导。

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