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酒精分子耦合:一种用于调制钒基阴极非晶性以实现高倍率和耐用水系锌离子电池的通用方法。

Alcohol molecule coupling: A universal approach to modulating amorphousness in vanadium-based cathodes for high-rate and durable aqueous zinc-ion batteries.

作者信息

Song Haobin, Cui Yang-Feng, Li Yifan, Li Xueliang, Li Yixiang, Zhao Nan, Li Wenjing, Wu Chao, Xi Shibo, 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.

Institute of Sustainability for Chemical, Energy and Environment (ISCE2), Agency for Science, Technology and Research, 1 Pesek Road Jurong Island, Singapore 627833, Singapore.

出版信息

Sci Adv. 2025 May 23;11(21):eadt7502. doi: 10.1126/sciadv.adt7502.

DOI:10.1126/sciadv.adt7502
PMID:40408486
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12101504/
Abstract

Vanadium oxides (VOs) are promising cathode materials for aqueous batteries due to their high theoretical capacity, but they face challenges such as sluggish kinetics and V dissolution. To overcome these issues, we introduce a universal alcohol-based molecule coupling (AMC) method to regulate amorphousness and inhibit V dissolution in VOs (VO, VO, and VO), resulting in high-performance cathodes. The strategy enables alcohol molecules with different chain lengths (ethanol, isopropanol, and isobutanol) to couple with VOs by forming V─OH bonds under Lewis acid-based interactions, inducing controlled amorphization. Among these, isopropanol coupling stands out by enabling the formation of short-range ordered amorphous structure (SOA-VO/Ipr). This structure enhances the reaction kinetics and suppresses V dissolution. As a result, the SOA-VO/Ipr cathode achieves 219.4 mAh g at 100 A g, retains 92.6% capacity over 10,000 cycles, and delivers 228.8 mAh g at 9.1 A g under high loading (21.9 mg cm) over 3500 cycles, demonstrating a promising method for durable zinc-ion batteries.

摘要

钒氧化物(VOs)因其高理论容量而有望成为水系电池的阴极材料,但它们面临着诸如动力学迟缓以及钒溶解等挑战。为克服这些问题,我们引入了一种通用的基于醇的分子偶联(AMC)方法来调控非晶态并抑制VOs(VO、VO和VO)中的钒溶解,从而得到高性能阴极。该策略使具有不同链长的醇分子(乙醇、异丙醇和异丁醇)在基于路易斯酸的相互作用下通过形成V─OH键与VOs偶联,诱导可控的非晶化。其中,异丙醇偶联表现突出,能够形成短程有序的非晶结构(SOA-VO/Ipr)。这种结构增强了反应动力学并抑制了钒溶解。结果,SOA-VO/Ipr阴极在100 A g时实现了219.4 mAh g的比容量,在10000次循环中保持了92.6%的容量,并且在高负载(21.9 mg cm)下经过3500次循环后在9.1 A g时提供228.8 mAh g的比容量,证明了这是一种用于耐用锌离子电池的有前景的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e7/12101504/1fac4107499f/sciadv.adt7502-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e7/12101504/0f505af64d8f/sciadv.adt7502-f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e7/12101504/cf2462aab2a4/sciadv.adt7502-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e7/12101504/93e77f212072/sciadv.adt7502-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e7/12101504/1fac4107499f/sciadv.adt7502-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e7/12101504/0f505af64d8f/sciadv.adt7502-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e7/12101504/9ba2a24f9437/sciadv.adt7502-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e7/12101504/20a9a02fe887/sciadv.adt7502-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e7/12101504/cf2462aab2a4/sciadv.adt7502-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e7/12101504/93e77f212072/sciadv.adt7502-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e7/12101504/1fac4107499f/sciadv.adt7502-f6.jpg

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本文引用的文献

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Architecting VO with a Triune Crystal Water-Amorphous-Crystalline Feature for Robust Zinc-Ion Batteries.构建具有三元晶体水-非晶-晶体特性的VO用于高性能锌离子电池。
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用于先进水系锌离子电池的超快定制非晶态ZnVO,采用精确设计的人工原子层1T'-MoS阴极电解质界面
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