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用于高速率和超稳定水系锌-钒氧化物电池的多功能抗质子电解质

A Multifunctional Anti-Proton Electrolyte for High-Rate and Super-Stable Aqueous Zn-Vanadium Oxide Battery.

作者信息

Chen Yangwu, Ma Dingtao, Ouyang Kefeng, Yang Ming, Shen Sicheng, Wang Yanyi, Mi Hongwei, Sun Lingna, He Chuanxin, Zhang Peixin

机构信息

College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, 518060, People's Republic of China.

Institute of Microscale Optoelectronics, Shenzhen University, Shenzhen, 518060, People's Republic of China.

出版信息

Nanomicro Lett. 2022 Aug 2;14(1):154. doi: 10.1007/s40820-022-00907-4.

Abstract

Large volumetric expansion of cathode hosts and sluggish transport kinetics in the cathode-electrolyte interface, as well as dendrite growth and hydrogen evolution at Zn anode side are considered as the system problems that cause the electrochemical failure of aqueous Zn-vanadium oxide battery. In this work, a multifunctional anti-proton electrolyte was proposed to synchronously solve all those issues. Theoretical and experimental studies confirm that PEG 400 additive can regulate the Zn solvation structure and inhibit the ionization of free water molecules of the electrolyte. Then, smaller lattice expansion of vanadium oxide hosts and less associated by-product formation can be realized by using such electrolyte. Besides, such electrolyte is also beneficial to guide the uniform Zn deposition and suppress the side reaction of hydrogen evolution. Owing to the integrated synergetic modification, a high-rate and ultrastable aqueous Zn-VO/C battery can be constructed, which can remain a specific capacity of 222.8 mAh g after 6000 cycles at 5 A g, and 121.8 mAh g even after 18,000 cycles at 20 A g, respectively. Such "all-in-one" solution based on the electrolyte design provides a new strategy for developing high-performance aqueous Zn-ion battery.

摘要

阴极主体的大量体积膨胀以及阴极-电解质界面处缓慢的传输动力学,还有锌阳极侧的枝晶生长和析氢现象,都被认为是导致水系锌-钒氧化物电池发生电化学失效的系统问题。在这项工作中,提出了一种多功能抗质子电解质来同步解决所有这些问题。理论和实验研究证实,聚乙二醇400添加剂可以调节锌的溶剂化结构并抑制电解质中游离水分子的电离。然后,通过使用这种电解质,可以实现氧化钒主体较小的晶格膨胀和较少的相关副产物形成。此外,这种电解质也有利于引导锌的均匀沉积并抑制析氢副反应。由于综合的协同改性,可以构建一种高倍率且超稳定的水系锌-氧化钒/碳电池,在5 A g下循环6000次后其比容量可保持在222.8 mAh g,在20 A g下循环18000次后比容量甚至可达121.8 mAh g。这种基于电解质设计的“一体化”解决方案为开发高性能水系锌离子电池提供了一种新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34a0/9346040/3054660468fc/40820_2022_907_Sch1_HTML.jpg

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