Baonian Zhu , Yuefeng Yan , Jingzhe Hong , Yuhao Xia , Meixiu Song , Xiaoshuang Wang , Yanan Liu , Bo Zhong , Dongdong Liu , Tao Zhang , Xiaoxiao Huang
{"title":"加速质子输运调节低温含水锌金属电池共晶凝胶电解质中的动态氢键网络","authors":"Baonian Zhu , Yuefeng Yan , Jingzhe Hong , Yuhao Xia , Meixiu Song , Xiaoshuang Wang , Yanan Liu , Bo Zhong , Dongdong Liu , Tao Zhang , Xiaoxiao Huang","doi":"10.1016/j.jechem.2025.05.028","DOIUrl":null,"url":null,"abstract":"<div><div>Aqueous Zn-metal batteries (AZMBs) performance is hampered by freezing water at low temperatures, which hampers their multi-scenario application. Hydrogen bonds (HBs) play a pivotal role in water freezing, and proton transport is indispensable for the establishment of HBs. Here, the accelerated proton transport modulates the dynamic hydrogen bonding network of a Zn (BF<sub>4</sub>)<sub>2</sub>/EMIMBF<sub>4</sub> impregnated polyacrylamide/poly (vinyl alcohol)/xanthan gum dual network eutectic gel electrolyte (PPX-ILZSE) for low-temperature AZMBs. The PPX-ILZSE forms more HBs, shorter HBs lifetimes, higher tetrahedral entropy, and faster desolvation processes, as demonstrated by experimental and theoretical calculations. This enhanced dynamic proton transport promotes rapid cycling of HBs formation-failure, and for polyaniline cathode (PANI) abundant redox sites of proton, confers excellent low temperature electrochemical performance to the Zn//PANI full cell. Specific capacities for 1000 and 5000 cycles at 1 and 5 A g<sup>−1</sup> were 149.8 and 128.4 mA h g<sup>−1</sup> at room temperature, respectively. Furthermore, specific capacities of 131.1 mA h g<sup>−1</sup> (92.4% capacity retention) and 0.0066% capacity decay per lap were achieved for 3000 and 3500 laps at −30 and 40 °C, respectively, at 0.5 A g<sup>−1</sup>. Furthermore, in-situ protective layer of ZnOHF nano-arrays on the Zn anode surface to eliminate dendrite growth and accelerate Zn-ions adsorption and charge transfer.</div></div>","PeriodicalId":15728,"journal":{"name":"Journal of Energy Chemistry","volume":"109 ","pages":"Pages 325-336"},"PeriodicalIF":13.1000,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Accelerated proton transport modulates dynamic hydrogen bonding networks in eutectic gel electrolytes for low-temperature aqueous Zn-metal batteries\",\"authors\":\"Baonian Zhu , Yuefeng Yan , Jingzhe Hong , Yuhao Xia , Meixiu Song , Xiaoshuang Wang , Yanan Liu , Bo Zhong , Dongdong Liu , Tao Zhang , Xiaoxiao Huang\",\"doi\":\"10.1016/j.jechem.2025.05.028\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Aqueous Zn-metal batteries (AZMBs) performance is hampered by freezing water at low temperatures, which hampers their multi-scenario application. Hydrogen bonds (HBs) play a pivotal role in water freezing, and proton transport is indispensable for the establishment of HBs. Here, the accelerated proton transport modulates the dynamic hydrogen bonding network of a Zn (BF<sub>4</sub>)<sub>2</sub>/EMIMBF<sub>4</sub> impregnated polyacrylamide/poly (vinyl alcohol)/xanthan gum dual network eutectic gel electrolyte (PPX-ILZSE) for low-temperature AZMBs. The PPX-ILZSE forms more HBs, shorter HBs lifetimes, higher tetrahedral entropy, and faster desolvation processes, as demonstrated by experimental and theoretical calculations. This enhanced dynamic proton transport promotes rapid cycling of HBs formation-failure, and for polyaniline cathode (PANI) abundant redox sites of proton, confers excellent low temperature electrochemical performance to the Zn//PANI full cell. Specific capacities for 1000 and 5000 cycles at 1 and 5 A g<sup>−1</sup> were 149.8 and 128.4 mA h g<sup>−1</sup> at room temperature, respectively. Furthermore, specific capacities of 131.1 mA h g<sup>−1</sup> (92.4% capacity retention) and 0.0066% capacity decay per lap were achieved for 3000 and 3500 laps at −30 and 40 °C, respectively, at 0.5 A g<sup>−1</sup>. 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引用次数: 0
摘要
含水锌金属电池(azmb)的性能受到低温冻结水的影响,这阻碍了其多场景应用。氢键在水的冻结过程中起着至关重要的作用,而氢键的建立离不开质子的输运。加速质子输运调节了Zn (BF4)2/EMIMBF4浸渍聚丙烯酰胺/聚乙烯醇/黄原胶双网络共晶凝胶电解质(PPX-ILZSE)用于低温azmb的动态氢键网络。实验和理论计算表明,PPX-ILZSE形成更多的HBs,更短的HBs寿命,更高的四面体熵和更快的脱溶过程。这种增强的动态质子传输促进了HBs形成失效的快速循环,并且由于聚苯胺阴极(PANI)中质子的丰富氧化还原位点,赋予了Zn//PANI充满电池优异的低温电化学性能。在1和5 A g−1下,室温下1000和5000次循环的比容量分别为149.8和128.4 mA h g−1。此外,在- 30°C和40°C下,在0.5 A g - 1下,在3000圈和3500圈时,每圈的比容量分别达到131.1 mA h g - 1(92.4%的容量保留)和0.0066%的容量衰减。此外,在锌阳极表面原位放置了一层ZnOHF纳米阵列保护层,消除了枝晶的生长,加速了Zn离子的吸附和电荷转移。
Accelerated proton transport modulates dynamic hydrogen bonding networks in eutectic gel electrolytes for low-temperature aqueous Zn-metal batteries
Aqueous Zn-metal batteries (AZMBs) performance is hampered by freezing water at low temperatures, which hampers their multi-scenario application. Hydrogen bonds (HBs) play a pivotal role in water freezing, and proton transport is indispensable for the establishment of HBs. Here, the accelerated proton transport modulates the dynamic hydrogen bonding network of a Zn (BF4)2/EMIMBF4 impregnated polyacrylamide/poly (vinyl alcohol)/xanthan gum dual network eutectic gel electrolyte (PPX-ILZSE) for low-temperature AZMBs. The PPX-ILZSE forms more HBs, shorter HBs lifetimes, higher tetrahedral entropy, and faster desolvation processes, as demonstrated by experimental and theoretical calculations. This enhanced dynamic proton transport promotes rapid cycling of HBs formation-failure, and for polyaniline cathode (PANI) abundant redox sites of proton, confers excellent low temperature electrochemical performance to the Zn//PANI full cell. Specific capacities for 1000 and 5000 cycles at 1 and 5 A g−1 were 149.8 and 128.4 mA h g−1 at room temperature, respectively. Furthermore, specific capacities of 131.1 mA h g−1 (92.4% capacity retention) and 0.0066% capacity decay per lap were achieved for 3000 and 3500 laps at −30 and 40 °C, respectively, at 0.5 A g−1. Furthermore, in-situ protective layer of ZnOHF nano-arrays on the Zn anode surface to eliminate dendrite growth and accelerate Zn-ions adsorption and charge transfer.
期刊介绍:
The Journal of Energy Chemistry, the official publication of Science Press and the Dalian Institute of Chemical Physics, Chinese Academy of Sciences, serves as a platform for reporting creative research and innovative applications in energy chemistry. It mainly reports on creative researches and innovative applications of chemical conversions of fossil energy, carbon dioxide, electrochemical energy and hydrogen energy, as well as the conversions of biomass and solar energy related with chemical issues to promote academic exchanges in the field of energy chemistry and to accelerate the exploration, research and development of energy science and technologies.
This journal focuses on original research papers covering various topics within energy chemistry worldwide, including:
Optimized utilization of fossil energy
Hydrogen energy
Conversion and storage of electrochemical energy
Capture, storage, and chemical conversion of carbon dioxide
Materials and nanotechnologies for energy conversion and storage
Chemistry in biomass conversion
Chemistry in the utilization of solar energy