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螯合封端的纳米银锌双界面重塑用于可逆无枝晶锌负极的局部环境。

Chelate-Capped Nano-AgZn Dual Interphase Remodeling the Local Environment for Reversible Dendrite-Free Zinc Anode.

作者信息

Luo Yuqing, Hu Jiugang, Cai Shan, Ding Kuixing, Hu Xiaochun, Fu Yanan, Zou Guoqiang, Hou Hongshuai, Ji Xiaobo

机构信息

College of Chemistry and Chemical Engineering, Central South University, Changsha, 410083, China.

School of Energy Science and Engineering, Central South University, Changsha, 410083, China.

出版信息

Small. 2023 Sep;19(39):e2303268. doi: 10.1002/smll.202303268. Epub 2023 May 24.

Abstract

Rechargeable aqueous zinc-ion batteries (AZIBs) are among the most promising candidates for next-generation energy-storage devices. However, the large voltage polarisation and infamous dendrite growth hinder the practical application of AZIBs owing to their complex interfacial electrochemical environment. In this study, a hydrophobic zinc chelate-capped nano-silver (HZC-Ag) dual interphase is fabricated on the zinc anode surface using an emulsion-replacement strategy. The multifunctional HZC-Ag layer remodels the local electrochemical environment by facilitating the pre-enrichment and de-solvation of zinc ions and inducing homogeneous zinc nucleation, thus resulting in reversible dendrite-free zinc anodes. The zinc deposition mechanism on the HZC-Ag interphase is elucidated by density functional theory (DFT) calculations, dual-field simulations, and in situ synchrotron X-ray radiation imaging. The HZC-Ag@Zn anode exhibited superior dendrite-free zinc stripping/plating performance and an excellent lifespan of >2000 h with ultra-low polarisation of ≈17 mV at 0.5 mA cm . Full cells coupled with a MnO cathode showed significant self-discharge inhibition, excellent rate performance, and improved cycling stability for >1000 cycles. Therefore, this multifunctional dual interphase may contribute to the design and development of dendrite-free anodes for high-performance aqueous metal-based batteries.

摘要

可充电水系锌离子电池(AZIBs)是下一代储能装置中最具潜力的候选者之一。然而,由于其复杂的界面电化学环境,较大的电压极化和臭名昭著的枝晶生长阻碍了AZIBs的实际应用。在本研究中,采用乳液置换策略在锌阳极表面制备了一种疏水锌螯合物包覆的纳米银(HZC-Ag)双界面。多功能HZC-Ag层通过促进锌离子的预富集和去溶剂化以及诱导均匀的锌成核来重塑局部电化学环境,从而产生可逆的无枝晶锌阳极。通过密度泛函理论(DFT)计算、双场模拟和原位同步辐射X射线辐射成像阐明了锌在HZC-Ag界面上的沉积机制。HZC-Ag@Zn阳极表现出优异的无枝晶锌剥离/电镀性能和超过2000小时的优异寿命,在0.5 mA cm 下极化超低,约为17 mV。与MnO阴极耦合的全电池表现出显著的自放电抑制、优异的倍率性能和超过1000次循环的改善的循环稳定性。因此,这种多功能双界面可能有助于设计和开发用于高性能水系金属基电池的无枝晶阳极。

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