钒
青铜色
铝
无机化学
离子
水溶液
铵
材料科学
化学
冶金
物理化学
有机化学
作者
Vishnu Priya H. Radhakantha,S.K. Pradhan,Aninda J. Bhattacharyya
标识
DOI:10.1021/acs.jpcc.4c06806
摘要
Rechargeable aluminum-ion batteries (AIBs) are promising alternatives to lithium-based batteries due to their competitive energy densities. Aqueous AIBs enable the use of electrode materials with open-framework structures and large interlayer spacings, which facilitate aluminum ion insertion and extraction. Herein, we explore ammonium vanadate (NH4V4O10; NVO) with a high interlayer spacing of ∼9.4 Å as a potential positive electrode for AIBs. The material demonstrates an initial high discharge capacity of 210 mA h g–1 in 1 M AlCl3 electrolyte but degrades due to structural distortion from the strain induced by the intercalating [Al(H2O)6]3+ cation. The effects of ammonium salt additives (NH4X: X = Cl, F, CH3CO2, HCO2) on the electrochemical performance are investigated, with a detailed focus on NH4Cl, demonstrating notable improvements in structural stability over 1 M AlCl3. Ex situ XRD, Fourier transform infrared, X-ray photoelectron spectroscopy, and inductively coupled plasma-optical emission spectrometry analyses reveal partial stabilization of the NVO structure and enhanced cyclability over a few tens of cycles. Solvent composition adjustments with 1 M AlCl3 as the salt showed similar trends. This work, in addition to identifying optimal Al3+ intercalating hosts, emphasizes the critical role of electrolytes in advancing aqueous AIB technologies.
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