水溶液
化学
X射线光电子能谱
铜
无机化学
电解质
极化(电化学)
离子
铵
普鲁士蓝
电化学
傅里叶变换红外光谱
电极
化学工程
物理化学
有机化学
工程类
作者
Xikun Zhang,Maoting Xia,Tingting Liu,Na Peng,Haoxiang Yu,Runtian Zheng,Liyuan Zhang,Miao Shui,Jie Shu
标识
DOI:10.1016/j.cej.2020.127767
摘要
Rechargeable aqueous batteries have aroused increasing attention as an effective energy strategy. In this research, non-metallic ammonium ions are reported as a highly efficient charge carrier to reversible insert into NH4+-rich copper hexacyanoferrate (N-CuHCF) in aqueous NH4NO3 electrolyte. It is worth noting that N-CuHCF displays remarkable rate performance with no obvious capacity loss (60.0 mAh g−1 at 1 C, 59.0 mAh g−1 at 50 C) and negligible voltage polarization (∼0.1 V) from 1 to 50 C. Even at ultra-high rate (≥100 C), N-CuHCF still demonstrates favorable long-life cycling performance. For example, capacity retentions of 91.5% and 86.5% are achieved over 17,000 and 20,000 cycles at 100 and 180 C, respectively. Furthermore, XRD, FTIR, and XPS reveal the essence of reversible redox reaction and stable structure of N-CuHCF based on Fe3+/Fe2+ and Cu2+/Cu+ couples. Hence, the rechargeable aqueous batteries based on the infinite ammonium ion and the stable Prussian blue analogues provide a novel imagine for large-scale and fast energy applications.
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