Journal
CHEMICAL ENGINEERING JOURNAL
Volume 421, Issue -, Pages -Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2020.127767
Keywords
Aqueous battery; Ammonium ion storage; Prussian blue analogues; High rate; Reversible electrochemical reaction
Categories
Funding
- NSAF Joint Fund [U1830106]
- Ningbo S& I Innovation 2025 Major Special Program [2018B10061]
- K.C. Wong Magna Fund in Ningbo University
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The research shows that non-metallic ammonium ions can be an efficient charge carrier to reversible insert into NH4+-rich copper hexacyanoferrate, achieving excellent rate performance and long cycling life. XRD, FTIR, and XPS reveal the reversible redox reaction essence and stable structure of N-CuHCF based on Fe3+/Fe2+ and Cu2+/Cu+ couples, providing a new option for large-scale and fast energy applications.
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 (similar to 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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