Affiliation:
1. College of Chemistry and Molecular Sciences Wuhan University Wuhan 430072 China
2. Department of Chemistry Massachusetts Institute of Technology Cambridge MA 02139 USA
3. The Institute for Advanced Studies (IAS) Wuhan University Wuhan 430072 China
4. School of Materials Science and Engineering Wuhan University of Technology Wuhan 430070 China
Abstract
AbstractAqueous ammonium‐ion batteries (AIBs) are considered a promising alternative for large‐scale energy storage due to their cost‐effectiveness and high safety. Prussian blue analogues (PBAs) are widely regarded as potential cathode materials for AIBs because of their high working potential and stable 3D framework. However, the low capacity of PBAs (≈60 mAh g−1 in the existing reported works) hinders their further development. Herein, the ion insertion is first proposed to double the capacity of PBAs by unlocking the inert‐site. Using NH4+‐rich copper hexacyanoferrate as a representative, trace amounts of induced ion in the electrolyte can change the electronic states of atoms at the inert site to achieve much higher capacity. What's more, the construction of NH4+‐rich high‐entropy Prussian blue (N‐HEPBA) further facilitates structural stability. N‐HEPBA unlocked by corresponding induced ions can exhibit an impressive specific capacity (129 mAh g−1 at 0.1 A g−1), which is the highest and approximately twice that of reported PBAs for aqueous AIBs. Meanwhile, it delivers excellent cycling stability with nearly 100% capacity retention achieved over 1000 cycles at 2 A g−1. This innovative unlocking method can provide an effective way to obtain high‐capacity PBAs in AIBs, thus promoting the development of large‐scale energy storage.
Funder
National Natural Science Foundation of China
Key Technologies Research and Development Program
Cited by
5 articles.
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