Preinserted Ammonium in MnO<sub>2</sub> to Enhance Charge Storage in Dimethyl Sulfoxide Based Zinc-Ion Batteries
- Authors
- Kao-ian, Wathanyu; Sangsawang, Jinnawat; Gopalakrishnan, Mohan; Wannapaiboon, Suttipong; Watwiangkham, Athis; Jungsuttiwong, Siriporn; Theerthagiri, Jayaraman; Choi, Myong Yong; Kheawhom, Soorathep
- Issue Date
- Aug-2024
- Publisher
- American Chemical Society
- Keywords
- wet nonaqueous; zinc-ion batteries; manganesedioxide; ammonium cation; charge disproportionation
- Citation
- ACS Applied Materials & Interfaces, v.16, no.42, pp 56926 - 56934
- Pages
- 9
- Indexed
- SCIE
SCOPUS
- Journal Title
- ACS Applied Materials & Interfaces
- Volume
- 16
- Number
- 42
- Start Page
- 56926
- End Page
- 56934
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/74130
- DOI
- 10.1021/acsami.4c07239
- ISSN
- 1944-8244
1944-8252
- Abstract
- Nonaqueous zinc-ion batteries (NZIBs) featuring manganese dioxide (MnO2) cathodes position themselves as viable options for large-scale energy storage systems. Herein, we demonstrate the use of ammonium cation as a preintercalant to improve the performance of the delta-MnO2 cathode in wet dimethyl sulfoxide based electrolytes. Employing in situ X-ray absorption spectroscopy, Raman spectroscopy, and synchrotron X-ray diffraction, we reveal that the integration of ammonium cations promotes the formation of NH-O-Mn networks. These networks are crucial for manipulating the distortion of the MnO6 octahedral units during discharging, thereby mitigating charge disproportionation, which is a primary limitation to MnO2's charge-storage efficiency. The modified MnO2, through this idea, displays a notable improvement in capacity (similar to 247 mAh/g) and can pass charge-discharge cycles up to 500 cycles with a capacity retention of 85%. These findings underscore the potential of modified MnO2 in advancing MnO2-based hosts for Zn-MnO2 batteries, marking significant progress toward next-generation energy storage solutions.
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