Decoding Dual Redox-Active Ammonium Molybdenum Sulfide for High-Capacity Hydrated Ammonium-Ion Storage
Aqueous nonmetallic ammonium-ion (NH4+) batteries (AmIBs) have emerged as one of the promising electrochemical energy storage candidates. However, their advancements have been hindered by the scarcity of high-performance host materials. Herein, a sulfur-rich ammonium molybdenum sulfide ((NH4)2Mo3S13·H2O, NMSH) is developed as an anode host for AmIBs. Theoretical and experimental results demonstrate that NMSH possesses a dual redox-active center (i.e., Mo4+ and S22–) displaying a high reversible specific capacity of ∼275 mAh g–1 at 0.1 A g–1, which outperforms the most reported ammonium-ion storage hosts. Even at 10 A g–1, this material shows a great rate capacity of 121 mAh g–1. Notably, the hydrated ammonium-ion storage mechanism with water co-intercalation/extraction is verified by various characterization technologies and theoretical simulation. The sulfur-rich NMSH facilitates ammonium-ion storage, thereby paving the way for exploring more energetic, efficient, and sustainable ammonium-ion batteries.
Authors
- Netanel Shpigel (ORCID: https://orcid.org/0000-0003-2657-8639)
- Huaiyu Shao (ORCID: https://orcid.org/0000-0001-9286-7071)
- Hang Ren (ORCID: https://orcid.org/0000-0002-9480-8881)
- Jinyao Yang
- Shengyang Dong
- Lifen Long
- Ying Yang (ORCID: https://orcid.org/0000-0002-4810-2976)
- Jing Li (ORCID: https://orcid.org/0000-0002-5627-4153)
- Langyuan Wu (ORCID: https://orcid.org/0000-0001-9042-9270)
- Zeyu Cao (ORCID: https://orcid.org/0000-0002-1566-2408)
Institutions
- Guangdong University of Technology (CN)
- Nanjing University of Information Science and Technology (CN)
- University of Macau (MO)
- Interface (United States) (US)
- Nanjing University of Science and Technology (CN)
- Advanced Materials and Devices (United States) (US)
- Ariel University (IL)
Publication Details
- Journal
- ACS Energy Letters
- Published
- 2025-11-21
- DOI
- https://doi.org/10.1021/acsenergylett.5c02680
- Primary Topic
- Advanced battery technologies research
- Type
- article
- Field-Weighted Citation Impact
- 0.00