Rechargeable Aqueous Mn‐Metal Battery Enabled by Inorganic–Organic Interfaces. (21st July 2022)
- Record Type:
- Journal Article
- Title:
- Rechargeable Aqueous Mn‐Metal Battery Enabled by Inorganic–Organic Interfaces. (21st July 2022)
- Main Title:
- Rechargeable Aqueous Mn‐Metal Battery Enabled by Inorganic–Organic Interfaces
- Authors:
- Yang, Qi
Qu, Xiaofeng
Cui, Huilin
He, Xincheng
Shao, Yuan
Zhang, Yong
Guo, Xun
Chen, Ao
Chen, Ze
Zhang, Rong
Kong, Duanyang
Shi, Zhicong
Liu, Jun
Qiu, Jieshan
Zhi, Chunyi - Abstract:
- Abstract: Aqueous batteries that use metal anodes exhibit maximum anodic capacity, whereas the energy density is still unsatisfactory partially due to the high redox potential of the metal anode. Current metal anodes are plagued by the dilemma that the redox potential of Zn is not low enough, whereas Al, Mg, and others with excessively low redox potential cannot work properly in aqueous electrolytes. Mn metal with a suitably low redox potential is a promising candidate, which was rarely explored before. Here, we report a rechargeable aqueous Mn‐metal battery enabled by a well‐designed electrolyte and robust inorganic–organic interfaces. The inorganic Sn‐based interface with a bottom‐up microstructure was constructed to preliminarily suppress water decomposition. With this bubble‐free interface, the organic interface can be formed via an esterification reaction of sucrose triggered by acyl chloride in the electrolyte, generating a dense physical shield that isolates water while permitting Mn 2+ diffusion. Hence, a Mn symmetric cell achieves a superior plating/stripping stability for 200 hours, and a Mn||V2 O5 battery maintains approximately 100 % capacity after 200 cycles. Moreover, the Mn||V2 O5 battery realizes a much higher output voltage than that of the Zn||V2 O5 battery, evidencing the possibility of increasing the energy density through using a Mn anode. This work develops a systematic strategy to stabilize a Mn‐metal anode for Mn‐metal batteries, opening a new doorAbstract: Aqueous batteries that use metal anodes exhibit maximum anodic capacity, whereas the energy density is still unsatisfactory partially due to the high redox potential of the metal anode. Current metal anodes are plagued by the dilemma that the redox potential of Zn is not low enough, whereas Al, Mg, and others with excessively low redox potential cannot work properly in aqueous electrolytes. Mn metal with a suitably low redox potential is a promising candidate, which was rarely explored before. Here, we report a rechargeable aqueous Mn‐metal battery enabled by a well‐designed electrolyte and robust inorganic–organic interfaces. The inorganic Sn‐based interface with a bottom‐up microstructure was constructed to preliminarily suppress water decomposition. With this bubble‐free interface, the organic interface can be formed via an esterification reaction of sucrose triggered by acyl chloride in the electrolyte, generating a dense physical shield that isolates water while permitting Mn 2+ diffusion. Hence, a Mn symmetric cell achieves a superior plating/stripping stability for 200 hours, and a Mn||V2 O5 battery maintains approximately 100 % capacity after 200 cycles. Moreover, the Mn||V2 O5 battery realizes a much higher output voltage than that of the Zn||V2 O5 battery, evidencing the possibility of increasing the energy density through using a Mn anode. This work develops a systematic strategy to stabilize a Mn‐metal anode for Mn‐metal batteries, opening a new door towards enhanced voltage of aqueous batteries. Abstract : Toward the energy upgrade of aqueous batteries, an aqueous Mn‐metal battery is reported for which the electrolyte and inorganic–organic interfaces were designed. The inorganic interface provides a bubble‐free environment for the organic interface formed by esterification. The Mn||Mn cell shows a life of 200 h, and the Mn||V2 O5 battery realizes a higher output voltage than the Zn||V2 O5 counterpart. This work paves the way for Mn‐anode and energetic aqueous batteries. … (more)
- Is Part Of:
- Angewandte Chemie. Volume 134:Number 35(2022)
- Journal:
- Angewandte Chemie
- Issue:
- Volume 134:Number 35(2022)
- Issue Display:
- Volume 134, Issue 35 (2022)
- Year:
- 2022
- Volume:
- 134
- Issue:
- 35
- Issue Sort Value:
- 2022-0134-0035-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-07-21
- Subjects:
- Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ange.202206471 ↗
- Languages:
- English
- ISSNs:
- 0044-8249
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0902.000000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23440.xml