Boosted Mg−CO2 Batteries by Amine‐Mediated CO2 Capture Chemistry and Mg2+‐Conducting Solid‐electrolyte Interphases

Author:

Peng Chengxin1,Xue Linlin2,Zhao Zhengfei2,Guo Longyuan2,Zhang Chenyue2,Wang Aoxuan23,Mao Jianfeng4,Dou Shixue1,Guo Zaiping4ORCID

Affiliation:

1. School of Materials and chemistry Institute of Energy Materials Science University of Shanghai Science and Technology Shanghai 200093 China

2. Key Laboratory for Green Chemical Technology of Ministry of Education School of Chemical Engineering and Technology Tianjin University Tianjin 300072 China

3. Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education) College of Chemistry Nankai University Tianjin 300071 China

4. School of Chemical Engineering The University of Adelaide Adelaide SA 5005 Australia

Abstract

AbstractMg−CO2 battery has been considered as an ideal system for energy conversion and CO2 fixation. However, its practical application is significantly limited by the poor reversibility and sluggish kinetics of CO2 cathode and Mg anode. Here, a new amine mediated chemistry strategy is proposed to realize a highly reversible and high‐rate Mg−CO2 battery in conventional electrolyte. Judiciously combined experimental characterization and theoretical computation unveiled that the introduced amine could simultaneously modify the reactant state of CO2 and Mg2+ to accelerate CO2 cathodic reactions on the thermodynamic‐kinetic levels and facilitate the formation of Mg2+‐conductive solid‐electrolyte interphase (SEI) to enable highly reversible Mg anode. As a result, the Mg−CO2 battery exhibits boosted stable cyclability (70 cycles, more than 400 h at 200 mA g−1) and high‐rate capability (from 100 to 2000 mA g−1 with 1.5 V overpotential) even at −15 °C. This work opens a newly promising avenue for advanced metal‐CO2 batteries.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Medicine

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