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A well-defined dual Mn-site based metal-organic framework to promote CO2 reduction/evolution in Li-CO2 batteries.

Long-Zhang DongYu ZhangYun-Feng LuLei ZhangXin HuangJian-Hui WangJiang LiuShun-Li LiYa-Qian Lan
Published in: Chemical communications (Cambridge, England) (2021)
A series of Li-CO2 battery cathode materials are reported based on metal-organic frameworks with dual-metal sites containing a metalloporphyrin and a metal-coordinated pyrazole. MnTPzP-Mn demonstrates a low voltage hysteresis of 1.05 V at 100 mA g-1 and good stability of 90 cycles at 200 mA g-1. Among them, the Mn-coordinated pyrazole site can promote the effective decomposition of Li2CO3, and the Mn-metalloporphyrin site contributes to the activation of CO2. This is the first example of using a crystalline cathode material with a well-defined structure to reveal natural catalytic sites for CO2 reduction/evolution reactions under aprotic conditions in Li-CO2 batteries.
Keyphrases
  • metal organic framework
  • ion batteries
  • solid state
  • molecular docking
  • ionic liquid
  • dna methylation
  • crystal structure