4.8 Article

Nanostructured Conductive Metal Organic Frameworks for Sustainable Low Charge Overpotentials in Li-Air Batteries

期刊

SMALL
卷 18, 期 4, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202102902

关键词

metal organic frameworks; Li-O; (2) batteries; electrocatalysis

资金

  1. Department of Energy, Office of Energy Efficiency and Renewable Energy, Vehicle Technologies Office
  2. National Science Foundation DMREF Grant [1729420]
  3. NSF [CBET 1800357]
  4. National Science Foundation CBET [1661038]
  5. Office of Science, Basic Energy Sciences, Materials Sciences and Engineering Division
  6. Argonne National Laboratory, a U.S. Department of Energy Office of Science laboratory [DE-AC02-06CH11357]
  7. CATSS project from the Knut and Alice Wallenberg Foundation [KAW 2016.0072]
  8. Swedish Research Council (VR) [2017-04321, 2016-04625]
  9. Directorate For Engineering
  10. Div Of Chem, Bioeng, Env, & Transp Sys [1661038] Funding Source: National Science Foundation

向作者/读者索取更多资源

This study discovered the outstanding characteristics of a conductive metal organic framework (c-MOF), which promotes the growth of nanocrystalline Li2O2 and enables fast discharge at high current rates. In addition, the structure of Li2O2 works synergistically with the redox mediator (RM) to achieve long cycle life and high capacity under high current densities.
Lithium-oxygen batteries are among the most attractive alternatives for future electrified transportation. However, their practical application is hindered by many obstacles. Due to the insulating nature of Li2O2 product and the slow kinetics of reactions, attaining sustainable low charge overpotentials at high rates becomes a challenge resulting in the battery's early failure and low round trip efficiency. Herein, outstanding characteristics are discovered of a conductive metal organic framework (c-MOF) that promotes the growth of nanocrystalline Li2O2 with amorphous regions. This provides a platform for the continuous growth of Li2O2 units away from framework, enabling a fast discharge at high current rates. Moreover, the Li2O2 structure works in synergy with the redox mediator (RM). The conductivity of the amorphous regions of the Li2O2 allows the RM to act directly on the Li2O2 surface instead of catalyst edges and then transport through the electrolyte to the Li2O2 surface. This direct charge transfer enables a small charge potential of <3.7 V under high current densities (1-2 A g(-1)) sustained for a long cycle life (100-300 cycles) for large capacities (1000-2000 mAh g(-1)). These results open a new direction for utilizing c-MOFs towards advanced energy storage systems.

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