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Conjugated Carbonyl Compounds as High-Performance Cathode Materials for Rechargeable Batteries

期刊

CHEMISTRY OF MATERIALS
卷 31, 期 21, 页码 8582-8612

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.9b03109

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资金

  1. National Natural Science Foundation, China [21773057, U1704142, 21403057]
  2. Postdoctoral Science Foundation, China [2017M621833]
  3. Program for Innovative Team (in Science and Technology) in University of Henan Province, China [17IRTSTHNO03]
  4. Program for Science and Technology Innovation Talents in Universities of Henan Province, China [18HASTIT008]
  5. Zhongyuan Thousand People Plan-The Zhongyuan Youth Talent Support Program (in Science and Technology), China [ZYQR201810139]
  6. Cultivation Plan for Young Core Teachers in Universities of Henan Province, China [2016GGJS-068]
  7. Fundamental Research Funds for the Henan Provincial Colleges and Universities in Henan University of Technology, China [2018RCJH01]

向作者/读者索取更多资源

In search for novel cathode materials for lithium, sodium, and potassium ion batteries, organic electrode materials are expected to be the next powerful candidates owing to their high theoretical capacity, facile synthesis, low cost, and structural diversity. However, reports concerning organic compounds are not common compared to those concerning inorganic compounds in both research and commercial applications. New requirements for rechargeable batteries, such as low production cost and natural abundance, also preclude us from focusing on heavy and toxic metals, which still impose cost and resource constraints. Undoubtedly, organic carbonyl compounds featuring multielectron reactions and reaction reversibility are quite suitable for meeting these needs. In this review, an overview of the recent efforts on carbonyl materials containing small molecules and polymers is provided. In addition, some strategies to resolve the main problems, such as the dissolution of active organic chemicals into organic electrolytes, low discharge voltage, and low electronic conductivity, are discussed.

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