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Halogen-powered static conversion chemistry

delete2024-04-26
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PRE
AI
李
李新亮 (Xinliang Li) *
W
Wenyu Xu
C
Chunyi Zhi *
DOI:10.1038/s41570-024-00597-zdelete
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Abstract

Abstract

En 中文
Halogen-powered static conversion batteries (HSCBs) thrive in energy storage applications. They fall into the category of secondary non-flow batteries and operate by reversibly changing the chemical valence of halogens in the electrodes or/and electrolytes to transfer electrons, distinguishing them from the classic rocking-chair batteries. The active halide chemicals developed for these purposes include organic halides, halide salts, halogenated inorganics, organic-inorganic halides and the most widely studied elemental halogens. Aside from this, various redox mechanisms have been discovered based on multi-electron transfer and effective reaction pathways, contributing to improved electrochemical performances and stabilities of HSCBs. In this Review, we discuss the status of HSCBs and their electrochemical mechanism-performance correlations. We first provide a detailed exposition of the fundamental redox mechanisms, thermodynamics, conversion and catalysis chemistry, and mass or electron transfer modes involved in HSCBs. We conclude with a perspective on the challenges faced by the community and opportunities towards practical applications of high-energy halogen cathodes in energy-storage devices. Substantial progress in halide chemicals and redox mechanisms has spawned a boom in halogen-powered static conversion batteries. This Review tracks the natural benefits and intricate redox behaviour of halogen conversion chemistry, highlighting its pivotal role in electrochemical energy storage.
Keywords:
REDOX CHEMISTRY
ENERGY-DENSITY
BATTERY
PERFORMANCE
INTERCALATION
ELECTROLYTES
INTERHALOGEN
PERSPECTIVE
GRAPHITE
DESIGN

Journal

Nature Reviews Chemistry cover
Nature Reviews Chemistry
IF:
51.7
Papers:
1.0K
Citations:
1.6W

Organization

Z
Zhengzhou University
Scholars:
6.8W
Papers: 4.4W
Citations: 8.5W
C
City University of Hong Kong
Scholars:
2.3W
Papers: 3.0W
Citations: 6.1W
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