Selenium-Anchored Chlorine Redox Chemistry in Aqueous Zinc Dual-Ion Batteries
© 2023 Wiley-VCH GmbH..
Chlorine-based batteries with Cl0 to Cl- redox reaction (ClRR) are promising for high-performance energystorage due to their high redox potential and large theoretical capacity. However, the inherent gas-liquid conversion feature of ClRR together with poor Cl fixation can cause Cl2 leakage, reducing battery reversibility. Herein, we utilize a Se-based organic molecule, diphenyl diselenide (di-Ph-Se), as the Cl anchoring agent and realize an atomic level-Cl fixation through chalcogen-halogencoordinating chemistry. The promoted Cl fixation, with two oxidized Cl0 anchoring on a single Ph-Se, and the multivalence conversion of Se contributeto a six-electron conversion process with up to 507 mAh g-1 and an average voltage of 1.51 V, as well as a high energy density of 665 Wh Kg-1 . Based on the superior reversibility of thedeveloped di-Ph-Se electrode with ClRR, a remarkable rate performance (205 mAh g-1 at 5 A g-1 ) and cycling performance (capacity retention of 77.3 % after 500cycles) are achieved. Significantly, the pouch cell delivers a record arealcapacity of up to 6.87 mAh cm-2 and extraordinary self-discharge performance. This chalcogen-halogen coordination chemistry between the Se electrode and Cl provides a new insight for developing reversible and efficientbatteries with halogen redox reactions.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2024 |
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Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - volume:36 |
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Enthalten in: |
Advanced materials (Deerfield Beach, Fla.) - 36(2024), 6 vom: 07. Feb., Seite e2309330 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Chen, Ze [VerfasserIn] |
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Links: |
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Themen: |
Aqueous batteries |
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Anmerkungen: |
Date Revised 08.02.2024 published: Print-Electronic Citation Status PubMed-not-MEDLINE |
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doi: |
10.1002/adma.202309330 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM365008567 |
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520 | |a Chlorine-based batteries with Cl0 to Cl- redox reaction (ClRR) are promising for high-performance energystorage due to their high redox potential and large theoretical capacity. However, the inherent gas-liquid conversion feature of ClRR together with poor Cl fixation can cause Cl2 leakage, reducing battery reversibility. Herein, we utilize a Se-based organic molecule, diphenyl diselenide (di-Ph-Se), as the Cl anchoring agent and realize an atomic level-Cl fixation through chalcogen-halogencoordinating chemistry. The promoted Cl fixation, with two oxidized Cl0 anchoring on a single Ph-Se, and the multivalence conversion of Se contributeto a six-electron conversion process with up to 507 mAh g-1 and an average voltage of 1.51 V, as well as a high energy density of 665 Wh Kg-1 . Based on the superior reversibility of thedeveloped di-Ph-Se electrode with ClRR, a remarkable rate performance (205 mAh g-1 at 5 A g-1 ) and cycling performance (capacity retention of 77.3 % after 500cycles) are achieved. Significantly, the pouch cell delivers a record arealcapacity of up to 6.87 mAh cm-2 and extraordinary self-discharge performance. This chalcogen-halogen coordination chemistry between the Se electrode and Cl provides a new insight for developing reversible and efficientbatteries with halogen redox reactions | ||
650 | 4 | |a Journal Article | |
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650 | 4 | |a zinc batteries | |
650 | 4 | |a zinc-ion batteries | |
700 | 1 | |a Hou, Yue |e verfasserin |4 aut | |
700 | 1 | |a Wang, Yiqiao |e verfasserin |4 aut | |
700 | 1 | |a Wei, Zhiquan |e verfasserin |4 aut | |
700 | 1 | |a Chen, Ao |e verfasserin |4 aut | |
700 | 1 | |a Li, Pei |e verfasserin |4 aut | |
700 | 1 | |a Huang, Zhaodong |e verfasserin |4 aut | |
700 | 1 | |a Li, Nan |e verfasserin |4 aut | |
700 | 1 | |a Zhi, Chunyi |e verfasserin |4 aut | |
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