d-Orbital Induced Electronic Structure Reconfiguration toward Manipulating Electron Transfer Pathways of Metallo-Porphyrin for Enhanced AlCl2 + Storage

© 2024 Wiley‐VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 36(2024), 45 vom: 21. Nov., Seite e2409904
1. Verfasser: Jiao, Shuqiang (VerfasserIn)
Weitere Verfasser: Han, Xue, Bu, Xudong, Huang, Zheng, Li, Shijie, Wang, Wei, Wang, Mingyong, Liu, Yunpeng, Song, Wei-Li
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2024
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article aluminum ion battery high specific capacity metallo‐porphyrin compounds organic positive electrode
Beschreibung
Zusammenfassung:© 2024 Wiley‐VCH GmbH.
The positive electrodes of non-aqueous aluminum ion batteries (AIBs) frequently encounter significant issues, for instance, low capacity in graphite (mechanism: anion de/intercalation and large electrode deformation induced) and poor stability in inorganic positive electrodes (mechanism: multi-electron redox reaction and dissolution of active materials induced). Here, metallo-porphyrin compounds (employed Fe2+, Co2+, Ni2+, Cu2+, and Zn2+ as the ion centers) are introduced to effectively enhance both the cycling stability and reversible capacity due to the formation of stable conjugated metal-organic coordination and presence of axially coordinated active sites, respectively. With the regulation of electronic energy levels, the d-orbitals in the redox reactions and electron transfer pathways can be rearranged. The 5,10,15,20-tetraphenyl-21H,23H-porphine nickle(II) (NiTPP) presents the highest specific capacity (177.1 mAh g-1), with an increment of 32.1% and 77.1% in comparison with the capacities of H2TPP and graphite, respectively, which offers a new route for developing high-capacity positive electrodes for stable AIBs
Beschreibung:Date Revised 07.11.2024
published: Print-Electronic
Citation Status PubMed-not-MEDLINE
ISSN:1521-4095
DOI:10.1002/adma.202409904