Polymers Bearing Catechol Pendants as Universal Hosts for Aqueous Rechargeable H+, Li-Ion, and Post-Li-ion (Mono-, Di-, and Trivalent) Batteries
Source abstract
Abstract
Organic electrode materials capable of reversible coordination/uncoordination of both mono- and multivalent ions in aqueous electrolytes are desired to develop safe, sustainable, and cost-effective water-based batteries. Here, we demonstrate the universality of bioinspired redox-active polymers bearing catechol pendants to reversibly coordinate/uncoordinate numerous cations including H+ and Li+ to Zn2+ and Al3+ with fast kinetics and ultralong cyclability. This unprecedented versatility is based on a catecholato–metal cation complex (Cat2–(mMn+)) charge storage mechanism that dictates the overall electrochemistry: formation of stronger complexes in M+ < M2+ < M3+ order resulted in a huge redox potential increment that might be used to tune the operating voltage of the battery.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced battery technologies research · Advanced Battery Materials and Technologies · Advancements in Battery Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Electrochemical Processes Unit, IMDEA Energy Institute, Avenida Ramón de la Sagra 3, 28935 Móstoles, Spain
Centre for Education and Research on Macromolecules (CERM), CESAM Research Unit, Department of Chemistry, University of Liege, Allée de la Chimie B6A, 4000 Liège, Belgium
Funding
Ministerio de Econom?a y Competitividad · Fonds De La Recherche Scientifique - FNRS · Comunidad de Madrid
References (30)
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