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Synthesis of Poly(1,4‐anthraquinone) Using Catalytic Amounts of Nickel

Adler, Florin; Pinto-Bautista, Sebastián; Lorenz, Christoph; Hinrichs, Lars; Weil, Marcel 1; Esser, Birgit
1 Institut für Technikfolgenabschätzung und Systemanalyse (ITAS), Karlsruher Institut für Technologie (KIT)

Abstract:

Multivalent metal batteries are attractive options to diversify energy storage options offering higher sustainability, but the high charge density of multivalent ions poses challenges to electrode materials. Organic electrode materials are currently the best-performing candidates, and among them, poly(1,4-anthraquinone) (P14AQ) shows excellent electrochemical properties. This holds in particular for magnesium-ion batteries, where the polymer displays reversible insertion of Mg2+ ions with high cycling stability. The conventional synthesis of P14AQ, however, employs stoichiometric amounts of bis(cycloocta-1,5-diene)nickel(0) (Ni(COD)2), which is an air- and light-sensitive and expensive chemical, and therefore lacks sustainability. Herein a synthetic route to P14AQ is presented that uses only catalytic amounts of dibromobis(triphenylphosphine)nickel(II) (NiBr2(PPh3)2). This route – in addition to being more cost-efficient and less toxic – results in higher yields and polymer molecular weights. A life-cycle assessment (LCA) comparing the new and conventional polymerization methods shows that regarding the environmental impact categories climate change, human toxicity, and cumulative energy demand, the new method brings significant improvement.


Verlagsausgabe §
DOI: 10.5445/IR/1000184663
Veröffentlicht am 15.09.2025
Cover der Publikation
Zugehörige Institution(en) am KIT Institut für Technikfolgenabschätzung und Systemanalyse (ITAS)
Publikationstyp Zeitschriftenaufsatz
Publikationsmonat/-jahr 09.2025
Sprache Englisch
Identifikator ISSN: 2198-3844
KITopen-ID: 1000184663
HGF-Programm 37.11.02 (POF IV, LK 01) Societally-Feasible Transformation Pathways
Erschienen in Advanced Science
Verlag Wiley Open Access
Band 12
Heft 36
Seiten e06251
Vorab online veröffentlicht am 21.07.2025
Nachgewiesen in Web of Science
OpenAlex
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Scopus
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