Coupling Ferricyanide/Ferrocyanide Redox Mediated Recycling Spent LiFePO4 with Hydrogen Production.

electrocatalysis * anodic electrooxidation * hydrogen production * lithium recovery * spent LiFePO4

Journal

Angewandte Chemie (International ed. in English)
ISSN: 1521-3773
Titre abrégé: Angew Chem Int Ed Engl
Pays: Germany
ID NLM: 0370543

Informations de publication

Date de publication:
16 Jan 2024
Historique:
revised: 01 01 2024
received: 29 11 2023
accepted: 16 01 2024
medline: 16 1 2024
pubmed: 16 1 2024
entrez: 16 1 2024
Statut: aheadofprint

Résumé

Replacing the oxygen evolution reaction with thermodynamically more favorable alternative oxidation reactions offers a promising alternative to reduce the energy consumption of hydrogen production. However, questions remain regarding the economic viability of alternative oxidation reactions for industrial-scale hydrogen production. Here, we propose an innovative cost-effective, environment-friendly and energy-efficient strategy for simultaneous recycling of spent LiFePO4 (LFP) batteries and hydrogen production by coupling the spent LFP-assisted ferricyanide/ferrocyanide ([Fe(CN)6]4-/[Fe(CN)6]3-) redox reaction. The onset potential for the electrooxidation of [Fe(CN)6]4- to [Fe(CN)6]3- is low at 0.87 V. Operando Raman and UV-visible spectroscopy confirm that the presence of LFP in the electrolyte allows for the rapid reduction of [Fe(CN)6]3- to [Fe(CN)6]4-, thereby completing the [Fe(CN)6]4-/[Fe(CN)6]3- redox cycle as well as facilitating the conversion of spent LiFePO4 into LiOH·H2O and FePO4. The electrolyzer consumes 3.6 kWh of electricity per cubic meter of H2 produced at 300 mA cm-2, which is 43% less than conventional water electrolysis. Additionally, this recycling pathway for spent LFP batteries not only minimizes chemical consumption and prevents secondary pollution but also presents significant economic benefits.

Identifiants

pubmed: 38226789
doi: 10.1002/anie.202318248
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e202318248

Informations de copyright

© 2024 Wiley-VCH GmbH.

Auteurs

Xin Jia (X)

Harbin Institute of Technology, School of Materials Science and Engineering, No. 92, West Dazhi Street, 150001, Harbin, Heilongjiang,, CHINA.

Hongjun Kang (H)

Harbin Institute of Technology, School of Chemistry and Chemical Engineering, No. 92, West Dazhi Street, 150001, Harbin, Heilongjiang, CHINA.

Guangyao Hou (G)

Harbin Institute of Technology, School of Materials Science and Engineering, No. 92, West Dazhi Street, 150001, Harbin, Heilongjiang, CHINA.

Weiran Wu (W)

Harbin Institute of Technology, School of Chemistry and Chemical Engineering, 92 Dazhi Street, Nangang District, 150001, Harbin, CHINA.

Songtao Lu (S)

Harbin Institute of Technology, School of Chemistry and Chemical Engineering, No. 92, West Dazhi Street, 150001, Harbin, Heilongjiang, CHINA.

Yang Li (Y)

Harbin Institute of Technology, School of Chemistry and Chemical Engineering, CHINA.

Qing Wang (Q)

National University of Singapore, Department of Materials Science and Engineering, Lower Kent Ridge Rd, 119260, SINGAPORE.

Wei Qin (W)

Harbin Institute of Technology, School of Materials Science and Engineering, No. 92, West Dazhi Street, 150001, Harbin, Heilongjiang,, CHINA.

Xiaohong Wu (X)

Harbin Institute of Technology, Chemistry, 92 Dazhi Street, Nangang District, 150001, Harbin, CHINA.

Classifications MeSH