Your browser doesn't support javascript.
loading
Coupling Ferricyanide/Ferrocyanide Redox Mediated Recycling Spent LiFePO4 with Hydrogen Production.
Jia, Xin; Kang, Hongjun; Hou, Guangyao; Wu, Weiran; Lu, Songtao; Li, Yang; Wang, Qing; Qin, Wei; Wu, Xiaohong.
Afiliação
  • Jia X; School of Materials Science and Engineering, Harbin Institute of Technology, 150001, Harbin, China.
  • Kang H; School of Materials Science and Engineering, Harbin Institute of Technology, 150001, Harbin, China.
  • Hou G; School of Chemistry and Chemical Engineering, Harbin Institute of Technology, 150001, Harbin, China.
  • Wu W; School of Materials Science and Engineering, Harbin Institute of Technology, 150001, Harbin, China.
  • Lu S; School of Chemistry and Chemical Engineering, Harbin Institute of Technology, 150001, Harbin, China.
  • Li Y; School of Chemistry and Chemical Engineering, Harbin Institute of Technology, 150001, Harbin, China.
  • Wang Q; School of Chemistry and Chemical Engineering, Harbin Institute of Technology, 150001, Harbin, China.
  • Qin W; Department of Materials Science and Engineering, National University of Singapore, 117576, Singapore, Singapore.
  • Wu X; School of Materials Science and Engineering, Harbin Institute of Technology, 150001, Harbin, China.
Angew Chem Int Ed Engl ; 63(10): e202318248, 2024 Mar 04.
Article em En | MEDLINE | ID: mdl-38226789
ABSTRACT
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 ⋅ H2 O 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.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article