Your browser doesn't support javascript.
loading
Upcycling of Spent LiFePO4 Cathodes to Heterostructured Electrocatalysts for Stable Direct Seawater Splitting.
Li, Zhen; Li, Mengting; Chen, Yiqun; Ye, Xucun; Liu, Mengjie; Lee, Lawrence Yoon Suk.
Afiliação
  • Li Z; The Hong Kong Polytechnic University, Applied Biology and Chemical Technology, HONG KONG.
  • Li M; The Hong Kong Polytechnic University, Applied Biology and Chemical Technology, HONG KONG.
  • Chen Y; The Hong Kong Polytechnic University, Applied Biology and Chemical Technology, HONG KONG.
  • Ye X; The Hong Kong Polytechnic University, Applied Biology and Chemical Technology, HONG KONG.
  • Liu M; The Hong Kong Polytechnic University, Applied Biology and Chemical Technology, HONG KONG.
  • Lee LYS; The Hong Kong Polytechnic University, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, ., Hung Hom, HONG KONG.
Angew Chem Int Ed Engl ; : e202410396, 2024 Aug 08.
Article em En | MEDLINE | ID: mdl-39115462
ABSTRACT
The pursuit of carbon-neutral energy has intensified the interest in green hydrogen production from direct seawater electrolysis, given the scarcity of freshwater resources. While Ni-based catalysts are known for their robust activity in alkaline water oxidation, their catalytic sites are prone to rapid degradation in the chlorine-rich environments of seawater, leading to limited operation time. Herein, we report a Ni(OH)2 catalyst interfaced with laser-ablated LiFePO4 (Ni(OH)2/L-LFP), derived from spent Li-ion batteries (LIBs), as an effective and stable electrocatalyst for direct seawater oxidation. Our comprehensive analyses reveal that the PO43- species, formed around L-LFP, effectively repels Cl- ions during seawater oxidation, mitigating corrosion. Simultaneously, the interface between in situ generated NiOOH and Fe3(PO4)2 enhances OH- adsorption and electron transfer during the oxygen evolution reaction. This synergistic effect leads to a low overpotential of 237 mV to attain a current density of 10 mA cm-2 and remarkable durability, with only a 3.3 % activity loss after 600 h at 100 mA cm-2 in alkaline seawater. Our findings present a viable strategy for repurposing spent LIBs into high-performance catalysts for sustainable seawater electrolysis, contributing to the advancement of green hydrogen production technologies.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article