Coordination Chemistry Modulation of LaFeO3 as a Promising Anode Material for Nickel‐Metal Batteries
Source abstract
Abstract
Abstract Perovskite oxide LaFeO3 (LFO) has emerged as a highly promising anode material for nickel‐metal hydride (Ni‐MH) batteries, owing to its friendly characteristics and cost‐effectiveness. Nevertheless, the practical application of LFO in Ni‐MH batteries faces two major limitations: insufficient electronic conductivity and unsatisfactory specific capacity. To address these issues, the aluminum (Al) and cobalt (Co) doped LaFeO3 materials are synthesized in this contribution via high‐temperature solid state reactions. The doping of Al and Co enhances the covalent interaction between the 3p orbitals of the dopants and the O2p orbitals, facilitating electron migration and thereby improving the material's electrical conductivity, which in turn enhances its discharge performance. After Al and Co modification, the maximum discharge capacity of LFO increased from 178.8 to 314.8 mAh g−1, while the high‐rate discharge performance (HRD) improved from 11.2% to 66.1%. Moreover, after 100 cycles, the discharge capacity reached 223 mAh g−1, significantly higher than that of the undoped sample (98 mAh g−1). This work proposes an effective strategy to enhance the electrochemical performance of materials by employing doping to shorten electron transport pathways and improve electrical conductivity.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Molten salt chemistry and electrochemical processes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Shaanxi Key Laboratory of Macromolecular Science and Technology School of Chemistry and Chemical Engineering Northwestern Polytechnical University Xi'an 710072 China
Fujian Blue Ocean & Black Stone Technology Co. Ltd. Changtai 363900 China
Funding
Fundamental Research Funds for the Central Universities · Postdoctoral Research Foundation of China · Innovative Research Group Project of the National Natural Science Foundation of China
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