Electrolyzed Ni(OH)2 Precursor Sintered with LiOH/LiNiO3 Mixed Salt for Structurally and Electrochemically Stable Cobalt-Free LiNiO2 Cathode Materials
Source abstract
Abstract
Cobalt-free LiNiO2 cathode materials offer a higher energy density at a lower cost than high Co-containing cathode materials. However, Ni(OH)2 precursors for LiNiO2 cathodes are traditionally prepared by the coprecipitation method, which is expensive, complex, and time-consuming. Herein, we report a fast, facile, and inexpensive electrolysis process to prepare a Ni(OH)2 precursor, which was mixed with LiOH/LiNO3 salts to obtain a LiNiO2 cathode material. A combination of advanced characterization techniques revealed that the LiNiO2 cathode material prepared in this way exhibited an excellent layered structure with negligible Li/Ni site mixing and surface structural distortion. Electrochemical cycling of the LiNiO2 cathode material showed an initial discharge capacity of 235.2 mA h/g and a capacity retention of 80.2% after 100 cycles (at 1 C) between 2.75 and 4.3 V. The degradation of the cycling performance of the LiNiO2 cathode material was mainly attributed to the formation of a surface solid–electrolyte interface and a ∼5 nm rock salt-like structure, while the bulk structure of the cathode after cycling was generally stable.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Supercapacitor Materials and Fabrication
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Songshan Lake Materials Laboratory, Dongguan 523808, Guangdong, People’s Republic of China
Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China
Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing 100049, China
Funding
Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China
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