Rechargeable lithium-ion batteries (LIBs) are critical for enabling sustainable energy storage. The capacity of cathode materials is a major limiting factor in the LIB performance, and doping has emerged as an effective strategy for enhancing the electrochemical properties of nickel-rich layered oxides such as NCM811. In this study, boron is homogeneously incorporated into the tetrahedral site of NCM811 through co-precipitation, leading to an inductive effect on transition metal (TM)-O-B bonds that delayed structural collapse and reduced oxygen release.
View Article and Find Full Text PDFThe high-voltage oxygen redox activity of Li-rich layered oxides enables additional capacity beyond conventional transition metal (TM) redox contributions and drives the development of positive electrode active materials in secondary Li-based batteries. However, Li-rich layered oxides often face voltage decay during battery operation. In particular, although Li-rich positive electrode active materials with a high nickel content demonstrate improved voltage stability, they suffer from poor discharge capacity.
View Article and Find Full Text PDFAs the demand for lithium-ion batteries (LIBs) continues to increase, there is a growing focus on recycling these battery wastes. Among the existing recycling methods, direct recycling is considered a promising approach, because it allows waste to be returned directly to production. One crucial step in this process is the pretreatment, which involves separating the active materials from the current collector.
View Article and Find Full Text PDFLithium thiophosphates are a promising class of solid electrolyte (SE) materials for all-solid-state batteries (ASSBs) due to their high Li-ion conductivity. Yet, the practical application of lithium thiophosphates is hindered by their chemical instability, which remains a prevalent challenge in the field. Oxygen substitution has been discussed in the literature as a promising strategy to enhance stability.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2024
The simultaneous intercalation of protons and Zn ions in aqueous electrolytes presents a significant obstacle to the widespread adoption of aqueous zinc ion batteries (AZIBs) for large-scale use, a challenge that has yet to be overcome. To address this, we have developed a MnO/tetramethylammonium (TMA) superstructure with an enlarged interlayer spacing, designed specifically to control H/Zn co-intercalation in AZIBs. Within this superstructure, the pre-intercalated TMA ions work as spacers to stabilize the layered structure of MnO cathodes and expand the interlayer spacing substantially by 28 % to 0.
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