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Structural degradation and surface chemical instability are dominant issues of Ni-rich layered cathodes, which trigger capacity fading and safety concerns, hindering the extensive application of Ni-rich cathodes toward high-energy, long-life lithium-ion batteries. Here, by combining trace Ta doping and an ultrathin Zr-Y mixed oxide coating, an integrated modification strategy significantly improves the cycling and thermal stability of Ni-rich LiNiCoAlO (NCA) cathodes. The integrated modified Ni-rich cathode provides an unprecedented comprehensive performance with a high discharge capacity of 212.2 mA h g at 0.1 , an 88.6% cycling retention after 500 cycles at 1 , and a high exothermic peak temperature of 261 °C compared with the pristine NCA cathode (67.4% capacity retention for 500 cycles and 221 °C for the exothermic peak). Further mechanism studies illustrate that a dual-structural surface constructed of a rock salt surface induced by Ta doping and ultrathin Zr-Y mixed oxide coating jointly suppresses surface side reactions between cathodes and electrolytes. Moreover, trace Ta doping in the bulk stabilizes the bulk structure and prevents mechanical cracks. This study highlights the importance of comprehensive modification of the bulk and surface for improving the electrochemical performance and provides a potential optimizing strategy for the commercialization of high-capacity Ni-rich cathode materials.
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http://dx.doi.org/10.1021/acsami.2c07453 | DOI Listing |
Dalton Trans
September 2025
School of Education, Can Tho University, 3-2 Road, Can Tho City 900000, Vietnam.
Enhancement of the performance of lithium-ion batteries is a critical strategy for addressing the challenges associated with cost and raw materials. By doping boron (B), aluminum (Al), and aluminum/boron (Al/B) utilizing the sol-gel method, we demonstrate a substantial improvement in the cycling performance of Ni-rich lithium nickel manganese cobalt oxide (NMC) as an electrode. While the initial specific capacitance of the doped samples may be lower than that of the pristine NMC, these samples demonstrate a notable increase in specific capacitance during subsequent cycles, reaching a peak around the 10 cycle and nearing the highest specific capacitance observed in NMC cathodes.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Department of Chemical Engineering, Shanghai Electrochemical Energy Devices Research Center, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai, 200240, China.
High-energy lithium-ion batteries necessitate stable Ni-rich layered cathodes, yet critical challenges such as lattice distortion and surface structure collapse remain unresolved. While conventional high-valence doping greatly alleviates surface degradations, it is ineffective in stabilizing bulk lattice due to dopant segregation. Here, we propose a slightly Li-rich (SLR) lattice design by partially substituting transition-metal (TM) ions with Li ions in TM layers, reducing electrostatic repulsion against high-valence dopants.
View Article and Find Full Text PDFSmall
September 2025
Department of Energy Science, Sungkyunkwan University, Suwon, Gyeonggi-do, 16419, Republic of Korea.
Water-washing effectively removes surface residual lithium from high-Ni LiNiCoMnO (NCM) cathodes; however, it inevitably degrades the electrochemical performance. To address this issue, integrated strategies targeting the conversion of surface residual lithium into artificial coating layers on high-Ni NCM cathodes have been proposed; however, these require further processing, thus hindering their industrial application. This study proposes a trailblazing strategy for directly converting residual lithium into a LiF layer simultaneously formed on both the surface of secondary particles and the interfaces between the primary particles of high-Ni NCM, without requiring further processing.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
College of Chemistry, Huazhong Agricultural University, Wuhan 430070, China.
High-nickel LiNiCoMnO (NCM83) cathodes suffer from interfacial instability resulting from cathode-electrolyte reactions and anisotropic mechanical strain within secondary particles. Herein, we present a mechanically adaptive cathode-electrolyte interphase (CEI) engineered via a dynamic covalent network that features a supramolecular ion-conducting polyurethane ureido-pyrimidinone (SPU-UPy) elastomer. The dynamic network integrates cooperative hydrogen bonds and disulfide bonds and imparts exceptional mechanical resilience and autonomous self-healing capabilities that allow it to accommodate volume fluctuations without compromising structural integrity.
View Article and Find Full Text PDFAdv Sci (Weinh)
August 2025
Guangzhou Key Laboratory for Surface Chemistry of Energy Materials, New Energy Research Institute, School of Environment and Energy, South China University of Technology, Guangzhou, 510006, P. R. China.
Under prolonged high-voltage cycling, single-crystalline Ni-rich cathodes are prone to severe transition metal dissolution, irreversible phase transformations, and reduced structural stability, which significantly hinder their practical application. Hence, a dual-modification strategy is proposed and implemented for single-crystalline LiNiCoMnO (SCNCM90) cathodes by introducing Al/B gradient co-doping and an AlBO surface coating to mitigate anisotropic structural changes. The subsurface Al/B gradient doping induces a lithium-rich vacancy disordered structure, which effectively suppresses the H2-H3 phase transition, while suppressing lattice strain and mechanical degradation.
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