In this study, severe cracking occurred during an investigation of the direct hot rolling of industrial electrolytic nickel plates. To determine the cause of hot-rolling cracking, the microstructure phase composition was analyzed through the utilization of various techniques, including optical microscopy, scanning electron microscopy, electron backscattering diffraction, transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS) and electron probe micro-analysis. The comparative microstructural analysis took place between specimens heat treated in atmospheric and vacuum environments. The characterization and analysis of the hot-rolled plates considered the crack microstructure and fracture morphology. It was shown that holes appeared along the large angular grain boundaries after annealing at 1100 °C for 8 h. Possible reason: In a high-temperature environment, the decomposition of residual additives in the electrolytic nickel releases oxidizing gases, which oxidizes the grain boundaries. The reaction with carbon diffused into the grain boundaries and produced carbon monoxide gas, which induced holes and severely reduced the grain boundary plasticity. The heat treatment time did not need to be very long for severe grain boundary degradation to occur. After severe cavitation, the electrolytic nickel was severely cracked at grain boundaries cracks due to a shear force, and brittle fractures occurred along grains with very low plasticity.
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http://dx.doi.org/10.3390/ma17174428 | DOI Listing |
J Colloid Interface Sci
December 2024
Key Laboratory of New Energy Development and Energy Storage Technology of Handan, College of Materials Science and Engineering, Hebei University of Engineering, Handan 056038, People's Republic of China.
Herein, a novel composite solid-state polymer electrolytes (CSEs) was regulated by introducing CoNi-MOF (Metal-organic framework) @NiPc (Nickel phthalocyanine) nanofiller (CMN) into PEO (polyethylene oxide) matrix. In this novel system, the NiPc uniformly wrapped around the surface of MOF through hydrogen bond bridging, avoiding the agglomeration of the MOF particles. The chemisorption between Ni in NiPc and the O atoms in the bis(triffuoromethanesulfonyl)imide anion (TFSI) restricted the mobility of the anions within the CSEs, which improved the release of Li ions from the NiPcLi.
View Article and Find Full Text PDFACS Nano
January 2025
Soft Foundry Institute, Seoul National University, Seoul 08826, Republic of Korea.
Nickel-rich NCM cathode materials promise lithium-ion batteries with a high energy density. However, an increased Ni fraction in the cathode leads to complex phase transformations with electrode-electrolyte side reactions, which cause rapid capacity fading. Here, we show that an initial formation cycle at 0.
View Article and Find Full Text PDFSmall
January 2025
School of Materials Science and Engineering, Guangdong Provincial Key Laboratory of Advanced Energy Storage Materials, South China University of Technology, Guangzhou, 510640, China.
Ultrahigh-nickel layered oxide cathodes (≥90% nickel) possess exceptionally high discharge capacities, which can significantly improve the energy density of lithium-ion batteries and alleviate the driving range anxiety of electric vehicles. However, the high interfacial reactivity of ultrahigh-nickel cathodes, especially the detrimental side reactions with harmful acidic species like HF in the electrolyte, can deteriorate the battery interface and reduce the cycle life, hindering their practical application. In this study, 3-isocyanatopropyltrimethoxysilane (PTTS-NCO) is introduced as the electrolyte additive, which can effectively scavenge the harmful acidic species in the electrolyte and form a protective surface layer at the electrode/electrolyte interface, thereby enhancing the electrochemical performance of the battery (NCM90/Li).
View Article and Find Full Text PDFInorg Chem
January 2025
College of Environment and Materials Engineering, Yantai University, Yantai 264005, China.
As an attractive optical/heat dynamic management technology, reversible metal electrodeposition/dissolution electrochromism (RME-EC) shows many advantages, including high optical modulation amplitude, wide modulation band, and color neutrality, but also suffers from performance degradation because of uneven dendritic metal deposition as well as the formation/accumulation of isolated metal debris. In this paper, a facile RME-EC system is established in a green and affordable aqueous electrolyte, by making good use of the nondendritic Ni-Cu codeposition. Furthermore, an in situ self-healing strategy is further established by activating the Br/Br couple of the Br-containing electrolyte to improve the EC performance.
View Article and Find Full Text PDFACS Nano
January 2025
Department of Chemistry, Collaborative Innovation Center of Chemistry for Energy Materials, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Institute of New Energy, Fudan University, Shanghai 200438, China.
The utilization of sulfide-based solid electrolytes represents an attractive avenue for high safety and energy density all-solid-state batteries. However, the potential has been impeded by electrochemical and mechanical stability at the interface of oxide cathodes. Plastic crystals, a class of organic materials exhibiting remarkable elasticity, chemical stability, and ionic conductivity, have previously been underutilized due to their susceptibility to dissolution in liquid electrolytes.
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