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Cobalt tetraoxide (CoO) is regarded as a promising anode material for Li-ion batteries owing to its high theoretical capacity (890 mAh g), simple preparation, and controllable morphology. Nanoengineering has been proven to be an effective method for producing high-performance electrode materials. However, systematic research on the influence of material dimensionality on battery performance is lacking. Herein, we prepared CoO with various dimensionalities (one-dimensional (1D) CoO nanorod (NR), two-dimensional (2D) CoO nanosheet (NS), three-dimensional (3D) CoO nanocluster (NC), and 3D CoO nanoflower (NF)) using a simple solvothermal heat treatment method, and their morphologies were controlled by varying the precipitator type and solvent composition. The 1D CoO NR and 3D samples (3D CoO NC and 3D CoO NF) exhibited poor cyclic and rate performances, respectively, while the 2D CoO NS exhibited the best electrochemical performance. The mechanism analysis revealed that the cyclic stability and rate performance of the CoO nanostructures are closely related to their intrinsic stability and interfacial contact performance, respectively, and the 2D thin-sheet structure can achieve an optimal balance between the two, resulting in the best performance. This work presents a comprehensive study on the effect of dimensionality on the electrochemical performance of CoO anodes, providing a new concept for the nanostructure design of conversion-type materials.
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http://dx.doi.org/10.1016/j.jcis.2023.05.053 | DOI Listing |
Int J Biol Macromol
September 2025
College of Materials Engineering, Fujian Agriculture and Forestry University, Fuzhou, 350002, China. Electronic address:
Lignin, a negatively charged, three-dimensional natural biopolymer, serves as an ideal support for metal catalysts due to its abundant functional groups and tunable chemical properties, which enable strong metal coordination and effective immobilization. Herein, we demonstrate a lignin-mediated Co/O co-doped AgS, symbolized as L-AgCoOS, bimetal oxysulfide catalyst via a facile hydrolysis method for the efficient reduction of toxic phenolic compounds (4-nitrophenol, 4-NP), organic dyes (methyl orange (MO), methylene blue (MB), rhodamine B (RhB), and heavy metal ions Cr(VI)) under dark conditions. Lignin, used to immobilize catalysts, also contributes to increasing the number of active catalytic sites and enhancing catalytic activity.
View Article and Find Full Text PDFLangmuir
September 2025
School of Light Industry Science and Engineering, Beijing Technology and Business University, Beijing 100048, People's Republic of China.
The study of the self-assembly of surfactants in aqueous solutions, though a traditional field, remains fascinating and full of novelty. In this article, the anionic perfluorodecanoic acid surfactant (PFA) is separately complexed with three hydroxyalkylamines (monoethanolamine (MEA), diethylamine (DEA), and triethanolamine (TEA)) in aqueous solutions. The transformation of aggregate morphologies from spherical unilamellar to nanotubes and then to spherical bilamellar is observed at room temperature, which is confirmed by cryo-transmission electron microscopy (cryo-TEM).
View Article and Find Full Text PDFAdv Mater
September 2025
School of Materials Science and Engineering, Anhui University, Hefei, 230601, China.
Modulating the electronic structure of catalysts to maximize their power holds the key to address the challenges faced by zinc-iodine batteries (ZIBs), including the shuttle effect and slow redox kinetics at the iodine cathode. Herein, oxygen vacancies is innovatively introduced into CoO lattice to create high-spin-state Co active sites in nonstoichiometric CoO nanocrystals supported by carbon nanofibers (H-CoO/CNFs). This simple strategy intensifies crystal field splitting of Co 3d orbitals, optimizing the spin-orbital coupling between Co 3d orbitals and iodine species.
View Article and Find Full Text PDFACS Omega
September 2025
Research Laboratory in bionanomaterials, LPbio, Department of Chemistry, Federal University of Viçosa, 36570-900 Viçosa, Minas Gerais, Brazil.
Herein, it is reported the synthesis of a niobium-based metal-organic framework (MOF), [Nb-(Bez-(COO))] , for the extraction of caffeine from surface waters. The material was synthesized and characterized by Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, scanning electron microscopy (SEM), X-ray diffraction (XRD), and Brunauer-Emmett-Teller (BET) analysis, which confirmed the coordination between the ligand (1,4-benzenodicarboxylic, (Bez-(COO))) and niobium (Nb) with a morphology composed of hexagonal rods, high crystallinity, and a surface area of 94.7 m g.
View Article and Find Full Text PDFDalton Trans
September 2025
Instituto de Química, Universidad Nacional Autónoma de México, Circuito Interior, CU, Ciudad de México, 04510, Mexico.
Synthesis, characterization, and electrocatalytic water oxidation studies of the cubane-type complexes [(μ-)CoCl(MeOH)] (1) and [(μ-)CoCl(MeOH)] (2) are herein reported. Cubanes 1 and 2 were obtained in high yields under mild conditions by self-assembly of the ligands = 1--2-benzimidazolylmethanol and = 1-methyl-2-benzimidazolylmethanol with CoCl·6HO in basic methanolic solution. Both compounds feature a cubane-type structure in which the central {CoO} units are built by four Co centers coordinated by alkoxide-bridged oxygen and nitrogen atoms from the deprotonated ligands and stabilized by MeOH molecules and chloride ions.
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