ABSTRACT
Recently, Ni-rich LiNixCoyMn1-x-yO2 (x ≥ 0.8) draw significant research attention as cathode materials in lithium-ion batteries due to their superiority in energy density. However, the oxygen release and the transition metals (TMs) dissolution during the (dis)charging process lead to serious safety issues and capacity loss, which highly prevent its application. In this work, we systematically explored the stability of lattice oxygen and TM sites in LiNi0.8Co0.1Mn0.1O2(NCM811) cathode via investigating various vacancy formations during lithiation/delithiation, and properties such as the number of unpaired spins (NUS), net charges, and d band center were comprehensively studied. In the process of delithiation (x = 1 â 0.75 â 0), the vacancy formation energy of lattice oxygen [Evac(O)] has been identified to follow the order of Evac(O-Mn) > Evac(O-Co) > Evac(O-Ni), and Evac(TMs) shows a consistent trend with the sequence of Evac(Mn) > Evac(Co) > Evac(Ni), demonstrating the importance of Mn to stabilize the structural skeleton. Furthermore, the |NUS| and net charge are proved to be good descriptors for measuring Evac(O/TMs), which show linear correlations with Evac(O) and Evac(TMs), respectively. Li vacancy plays a pivotal role on Evac(O/TMs). Evac(O/TMs) at x = 0.75 vary extremely between the NiCoMnO layer (NCM layer) and the NiO layer (Ni layer), which correlates well with |NUS| and net charge in the NCM layer but aggregates in a small region in the Ni layer due to the effect of Li vacancies. In general, this work provides an in-depth understanding of the instability of lattice oxygen and transition metal sites on the (104) surface of Ni-rich NCM811, which might give new insights into oxygen release and transition metal dissolution in this system.
ABSTRACT
A novel heterostructured material, cobalt phosphate-SiO2 mesostructured cellular foams (CoPO-MCF), was successfully synthesized by in situ growth. The material was characterized by X-ray diffraction (XRD), nitrogen sorption, temperature-programmed reduction (H2-TPR and CO-TPR), temperature-programmed desorption of NH3 (NH3-TPD), and X-ray photoelectron spectroscopy (XPS). A ruthenium precursor was readily introduced and highly dispersed on the CoPO nanophases of the CoPO-MCF through an impregnation method. The resulting Ru/CoPO-MCF catalyst exhibited high catalytic activity for the oxidation of vinyl chloride (VC). The results of three consecutive runs and long-term tests showed high stability of the Ru/CoPO-MCF for the catalytic oxidation of VC. The unique heterostructures of the CoPO-MCF not only improve the reducibility and acidity of the MCF but also strengthen the interaction between ruthenium oxide nanoparticles and the CoPO-MCF support, which contributes to the enhanced catalytic performance.
