4.7 Article

Novel NASICON-typed porous Ni1.5V2(PO4)3/C and Mn1.5V2(PO4)3/C as anode materials for lithium-ion batteries: Crystal structure and electrochemical lithiation/delithiation reaction mechanism

Journal

JOURNAL OF ENERGY STORAGE
Volume 70, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.est.2023.107889

Keywords

NaSICon; XPS; Operando; Jahn-Teller distortion; Energy storage; Batteries

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Novel porous NaSICon-typed phosphate materials Ni1.5V2(PO4)3/C and Mn1.5V2(PO4)3/C were synthesized as anode materials for Li-ion batteries. These materials exhibited reversible conversion mechanism, high cycling stability at high rates, and good rate capability performances. In operando XRD and X-ray photoelectron spectroscopy were used to investigate the structural changes and SEI growth affecting the electrochemical performances of the materials, providing insights into the lithiation/delithiation reaction mechanism.
Novel porous NaSICon-typed phosphate materials Ni1.5V2(PO4)3/C (NVP/C) and Mn1.5V2(PO4)3/C (MVP/C) are introduced as anode materials for Li-ion batteries. The materials were prepared via sol-gel method with annealing under argon flow. The structural, morphological, and electrochemical investigations of the materials as anodes for Li-ion batteries were conducted. The samples crystallized in a distorted triclinic system with a P1 space group. The two synthesized anode materials exhibited a conversion mechanism, displaying reversible initial charge capacities of 495 mAh.g- 1 and 550 mAh.g- 1 at 0.2C rate for NVP/C and MVP/C, respectively. Both materials showed better cycling stability at high rates and good rate capability performances with high coulombic efficiencies. For long term cycling, the materials can maintain a good reversible capacity for 1000 cycles, although a continuous decrease was noticed during the first cycles. The structural changes and the SEI growth impacting the electrochemical performances of the materials were evidenced via in operando XRD and X-ray photoelectron spectroscopy, leading to the understanding of the lithiation/delithiation reaction mechanism involved in the studied phosphates.

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