Full Potential Catalysis of Co0.4Ni1.6P-V/CNT with Phosphorus Vacancies for Li2S1-2 Deposition/Decomposition and S8/Li2S n (3 n 8) Conversion in Li-S Batteries
ACS APPLIED MATERIALS & INTERFACES(2023)
Abstract
The slow kinetics of polysulfide conversions hinders the commercial progress of Li-S batteries. The introduction of high-efficiency catalysts accelerates heterogeneous reactions and enhances the utilization of S. The full potential of the Co0.4Ni1.6P-V/CNT-modified separator catalyzes the all-process reactions of the S electrode and increases the rates and cycling lives of the batteries. The two-site synergistic effect of Co0.4Ni1.6P-V/CNT regulates the catalytic activity, and the phosphorus vacancies enrich the active sites. The higher electron density at the Co and Ni double sites increases chemisorption of the Co0.4Ni1.6P-V/CNT on Li2S n (1 <= n <= 4), stretches and breaks the Li-S and Ni-S bonds during Li2S decomposition, and reduces the energy barrier for Li2S decomposition. The cyclic voltammograms of the asymmetric batteries demonstrated that Co0.4Ni1.6P-V/CNT also catalyzed the Li2S n S-8 (3 <= n <= 8) reaction, realizing the full catalytic potential of the Li-S batteries. Increased Li+ diffusion/migration in the Co0.4Ni1.6P-V/CNT-modified separator ensured fast electrochemical reactions. The excellent catalytic effect of Co0.4Ni1.6P-V/CNT provided smaller polarization and superior rate performance, which led to high discharge specific capacities of 1511.9, 1172.6, 1006.0, 881.0, and 785.7 mA h g(-1) at current densities of 0.1, 0.2, 0.5, 1, and 2 mA cm(-2) with sulfur loadings of 7.98 mg cm(-2), respectively. This approach involving simple crystal modulation and introduction of defects provides a new way to achieve the full catalytic potential of Li-S batteries.
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Key words
phosphorus vacancy,catalysis,full potential,separator,Li-S batteries
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