Dataset Information

Ni-CeO₂ Heterostructures in Li-S Batteries: A Balancing Act between Adsorption and Catalytic Conversion of Polysulfide.

ABSTRACT: Lithium-sulfur (Li-S) batteries have attracted considerable attention over the last two decades because of a high energy density and low cost. However, the wide application of Li-S batteries has been severely impeded due to the poor electrical conductivity of S, shuttling effect of soluble lithium polysulfides (LiPSs), and sluggish redox kinetics of S species, especially under high S loading. To address all these issues, a Ni-CeO₂ heterostructure-doped carbon nanofiber (Ni-CeO₂ -CNF) is developed as an S host that combines the strong adsorption with the high catalytic activity and the good electrical conductivity, where the LiPSs anchored on the heterostructure surface can directly gain electrons from the current collector and realize a fast conversion between S₈ and Li₂ S. Therefore, Li-S batteries with S@Ni-CeO₂ -CNF cathodes exhibit superior long-term cycling stability, with a capacity decay of 0.046% per cycle over 1000 cycles, even at 2 C. Noteworthy, under a sulfur loading up to 6 mg cm^-2 , a high reversible areal capacity of 5.3 mAh cm^-2 can be achieved after 50 cycles at 0.1 C. The heterostructure-modified S cathode effectively reconciles the thermodynamic and kinetic characteristics of LiPSs for adsorption and conversion, furthering the development of high-performance Li-S batteries.

SUBMITTER: Kong Y

PROVIDER: S-EPMC9189638 | biostudies-literature | 2022 Jun

REPOSITORIES: biostudies-literature

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Publications

Ni-CeO2 Heterostructures in Li-S Batteries: A Balancing Act between Adsorption and Catalytic Conversion of Polysulfide.

Kong Yang Y Ao Xin X Huang Xiao X Bai Jinglong J Zhao Shangquan S Zhang Jinyong J Tian Bingbing B

Advanced science (Weinheim, Baden-Wurttemberg, Germany) 20220412 17

Lithium-sulfur (Li-S) batteries have attracted considerable attention over the last two decades because of a high energy density and low cost. However, the wide application of Li-S batteries has been severely impeded due to the poor electrical conductivity of S, shuttling effect of soluble lithium polysulfides (LiPSs), and sluggish redox kinetics of S species, especially under high S loading. To address all these issues, a Ni-CeO2 heterostructure-doped carbon nanofiber (Ni-CeO2</ ...[more]

PMID: 35415972

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Project description:A SnO2/Ni/CNT nanocomposite was synthesized using a simple one-step hydrothermal method followed by calcination. A structural study via XRD shows that the tetragonal rutile structure of SnO2 is maintained. Further, X-ray photoelectron spectroscopy (XPS) and Raman studies confirm the existence of SnO2 along with CNTs and Ni nanoparticles. The electrochemical performance was investigated via cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic charge-discharge measurements. The nanocomposite has been used as an anode material for lithium-ion batteries. The SnO2/Ni/CNT nanocomposite exhibited an initial discharge capacity of 5312 mA h g-1 and a corresponding charge capacity of 2267 mA h g-1 during the first cycle at 50 mA g-1. Pristine SnO2 showed a discharge/charge capacity of 1445/636 mA h g-1 during the first cycle at 50 mA g-1. This clearly shows the effects of the optimum concentrations of CNTs and Ni. Further, the nanocomposite (SnNiCn) shows a discharge capacity as high as 919 mA h g-1 after 210 cycles at a current density of 400 mA g-1 in a Li-ion battery set-up. Thus, the obtained capacity from the nanocomposite is much higher compared to pristine SnO2. The higher capacity in the nanoheterostructure is due to the well-dispersed nanosized Ni-decorated stabilized SnO2 along with the CNTs, avoiding pulverization as a result of the volumetric change of the nanoparticles being minimized. The material accommodates huge volume expansion and avoids the agglomeration of nanoparticles during the lithiation and delithiation processes. The Ni nanoparticles can successfully inhibit Sn coarsening during cycling, resulting in the enhancement of stability during reversible conversion reactions. They ultimately enhance the capacity, giving stability to the nanocomposite and improving performance. Additionally, the material exhibits a lower Warburg coefficient and higher Li ion diffusion coefficient, which in turn accelerate the interfacial charge transfer process; this is also responsible for the enhanced stable electrochemical performance. A detailed mechanism is expressed and elaborated on to provide a better understanding of the enhanced electrochemical performance.

Dataset Information

Ni-CeO₂ Heterostructures in Li-S Batteries: A Balancing Act between Adsorption and Catalytic Conversion of Polysulfide.

Publications

Ni-CeO<sub>2</sub> Heterostructures in Li-S Batteries: A Balancing Act between Adsorption and Catalytic Conversion of Polysulfide.

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