Metal-Sulfur Battery with Field (Electric, Magnetic) Enhancement Mechanism
Chaoyue Zhang a b, Jinyuan Zhou b, Andreu Cabot a
a Catalonia Institute for Energy Research (IREC), Sant Adrià de Besos, 08930, Barcelona, Spain.
b School of physcis science and engineering, Lanzhou University,730000, Lanzhou, China.
Materials for Sustainable Development Conference (MATSUS)
Proceedings of MATSUS Spring 2024 Conference (MATSUS24)
#BATS - Toward sustainable batteries based on sulfur cathodes
Barcelona, Spain, 2024 March 4th - 8th
Organizers: Andreu Cabot, Pascale Chenevier and Alessandra Manzini
Invited Speaker, Chaoyue Zhang, presentation 131
DOI: https://doi.org/10.29363/nanoge.matsus.2024.131
Publication date: 18th December 2023

Field effect (Electric, Magnetic) enhancement of catalytic performance refers to improving the efficiency and activity of catalytic reactions through the application of external fields. The field effect can introduce an electric field or magnetic field on the surface of the catalyst to regulate the energy barrier, electron transfer rate and catalytic activity of the catalytic reaction. This method can provide an effective ways to enhance the performance of the catalyst and promote the catalytic reaction. Metal-sulfur batteries(Li, Na) have been widely studied by researchers due to their high theoretical specific capacity (1675 mA h g-1) and energy density (2600 Wh kg-1). Due to the "shuttle effect" caused by the solubility of its intermediate product polysulfide, battery failure is caused. In this context, we extend the field effect to the field of metal-sulfur batteries to reduce the polysulfide redox reaction kinetics barrier to achieve high-performance in metal-sulfur batteries.

1. Through external heat-assisted electric polarization, the traditional α-phase PVDF binder without ferroelectric effect is converted into β-phase PVDF with ferroelectric enhancement to anchor polysulfide through electrostatic interaction force while enhancing the lithium ion diffusion resistance. The structure of the PVDF film before and after polarization was analyzed through XRD, Raman and FTIR, and it was found that as polarization increased, PVDF gradually transformed from the α phase to the β phase. The modified electrode can still maintain stable capacity after 1000 cycles at 1 C, and the decay rate of specific capacity is only 0.038%.[1]
2. Apply a constant magnetic field outside the battery and use CoSx as the catalytic additive.[2] By exploring the impact of the magnetic field generated by the external magnet on the electrochemical performance of the battery, we found that the addition of the magnetic field can significantly improve the adsorption ability of polysulfides and the Li-S reaction kinetics. The CNF/CoSx/S electrode exhibits excellent electrochemical performance. In the presence of a magnetic field, even at a high current density of 2 C, CNF/CoSx/S dropped to 315 mA h g-1 after 8150 cycles, with a decay rate of only 0.0084% per cycle.
3. CoFe2O4 catalyst under an external magnetic field assists sodium-sulfur battery to realize high electrochemical performance.[3] This work details the process of growing CoFe2O4, VO2 and Co3O4 particles on the surface of CNF using a combination of electrospinning and hydrothermal processes. At the same time, this work systematically explores the process of the prepared cathode material catalyzing sodium polysulfides (SPSs) through ferromagnetic and paramagnetic catalysts under an external magnetic field. DFT calculations show that under a magnetic field, the adsorption energy of SPS on the ferromagnetic catalyst applying a magnetic field increases, and the kinetic barrier for SPS conversion decreases. Experimental results show that the spin-polarized Co ions in CoFe2O4 improve the ability to adsorb SPS and the electrocatalytic activity of SPS conversion. Experiments and theory have proven that the magnetic field can polarize the electrons of Co ions, thereby enhancing the adsorption of SPS and its catalytic conversion. The CNF/CoFe2O4/S cathode with spin polarization can last for 2700 cycles at 1 C, with a decay rate as low as 0.0039% per cycle. 

In summary, these works not only establish a new catalytic relationship and strategy for the field effect in the redox reaction kinetics of polysulfides, but also provide new ideas for applications in the field of efficient electrochemical energy storage.

A. Cabot thanks financial support from the Combenergy project (PID2019−105490RB−C32) from the Spanish Ministerio de Ciencia e Innovación. This work was supported by the National Natural Science Foundation of China (Grant Nos.: 61801200) and partially by the Fundamental Research Funds for the Central Universities (Grant Nos.: lzujbky−2021−it33). The authors also greatly acknowledge the support supported by the Supercomputing Center of Lanzhou University, China.

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