4.7 Article

Manipulating the electrocatalytic activity of sulfur cathode via distinct cobalt sulfides as sulfur host materials in lithium-sulfur batteries

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 622, 期 -, 页码 515-525

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2022.04.156

关键词

Cobalt sulfides; Defects; Electrocatalysis; In-situ XRD; Lithium-sulfur batteries

资金

  1. National Natural Science Foundation of China [21373189]
  2. Science and Technology Department of Henan Province [212102210586]
  3. Top-Notch Talents Program of Henan Agricultural University [30501035]

向作者/读者索取更多资源

This study focuses on the development of lithium-sulfur (Li-S) batteries by fabricating sulfur hosts with cheap and rapid sulfur reaction properties and inhibiting the shuttling effect of lithium polysulfides (LiPSs). Hollow cubic materials with nitrogen-doped carbon derived from Prussian blue analogues (PBA) precursor were prepared at different vulcanization temperatures. Among them, CoS1.097/MnS/NC@NC-600 showed the best performance in terms of adsorption ability and electrocatalytic activity, greatly improving the electrochemical performances of Li-S batteries.
For the better development of lithium-sulfur (Li-S) batteries, it is necessary to fabricate sulfur hosts with cheap, rapid sulfur reaction dynamic and inhibiting the shuttling effect of lithium polysulfides (LiPSs). Herein, four hollow cubic materials with two kinds of nitrogen-doped carbon derived from Prussian blue analogues (PBA) precursor, Co9S8/MnS/NC@NC-400, CoS2/MnS/NC@NC-500, CoS1.097/MnS/NC@NC-600 and CoS1.097/MnS/NC@NC-700, are reported when the vulcanization temperatures are regulated at 400 degrees C, 500 degrees C, 600 degrees C and 700 degrees C, respectively. Among them, Co9S8/MnS/NC@NC-400, CoS2/MnS/ NC@NC-500 and CoS1.097/MnS/NC@NC-600 have the similar hollow cubic structure, which can physically confine the LiPSs's shuttle, however, the Co vacancies of CoS1.097 in the CoS1.097/MnS/NC@NC-600 can promote the rearrangement of surface electrons, which is beneficial to the diffusion of Li+/e-, improving the electrochemical reaction kinetics. As for the CoS1.097/MnS/NC@NC-700 with the same substance but almost collapsed structure, the CoS1.097/MnS/NC@NC-600 can accommodate the volume expansion of sulfur conversion. In the four sulfur-host materials, the CoS1.097/MnS/NC@NC-600 not only displays the outstanding adsorption ability on LiPSs, but also presents the best electrocatalytic activity in the Li2S potentiostatic deposition experiments and active sulfur reduction/oxidation conversion reactions, greatly promoting the electrochemical performances of Li-S batteries. The S@CoS1.097/MnS/NC@NC-600 cathode can deliver 1010.2 mA h g-1 at 0.5 C and maintain 651.1 mA h g-1 after 200 cycles. In addition, the in-situ X-ray diffraction (in-situ XRD) test reveals that the sulfur conversion mechanism is the processes of the ocS8 -. Li2S -. /3-S8 (first cycle), then /3-S8 M Li2S during the subsequent cycles. Based on the fundamental understanding of the design and preparation of CoxSy/MnS/NC@NC hosts with the desired adsorption and catalysis functions, the work can provide new insights and reveal the defect-engineering to develop the advanced Li-S batteries.

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