硫黄
催化作用
材料科学
吸附
离解(化学)
合金
氧化还原
阴极
化学工程
无机化学
电导率
化学
物理化学
冶金
有机化学
工程类
作者
Xue‐Qin Song,Da Tian,Yue Qiu,Xun Sun,Bo Jiang,Chenghao Zhao,Yu Zhang,Lishuang Fan,Naiqing Zhang
标识
DOI:10.1016/j.ensm.2021.05.028
摘要
Transition metals (TMs) are attractive electrocatalysts for lithium-sulfur (Li-S) batteries due to their strong adsorption of sulfur species based on Lewis acid-base interactions and high intrinsic conductivity. However, S8 molecule undergoes dissociation on their surfaces, resulting in sulfur-poisoned TMs with reduced catalytic sites. We propose here an alloying strategy which changes the S adsorption sites and the corresponding binding energies, enabling intact adsorption of S8 as evidenced by theoretical and experimental results. Such merit renders Co-Te alloy a superior catalyst which effectively expedites the sulfur redox reactions and suppresses the shuttle effect. Consequently, the cathode with Co-Te alloy catalyst delivers an impressive rate capability of 898 mAh g−1 at 2 C together with a low capacity decay of 0.03% per cycle over 1000 cycles. Even the sulfur mass loading is up to 5.4 mg cm−2, a stable capacity of 5.0 mAh cm−2 can be still maintained after 100 cycles. Our work deepens the mechanism understanding of Li-S catalysis and opens a new avenue toward the design of poisoning-resistant electrocatalysts.
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