锂硫电池
材料科学
硫黄
溶解
沉积(地质)
锂(药物)
电池(电)
无机化学
化学工程
纳米技术
冶金
功率(物理)
化学
热力学
医学
古生物学
物理
沉积物
生物
工程类
内分泌学
作者
Dan You,Wenhao Yang,Yongshun Liang,Chunman Yang,Yiwei Yu,Ziyi Zhu,Xue Li,Yiyong Zhang,Yingjie Zhang
标识
DOI:10.1002/adfm.202421900
摘要
Abstract Promoting the sulfur reduction reaction (SRR) and sulfur evolution reaction (SER) kinetics is crucial for practical lithium–sulfur batteries. However, the electrode will be passivated by insulated Li 2 S if blindly accelerated the SRR kinetics, meanwhile, the high activation energy of Li 2 S will lead to premature the oxidation of Li 2 S (SER), achieving limited catalyst. Here, a nano‐nickel nitrogen‐doped carbon gel material (CG/Ni) induces the instantaneous nucleation, further endows Li 2 S fast ion/electron transfer, resulting porous 3D growth instead single lateral growth. Therefore, CG/Ni material avoids being passivated, accelerating the SRR kinetics. Meanwhile, CG/Ni decreases the delithiation barrier, thus, facilitating the Li 2 S dissociation. Both experiments and theory calculation prove that CG/Ni achieves efficient bidirectional catalysis. Consequently, CG/Ni cathode delivers a low‐capacity decay ratio of 0.047% per cycle for 900 cycles at 5 C. This work unlocks a bidirectional catalyst and provide new insight for high‐efficiency lithium–sulfur batteries.
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