多硫化物
材料科学
硫黄
硫化物
化学工程
电解质
阴极
碳纤维
锂(药物)
纳米技术
电极
复合材料
化学
复合数
冶金
工程类
内分泌学
物理化学
医学
作者
Xia Huang,Jiayong Tang,Bin Luo,Ruth Knibbe,Tongen Lin,Han Hu,Masud Rana,Yuxiang Hu,Xiaobo Zhu,Qinfen Gu,Dan Wang,Lianzhou Wang
标识
DOI:10.1002/aenm.201901872
摘要
Abstract As the lightest member of transition metal dichalcogenides, 2D titanium disulfide (2D TiS 2 ) nanosheets are attractive for energy storage and conversion. However, reliable and controllable synthesis of single‐ to few‐layered TiS 2 nanosheets is challenging due to the strong tendency of stacking and oxidation of ultrathin TiS 2 nanosheets. This study reports for the first time the successful conversion of Ti 3 C 2 T x MXene to sandwich‐like ultrathin TiS 2 nanosheets confined by N, S co‐doped porous carbon (TiS 2 @NSC) via an in situ polydopamine‐assisted sulfuration process. When used as a sulfur host in lithium–sulfur batteries, TiS 2 @NSC shows both high trapping capability for lithium polysulfides (LiPSs), and remarkable electrocatalytic activity for LiPSs reduction and lithium sulfide oxidation. A freestanding sulfur cathode integrating TiS 2 @NSC with cotton‐derived carbon fibers delivers a high areal capacity of 5.9 mAh cm −2 after 100 cycles at 0.1 C with a low electrolyte/sulfur ratio and a high sulfur loading of 7.7 mg cm −2 , placing TiS 2 @NSC one of the best LiPSs adsorbents and sulfur conversion catalysts reported to date. The developed nanospace‐confined strategy will shed light on the rational design and structural engineering of metal sulfides based nanoarchitectures for diverse applications.
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