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Gao, Xiao‐Tian; Xie, Ying; Zhu, Xiao‐Dong; Sun, Ke‐Ning; Xie, Xu‐Ming; Liu, Yi‐Tao; Yu, Jian‐Yong; Ding, Bin
Small (Weinheim an der Bergstrasse, Germany), October 11, 2018, Volume: 14, Issue: 41Journal Article
Being conductive and flexible, 2D transition metal nitrides and carbides (MXenes) can serve in Li–S batteries as sulfur hosts to increase the conductivity and alleviate the volume expansion. However, the surface functional groups, such as OH and F, weaken the ability of bare MXenes in the chemisorption of polysulfides. Besides, they create numerous hydrogen bonds which make MXenes liable to restack, resulting in substantial loss of active area and, thus, inaccessibility of ions and electrolyte. Herein, a facile, one‐step strategy is developed for the growth of TiO2 quantum dots (QDs) on ultrathin MXene (Ti3C2Tx) nanosheets by cetyltrimethylammonium bromide‐assisted solvothermal synthesis. These QDs act as spacers to isolate the MXene nanosheets from restacking, and preserve their 2D geometry which guarantees larger electrode–electrolyte contact area and higher sulfur loading. The stronger adsorption energy of polysulfides with TiO2 (than with Ti3C2Tx), as proven by density functional theory calculations, is essential for better on‐site polysulfide retention. The ultrathin nature and protected conductivity ensure rapid ion and electron diffusion, and the excellent flexibility maintains high mechanical integrity. In result, the TiO2 QDs@MXene/S cathode exhibits significantly improved long‐term cyclability and rate capability, disclosing a new opportunity toward fast and stable Li–S batteries. TiO2 quantum dots (QDs) are grown on ultrathin MXene nanosheets by a facile, one‐step strategy through cetyltrimethylammonium bromide‐assisted solvothermal synthesis, resulting in TiO2 QDs@MXene nanohybrids that serve as a high‐performance sulfur host toward fast and stable Li–S batteries.
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