Yang Xiao-Xia, Du Wen-Zheng, Li Xu-Ting, Zhang Yang, Qian Zhao, Biggs Mark James, Hu Cheng
Key Laboratory for Liquid-Solid Structural Evolution and Processing of Materials (Ministry of Education), School of Materials Science and Engineering, Shandong University, Ji'nan, 250061, Shandong, P. R. China.
College of Science and Technology, Nottingham Trent University, Nottingham, NG11 8NS, United Kingdom.
ChemSusChem. 2020 Jun 8;13(11):3034-3044. doi: 10.1002/cssc.202000648. Epub 2020 Apr 17.
An efficient Li-S redox catalyst consisting of MWCNTs covalently modified by cobalt(II) tetraaminophthalocyanines (TaPcCo-MWCNTs) is developed. Effective lithium polysulfide (LiPS) capturing is enabled by the lithiophilic N-containing phthalocyanine rings and the sulfiphilic Co central atoms. This adsorption geometry utilizes the Co unoccupied d-orbitals as electron super-exchange highways. Elevated kinetics of LiPSs reactions in the liquid phase as well as liquid-solid transitions were revealed by electrochemical measurements and density functional theory calculations. Uniform deposition of Li S films was also observed, which preserves cathode integrity and sulfur utilization during cell cycling. The catalyzed sulfur redox is also significantly facilitated by the fast electron and Li-ion transport to and from the reaction sites through the conductive MWCNT skeletons and the lithiophilic substituent amino groups on TaPcCo. With 6 wt % addition of TaPcCo-MWCNT in the cathode coatings, high sulfur utilization is achieved with areal sulfur loadings of up to 7 mg cm . Stable long-term cycling is achieved at 1 C at a sulfur loading of 5 mg cm , with an initial areal capacity of 4.4 mAh cm retention of 3.5 mAh cm after 500 cycles. Considering the high structural diversity of phthalocyanines macromolecules, this study provides opportunities for a new class of Li-S catalysts.
开发了一种由钴(II)四氨基酞菁共价修饰的多壁碳纳米管(TaPcCo-MWCNTs)组成的高效锂硫氧化还原催化剂。亲锂的含氮酞菁环和亲硫的钴中心原子实现了有效的多硫化锂(LiPS)捕获。这种吸附几何结构利用钴的未占据d轨道作为电子超级交换通道。通过电化学测量和密度泛函理论计算揭示了液相中LiPS反应以及液固转变的动力学增强。还观察到Li-S薄膜的均匀沉积,这在电池循环过程中保持了阴极的完整性和硫的利用率。通过快速的电子和锂离子通过导电的MWCNT骨架以及TaPcCo上的亲锂取代基氨基往返于反应位点的传输,催化的硫氧化还原也得到了显著促进。在阴极涂层中添加6 wt%的TaPcCo-MWCNT时,在高达7 mg cm的面硫负载下实现了高硫利用率。在硫负载为5 mg cm时,在1 C下实现了稳定的长期循环,初始面容量为4.4 mAh cm,500次循环后保留3.5 mAh cm。考虑到酞菁大分子的高度结构多样性,本研究为新型锂硫催化剂提供了机会。