Yan Zichao, Liang Yaru, Hua Weibo, Zhang Xia-Guang, Lai Weihong, Hu Zhe, Wang Wanlin, Peng Jian, Indris Sylvio, Wang Yunxiao, Chou Shu-Lei, Liu Huakun, Dou Shi-Xue
Institute for Superconducting and Electronic Materials, University of Wollongong, Innovation Campus, Squires Way, North Wollongong, New South Wales 2500, Australia.
Powder Metallurgy Research Institute State Key Laboratory of Powder Metallurgy, Central South University, Lushan South Road, Changsha 410083, P.R. China.
ACS Nano. 2020 Aug 25;14(8):10284-10293. doi: 10.1021/acsnano.0c03737. Epub 2020 Jul 30.
Electrode materials with high conductivity, strong chemisorption, and catalysis toward polysulfides are recognized as key factors for metal-sulfur batteries. Nevertheless, the construction of such functional material is a challenge for room-temperature sodium-sulfur (RT-Na/S) batteries. Herein, a multiregion Janus-featured CoP-Co structure obtained sequential carbonization-oxidation-phosphidation of heteroseed zeolitic imidazolate frameworks is introduced. The structural virtues include a heterostructure existing in a CoP-Co structure and a conductive network of N-doped porous carbon nanotube hollow cages (NCNHCs), endowing it with superior conductivity in both the short- and long-range and strong polarity toward polysulfides. Thus, the S@CoP-Co/NCNHC cathode exhibits superior electrochemical performance (448 mAh g remained for 700 times cycling under 1 A g) and an optimized redox mechanism in polysulfides conversion. Density functional theory calculations present that the CoP-Co structure optimizes bond structure and bandwidth, whereas the pure CoP is lower than the corresponding Fermi level, which could essentially benefit the adsorptive capability and charge transfer from the CoP-Co surface to NaS and therefore improve its affinity to polysulfides.
具有高导电性、对多硫化物有强化学吸附和催化作用的电极材料被认为是金属硫电池的关键因素。然而,对于室温钠硫(RT-Na/S)电池而言,构建这种功能材料是一项挑战。在此,我们介绍了一种通过对异质晶种沸石咪唑酯骨架进行顺序碳化-氧化-磷化而获得的多区域Janus结构CoP-Co结构。其结构优点包括存在于CoP-Co结构中的异质结构以及N掺杂多孔碳纳米管空心笼(NCNHCs)的导电网络,使其在短程和长程都具有优异的导电性以及对多硫化物的强极性。因此,S@CoP-Co/NCNHC正极表现出优异的电化学性能(在1 A g下循环700次后仍有448 mAh g)以及在多硫化物转化过程中的优化氧化还原机制。密度泛函理论计算表明,CoP-Co结构优化了键结构和带宽,而纯CoP低于相应的费米能级,这从本质上有利于吸附能力以及从CoP-Co表面到NaS的电荷转移,因此提高了其对多硫化物的亲和力。