Mahankali Kiran, Thangavel Naresh Kumar, Gopchenko Daryna, Arava Leela Mohana Reddy
Department of Mechanical Engineering, Wayne State University, 5050 Anthony Wayne Drive, Detroit, Michigan 48202, United States.
ACS Appl Mater Interfaces. 2020 Jun 17;12(24):27112-27121. doi: 10.1021/acsami.0c04281. Epub 2020 Jun 4.
Curtailing the polysulfide shuttle by anchoring the intermediate lithium polysulfides (LiPS) within the electrode structure is essential to impede the rapid capacity fade in lithium-sulfur (Li-S) batteries. While most of the contemporary Li-S cathode surfaces are capable of entrapping certain LiPS, developing a unique electrode material that can adsorb all the intermediates of sulfur redox is imperative. Herein, we report doping of the MoS atomic structure with nickel (Ni@1TMoS) to modulate its absorption capability toward all LiPS and function as an electrocatalyst for Li-S redox. Detailed in situ and ex situ spectroscopic analysis revealed that both Ni and Mo sites chemically anchor all the intermediate of LiPS. Electrochemical studies and detailed kinetics analysis suggested that the conversion of liquid LiPS to solid end products are facilitated on the Ni@1TMoS electrocatalytic surface. Further, the employment of the Ni@1TMoS electrocatalyst enhances the Li diffusion coefficient, thus contributing to the realization of a high capacity of 1107 mA h g at 0.2C with a very limited capacity fade of 0.19% per cycle for over 100 cycles. In addition, this cathode demonstrated an excellent high rate and long cycling performance for over 300 cycles at a 1C rate.
通过将中间产物多硫化锂(LiPS)锚定在电极结构中来抑制多硫化物穿梭效应对于阻止锂硫(Li-S)电池中快速的容量衰减至关重要。虽然大多数当代Li-S阴极表面能够捕获某些LiPS,但开发一种能够吸附硫氧化还原所有中间产物的独特电极材料势在必行。在此,我们报道了用镍对MoS原子结构进行掺杂(Ni@1TMoS),以调节其对所有LiPS的吸附能力,并作为Li-S氧化还原的电催化剂。详细的原位和非原位光谱分析表明,Ni和Mo位点都能化学锚定LiPS的所有中间产物。电化学研究和详细的动力学分析表明,在Ni@1TMoS电催化表面上,液态LiPS向固态最终产物的转化得到了促进。此外,使用Ni@1TMoS电催化剂提高了Li扩散系数,从而有助于在0.2C下实现1107 mA h g的高容量,在超过100个循环中每循环容量衰减非常有限,仅为0.19%。此外,这种阴极在1C速率下超过300个循环表现出优异的高倍率和长循环性能。