Department of Mechanical and Aerospace Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong.
Nanoscale. 2018 Dec 21;10(47):22549-22559. doi: 10.1039/c8nr07106c. Epub 2018 Nov 27.
Lithium-oxygen batteries (LOBs) possess the highest theoretical specific density among all types of lithium batteries, making them ideal candidates to replace the current Li ion batteries for next-generation electric vehicle applications. However, designing highly active catalysts with high electronic conductivities to kinetically accelerate the sluggish oxygen reduction/evolution reactions (ORR/OER) is still a big challenge. This work was dedicated to developing two-dimensional (2D) trigonal phase MoS (1T-MoS) nanosheets as a highly active electrocatalyst for LOBs for the first time. Metallic 1T-MoS prepared via in situ liquid-redox intercalation and exfoliation was hybridized with functionalized carbon nanotubes (CNTs) to form freestanding, binder-free oxygen electrodes. The 1T-MoS/CNT electrode exhibited excellent electrochemical performances with a high reversible capacity of 500 mA h g at a current density of 200 mA g for more than 100 cycles owing to the catalytically active surfaces of 1T-MoS accessible by Li ions and O. Density functional theory (DFT) calculations identified the catalytically active basal planes in 1T-MoS during the ORR as well as the initial ORR path during LOB cycles. The results based on the rotational ring disk electrode (RRDE) experiments also supported the findings from the DFT calculations, where the 1T-MoS basal planes are active for both the ORR and OER, not the semiconducting hexagonal MoS (2H-MoS) whose edges are only electrocatalytically active. This study sheds light on the use of metallic 1T-MoS as a multifunctional oxygen electrocatalyst for LOB applications with enhanced ORR and OER activities.
锂-氧电池(LOBs)在所有类型的锂电池中具有最高的理论比能量密度,是下一代电动汽车应用中替代现有锂离子电池的理想候选材料。然而,设计具有高电子电导率的高活性催化剂来动力学加速缓慢的氧还原/氧化反应(ORR/OER)仍然是一个巨大的挑战。本工作首次致力于开发二维(2D)三角相 MoS(1T-MoS)纳米片作为 LOB 的高活性电催化剂。通过原位液-氧化还原插层和剥离制备的金属 1T-MoS 与功能化碳纳米管(CNTs)杂交,形成独立的、无粘结剂的氧气电极。由于 Li 离子和 O 可到达 1T-MoS 的催化活性表面,1T-MoS/CNT 电极表现出优异的电化学性能,在 200 mA g 的电流密度下具有 500 mA h g 的可逆容量,循环 100 次以上。密度泛函理论(DFT)计算确定了 1T-MoS 在 ORR 过程中的催化活性基面以及 LOB 循环过程中的初始 ORR 路径。基于旋转环盘电极(RRDE)实验的结果也支持了 DFT 计算的结果,其中 1T-MoS 的基面既对 ORR 又对 OER 具有活性,而不是半导体六方相 MoS(2H-MoS),其边缘仅对电催化具有活性。这项研究揭示了将金属 1T-MoS 用作 LOB 应用的多功能氧气电催化剂,以提高 ORR 和 OER 活性。