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Metallic MoS2 nanosheets: multifunctional electrocatalyst for the ORR, OER and Li-O-2 batteries

机译:金属二硫化钼nanosheets:多功能electrocatalyst奥尔,OER和Li-O-2电池

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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 MoS2 (1T-MoS2) nanosheets as a highly active electrocatalyst for LOBs for the first time. Metallic 1T-MoS2 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-MoS2/CNT electrode exhibited excellent electrochemical performances with a high reversible capacity of 500 mA h g(-1) at a current density of 200 mA g(-1) for more than 100 cycles owing to the catalytically active surfaces of 1T-MoS2 accessible by Li+ ions and O-2. Density functional theory (DFT) calculations identified the catalytically active basal planes in 1T-MoS2 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-MoS2 basal planes are active for both the ORR and OER, not the semiconducting hexagonal MoS2 (2H-MoS2) whose edges are only electrocatalytically active. This study sheds light on the use of metallic 1T-MoS2 as a multifunctional oxygen electrocatalyst for LOB applications with enhanced ORR and OER activities.
机译:Lithium-oxygen电池(lob)拥有最高理论具体的密度在所有类型的锂电池,使他们的理想候选人替换当前锂离子新一代电动汽车电池应用程序。催化剂的电子导率高活动加速迟缓的氧气减少/(奥尔/ OER)仍在进化反应一个巨大的挑战。发展中二维(2 d)三方晶系的阶段二硫化钼(1 t-mos2) nanosheets高度活跃第一次electrocatalyst为lob。通过原位金属1 t-mos2准备liquid-redox夹层和剥落与功能化碳纳米管杂化(碳纳米管)形成独立,binder-free氧气电极。优秀的电化学性能较高的可逆容量500毫安h g (1)200毫安的电流密度超过100 g (1)周期由于表面催化地活跃1被李+离子和0 2 t-mos2访问。密度泛函理论(DFT)计算确定了催化地活性基底的飞机在1 t-mos2奥尔以及初始奥尔路径在LOB周期。旋转环盘电极(RRDE)实验的结果也支持DFT计算,1 t-mos2基底的飞机奥尔和OER是活跃的,不是吗半导体六角二硫化钼(2 h-mos2)的边只有electrocatalytically活跃。研究揭示了金属1 t-mos2的使用作为一个多功能氧electrocatalyst增强的奥尔和OER LOB应用程序活动。

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