Lu Huibing, Yang Caihong, Li Cunjun, Wang Linjiang, Wang Hai
Ministry-Province Jointly-Constructed Cultivation Base for State Key Laboratory of Processing for Non-Ferrous Metal and Featured Materials , Guangxi Zhuang Autonomous Region , Guilin 541004 , China.
ACS Appl Mater Interfaces. 2019 Apr 10;11(14):13405-13415. doi: 10.1021/acsami.9b00824. Epub 2019 Apr 1.
α-MoO has gained growing attention as an anode material of lithium-ion batteries (LIBs) because it has a high theoretical specific capacity of 1111 mA h g and unique layer structure. However, the electrochemical reactions of MoO exhibit sluggish kinetics and structural instability caused by pulverization during charge and discharge. Herein, we report new two-dimensional Cr-doped MoO(OH) (doped MoO(OH)) ultrathin nanosheets prepared by a facile hydrothermal process. The formation of the ultrathin nanosheets was clarified by a "doping-adsorption" model. Compared with doped MoO, doped MoO(OH) has larger expanded spacing of the {0 l0} crystal planes for fast Li storage. The electrodes after cycling were investigated by ex situ transmission electron microscopy in combination with X-ray photoelectron spectroscopy analysis to reveal the reversible conversion reaction mechanism of doped MoO(OH) nanosheets. Interestingly, for doped MoO(OH) nanosheet electrodes, it was found that the as-formed intermediate Li MoO nanodots were well-dispersed in the mesoporous amorphous matrix and had an expanded (040) crystal plane after 10 cycles. These unique structural features increased the effective surface of intermediate products Li MoO to react with Li and shortened the diffusion length and thus promoted the electrochemical reactions of doped MoO(OH). Additionally, the presence of Cr also played a critical role in the reversible decomposition of LiO and enhanced specific capacity. When employed as an anode in LIBs, doped MoO(OH) nanosheets show superior reversible capacity (294 mA h g at 10 A g after 2000 cycles). Moreover, the reversible capacity after electrochemical activation is quite stable throughout the cycling, thereby presenting a potential candidate anode material for LIBs.
α-MoO作为锂离子电池(LIBs)的负极材料受到越来越多的关注,因为它具有1111 mA h g的高理论比容量和独特的层状结构。然而,MoO的电化学反应表现出缓慢的动力学和充放电过程中因粉化导致的结构不稳定性。在此,我们报道了通过简便的水热法制备的新型二维Cr掺杂MoO(OH)(掺杂MoO(OH))超薄纳米片。通过“掺杂-吸附”模型阐明了超薄纳米片的形成过程。与掺杂MoO相比,掺杂MoO(OH)具有更大的{0 l0}晶面扩展间距,有利于快速储锂。通过非原位透射电子显微镜结合X射线光电子能谱分析对循环后的电极进行研究,以揭示掺杂MoO(OH)纳米片的可逆转化反应机理。有趣的是,对于掺杂MoO(OH)纳米片电极,发现形成的中间产物Li MoO纳米点在介孔无定形基质中分散良好,并且在10次循环后(040)晶面有所扩展。这些独特的结构特征增加了中间产物Li MoO与Li反应的有效表面积,缩短了扩散长度,从而促进了掺杂MoO(OH)的电化学反应。此外,Cr的存在对LiO的可逆分解和比容量的提高也起到了关键作用。当用作LIBs的负极时,掺杂MoO(OH)纳米片表现出优异的可逆容量(2000次循环后在10 A g下为294 mA h g)。此外,电化学活化后的可逆容量在整个循环过程中相当稳定,从而成为LIBs潜在的候选负极材料。