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原位催化生长大面积多层石墨烯/二硫化钼异质结。

In situ catalytic growth of large-area multilayered graphene/MoS2 heterostructures.

机构信息

1] School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, China [2].

School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.

出版信息

Sci Rep. 2014 Apr 14;4:4673. doi: 10.1038/srep04673.

Abstract

Stacking various two-dimensional atomic crystals on top of each other is a feasible approach to create unique multilayered heterostructures with desired properties. Herein for the first time, we present a controlled preparation of large-area graphene/MoS2 heterostructures via a simple heating procedure on Mo-oleate complex coated sodium sulfate under N2 atmosphere. Through a direct in situ catalytic reaction, graphene layer has been uniformly grown on the MoS2 film formed by the reaction of Mo species with Species, which is from the carbothermal reduction of sodium sulfate. Due to the excellent graphene "painting" on MoS2 atomic layers, the significantly shortened lithium ion diffusion distance and the markedly enhanced electronic conductivity, these multilayered graphene/MoS2 heterostructures exhibit high specific capacity, unprecedented rate performance and outstanding cycling stability, especially at a high current density, when used as an anode material for lithium batteries. This work provides a simple but efficient route for the controlled fabrication of large-area multilayered graphene/metal sulfide heterostructures with promising applications in battery manufacture, electronics or catalysis.

摘要

将各种二维原子晶体堆叠在一起是一种可行的方法,可以创建具有所需性质的独特多层异质结构。在此,我们首次通过在氮气气氛下,在钼辛酸复合物涂覆的硫酸钠上进行简单的加热处理,来控制大面积石墨烯/ MoS2 异质结构的制备。通过直接的原位催化反应,石墨烯层已均匀地生长在由 Mo 物种与来自硫酸钠的碳热还原的物种反应形成的 MoS2 薄膜上。由于石墨烯在 MoS2 原子层上的优异“涂覆”效果,显著缩短了锂离子的扩散距离,并显著提高了电子电导率,这些多层石墨烯/ MoS2 异质结构表现出高比容量、前所未有的倍率性能和出色的循环稳定性,尤其是在高电流密度下,可用作锂电池的阳极材料。这项工作为控制大面积多层石墨烯/金属硫化物异质结构的制备提供了一种简单但有效的途径,有望在电池制造、电子或催化等领域得到应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b14/3985074/75575aa24963/srep04673-f1.jpg

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