超晶格
异质结
范德瓦尔斯力
材料科学
亚稳态
钴
相(物质)
化学物理
凝聚态物理
纳米技术
化学
光电子学
分子
物理
有机化学
冶金
作者
Kunkun Nie,Na Li,Binjie Li,Yanling Yuan,Yujia Zhang,Pei Liu,Shaokun Chong,Jun Hu,Z.Y. Liu,Wei Huang
标识
DOI:10.1016/j.cej.2023.146066
摘要
Van der Waals superlattice heterostructure with different two-dimensional (2D) nanosheets provides a promising way to exploit the intrinsic properties of both 2D components. However, developing efficient methods for precisely constructing ordered/controlled layer sequence superlattice heterostructures has always been challenging. Here, we report a facile strategy for the preparation of single-atomic cobalt anchored 1T-MoS2/carbon (Co-1T-MoS2/C) heterostructure with a well-ordered superlattice of alternating Co-1T-MoS2 and C nanosheets at a molecular level. The coordination of Co atoms on the 1T-MoS2 matrix and its effect on the phase transformation of MoS2 has been systematically investigated. Importantly, the Co atoms can efficiently improve the metastable 1T phase stability of MoS2. As a proof-of-concept application, the obtained Co-1T-MoS2/C is employed as an electrocatalyst for overall water splitting in alkaline conditions. The rapid interfacial charge transfer and abundant active catalytic sites, coupled with the contribution of the single-atomic Co sites enable the Co-1T-MoS2/C superlattice heterostructure to exhibit excellent performance. The assembled Pt/C||Co-1T-MoS2/C cell needs only 1.57 V to reach the current density of 10 mA/cm2. Our research strategy provides a feasible path for the design of 2D-2D van der Waals superlattice heterostructures and further broadens their applications.
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