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Design of two-dimensional, ultrathin MoS₂ nanoplates fabricated within one-dimensional carbon nanofibers with thermosensitive morphology: high-performance electrocatalysts for the hydrogen evolution reaction.

Authors :
Zhu H
Lyu F
Du M
Zhang M
Wang Q
Yao J
Guo B
Source :
ACS applied materials & interfaces [ACS Appl Mater Interfaces] 2014 Dec 24; Vol. 6 (24), pp. 22126-37. Date of Electronic Publication: 2014 Dec 04.
Publication Year :
2014

Abstract

Two-dimensional MoS2 nanoplates within carbon nanofibers (CNFs) with monolayer thickness, nanometer-scale dimensions and abundant edges are fabricated. This strategy provides a well-defined pathway for the precise design of MoS2 nanomaterials, offering control over the evolution of MoS2 morphology from nanoparticles to nanoplates as well as from mono- to several-layer structures, over a lateral dimension range of 5 to 70 nm. CNFs play an important role in confining the growth of MoS2 nanoplates, leading to increases in the amount of exposed edge sites while hindering the stacking and aggregation of MoS2 layers, and accelerating electron transfer. The controlled growth of MoS2 nanoplates embedded in CNFs is leveraged to demonstrate structure-dependent catalytic activity in the hydrogen evolution reaction (HER). The results suggest that increases in the number of layers and the lateral dimension result in a decrease in HER activity as a general rule. Single-layer MoS2 nanoplates with abundant edges and a lateral dimension of 7.3 nm demonstrated the lowest hydrogen evolution reaction overpotential of 93 mV (J = 10 mA/cm(2)), the highest current density of 80.3 mA/cm(2) at η = 300 mV and the smallest Tafel slope of 42 mV/decade. The ability of MoS2-CNFs hybrids to act as nonprecious metal catalysts indicates their promise for use in energy-related electrocatalytic applications.

Details

Language :
English
ISSN :
1944-8252
Volume :
6
Issue :
24
Database :
MEDLINE
Journal :
ACS applied materials & interfaces
Publication Type :
Academic Journal
Accession number :
25420219
Full Text :
https://doi.org/10.1021/am505544g