| Literature DB >> 26765150 |
Ping Li1, Zhi Yang1, Juanxia Shen1, Huagui Nie1, Qiran Cai2, Luhua Li2, Mengzhan Ge1, Cancan Gu1, Xi'an Chen1, Keqin Yang1, Lijie Zhang1, Ying Chen2, Shaoming Huang1.
Abstract
Electrochemically splitting water for hydrogen evolution reaction (HER) has been viewed as a promising approach to produce renewable and clean hydrogen energy. However, searching for cheap and efficient HER electrocatalysts to replace the currently used Pt-based catalysts remains an urgent task. Herein, we develop a one-step carbon nanotube (CNT) assisted synthesis strategy with CNTs' strong adsorbability to mediate the growth of subnanometer-sized MoS(x) on CNTs. The subnanometer MoS(x)-CNT hybrids achieve a low overpotential of 106 mV at 10 mA cm(-2), a small Tafel slope of 37 mV per decade, and an unprecedentedly high turnover frequency value of 18.84 s(-1) at η = 200 mV among all reported non-Pt catalysts in acidic conditions. The superior performance of the hybrid catalysts benefits from the presence of a higher number of active sites and the abundant exposure of unsaturated S atoms rooted in the subnanometer structure, demonstrating a new class of subnanometer-scale catalysts.Entities:
Keywords: carbon nanotubes; electrocatalysts; hydrogen evolution reaction; molybdenum sulfide; subnanometer
Year: 2016 PMID: 26765150 DOI: 10.1021/acsami.5b08816
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229