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Nitrogen-Plasma-Treated Continuous Monolayer MoS(2) for Improving Hydrogen Evolution Reaction

[Image: see text] Theoretically, the edges of a MoS(2) flake and S-vacancy within the lattice have nearly zero Gibbs free energy for hydrogen adsorption, which is essentially correlated to the exchange currents in hydrogen evolution reaction (HER). However, MoS(2) possesses insufficient active sites...

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Detalles Bibliográficos
Autores principales: Nguyen, Anh Duc, Nguyen, Tri Khoa, Le, Chinh Tam, Kim, Sungdo, Ullah, Farman, Lee, Yangjin, Lee, Sol, Kim, Kwanpyo, Lee, Dooyong, Park, Sungkyun, Bae, Jong-Seong, Jang, Joon I., Kim, Yong Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921679/
https://www.ncbi.nlm.nih.gov/pubmed/31867547
http://dx.doi.org/10.1021/acsomega.9b03205
Descripción
Sumario:[Image: see text] Theoretically, the edges of a MoS(2) flake and S-vacancy within the lattice have nearly zero Gibbs free energy for hydrogen adsorption, which is essentially correlated to the exchange currents in hydrogen evolution reaction (HER). However, MoS(2) possesses insufficient active sites (edges and S-vacancies) in pristine form. Interestingly, active sites can be effectively engineered within the continuous MoS(2) sheets by treating it with plasma in a controlled manner. Here, we employed N(2) plasma on a large-area continuous-monolayer MoS(2) synthesized via metal–organic chemical vapor deposition to acquire maximum active sites that are indeed required for an efficient HER performance. The MoS(2) samples with maximum active sites were acquired by optimizing the plasma exposure time. The newly induced edges and S-vacancies were directly verified by high-resolution transmission electron microscopy. The 20 min treated MoS(2) sample showed maximum active sites and thereby maximum HER activity, onset overpotential of ∼−210 mV vs reversible hydrogen electrode (RHE), and Tafel slope of ∼89 mV/dec. Clearly, the above results show that this approach can be employed for improving the HER efficiency of large-scale MoS(2)-based electrocatalysts.