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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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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
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author 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
author_facet 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
author_sort Nguyen, Anh Duc
collection PubMed
description [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.
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spelling pubmed-69216792019-12-20 Nitrogen-Plasma-Treated Continuous Monolayer MoS(2) for Improving Hydrogen Evolution Reaction 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 ACS Omega [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. American Chemical Society 2019-12-03 /pmc/articles/PMC6921679/ /pubmed/31867547 http://dx.doi.org/10.1021/acsomega.9b03205 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle 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
Nitrogen-Plasma-Treated Continuous Monolayer MoS(2) for Improving Hydrogen Evolution Reaction
title Nitrogen-Plasma-Treated Continuous Monolayer MoS(2) for Improving Hydrogen Evolution Reaction
title_full Nitrogen-Plasma-Treated Continuous Monolayer MoS(2) for Improving Hydrogen Evolution Reaction
title_fullStr Nitrogen-Plasma-Treated Continuous Monolayer MoS(2) for Improving Hydrogen Evolution Reaction
title_full_unstemmed Nitrogen-Plasma-Treated Continuous Monolayer MoS(2) for Improving Hydrogen Evolution Reaction
title_short Nitrogen-Plasma-Treated Continuous Monolayer MoS(2) for Improving Hydrogen Evolution Reaction
title_sort nitrogen-plasma-treated continuous monolayer mos(2) for improving hydrogen evolution reaction
url 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
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