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Escalating Catalytic Activity for Hydrogen Evolution Reaction on MoSe(2)@Graphene Functionalization
Developing highly efficient and durable hydrogen evolution reaction (HER) electrocatalysts is crucial for addressing the energy and environmental challenges. Among the 2D-layered chalcogenides, MoSe(2) possesses superior features for HER catalysis. The van der Waals attractions and high surface ener...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10384179/ https://www.ncbi.nlm.nih.gov/pubmed/37513150 http://dx.doi.org/10.3390/nano13142139 |
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author | Bui, Hoa Thi Lam, Nguyen Duc Linh, Do Chi Mai, Nguyen Thi Chang, HyungIl Han, Sung-Hwan Oanh, Vu Thi Kim Pham, Anh Tuan Patil, Supriya A. Tung, Nguyen Thanh Shrestha, Nabeen K. |
author_facet | Bui, Hoa Thi Lam, Nguyen Duc Linh, Do Chi Mai, Nguyen Thi Chang, HyungIl Han, Sung-Hwan Oanh, Vu Thi Kim Pham, Anh Tuan Patil, Supriya A. Tung, Nguyen Thanh Shrestha, Nabeen K. |
author_sort | Bui, Hoa Thi |
collection | PubMed |
description | Developing highly efficient and durable hydrogen evolution reaction (HER) electrocatalysts is crucial for addressing the energy and environmental challenges. Among the 2D-layered chalcogenides, MoSe(2) possesses superior features for HER catalysis. The van der Waals attractions and high surface energy, however, stack the MoSe(2) layers, resulting in a loss of edge active catalytic sites. In addition, MoSe(2) suffers from low intrinsic conductivity and weak electrical contact with active sites. To overcome the issues, this work presents a novel approach, wherein the in situ incorporated diethylene glycol solvent into the interlayers of MoSe(2) during synthesis when treated thermally in an inert atmosphere at 600 °C transformed into graphene (Gr). This widened the interlayer spacing of MoSe(2), thereby exposing more HER active edge sites with high conductivity offered by the incorporated Gr. The resulting MoSe(2)-Gr composite exhibited a significantly enhanced HER catalytic activity compared to the pristine MoSe(2) in an acidic medium and demonstrated a superior HER catalytic activity compared to the state-of-the-art Pt/C catalyst, particularly at a high current density beyond ca. 55 mA cm(−2). Additionally, the MoSe(2)-Gr catalyst demonstrated long-term electrochemical stability during HER. This work, thus, presents a facile and novel approach for obtaining an efficient MoSe(2) electrocatalyst applicable in green hydrogen production. |
format | Online Article Text |
id | pubmed-10384179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103841792023-07-30 Escalating Catalytic Activity for Hydrogen Evolution Reaction on MoSe(2)@Graphene Functionalization Bui, Hoa Thi Lam, Nguyen Duc Linh, Do Chi Mai, Nguyen Thi Chang, HyungIl Han, Sung-Hwan Oanh, Vu Thi Kim Pham, Anh Tuan Patil, Supriya A. Tung, Nguyen Thanh Shrestha, Nabeen K. Nanomaterials (Basel) Article Developing highly efficient and durable hydrogen evolution reaction (HER) electrocatalysts is crucial for addressing the energy and environmental challenges. Among the 2D-layered chalcogenides, MoSe(2) possesses superior features for HER catalysis. The van der Waals attractions and high surface energy, however, stack the MoSe(2) layers, resulting in a loss of edge active catalytic sites. In addition, MoSe(2) suffers from low intrinsic conductivity and weak electrical contact with active sites. To overcome the issues, this work presents a novel approach, wherein the in situ incorporated diethylene glycol solvent into the interlayers of MoSe(2) during synthesis when treated thermally in an inert atmosphere at 600 °C transformed into graphene (Gr). This widened the interlayer spacing of MoSe(2), thereby exposing more HER active edge sites with high conductivity offered by the incorporated Gr. The resulting MoSe(2)-Gr composite exhibited a significantly enhanced HER catalytic activity compared to the pristine MoSe(2) in an acidic medium and demonstrated a superior HER catalytic activity compared to the state-of-the-art Pt/C catalyst, particularly at a high current density beyond ca. 55 mA cm(−2). Additionally, the MoSe(2)-Gr catalyst demonstrated long-term electrochemical stability during HER. This work, thus, presents a facile and novel approach for obtaining an efficient MoSe(2) electrocatalyst applicable in green hydrogen production. MDPI 2023-07-23 /pmc/articles/PMC10384179/ /pubmed/37513150 http://dx.doi.org/10.3390/nano13142139 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Bui, Hoa Thi Lam, Nguyen Duc Linh, Do Chi Mai, Nguyen Thi Chang, HyungIl Han, Sung-Hwan Oanh, Vu Thi Kim Pham, Anh Tuan Patil, Supriya A. Tung, Nguyen Thanh Shrestha, Nabeen K. Escalating Catalytic Activity for Hydrogen Evolution Reaction on MoSe(2)@Graphene Functionalization |
title | Escalating Catalytic Activity for Hydrogen Evolution Reaction on MoSe(2)@Graphene Functionalization |
title_full | Escalating Catalytic Activity for Hydrogen Evolution Reaction on MoSe(2)@Graphene Functionalization |
title_fullStr | Escalating Catalytic Activity for Hydrogen Evolution Reaction on MoSe(2)@Graphene Functionalization |
title_full_unstemmed | Escalating Catalytic Activity for Hydrogen Evolution Reaction on MoSe(2)@Graphene Functionalization |
title_short | Escalating Catalytic Activity for Hydrogen Evolution Reaction on MoSe(2)@Graphene Functionalization |
title_sort | escalating catalytic activity for hydrogen evolution reaction on mose(2)@graphene functionalization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10384179/ https://www.ncbi.nlm.nih.gov/pubmed/37513150 http://dx.doi.org/10.3390/nano13142139 |
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