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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...

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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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
Descripción
Sumario: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.