Escalating Catalytic Activity for Hydrogen Evolution Reaction on MoSe2@Graphene Functionalization

Author:

Bui Hoa Thi1,Lam Nguyen Duc1,Linh Do Chi1,Mai Nguyen Thi1,Chang HyungIl2ORCID,Han Sung-Hwan2,Oanh Vu Thi Kim3,Pham Anh Tuan4,Patil Supriya A.5,Tung Nguyen Thanh1ORCID,Shrestha Nabeen K.6

Affiliation:

1. Institute of Materials Science, Vietnam Academy of Science and Technology, Hanoi 100000, Vietnam

2. Department of Chemistry, Hanyang University, 222, Wangsimni-ro, Seongdong-gu, Seoul 04763, Republic of Korea

3. Institute of Physic and Graduate University of Science and Technology, Vietnam Academy of Science and Technology, Hanoi 100000, Vietnam

4. Institute of Engineering and Technology, Thu Dau Mot University, Binh Duong 75000, Vietnam

5. Department of Nanotechnology and Advanced Materials Engineering, Sejong University, Seoul 05006, Republic of Korea

6. Division of Physics and Semiconductor Science, Dongguk University, Seoul 04620, Republic of Korea

Abstract

Developing highly efficient and durable hydrogen evolution reaction (HER) electrocatalysts is crucial for addressing the energy and environmental challenges. Among the 2D-layered chalcogenides, MoSe2 possesses superior features for HER catalysis. The van der Waals attractions and high surface energy, however, stack the MoSe2 layers, resulting in a loss of edge active catalytic sites. In addition, MoSe2 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 MoSe2 during synthesis when treated thermally in an inert atmosphere at 600 °C transformed into graphene (Gr). This widened the interlayer spacing of MoSe2, thereby exposing more HER active edge sites with high conductivity offered by the incorporated Gr. The resulting MoSe2-Gr composite exhibited a significantly enhanced HER catalytic activity compared to the pristine MoSe2 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 MoSe2-Gr catalyst demonstrated long-term electrochemical stability during HER. This work, thus, presents a facile and novel approach for obtaining an efficient MoSe2 electrocatalyst applicable in green hydrogen production.

Funder

Vietnam Academy of Science and Technology

Publisher

MDPI AG

Subject

General Materials Science,General Chemical Engineering

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