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
Institute of Materials Science, Vietnam Academy of Science and Technology, Hanoi 100000, Vietnam.
Department of Chemistry, Hanyang University, 222, Wangsimni-ro, Seongdong-gu, Seoul 04763, Republic of Korea.
Nanomaterials (Basel). 2023 Jul 23;13(14):2139. doi: 10.3390/nano13142139.
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 possesses superior features for HER catalysis. The attractions and high surface energy, however, stack the MoSe layers, resulting in a loss of edge active catalytic sites. In addition, MoSe 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 during synthesis when treated thermally in an inert atmosphere at 600 °C transformed into graphene (Gr). This widened the interlayer spacing of MoSe, thereby exposing more HER active edge sites with high conductivity offered by the incorporated Gr. The resulting MoSe-Gr composite exhibited a significantly enhanced HER catalytic activity compared to the pristine MoSe 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. Additionally, the MoSe-Gr catalyst demonstrated long-term electrochemical stability during HER. This work, thus, presents a facile and novel approach for obtaining an efficient MoSe electrocatalyst applicable in green hydrogen production.
开发高效且耐用的析氢反应(HER)电催化剂对于应对能源和环境挑战至关重要。在二维层状硫族化物中,MoSe在HER催化方面具有卓越特性。然而,其吸引力和高表面能会使MoSe层堆叠,导致边缘活性催化位点丧失。此外,MoSe存在本征电导率低以及与活性位点电接触弱的问题。为克服这些问题,本工作提出一种新颖方法,即在合成过程中原位将二甘醇溶剂引入MoSe的层间,当在600°C的惰性气氛中进行热处理时,二甘醇转变为石墨烯(Gr)。这拓宽了MoSe的层间距,从而暴露出更多具有由引入的Gr提供的高电导率的HER活性边缘位点。所得的MoSe-Gr复合材料在酸性介质中与原始MoSe相比表现出显著增强的HER催化活性,并且与最先进的Pt/C催化剂相比表现出优异的HER催化活性,特别是在超过约55 mA cm的高电流密度下。此外,MoSe-Gr催化剂在HER过程中表现出长期的电化学稳定性。因此,本工作提出了一种简便且新颖的方法来获得适用于绿色制氢的高效MoSe电催化剂。