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https://dspace.iiti.ac.in/handle/123456789/8177
Title: | S-Doped MoP Nanoporous Layer Toward High-Efficiency Hydrogen Evolution in pH-Universal Electrolyte |
Authors: | Pakhira, Srimanta |
Keywords: | Catalysts;Chemical vapor deposition;Computation theory;Density functional theory;Design for testability;Efficiency;Hydrogen production;Layered semiconductors;Molybdenum compounds;Computational studies;Hydrogen evolution;Hydrogen evolution reactions;Hydrogen generations;Nano-porous;Neutral electrolytes;Non-precious metal catalysts;Stability performance;Electrolytes |
Issue Date: | 2019 |
Publisher: | American Chemical Society |
Citation: | Liang, K., Pakhira, S., Yang, Z., Nijamudheen, A., Ju, L., Wang, M., . . . Yang, Y. (2019). S-doped MoP nanoporous layer toward high-efficiency hydrogen evolution in pH-universal electrolyte. ACS Catalysis, 9(1), 651-659. doi:10.1021/acscatal.8b04291 |
Abstract: | In this study, we report a nonprecious metal catalyst for high-efficiency hydrogen evolution reaction (HER). A self-organized S-doped MoP nanoporous layer (S-MoP NPL) is achieved through a facile electrochemical anodic process and a two-step chemical vapor deposition treatment, which was directly used as a binder-free catalyst for HER in pH-universal electrolytes. S-MoP NPL exhibits HER behavior with a low overpotential of 86 mV at 10 mA cm -1 and low Tafel slope of 34 mV dec -1 in acidic solution. Moreover, S-MoP NPL also shows high HER activity in basic and neutral electrolytes. Density functional theory (DFT) computations were carried out to support our experiment. The calculations show that the H 2 formation (via Volmer-Heyrovsky mechanism) from the reaction of a metal (Mo) absorbed hydride with a solvated proton is favored over S-MoP than MoS 2 . Both experimental and computational studies demonstrate that the extraordinary HER activity and stability performance displayed by a MoP catalyst can be enhanced by S-doping, opening up a promising paradigm for the conscious design of high-performance nonprecious metal catalyst for hydrogen generation. © 2018 American Chemical Society. |
URI: | https://doi.org/10.1021/acscatal.8b04291 https://dspace.iiti.ac.in/handle/123456789/8177 |
ISSN: | 2155-5435 |
Type of Material: | Journal Article |
Appears in Collections: | Department of Physics |
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