Morphology and surface chemistry engineering toward pH-universal catalysts for hydrogen evolution at high current density
Large-scale implementation of electrochemical hydrogen production requires several fundamental issues to be solved, including understanding the mechanism and developing inexpensive electrocatalysts that work well at high current densities. Here we address these challenges by exploring the roles of m...
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Veröffentlicht in: | Nature communications 2019-01, Vol.10 (1), p.269-269, Article 269 |
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Sprache: | eng |
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Zusammenfassung: | Large-scale implementation of electrochemical hydrogen production requires several fundamental issues to be solved, including understanding the mechanism and developing inexpensive electrocatalysts that work well at high current densities. Here we address these challenges by exploring the roles of morphology and surface chemistry, and develop inexpensive and efficient electrocatalysts for hydrogen evolution. Three model electrocatalysts are flat platinum foil, molybdenum disulfide microspheres, and molybdenum disulfide microspheres modified by molybdenum carbide nanoparticles. The last catalyst is highly active for hydrogen evolution independent of pH, with low overpotentials of 227 mV in acidic medium and 220 mV in alkaline medium at a high current density of 1000 mA cm
−2
, because of enhanced transfer of mass (reactants and hydrogen bubbles) and fast reaction kinetics due to surface oxygen groups formed on molybdenum carbide during hydrogen evolution. Our work may guide rational design of electrocatalysts that work well at high current densities.
Hydrogen production from water provides one avenue toward harnessing renewable energy, although large-scale implementation remains a challenge. Here, authors explore roles of morphology and surface chemistry, and develop efficient catalysts for hydrogen evolution at high current densities. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-018-07792-9 |