Fabrication of a Robust PEM Water Electrolyzer Based on Non‐Noble Metal Cathode Catalyst: [Mo 3 S 13 ] 2− Clusters Anchored to N‐Doped Carbon Nanotubes
Autor: | Karl Johann Jakob Mayrhofer, Simon Thiele, Melanie Bühler, Daniel Escalera-López, Chuyen Van Pham, Markus Bierling, Florian Speck, Serhiy Cherevko, Peter Holzapfel |
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Rok vydání: | 2020 |
Předmět: |
Materials science
Proton exchange membrane fuel cell 02 engineering and technology Carbon nanotube engineering.material 010402 general chemistry Electrochemistry 01 natural sciences 7. Clean energy law.invention Catalysis Biomaterials law General Materials Science Polarization (electrochemistry) Electrolysis General Chemistry 021001 nanoscience & nanotechnology 0104 chemical sciences Chemical engineering ddc:540 engineering Water splitting Noble metal ddc:620 0210 nano-technology ddc:600 Biotechnology |
Zdroj: | Small Small 16(37), 2003161 (2020). doi:10.1002/smll.202003161 |
ISSN: | 1613-6810 |
DOI: | 10.1002/smll.202003161 |
Popis: | High investment costs and a dependence on noble metal catalysts currently obstruct the large-scale implementation of proton exchange membrane water electrolyzers (PEMWEs) for converting fluctuating green electricity into chemical energy via water splitting. In this context, this work presents a high-performing and stable non-noble metal catalyst for the hydrogen evolution reaction (HER), consisting of [Mo3 S13 ]2- clusters supported on nitrogen doped carbon nanotubes (NCNTs). Strikingly, a significant electrochemically induced activation of the Mo3 S13 -NCNT catalyst at high current densities is observed in full cell configuration, enabling a remarkable current density of 4 A cm-2 at a cell voltage of 2.36 V. To the authors' knowledge, this is the highest reported value to date for a PEMWE full cell using a non-noble metal HER catalyst. Furthermore, only a minor degradation of 83 µV h-1 is observed during a stability test of 100 h constant current at 1 A cm-2 , with a nearly unchanged polarization behavior after the current hold. Catalyst stability and activity are additionally analyzed via online dissolution measurements. X-ray photoelectron spectroscopy examination of the catalyst before and after electrochemical application reveals a correlation between the electrochemical activation occurring via electrodissolution with changes in the molecular structure of the Mo3 S13 -NCNT catalyst. |
Databáze: | OpenAIRE |
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