4.6 Article

Molybdenum-supported amorphous MoS3 catalyst for efficient hydrogen evolution in solar-water-splitting devices

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 4, Issue 37, Pages 14204-14212

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6ta04789k

Keywords

-

Funding

  1. Ministry of Science and Technology [2014DFE60170]
  2. National Natural Science Foundation of China [61474065, 61504069, 61674084]
  3. Tianjin Research Key Program of Application Foundation and Advanced Technology [15JCZDJC31300]
  4. Key Project in the Science & Technology Pillar Program of Jiangsu Province [BE2014147-3]
  5. 111 Project [B16027]
  6. Specialized Research Fund for the PhD Program of Higher Education [20120031110039]

Ask authors/readers for more resources

We report molybdenum (Mo) metal-supported amorphous molybdenum sulfide (a-MoS3) catalysts with a porous and nanostructure nature, which exhibit excellent catalytic activity for the hydrogen evolution reaction (HER) in wired solar-water-splitting devices. Mo-supported a-MoS3 catalysts were prepared by wet chemically synthesizing a-MoS3 nanoparticles at room-temperature and then loading with Earth-abundant and scalable Mo metals sputtered at low temperature (100 degrees C). Electrochemical studies and applications in wired photoelectrochemical/photovoltaic (PEC-PV) solar-water-splitting devices reveal that the HER performance of wired PEC-PV solar-water-splitting devices can be efficiently enhanced with the proposed highly conductive Mo-supported a-MoS3 catalysts by enlarging the electrochemically active areas, accelerating the electron transport to active sites, and improving the charge transfer at the catalysts/electrolyte interfaces. The low-temperature preparation of highly active Mo-supported a-MoS3 catalysts paves the way to integrating them into various high-performance PV devices to develop highly efficient, scalable, low-cost, and monolithic PEC-PV solar-water-splitting devices.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available