Author
Listed:
- Dustin R. Cummins
(Materials Physics and Applications (MPA-11), Los Alamos National Laboratory
Chemical Engineering and Conn Center for Renewable Energy Research, University of Louisville)
- Ulises Martinez
(Materials Physics and Applications (MPA-11), Los Alamos National Laboratory)
- Andriy Sherehiy
(Chemical Engineering and Conn Center for Renewable Energy Research, University of Louisville)
- Rajesh Kappera
(Materials Physics and Applications (MPA-11), Los Alamos National Laboratory
Materials Science and Engineering, Rutgers University)
- Alejandro Martinez-Garcia
(Chemical Engineering and Conn Center for Renewable Energy Research, University of Louisville)
- Roland K. Schulze
(Materials Science and Technology (MST-6), Los Alamos National Laboratory)
- Jacek Jasinski
(Chemical Engineering and Conn Center for Renewable Energy Research, University of Louisville)
- Jing Zhang
(Materials Science and NanoEngineering, Rice University)
- Ram K. Gupta
(Chemistry, Pittsburg State University)
- Jun Lou
(Materials Science and NanoEngineering, Rice University)
- Manish Chhowalla
(Materials Science and Engineering, Rutgers University)
- Gamini Sumanasekera
(Chemical Engineering and Conn Center for Renewable Energy Research, University of Louisville)
- Aditya D. Mohite
(Materials Physics and Applications (MPA-11), Los Alamos National Laboratory)
- Mahendra K. Sunkara
(Chemical Engineering and Conn Center for Renewable Energy Research, University of Louisville)
- Gautam Gupta
(Materials Physics and Applications (MPA-11), Los Alamos National Laboratory)
Abstract
Hydrogen evolution reaction is catalysed efficiently with precious metals, such as platinum; however, transition metal dichalcogenides have recently emerged as a promising class of materials for electrocatalysis, but these materials still have low activity and durability when compared with precious metals. Here we report a simple one-step scalable approach, where MoOx/MoS2 core-shell nanowires and molybdenum disulfide sheets are exposed to dilute aqueous hydrazine at room temperature, which results in marked improvement in electrocatalytic performance. The nanowires exhibit ∼100 mV improvement in overpotential following exposure to dilute hydrazine, while also showing a 10-fold increase in current density and a significant change in Tafel slope. In situ electrical, gate-dependent measurements and spectroscopic investigations reveal that hydrazine acts as an electron dopant in molybdenum disulfide, increasing its conductivity, while also reducing the MoOx core in the core-shell nanowires, which leads to improved electrocatalytic performance.
Suggested Citation
Dustin R. Cummins & Ulises Martinez & Andriy Sherehiy & Rajesh Kappera & Alejandro Martinez-Garcia & Roland K. Schulze & Jacek Jasinski & Jing Zhang & Ram K. Gupta & Jun Lou & Manish Chhowalla & Gamin, 2016.
"Efficient hydrogen evolution in transition metal dichalcogenides via a simple one-step hydrazine reaction,"
Nature Communications, Nature, vol. 7(1), pages 1-10, September.
Handle:
RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms11857
DOI: 10.1038/ncomms11857
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