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Ultralow Loading (Single-Atom and Clusters) of the Pt Catalyst by Atomic Layer Deposition Using Dimethyl ((3,4-eta) N,N-dimethyl-3-butene-1-amine-N) Platinum (DDAP) on the High-Surface-Area Substrate for Hydrogen Evolution Reaction
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Title
Ultralow Loading (Single-Atom and Clusters) of the Pt Catalyst by Atomic Layer Deposition Using Dimethyl ((3,4-eta) N,N-dimethyl-3-butene-1-amine-N) Platinum (DDAP) on the High-Surface-Area Substrate for Hydrogen Evolution Reaction
Issued Date
2021-02
Citation
Ramesh, Rahul. (2021-02). Ultralow Loading (Single-Atom and Clusters) of the Pt Catalyst by Atomic Layer Deposition Using Dimethyl ((3,4-eta) N,N-dimethyl-3-butene-1-amine-N) Platinum (DDAP) on the High-Surface-Area Substrate for Hydrogen Evolution Reaction. Advanced Materials Interfaces, 8(3), 2001508. doi: 10.1002/admi.202001508
Type
Article
Author Keywords
atomic layer depositionhydrogen evolution reactionnitrogen‐incorporated carbon cloth substrateplatinum single‐atom catalystsultralow loading
Keywords
DOPED CARBONTHIN-FILMSOXIDEELECTROCATALYSTS
ISSN
2196-7350
Abstract
Single-atom Pt catalyst has seen a tremendous surge in the research community in very recent times. The minimum loading of such precious metal catalysts on high surface area substrates with effective performance toward catalyzing a reaction is indeed of great importance. Here, an alternative way is demonstrated to perform an ultralow loading of Pt catalyst by atomic layer deposition (ALD) using dimethyl ((3,4-η) N,N-dimethyl-3-butene-1-amine-N) platinum precursor (C8H19NPt). The ultralow loading of Pt catalyst is performed on highly porous nitrogen–carbon-powder coated carbon cloth (NC–CC) substrates by varying the number of ALD cycles (2 to 60), and their performance in electrochemical hydrogen evolution reaction (HER) is evaluated. The inductively coupled plasma-optical emission spectrometry provides the exact mass of the Pt catalyst, whereas, the transmission electron microscopy images confirm the uniform and homogeneous dispersion of platinum single-atoms and clusters (with an average size of <1 nm for ten ALD cycles) on the NC–CC substrate. It is further found that the mass activity of Pt catalyst (per microgram of Pt) toward HER is extraordinarily high for less number of ALD cycles (two and five), whereas, the overall performance (current density per geometrical area) becomes more and more improved with increasing the ALD cycles. © 2020 Wiley-VCH GmbH
URI
http://hdl.handle.net/20.500.11750/12821
DOI
10.1002/admi.202001508
Publisher
Wiley-VCH Verlag
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