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Direct immobilization of an atomically dispersed Pt catalyst by suppressing heterogeneous nucleation at 40 C
Direct deposition of isolated metal atoms onto substrates has been recognized as a simple route to obtain high performance supported atomically dispersed metals (SACs), however, the agglomeration driven by high surface energy is difficult to avoid. Herein, we demonstrate a one-pot solution synthesis...
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Published in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2019, Vol.7 (45), p.25779-25784 |
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Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Direct deposition of isolated metal atoms onto substrates has been recognized as a simple route to obtain high performance supported atomically dispersed metals (SACs), however, the agglomeration driven by high surface energy is difficult to avoid. Herein, we demonstrate a one-pot solution synthesis to obtain atomically dispersed platinum (Pt) supported on nitrogen (N)-doped mesoporous carbon (NMC) substrates (Pt/NMC-LT) by conducting the whole synthesis at 40 C, owing to the sluggish nucleation kinetics. We obtained the Pt/NMC-LT catalyst with superior electrochemical hydrogen evolution reaction (HER) activity and stability, in comparison with the NMC supported dominant Pt sub-nanometer cluster catalyst from solution synthesis at RT 25 C (Pt/NMC-RT) and commercial carbon supported Pt nanoparticle catalysts (Pt/C). Lower over-potential values (only 17.0 and 49.8 mV) are needed for high HER current densities (10 and 100 mA cm
2
, respectively), and no obvious degradation is observed after an accelerated durability test (ADT) for 5000 CV cycles.
Direct deposition of isolated metal atoms onto substrates has been recognized as a simple route to obtain high performance supported atomically dispersed metals (SACs), however, the agglomeration driven by high surface energy is difficult to avoid. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/c9ta07469d |