Journal
CHEMICAL ENGINEERING JOURNAL
Volume 438, Issue -, Pages -Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.135585
Keywords
Electrocatalyst; Palladium single atom; Palladium nanoparticle; Methanol oxidation reaction; Electronic structure regulation
Categories
Funding
- National Key Research and Development Program of China [2020YFC1909001]
- Strategic Priority Research Program of Chinese Academy of Sciences [XDA21070302]
- National Natural Science Foundation of China [51804291]
- Beijing Natural Science Foundation [2184127]
- Chinese Academy of Sciences [HZ2021013]
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This study develops a unique composite catalyst comprised of partial Pd nanoparticles and partial Pd single atoms for commercially viable direct methanol fuel cells. The catalyst exhibits remarkable activity and long-time stability in alkaline solution for the methanol oxidation reaction.
For commercially viable direct methanol fuel cells, electrocatalysts play a crucial role in motivating the sluggish methanol oxidation reaction (MOR) over anode. Unfortunately, the large-scale applications of current MOR catalysts are hampered by their poor tolerance to poisoning and fast activity degradation. Herein, a unique composite catalyst comprised of partial Pd nanoparticles and partial Pd single atoms (Pd-NPs/Pd-N-x@C) is developed. The as-fabricated catalyst exhibits remarkable activity of 9.45 mA.cm(-2) towards MOR in alkaline solution, which is 7.05 and 3.92 times that of commercial Pd/C and nanoparticle type (Pd-NPs@C) electro-catalysts, respectively. Impressively, the Pd-NPs/Pd-N-x@C shows the highest long-time stability with 90.38% and 89.8% of the initial activity retained after 3600 s chronoamperometry (CA) test and 2000 cycles of cyclic voltammetry (CV) measurements with accelerated durability test (ADT), respectively. Combined with high-angle annular darkfield scanning transmission electron microscopy (HAADF-STEM), X-ray adsorption fine structure (XAFS) spectra and X-ray photoelectron spectroscopy (XPS) analyses, the superior performance of Pd-NPs/Pd-N-x@C can be ascribed to the synergistic effect from the Pd single atoms, N-doped carbon supports and Pd nanoparticles. Notably, the embedded Pd single atoms are liable to transfer electrons to the substrate due to the electronic metal-support interactions (EMSI) and the charge transfer between Pd nanoparticles and carbon supports is suppressed, inducing a weak adsorption strength of poisonous carbonous intermediate species on active Pd nanoparticles and improved poisoning tolerance in MOR process, which is verified by density functional theory (DFT) calculations as well as CO-stripping voltammetry experiments. This work not only con-tributes the first example of a synergistic catalyst between nanoparticles and single atoms for MOR but also deepens the knowledge on the metal-support interaction.
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