2018
DOI: 10.3390/catal8080329
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Oxygen Reduction Reaction and Hydrogen Evolution Reaction Catalyzed by Pd–Ru Nanoparticles Encapsulated in Porous Carbon Nanosheets

Abstract: Developing bi-functional electrocatalysts for both oxygen reduction reaction (ORR) and hydrogen evolution reaction (HER) is crucial for enhancing the energy transfer efficiency of metal-air batteries and fuel cells, as well as producing hydrogen with a high purity. Herein, a series of Pd-Ru alloyed nanoparticles encapsulated in porous carbon nanosheets (CNs) were synthesized and employed as a bifunctional electrocatalyst for both ORR and HER. The TEM measurements showed that Pd-Ru nanoparticles, with a size of… Show more

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Cited by 49 publications
(30 citation statements)
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“…Figure c represents the amount of evolved hydrogen with time and dividing the experimental result by calculated value provides an extremely high efficiency of 99.4 %. The intrinsic figure of merit for HER electrocatalysts, the TOF of AgNi‐5 at 50 mV (versus RHE) is found to be 2.1 H 2 s −1 and at 150 mV (versus RHE) it is 14.6 H 2 s −1 (Supporting Information, Discussion S2), which is at par or larger than the best HER electrocatalysts reported till date (Supporting Information, Table S3) . AgNi‐5 NCs is also found to be remarkably stable both at pH 0 and pH 14 under operational conditions at −0.15 V overpotential for 5 days (Figure d), with no apparent change in its intertwined morphology (Figure d inset).…”
Section: Resultsmentioning
confidence: 82%
“…Figure c represents the amount of evolved hydrogen with time and dividing the experimental result by calculated value provides an extremely high efficiency of 99.4 %. The intrinsic figure of merit for HER electrocatalysts, the TOF of AgNi‐5 at 50 mV (versus RHE) is found to be 2.1 H 2 s −1 and at 150 mV (versus RHE) it is 14.6 H 2 s −1 (Supporting Information, Discussion S2), which is at par or larger than the best HER electrocatalysts reported till date (Supporting Information, Table S3) . AgNi‐5 NCs is also found to be remarkably stable both at pH 0 and pH 14 under operational conditions at −0.15 V overpotential for 5 days (Figure d), with no apparent change in its intertwined morphology (Figure d inset).…”
Section: Resultsmentioning
confidence: 82%
“…The high intense metallic deconvoluted peaks of Pd 0 3d 5/2 and Pd 0 3d 3/2 are attributed at the binding energies of 336.49 and 341.91 eV, while the less intense oxidized deconvoluted peaks of Pd 2+ 3d 5/2 and Pd 2+ 3d 3/2 are attributed at 331.01 and 342.68 eV, respectively. 44 The deconvoluted Ti 2p spectra in Figure 3H exhibited two main spin-orbit split peaks of Ti p 3/2 and Ti p 1/2 at the binding energies of 457.3 and 462.5 eV, respectively. The deconvoluted peaks of Ti-C (sp 3 ), Ti 2+ , and Ti-O are attributed to the binding energies of 458.13, 460.85, and 463.27 eV, respectively, that are correlated with the chemical state of the MXene.…”
Section: Formation Mechanism Of the Pd-ru/mxene Catalystmentioning
confidence: 92%
“…Catalyst supports require properties, such as high surface area and high electronic conductivity, to maintain high catalytic activity [13]. While platinum remains an efficient electrocatalyst [14], carbon black degrades over time decreasing durability and increasing the cost of the catalyst due to the need for regeneration [15]. Possible replacements for carbon black are carbon tubule membranes [16], ordered porous carbon [17], graphite nanofibers [18], films of C60 clusters [19], hard carbon spherules [20], and carbon nanotubes [21].…”
Section: Introductionmentioning
confidence: 99%