AI Article Synopsis

  • A new electrocatalyst made from yttrium oxide and palladium nanoparticles was created using a sodium borohydride reduction method, optimizing the ratio of these materials to enhance performance.
  • Characterization techniques like XPS, TEM, and XRD confirmed that the best-performing electrocatalyst, PdY/rGO, had the highest current density and lowest onset potential compared to other standards.
  • The presence of yttrium oxide improved the structure and properties of the catalyst, resulting in greater stability, resistance to CO poisoning, and a larger electrochemically active surface area.

Article Abstract

A highly efficient and stable electrocatalyst comprised of yttrium oxide (YO) and palladium nanoparticles has been synthesized a sodium borohydride reduction approach. The molar ratio of Pd and Y was varied to fabricate various electrocatalysts and the oxidation reaction of formic acid was checked. X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), and X-ray powder diffraction (XRD) are used to characterize the synthesized catalysts. Among the synthesized catalysts (PdY/rGO), the optimized catalyst , PdY/rGO exhibits the highest current density (106 mA cm) and lowest onset potential compared to Pd/rGO (28.1 mA cm) and benchmark Pd/C (21.7 mA cm). The addition of YO to the rGO surface results in electrochemically active sites due to the improved geometric structure and bifunctional components. The electrochemically active surface area 119.4 m g is calculated for PdY/rGO, which is ∼1.108, ∼1.24, ∼1.47 and 1.55 times larger than PdY/rGO, PdY/rGO, Pd/C and Pd/rGO, respectively. The redesigned Pd structures on YO-promoted rGO give exceptional stability and enhanced resistance to CO poisoning. The outstanding electrocatalytic performance of the PdY/rGO electrocatalyst is ascribed to uniform dispersion of small size palladium nanoparticles which is possibly due to the presence of yttrium oxide.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10184137PMC
http://dx.doi.org/10.1039/d3ra01929bDOI Listing

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