Citation:
Meiying Lv, Wenpeng Li, Huiling Liu, Wenjuan Wen, Guang Dong, Jinghua Liu, Kaichen Peng. Enhancement of the formic acid electrooxidation activity of palladium using graphene/carbon black binary carbon supports[J]. Chinese Journal of Catalysis,
;2017, 38(5): 939-947.
doi:
10.1016/S1872-2067(17)62834-1
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Combinations of graphene (Gr) and carbon black (C) were employed as binary carbon supports to fabricate Pd-based electrocatalysts via one-pot co-reduction with Pd2+. The electrocatalytic performance of the resulting Pd/Gr-C catalysts during the electrooxidation of formic acid was assessed. A Pd/Gr0.3C0.7 (Gr oxide:C = 3:7, based on the precursor mass ratio) electrocatalyst exhibited better catalytic performance than both Pd/C and Pd/Gr catalysts. The current density generated by the Pd/Gr0.3C0.7 catalyst was as high as 102.14 mA mgPd-1, a value that is approximately 3 times that obtained from the Pd/C (34.40 mA mgPd-1) and 2.6 times that of the Pd/Gr material (38.50 mA mgPd-1). The anodic peak potential of the Pd/Gr0.3C0.7 was 120 mV more negative than that of the Pd/C and 70 mV more negative than that of the Pd/Gr. Scanning electron microscopy images indicated that the spherical C particles accumulated on the wrinkled graphene surfaces to form C cluster/Gr hybrids having three-dimensional nanostructures. X-ray photoelectron spectroscopy data confirmed the interaction between the Pd metal and the binary Gr-C support. The Pd/Gr0.3C0.7 also exhibited high stability, and so is a promising candidate for the fabrication of anodes for direct formic acid fuel cells. This work demonstrates a simple and cost-effective method for improving the performance of Pd-based electrocatalysts, which should have potential industrial applications.
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Keywords:
- Binary carbon support,
- Palladium,
- Graphene,
- Carbon black,
- Formic acid oxidation,
- Fuel cell
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