4.6 Article

Co-existence of Pd, Bi2O3 and CuO supported on porous activated biocarbon for electrochemical conversion and energy storage

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NEW JOURNAL OF CHEMISTRY
卷 45, 期 37, 页码 17603-17616

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d1nj02184b

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  1. CSIR
  2. NRF
  3. CSIR-Nanostructured (NSNM) unit

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The combination of metal oxides and activated carbon in Pd-AC/Bi2O3/CuO catalyst shows enhanced catalytic behavior and activity for ethanol electro-oxidation and energy storage. The catalyst exhibits high current densities, capacitive j, good electrochemical reversibility, and quick delivery of stored charges, indicating superior energy delivery capability.
The co-existence of metal oxides (MO) and activated carbon (AC) causes changes in the catalytic behaviour and activity which would contribute greatly to a number of applications. Pd-AC/Bi2O3/CuO synthesized via the green process was used as a catalyst for electro-oxidation of ethanol and energy storage. Carbonization at 800 degrees C and hydrothermal treatment in a microwave oven yielded biocarbon (BC) from banana peels with mesoporous and high surface area (690.42 m(2) g(-1)). Cyclic voltammetry (CV), galvanostatic charge-discharge, electrochemical impedance spectroscopy, and chronoamperometry were used to assess the electroactivity of the catalyst (CA). CV of Pd-AC/Bi2O3/CuO revealed 40% enhanced current densities (j) in ethanol electro-oxidation compared to that of the prepared Pd/AC, while the j determined at 20 min of CA measurements was 60% higher than those of the other prepared catalysts. Among the other catalysts, Pd-AC/Bi2O3/CuO revealed high capacitive j and confirmed the near ideal capacitive behaviour with good electrochemical reversibility while the calculated C-sp of the electrode system was found to be 369.1 F g(-1) at 0.95 mA cm(-2). The calculated time constant (tau(0)) value for Pd-AC/Bi2O3/CuO was higher, 390 ms, implying that the catalyst performs better with quick delivery of stored charges indicating better energy delivery capability.

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