电催化剂
甲醇
石墨烯
氧化物
钯
甲酸
制作
材料科学
氮气
化学工程
纳米技术
无机化学
化学
催化作用
有机化学
电化学
电极
冶金
医学
替代医学
物理化学
病理
工程类
作者
Adil Amin Wani,Aamir Y. Bhat,Pravin P. Ingole,Mohsin Ahmad Bhat
标识
DOI:10.1021/acs.energyfuels.4c03642
摘要
Herein, we report a simple and highly reproducible synthetic strategy for the shape-directed growth of palladium (Pd) nanocubes supported over nitrogen-doped reduced graphene oxide (NrGO). Characterization of the Pd/NrGO composite by Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), energy-dispersive X-ray analysis (EDXA), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), X-ray diffraction (XRD), and Raman spectroscopy suggests that the composite has a uniform distribution of nanocube-shaped Pd clusters (with an average size of 8.14 nm) firmly anchored to the NrGO matrix. Cyclic voltammetry (CV), chronoamperometry (CA), and electrochemical impedance spectroscopy (EIS) were used to test the electrocatalytic performance and electrochemical stability of the Pd/NrGO composite toward the formic acid oxidation reaction (FAOR) and methanol oxidation reaction (MOR). The Pd/NrGO composite exhibits a better peak current density of 2.6 mA/cm2 (FAOR) and 2.2 mA/cm2 (MOR) as against commercial Pd/C (0.76 mA/cm2 for the FAOR, 1.6 mA/cm2 for the MOR) and Pt/C (0.63 mA/cm2 for the FAOR, 1.5 mA/cm2 for the MOR) with a much lower overpotential requirement for the onset of both the FAOR and MOR. The presented results clearly suggest that the electrochemical stability and electrocatalytic performance of the Pd/NrGO composite crafted for the present work are sufficient to qualify it as a promising alternative of Pt-based anode materials for commercially relevant DFAFCs and DMFCs.
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