氧化铈/类洋葱碳负载pd基催化剂在碱性介质中氧化异丙醇的电催化性能及DFT研究

IF 3.2 3区 化学 Q2 CHEMISTRY, PHYSICAL
Desalegn Nigatu Gemechu, Aderemi B. Haruna, Ahmed Mustefa Mohammed, Yedilfana Setarge Mekonnen* and Kenneth I. Ozoemena*, 
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引用次数: 0

摘要

研究了类洋葱碳(OLC)负载的pd基催化剂在碱性介质(直接异丙醇燃料电池(DIFC))中氧化异丙醇(IPA)的电催化性能。所合成和评价的催化剂有PdNi/OLC、Pd/CeO2/OLC和PdNi/CeO2/OLC,其性能均与市售Pd/C相当。采用x射线衍射(XRD)、场发射扫描电镜(FE-SEM)耦合能量色散x射线(EDX)、高分辨率透射电镜(HRTEM)、x射线光电子能谱(XPS)等理化分析方法对样品进行了表征。电化学测量采用循环伏安法(CV)、计时伏安法(CA)、线性扫描伏安法(LSV)和电化学阻抗谱法(EIS)。CV测试和Tafel分析结果表明,PdNi/CeO2/OLC具有最高的电流响应,起始电位为- 0.69 V,动力学活性为136.9 mV/dec。计时安培测试证实,PdNi/CeO2/OLC具有优异的稳定性和抗毒性能,可在较长时间内实现稳定的电流密度。EIS显示PdNi/CeO2/OLC的电荷转移电阻(Rct)最低,反映了更有效的电子转移。含Ni催化剂的Tafel斜率也较低(PdNi/OLC为121.5 mV/dec, PdNi/CeO2/OLC为136.9 mV/dec),表明Ni的加入改善了反应动力学。密度泛函理论(DFT)计算表明,Ni加入Pd增强了电子给能,而CeO2的支持增强了电子给能。这种协同作用改善了IPA的吸附和反应动力学,从而提高了电催化性能。这些发现表明,将Pd与Ni合金化并将其负载在CeO2上,可以显著提高醇氧化过程中的电催化活性、稳定性和质量传输。PdNi/CeO2/OLC催化剂是DIFC应用的一个很有前途的候选者,具有高效率,耐用性和低起爆潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrocatalytic Properties and DFT Studies of Pd-Based Catalysts Supported on Ceria/Onion-like Carbon for Isopropanol Oxidation in Alkaline Medium

This study investigated the electrocatalytic performance of Pd-based catalysts supported on onion-like carbon (OLC) for isopropanol (IPA) oxidation in alkaline media (a direct isopropanol fuel cells (DIFC)). The synthesized and evaluated catalysts included PdNi/OLC, Pd/CeO2/OLC, and PdNi/CeO2/OLC, all of which demonstrated performances comparable to that of commercial Pd/C. These samples are characterized by physicochemical analytical methods such as X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM) coupled with energy-dispersive X-ray (EDX), high resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS). Electrochemical measurements were also carried out using cyclic voltammetry (CV), chronoamperometry (CA), linear sweep voltammetry (LSV) and electrochemical impedance spectroscopy (EIS). The CV tests and Tafel analysis results revealed that PdNi/CeO2/OLC exhibited the highest current response with an onset potential of −0.69 V and better kinetic activity of 136.9 mV/dec respectively. Chronoamperometric tests confirmed that PdNi/CeO2/OLC maintains superior stability and antipoisoning properties, achieving stable current densities over extended periods. EIS showed the lowest charge transfer resistance (Rct) for PdNi/CeO2/OLC, reflecting more efficient electron transfer. The Ni-containing catalysts also exhibit lower Tafel slopes (121.5 mV/dec for PdNi/OLC and 136.9 mV/dec for PdNi/CeO2/OLC), indicating improved reaction kinetics due to Ni. Density functional theory (DFT) calculations suggest that Ni incorporation into Pd enhances electron donation, which is enhanced by the CeO2 support. This synergy improves IPA adsorption and reaction kinetics, leading to enhanced electrocatalytic performance. These findings demonstrate that alloying Pd with Ni and supporting it on CeO2 significantly boosts electrocatalytic activity, stability, and mass transport in alcohol oxidation. The PdNi/CeO2/OLC catalyst is a promising candidate for DIFC applications, offering high efficiency, durability, and a low onset potential.

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来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
期刊介绍: The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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