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Formic acid electrooxidation on thallium-decorated shape-controlled platinum nanoparticles: an improvement in electrocatalytic activity

机译:th修饰的形状可控铂纳米粒子上的甲酸电氧化:电催化活性的提高

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摘要

Thallium modified shape-controlled Pt nanoparticles were prepared and their electrocatalytic activity towards formic acid electrooxidation was evaluated in 0.5 M sulfuric acid. The electrochemical and in situ FTIR spectroscopic results show a remarkable improvement in the electrocatalytic activity, especially in the low potential region (around 0.1–0.2 V vs. RHE). Cubic Pt nanoparticles modified with Tl were found to be more active than the octahedral Pt ones in the entire range of Tl coverages and potential windows. In situ FTIR spectra indicate that the promotional effect produced by Tl results in the inhibition of the poisoning step leading to COads, thus improving the onset potential for the complete formic acid oxidation to CO2. Chronoamperometric experiments were also performed at 0.2 V to evaluate the stability of the electrocatalysts at constant potential. Finally, experiments with different concentrations of formic acid (0.05–1 M) were also carried out. In all cases, Tl-modified cubic Pt nanoparticles result to be the most active. All these facts reinforce the importance of controlling the surface structure of the electrocatalysts to optimize their electrocatalytic properties.
机译:制备了modified修饰的形状控制的Pt纳米粒子,并在0.5 M硫酸中评估了其对甲酸电氧化的电催化活性。电化学和原位FTIR光谱结果显示出电催化活性的显着改善,尤其是在低电势区域(相对于RHE约为0.1–0.2 V)。发现在整个T1覆盖率和潜在窗口范围内,用T1改性的立方Pt纳米颗粒比八面体Pt纳米颗粒更具活性。原位FTIR光谱表明,由T1产生的促进作用导致对导致COads的中毒步骤的抑制,从而提高了将甲酸完全氧化为CO2的起始潜力。还在0.2 V时进行了计时安培实验,以评估电催化剂在恒定电位下的稳定性。最后,还进行了不同浓度甲酸(0.05-1 M)的实验。在所有情况下,T1改性的立方Pt纳米颗粒都具有最强的活性。所有这些事实增强了控制电催化剂的表面结构以优化其电催化性能的重要性。

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