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铊修饰的形状可控铂纳米颗粒上的甲酸电氧化:电催化活性的提高

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

作者信息

Busó-Rogero Carlos, Perales-Rondón Juan V, Farias Manuel J S, Vidal-Iglesias Francisco J, Solla-Gullon Jose, Herrero Enrique, Feliu Juan M

机构信息

Instituto de Electroquímica, Universidad de Alicante, Ap. 99 E-03080, Alicante, Spain.

出版信息

Phys Chem Chem Phys. 2014 Jul 21;16(27):13616-24. doi: 10.1039/c4cp00304g. Epub 2014 Mar 18.

Abstract

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.

摘要

制备了铊修饰的形状可控铂纳米颗粒,并在0.5 M硫酸中评估了它们对甲酸电氧化的电催化活性。电化学和原位傅里叶变换红外光谱结果表明,电催化活性有显著提高,特别是在低电位区域(相对于可逆氢电极约为0.1 - 0.2 V)。发现在整个铊覆盖范围和电位窗口内,用铊修饰的立方铂纳米颗粒比八面体铂纳米颗粒更具活性。原位傅里叶变换红外光谱表明,铊产生的促进作用导致抑制了生成吸附态一氧化碳的中毒步骤,从而提高了甲酸完全氧化为二氧化碳的起始电位。还在0.2 V下进行了计时电流实验,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,铊修饰的立方铂纳米颗粒都是最具活性的。所有这些事实都强化了控制电催化剂表面结构以优化其电催化性能的重要性。

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