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Electrochemical observation of ligand effects on oxygen reduction at ligand-stabilized Pt nanoparticle electrocatalysts

机译:配体稳定的Pt纳米粒子电催化剂上配体对氧还原的电化学观察

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摘要

We investigate the effect of triphenylphosphine triphosphonate, TPPTP, on the electrocatalytic activity for the oxygen reduction reaction (ORR) at ligand-stabilized Pt nanoparticles (Pt-2.1 nm-TPPTP). The Pt-2.1 nm-TPPTP catalyst supported on Vulcan carbon (VC) (Pt-2.1 mm-TPPTP/VC) adsorbs and desorbs oxygen +40 mV vs the potential for bare Pt nanoparticles supported on VC (Pt-2.4 nm/VC), as measured by cyclic voltammetry in Ar-saturated 0.1 M HClO4. The area-specific ORR activity (i(s)) of Pt in the Pt-2.1-TPPTP/VC catalyst is similar to 22% higher than that of Pt-2.4 nm/VC, as measured by rotating disk electrode voltammetry. These results suggest that the TPPTP ligand weakens the Pt-O bond, resulting in the observed kinetic enhancement of the ORR.
机译:我们研究了三苯基膦三膦酸酯TPPTP对配体稳定的Pt纳米颗粒(Pt-2.1 nm-TPPTP)上的氧还原反应(ORR)的电催化活性。 Vulcan碳(VC)上负载的Pt-2.1 nm-TPPTP催化剂(Pt-2.1 mm-TPPTP / VC)吸附和解吸氧气+40 mV,而VC上负载的裸Pt纳米颗粒的潜力(Pt-2.4 nm / VC)通过循环伏安法在Ar饱和的0.1 M HClO4中测量。通过旋转盘电极伏安法测得,Pt-2.1-TPPTP / VC催化剂中Pt的比表面积ORR活性比Pt-2.4 nm / VC高22%。这些结果表明TPPTP配体削弱了Pt-O键,从而导致观察到的ORR动力学增强。

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