Jayaraman Shrisudersan, Jaramillo Thomas F, Baeck Sung-Hyeon, McFarland Eric W
Mitsubishi Chemical Center for Advanced Materials and Department of Chemical Engineering, University of California, Santa Barbara, California 93106, USA.
J Phys Chem B. 2005 Dec 8;109(48):22958-66. doi: 10.1021/jp053053h.
Several compositions of Pt-WO3 catalysts were synthesized and characterized for the electro-oxidation of methanol and CO. The surface morphologies of the catalysts were found to be dependent on the composition. X-ray energy dispersive spectroscopy and X-ray photoelectron spectroscopy results suggest a surface enrichment of WO3 in the codeposited Pt-WO3 catalysts. Cyclic voltammetry and chronoamperometry in methanol show an improvement in catalytic activity for the Pt-WO3 catalysts. A significant improvement in the poison tolerance toward CO and other organic intermediates was observed in the mixed metal-metal oxide catalyst. The catalytic performance of the different compositions was directly compared by normalization of the current to active sites. CO-stripping voltammetry suggests the involvement of WO3 in the catalytic process as opposed to a mere physical effect as suggested by previous work. A possible mechanism for this improvement is proposed based on the electrochemical data.
合成了几种Pt-WO₃催化剂组合物,并对其用于甲醇和CO电氧化的性能进行了表征。发现催化剂的表面形态取决于其组成。X射线能量色散光谱和X射线光电子能谱结果表明,共沉积的Pt-WO₃催化剂表面存在WO₃富集现象。甲醇中的循环伏安法和计时电流法表明,Pt-WO₃催化剂的催化活性有所提高。在混合金属-金属氧化物催化剂中,观察到对CO和其他有机中间体的抗毒性能有显著改善。通过将电流归一化到活性位点,直接比较了不同组成的催化性能。CO溶出伏安法表明,与先前工作所提出的仅仅是物理效应不同,WO₃参与了催化过程。基于电化学数据,提出了这种性能改善的可能机制。