Department of Applied Physics and Competence Centre for Catalysis, Chalmers University of Technology, SE-41296 Göteborg, Sweden.
ACS Nano. 2011 Apr 26;5(4):2547-58. doi: 10.1021/nn1021692. Epub 2011 Mar 31.
Aiming at the investigation of spillover and transport effects in electrocatalytic reactions on bimetallic catalyst electrodes, we have prepared novel, nanostructured electrodes consisting of arrays of homogeneously distributed pairs of Pt and Ru nanodisks of uniform size and with controlled separation on planar glassy carbon substrates. The nanodisk arrays (disk diameter ≈ 60 nm) were fabricated by hole-mask colloidal lithography; the separation between pairs of Pt and Ru disks was varied from -25 nm (overlapping) via +25 nm to +50 nm. Morphology and (surface) composition of the Pt/Ru nanodisk arrays were characterized by scanning electron microscopy, energy dispersive X-ray analysis, and X-ray photoelectron spectroscopy, the electrochemical/electrocatalytic properties were explored by cyclic voltammetry, CO(ad) monolayer oxidation ("CO(ad) stripping"), and potentiodynamic hydrogen oxidation. Detailed analysis of the CO(ad) oxidation peaks revealed that on all bimetallic pairs these cannot be reproduced by superposition of the peaks obtained on electrodes with Pt/Pt or Ru/Ru pairs, pointing to effective Pt-Ru interactions even between rather distant pairs (50 nm). Possible reasons for this observation and its relevance for the understanding of previous reports of highly active catalysts with separate Pt and Ru nanoparticles are discussed. The results clearly demonstrate that this preparation method is perfectly suited for fabrication of planar model electrodes with well-defined arrays of bimetallic nanodisk pairs, which opens up new possibilities for model studies of electrochemical/electrocatalytic reactions.
针对双金属催化剂电极上电催化反应中的溢出和传输效应的研究,我们制备了新型的纳米结构电极,该电极由均匀尺寸且在平面玻璃碳基底上具有受控间隔的 Pt 和 Ru 纳米盘均匀分布的对的阵列组成。纳米盘阵列(盘直径≈60nm)通过孔掩模胶体光刻法制备;Pt 和 Ru 纳米盘对之间的间隔可以从-25nm(重叠)变化到+25nm 再到+50nm。Pt/Ru 纳米盘阵列的形貌和(表面)组成通过扫描电子显微镜、能量色散 X 射线分析和 X 射线光电子能谱进行了表征,电化学/电催化性质通过循环伏安法、CO(ad)单层氧化(“CO(ad)剥离”)和动电位氢氧化进行了研究。对 CO(ad)氧化峰的详细分析表明,在所有双金属对中,这些峰都不能通过将具有 Pt/Pt 或 Ru/Ru 对的电极上获得的峰叠加来重现,这表明即使在相隔较远的对(50nm)之间也存在有效的 Pt-Ru 相互作用。讨论了观察到这种相互作用的可能原因及其对理解具有独立 Pt 和 Ru 纳米粒子的高活性催化剂的先前报道的相关性。结果清楚地表明,这种制备方法非常适合于制造具有定义明确的双金属纳米盘对的平面模型电极,这为电化学/电催化反应的模型研究开辟了新的可能性。