Guerin Samuel, Hayden Brian E, Pletcher Derek, Rendall Michael E, Suchsland Jens-Peter
School of Chemistry, University of Southampton, Southampton SO17 1BJ, UK.
J Comb Chem. 2006 Sep-Oct;8(5):679-86. doi: 10.1021/cc060041c.
A novel high-throughput technique has been developed for the investigation of the influence of supported metal particle size and the support on electrocatalytic activity. Arrays with a gradation of catalyst particle sizes are fabricated in a physical vapor deposition system that also allows selection of the support material. Simultaneous electrochemical measurements at all electrodes in the array, together with determination of the actual particle size distribution on each of the electrodes by transmission electron microscopy (TEM), then allows rapid determination of the activity as a function of catalyst center size. The procedure is illustrated using data for the reduction of oxygen on gold nanoparticles supported on both substoichiometric titanium dioxide (TiO(x)()) and carbon and the conclusions are verified using voltammetry at rotating disk electrodes. Gold centers with diameters in the range 1.4-6.3 nm were investigated and it is demonstrated that, with both supports, the catalytic activity for oxygen reduction decays rapidly for particle sizes below 3.0 nm. This may be observed as a decrease in current at constant potential or an increase in the overpotential for oxygen reduction.
已开发出一种新型高通量技术,用于研究负载型金属颗粒尺寸和载体对电催化活性的影响。在物理气相沉积系统中制备具有渐变催化剂颗粒尺寸的阵列,该系统还允许选择载体材料。对阵列中所有电极同时进行电化学测量,并通过透射电子显微镜(TEM)测定每个电极上实际的颗粒尺寸分布,然后可以快速确定活性与催化剂中心尺寸的函数关系。使用在亚化学计量二氧化钛(TiO(x))和碳上负载的金纳米颗粒上氧气还原的数据来说明该过程,并使用旋转圆盘电极上的伏安法验证结论。研究了直径在1.4 - 6.3 nm范围内的金中心,结果表明,对于这两种载体,当颗粒尺寸低于3.0 nm时,氧还原的催化活性迅速下降。这可以表现为在恒定电位下电流的降低或氧还原过电位的增加。