Kolagatla Srikanth, Subramanian Palaniappan, Schechter Alex
Department of Chemical Sciences, Ariel University, Ariel, 40700, Israel.
ChemSusChem. 2019 Jun 21;12(12):2708-2714. doi: 10.1002/cssc.201900656. Epub 2019 Jun 6.
Electrochemical scanning probe microscopies have become valuable experimental tools, owing to their capability of capturing topographic features in addition to mapping the electrochemical activity of nanoscale oxygen reduction catalysts. However, most scanning probe techniques lack the ability to correlate topographic features with the electrochemical oxygen reduction and peroxide formation in real time. In this report, we show that it is indeed possible to construct high-resolution catalytic current maps at an electrified solid-liquid interface by placing a specially made Au-coated SiO Pt atomic force microscopy and scanning electrochemical microscopy (AFM-SECM) dual electrode tip approximately 4-8 nm above the reaction center. The catalytic current measured every 16 nm and high collection efficiency (≈90 %) of the reverse current of peroxide byproducts was also demonstrated with the help of the dual electrode tip. Simultaneous oxygen reduction and intermediate peroxide oxidation current mapping was demonstrated using this Au-coated SiO Pt probe on two model surfaces, namely highly oriented pyrolytic graphite and Pt nanoparticles (NPs) supported on a glassy carbon surface.
电化学扫描探针显微镜已成为有价值的实验工具,这得益于其除了能够绘制纳米级氧还原催化剂的电化学活性外,还具备捕捉形貌特征的能力。然而,大多数扫描探针技术缺乏实时关联形貌特征与电化学氧还原及过氧化物形成的能力。在本报告中,我们表明,通过将特制的金涂层二氧化硅铂原子力显微镜和扫描电化学显微镜(AFM-SECM)双电极尖端置于反应中心上方约4-8纳米处,确实有可能在带电的固液界面构建高分辨率催化电流图。借助双电极尖端,还展示了每16纳米测量一次的催化电流以及过氧化物副产物反向电流的高收集效率(约90%)。使用这种金涂层二氧化硅铂探针在两个模型表面,即高度取向热解石墨和玻碳表面负载的铂纳米颗粒(NPs)上,演示了同时进行氧还原和中间过氧化物氧化电流映射。