Wieser Philipp Aldo, Moser David, Gollas Bernhard, Amenitsch Heinz
Institute of Inorganic Chemistry, Graz University of Technology, Graz 8010, Austria.
Institute of Electron Microscopy and Nanoanalysis, Graz University of Technology, Graz 8010, Austria.
ACS Appl Mater Interfaces. 2023 Oct 11;15(40):47604-47614. doi: 10.1021/acsami.3c03316. Epub 2023 Sep 28.
We have used grazing incidence small-angle X-ray scattering (GISAXS) to monitor structural changes during templated electrodeposition of mesoporous platinum films on gold electrodes from a ternary lyotropic liquid crystalline mixture of aqueous hexachloroplatinic acid and the diblock copolymer surfactant Brij56. While the cylindrical micelles of the lyotropic liquid crystal (LLC) in the hexagonal phase have a center-to-center distance of 7.5 nm with a preferential alignment parallel to the electrode surface, the electrodeposited platinum films contain highly ordered mesopores arranged in a 2D hexagonal structure, with a center-to-center distance of about 8.5 nm and a preferential orientation perpendicular to the electrode surface. The progression of structural changes of the LLC template and the deposited mesoporous Pt could be monitored for the first time by GISAXS: within the first 14 s of deposition, a nucleation burst of Pt coincides with a loss of preferential alignment of the LLC. Initially, the morphology of the 2-dimensionally nucleated Pt replicates the Au substrate. During the following 5 to 7 min, the growth morphology of the Pt film changes, and vertically aligned mesopores form. Our results indicate mutual interaction between the species involved in the electrodeposition and the LLC template, leading to a partial loss of horizontal orientation of the LLC during Pt nucleation before vertical rearrangement of the micelles to the electrode surface. The vertically aligned mesopores in the Pt and the possibility to produce freestanding films make these materials interesting in fields such as electrocatalysis, energy harvesting, and nanofluidics.
我们使用掠入射小角X射线散射(GISAXS)来监测在金电极上通过六氯铂酸水溶液与二嵌段共聚物表面活性剂Brij56的三元溶致液晶混合物进行介孔铂膜模板电沉积过程中的结构变化。虽然六方相溶致液晶(LLC)的圆柱形胶束中心距为7.5 nm,且优先平行于电极表面排列,但电沉积的铂膜包含高度有序的介孔,排列成二维六方结构,中心距约为8.5 nm,且优先垂直于电极表面取向。通过GISAXS首次监测到了LLC模板和沉积的介孔铂的结构变化过程:在沉积的前14秒内,铂的成核爆发与LLC优先排列的丧失同时发生。最初,二维成核铂的形态复制了金基底。在接下来的5到7分钟内,铂膜的生长形态发生变化,垂直排列的介孔形成。我们的结果表明,电沉积过程中涉及的物质与LLC模板之间存在相互作用,导致在铂成核过程中LLC的水平取向部分丧失,然后胶束垂直重新排列到电极表面。铂中垂直排列的介孔以及制备独立膜的可能性使得这些材料在电催化、能量收集和纳米流体等领域具有吸引力。