Park Seongeun, Shviro Meital, Hartmann Heinrich, Besmehn Astrid, Mayer Joachim, Stolten Detlef, Carmo Marcelo
Institute of Energy and Climate Research, Electrochemical Process Engineering (IEK-14), Forschungszentrum Jülich GmbH, 52425 Jülich, Germany.
Central Institute for Engineering, Electronics and Analytics (ZEA-3), Forschungszentrum Jülich GmbH, 52425 Jülich, Germany.
ACS Appl Mater Interfaces. 2021 Mar 24;13(11):13576-13585. doi: 10.1021/acsami.0c23026. Epub 2021 Mar 12.
Low-cost, highly active, and highly stable catalysts are desired for the generation of hydrogen and oxygen using water electrolyzers. To enhance the kinetics of the oxygen evolution reaction in an acidic medium, it is of paramount importance to redesign iridium electrocatalysts into novel structures with organized morphology and high surface area. Here, we report on the designing of a well-defined and highly active hollow nanoframe based on iridium. The synthesis strategy was to control the shape of nickel nanostructures on which iridium nanoparticles will grow. After the growth of iridium on the surface, the next step was to etch the nickel core to form the NiIr hollow nanoframe. The etching procedure was found to be significant in controlling the hydroxide species on the iridium surface and by that affecting the performance. The catalytic performance of the NiIr hollow nanoframe was studied for oxygen evolution reaction and shows 29 times increased iridium mass activity compared to commercially available iridium-based catalysts. Our study provides novel insights to control the fabrication of iridium-shaped catalysts using 3d transition metal as a template and via a facile etching step to steer the formation of hydroxide species on the surface. These findings shall aid the community to finally create stable iridium alloys for polymer electrolyte membrane water electrolyzers, and the strategy is also useful for many other electrochemical devices such as batteries, fuel cells, sensors, and solar organic cells.
使用水电解槽产生氢气和氧气需要低成本、高活性和高稳定性的催化剂。为了提高酸性介质中析氧反应的动力学,将铱电催化剂重新设计成具有规整形态和高表面积的新型结构至关重要。在此,我们报道了一种基于铱的结构明确且高活性的中空纳米框架的设计。合成策略是控制铱纳米颗粒将在其上生长的镍纳米结构的形状。在铱在表面生长之后,下一步是蚀刻镍核以形成NiIr中空纳米框架。发现蚀刻过程对于控制铱表面的氢氧化物种类并由此影响性能具有重要意义。研究了NiIr中空纳米框架在析氧反应中的催化性能,结果表明与市售铱基催化剂相比,铱质量活性提高了29倍。我们的研究为使用3d过渡金属作为模板并通过简便的蚀刻步骤来控制铱形催化剂的制备提供了新的见解,以引导表面氢氧化物种类的形成。这些发现将有助于该领域最终为聚合物电解质膜水电解槽制造稳定的铱合金,并且该策略对许多其他电化学装置(如电池、燃料电池、传感器和太阳能有机电池)也有用。