Xue Song, Haid Richard W, Kluge Regina M, Ding Xing, Garlyyev Batyr, Fichtner Johannes, Watzele Sebastian, Hou Shujin, Bandarenka Aliaksandr S
Physics of Energy Conversion and Storage, Physik-Department, Technische Universität München, James-Franck-Strasse 1, 85748, Garching, Germany.
Catalysis Research Center TUM, Ernst-Otto-Fischer-Strasse 1, 85748, Garching, Germany.
Angew Chem Int Ed Engl. 2020 Jun 26;59(27):10934-10938. doi: 10.1002/anie.202000383. Epub 2020 Apr 30.
Herein, we demonstrate an easy way to improve the hydrogen evolution reaction (HER) activity of Pt electrodes in alkaline media by introducing Ni-Fe clusters. As a result, the overpotential needed to achieve a current density of 10 mA cm in H -saturated 0.1 m KOH is reduced for the model single-crystal electrodes down to about 70 mV. To our knowledge, these modified electrodes outperform any other reported electrocatalysts tested under similar conditions. Moreover, the influence of 1) Ni to Fe ratio, 2) cluster coverage, and 3) the nature of the alkali-metal cations present in the electrolyte on the HER activity has been investigated. The observed catalytic performance likely originates from both the improved water dissociation at the Ni-Fe clusters and the subsequent optimal hydrogen adsorption and recombination at Pt atoms present at the Ni-Fe/Pt boundary.
在此,我们展示了一种通过引入镍铁簇来提高铂电极在碱性介质中析氢反应(HER)活性的简便方法。结果,对于模型单晶电极,在氢气饱和的0.1 m KOH中实现10 mA cm电流密度所需的过电位降低至约70 mV。据我们所知,这些修饰电极在类似条件下的表现优于任何其他已报道的电催化剂。此外,还研究了1)镍与铁的比例、2)簇覆盖率以及3)电解质中存在的碱金属阳离子的性质对析氢反应活性的影响。观察到的催化性能可能源于镍铁簇处水离解的改善以及随后在镍铁/铂边界处存在的铂原子上的最佳氢吸附和重组。