• Energy Research

LaNiO perovskite is a promising electrocatalyst for the oxygen reduction reaction (ORR). In this work we study the effects of several key structural and morphological features on the performance of LaNiO perovskites for the ORR. We have prepared a series of LaNiO oxides via soft chemistry and calcined the final materials at different temperatures from 500 to 1000 °C. With the aim of obtaining morphological and structural information relevant to their performance the prepared oxides have been thoroughly characterized by BET, Power Neutron Diffraction (PND), XRD, HRTEM, STEM-HAADF and XPS. We have analysed the effect of extrinsic (surface area and particle size) and intrinsic factors (formation of oxygen vacancies, Ni oxidation states and occupancy of the e levels) on the current densities and specific activity, respectively, of several samples of LaNiO. The catalysts with higher catalytic activity are those in which the perovskite structure is properly formed, but display high surface areas. María Retuerto acknowledges the Juan de la Cierva program of the Spanish Ministry of Economy and Competitiveness for a grant (FPDI-2013-17582). Economic support from projects ENE2013-42322-R from the Spanish Ministry of Economy and Competitiveness, and project 201480E122 from the CSIC are also acknowledged. Project S2013/MAE-2882 is also acknowledged. J. A. Alonso and M. Teresa Fernández-Diaz thank the financial support of the Spanish Ministry of Science and Innovation to the project MAT2013-41099-R. Amaru González acknowledges the SECAT for a grant.

The demand of green hydrogen, that is, the hydrogen produced from water electrolysis, is expected to increase dramatically in the coming years. State‐of‐the‐art proton exchange membrane water electrolysis (PEMWE) uses high loadings of platinum group metals, such as Pt in the electrode where hydrogen is produced. Alternative electrodes based on phosphides, sulfides, nitrides, and other low‐cost alternatives are under investigation. Herein, a simple process for the preparation of RuP electrodes with high activity for the hydrogen evolution reaction (HER) in acidic electrolyte is described. A straightforward one‐pot synthesis that yields RuP nanoparticles with fine‐tuned composition and stoichiometry is presented, as determined by multiple characterization techniques, including lab‐ and synchrotron‐based experiments and theoretical modeling. The RuP nanoparticles exhibit a high activity of 10 mA cm−2 at 36 mV overpotential and a Tafel slope of 30 mV dec−1, which is comparable to Pt/C. Moreover, a RuP catalyst‐coated membrane (CCM) with a low Ru loading of 0.6 mgRu cm−2 is produced and tested in a PEMWE cell configuration, yielding 1.7 A cm−2 at 2 V.

AbstractThe design of active and durable catalysts for the H2O/O2 interconversion is one of the major challenges of electrocatalysis for renewable energy. The oxygen evolution reaction (OER) is catalyzed by SrRuO3 with low potentials (ca. 1.35 VRHE), but the catalyst’s durability is insufficient. Here we show that Na doping enhances both activity and durability in acid media. DFT reveals that whereas SrRuO3 binds reaction intermediates too strongly, Na doping of ~0.125 leads to nearly optimal OER activity. Na doping increases the oxidation state of Ru, thereby displacing positively O p-band and Ru d-band centers, weakening Ru-adsorbate bonds. The enhanced durability of Na-doped perovskites is concomitant with the stabilization of Ru centers with slightly higher oxidation states, higher dissolution potentials, lower surface energy and less distorted RuO6 octahedra. These results illustrate how high OER activity and durability can be simultaneously engineered by chemical doping of perovskites.

Crystalline Ni5P4 evolves hydrogen with electrical-efficiency comparable to platinum—while being corrosion-resistant in both acid and base for >16 hours.