4.6 Article

Benchmarking Perovskite Electrocatalysts' OER Activity as Candidate Materials for Industrial Alkaline Water Electrolysis

Journal

CATALYSTS
Volume 10, Issue 12, Pages -

Publisher

MDPI
DOI: 10.3390/catal10121387

Keywords

perovskites; oxygen evolution reaction; alkaline water electrolysis; electrocatalysts

Funding

  1. European Commission [722614]
  2. Marie Curie Actions (MSCA) [722614] Funding Source: Marie Curie Actions (MSCA)

Ask authors/readers for more resources

The selection and evaluation of electrocatalysts as candidate materials for industrial alkaline water electrolysis is fundamental in the development of promising energy storage and sustainable fuels for future energy infrastructure. However, the oxygen evolution reaction (OER) activities of various electrocatalysts already reported in previous studies are not standardized. This work reports on the use of perovskite materials (LaFeO3, LaCoO3, LaNiO3, PrCoO3, Pr0.8Sr0.2CoO3, and Pr0.8Ba0.2CoO3) as OER electrocatalysts for alkaline water electrolysis. A facile co-precipitation technique with subsequent thermal annealing (at 700 degrees C in air) was performed. Industrial requirements and criteria (cost and ease of scaling up) were well-considered for the selection of the materials. The highest OER activity was observed in LaNiO3 among the La-based perovskites, and in Pr0.8Sr0.2CoO3 among the Pr-based perovskites. Moreover, the formation of double perovskites (Pr0.8Sr0.2CoO3 and Pr0.8Ba0.2CoO3) improved the OER activity of PrCoO3. This work highlights that the simple characterization and electrochemical tests performed are considered the initial step in evaluating candidate catalyst materials to be used for industrial alkaline water electrolysis.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Article Biochemistry & Molecular Biology

How half sandwich ruthenium compounds interact with DNA while not being hydrolyzed; a comparative study

Theodoros Tsolis, Konstantinos D. Papavasileiou, Spyridon A. Divanis, Vasilios S. Melissas, Achilleas Garoufis

JOURNAL OF INORGANIC BIOCHEMISTRY (2016)

Article Optics

Role of broadband-laser-pulse temporal extent in H2+ photodissociation

E. P. Benis, M. Bakarezos, N. A. Papadogiannis, M. Tatarakis, S. Divanis, C. O. Broin, L. A. A. Nikolopoulos

PHYSICAL REVIEW A (2012)

Article Electrochemistry

Synergistic effects in oxygen evolution activity of mixed iridium-ruthenium pyrochlores

Rebecca K. Pittkowski, Daniel F. Abbott, Roman Nebel, Spyridon Divanis, Emiliana Fabbri, Ivano E. Castelli, Thomas J. Schmidt, Jan Rossmeisl, Petr Krtil

Summary: Pyrochlore oxides containing both iridium and ruthenium in the B-site are promising catalysts for the oxygen evolution reaction (OER) in acidic media. The coexistence of Ir and Ru in the B-site enhances the catalytic activity, and the observed OER activity scales with the Ir-Ru bond distance. The addition of iridium and ruthenium suppresses the effect of the A-site cation radius on OER activity.

ELECTROCHIMICA ACTA (2021)

Article Chemistry, Physical

Engendering Unprecedented Activation of Oxygen Evolution via Rational Pinning of Ni Oxidation State in Prototypical Perovskite: Close Juxtaposition of Synthetic Approach and Theoretical Conception

Rebecca Pittkowski, Spyridon Divanis, Mariana Klementova, Roman Nebel, Shahin Nikman, Harry Hoster, Sanjeev Mukerjee, Jan Rossmeisl, Petr Krtil

Summary: Rational optimization of OER activity of catalysts based on LaNiO3 oxide is achieved by maximizing the presence of trivalent Ni in the surface structure. Theoretical predictions of high intrinsic OER activity structures related to LaNiO3 catalysts have been confirmed through the preparation of nanocrystalline LaNiO3-related materials. These materials show a dramatic improvement in OER activity and exhibit stable exfoliated surfaces in OER catalysis.

ACS CATALYSIS (2021)

Article Chemistry, Multidisciplinary

Synergistic effect of p-type and n-type dopants in semiconductors for efficient electrocatalytic water splitting

Tugce Kutlusoy, Spyridon Divanis, Rebecca Pittkowski, Riccardo Marina, Adrian M. Frandsen, Katerina Minhova-Macounova, Roman Nebel, Dongni Zhao, Stijn F. L. Mertens, Harry Hoster, Petr Krtil, Jan Rossmeisl

Summary: The main challenge for acidic water electrolysis is the lack of active and stable oxygen evolution catalysts based on abundant materials. This work presents a new design strategy for activating stable materials, deemed unsuitable due to their semiconducting nature. By adding both n-type and p-type dopants, the reactivity of the catalyst can be tuned to allow for oxygen adsorption and desorption under reaction conditions. Experimental verification on TiO2 suggests that co-substitution can be used to activate stable materials for acid water electrolysis catalysts.

CHEMICAL SCIENCE (2022)

Article Chemistry, Physical

Lifting the discrepancy between experimental results and the theoretical predictions for the catalytic activity of RuO2(110) towards oxygen evolution reaction

Spyridon Divanis, Adrian Malthe Frandsen, Tugce Kutlusoy, Jan Rossmeisl

Summary: Both RuO2 and IrO2 have shown high activity as OER catalysts, but DFT predictions have failed to explain the high activity of RuO2. The authors propose that this discrepancy is due to RuO2 utilizing a different reaction pathway compared to IrO2, which is supported by comparisons between experimental data, DFT data and the proposed reaction model.

PHYSICAL CHEMISTRY CHEMICAL PHYSICS (2021)

Article Chemistry, Multidisciplinary

Oxygen evolution reaction: a perspective on a decade of atomic scale simulations

Spyridon Divanis, Tugce Kutlusoy, Ida Marie Ingmer Boye, Isabela Costinela Man, Jan Rossmeisl

CHEMICAL SCIENCE (2020)

No Data Available