Perovskite Oxide as A New Platform for Efficient Electrocatalytic Nitrogen Oxidation

Author:

Zheng Hui1,Ma Ziwei1,Liu Yunxia2,Zhang Yizhe1,Ye Jinyu3,Debroye Elke4,Zhang Longsheng1,Liu Tianxi1,Xie Yi5ORCID

Affiliation:

1. Key Laboratory of Synthetic and Biological Colloids Ministry of Education School of Chemical and Material Engineering International Joint Research Laboratory for Nano Energy Composites Jiangnan University Wuxi 214122 China

2. School of Chemistry and Chemical Engineering Northwestern Polytechnical University Xi'an 710072 China

3. State Key Laboratory of Physical Chemistry of Solid Surfaces College of Chemistry and Chemical Engineering Xiamen University Xiamen 361005 China

4. Department of Chemistry, KU Leuven Celestijnenlaan 200F 3001 Leuven Belgium

5. Hefei National Research Center for Physical Sciences at the Microscale University of Science and Technology of China Hefei 230026 China

Abstract

AbstractElectrocatalytic nitrogen oxidation reaction (NOR) offers an efficient and sustainable approach for conversion of widespread nitrogen (N2) into high‐value‐added nitrate (NO3) under mild conditions, representing a promising alternative to the traditional approach that involves harsh Haber–Bosch and Ostwald oxidation processes. Unfortunately, due to the weak absorption/activation of N2 and the competitive oxygen evolution reaction, the kinetics of NOR process is extremely sluggish accompanied with low Faradaic efficiencies and NO3 yield rates. In this work, an oxygen‐vacancy‐enriched perovskite oxide with nonstoichiometric ratio of strontium and ruthenium (denoted as Sr0.9RuO3) was synthesized and explored as NOR electrocatalyst, which can exhibit a high Faradaic efficiency (38.6 %) with a high NO3 yield rate (17.9 μmol mg−1 h−1). The experimental results show that the amount of oxygen vacancies in Sr0.9RuO3 is greatly higher than that of SrRuO3, following the same trend as their NOR performance. Theoretical simulations unravel that the presence of oxygen vacancies in the Sr0.9RuO3 can render a decreased thermodynamic barrier toward the oxidation of *N2 to *N2OH at the rate‐determining step, leading to its enhanced NOR performance.

Funder

National Natural Science Foundation of China

Fonds Wetenschappelijk Onderzoek

Fundamental Research Funds for the Central Universities

H2020 European Research Council

Publisher

Wiley

Subject

General Chemistry,Catalysis

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