Suppression of Oxygen Vacancies in Rutile Ruo2 via In Situ Exsolution for Enhanced Water Electrocatalysis

Elemental vacancies are proposed as an effective approach to tuning the electronic structure of catalysts that are critical for energy conversion. However, for reactions such as the sluggish oxygen evolution reaction, the excess of oxygen vacancies (VO) is inevitable and detrimental to catalysts’ el...

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Main Authors: Huo, J. (Author), Li, G. (Author), Liu, J. (Author), Ma, D. (Author), Ma, J. (Author), Rao, J. (Author), Sun, W. (Author), Wang, Y. (Author), Xu, Q. (Author), Zhang, Y. (Author)
Format: Article
Language:English
Published: John Wiley and Sons Inc 2023
Subjects:
Online Access:View Fulltext in Publisher
LEADER 02866nam a2200493Ia 4500
001 10.1002-admi.202300279
008 230526s2023 CNT 000 0 und d
020 |a 21967350 (ISSN) 
245 1 0 |a Suppression of Oxygen Vacancies in Rutile Ruo2 via In Situ Exsolution for Enhanced Water Electrocatalysis 
260 0 |b John Wiley and Sons Inc  |c 2023 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1002/admi.202300279 
520 3 |a Elemental vacancies are proposed as an effective approach to tuning the electronic structure of catalysts that are critical for energy conversion. However, for reactions such as the sluggish oxygen evolution reaction, the excess of oxygen vacancies (VO) is inevitable and detrimental to catalysts’ electrochemical stability and activities, e.g., in the most active RuO2. While significant work is carried out to hinder the formation of VO, the development of a fast and efficient strategy is limited. Herein, a protection SrO layer produced successfully at the surface of RuO2 with the in situ exsolution method with perovskite SrRuO3 as the precatalyst, which could significantly hinder the generation of VO. Benefited from the suppression of VO, the surface-modified RuO2 requires a low overpotential of 290 mV at 100 mA cm−2, accompanied by remarkably high electrochemical stability (100 h) and Faraday efficiency (≈100%). Theoretical investigation reveals that the formation energy of VO in RuO2 is almost doubled in the exsolved RuO2 phase as a result of the weakened Ru-O bond covalency. This work not only provides insight into the structural evolution of perovskite oxide catalysts but also demonstrates the feasibility of controlling vacancy formation via in situ exsolution. © 2023 The Authors. Advanced Materials Interfaces published by Wiley-VCH GmbH. 
650 0 4 |a ]+ catalyst 
650 0 4 |a Catalysts 
650 0 4 |a Effective approaches 
650 0 4 |a Efficient strategy 
650 0 4 |a Electrocatalysis 
650 0 4 |a Electrochemical activities 
650 0 4 |a Electrochemical stabilities 
650 0 4 |a Electronic structure 
650 0 4 |a Electronic.structure 
650 0 4 |a exsolution 
650 0 4 |a Exsolution 
650 0 4 |a oxygen evolution reaction 
650 0 4 |a oxygen vacancies 
650 0 4 |a Oxygen vacancies 
650 0 4 |a Perovskite 
650 0 4 |a Precatalysts 
650 0 4 |a RuO 2 
650 0 4 |a Ruthenium compounds 
650 0 4 |a Strontium compounds 
650 0 4 |a Surface-modified 
650 0 4 |a Titanium dioxide 
700 1 0 |a Huo, J.  |e author 
700 1 0 |a Li, G.  |e author 
700 1 0 |a Liu, J.  |e author 
700 1 0 |a Ma, D.  |e author 
700 1 0 |a Ma, J.  |e author 
700 1 0 |a Rao, J.  |e author 
700 1 0 |a Sun, W.  |e author 
700 1 0 |a Wang, Y.  |e author 
700 1 0 |a Xu, Q.  |e author 
700 1 0 |a Zhang, Y.  |e author 
773 |t Advanced Materials Interfaces  |x 21967350 (ISSN)