AI Article Synopsis

  • Data mining in computational materials databases is increasingly used to discover new low-cost metal oxide (MO) electrocatalysts, but there are challenges in aligning data-driven predictions with experimental outcomes.
  • The study identifies Sb WO as a stable MO for oxygen reduction reactions (ORR) in acidic conditions but reveals unexpected instability under high-pH conditions, despite initial data suggesting otherwise.
  • Through advanced analysis, it is found that the surface of Sb WO changes during catalysis, forming a stable state that allows for effective ORR, highlighting the need for improved strategies that integrate both data mining and electrochemistry.

Article Abstract

Data mining from computational materials database has become a popular strategy to identify unexplored catalysts. Herein, the opportunities and challenges of this strategy are analyzed by investigating a discrepancy between data mining and experiments in identifying low-cost metal oxide (MO) electrocatalysts. Based on a search engine capable of identifying stable MOs at the pH and potentials of interest, a series of MO electrocatalysts is identified as potential candidates for various reactions. Sb WO attracted the attention among the identified stable MOs in acid. Based on the aqueous stability diagram, Sb WO is stable under oxygen reduction reaction (ORR) in acidic media but rather unstable under high-pH ORR conditions. However, this contradicts to the subsequent experimental observation in alkaline ORR conditions. Based on the post-catalysis characterizations, surface state analysis, and an advanced pH-field coupled microkinetic modeling, it is found that the Sb WO surface will undergo electrochemical passivation under ORR potentials and form a stable and 4e-ORR active surface. The results presented here suggest that though data mining is promising for exploring electrocatalysts, a refined strategy needs to be further developed by considering the electrochemistry-induced surface stability and activity.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10837344PMC
http://dx.doi.org/10.1002/advs.202305630DOI Listing

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