Abstract

Controlling the structure of catalysts at the atomic level provides an opportunity to establish detailed understanding of the catalytic form-to-function and realize new, non-equilibrium catalytic structures. Here, advanced thin-film deposition is used to control the atomic structure of La2/3Sr1/3MnO3, a well-known catalyst for the oxygen reduction reaction. The surface and sub-surface is customized, whereas the overall composition and d-electron configuration of the oxide is kept constant. Although the addition of SrMnO3 benefits the oxygen reduction reaction via electronic structure and conductivity improvements, SrMnO3 can react with ambient air to reduce the surface site availability. Placing SrMnO3 in the sub-surface underneath a LaMnO3 overlayer allows the catalyst to maintain the surface site availability while benefiting from improved electronic effects. The results show the promise of advanced thin-film deposition for realizing atomically precise catalysts, in which the surface and sub-surface structure and stoichiometry are tailored for functionality, over controlling only bulk compositions.

Highlights

  • 138 136 134 132 130 Binding energy

  • 20-nm thick La2/3Sr1/3MnO3 heterostructures were grown by molecular beam epitaxy (MBE) on TiO2terminated (001) SrTiO3 single-crystal substrates27. (001) was chosen as the low-energy termination of the perovskite structure which allows for a layer-by-layer growth

  • The structural integrity of the heterostructures were characterized using fourcircle X-ray diffraction (XRD), angle-resolved photoemission spectroscopy (ARPES), and transport measurements[28,29]. These results show that thin films studied in this article, thin films of low repeat units (n = 1 and 2), the LaMnO3 and SrMnO3 layers are commensurate to the substrate and the effects of interlayer strain are very small

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Summary

Objectives

The purpose of this article is to present a route to realize this concept via advanced thin-film deposition

Methods
Results
Conclusion

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