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<p>Precisely engineered nanoarchitectures can unlock new catalytic active sites. We introduce nanomace, a ceria (CeO<sub>2</sub>) nanostructure integrating cubic and rod-like domains within a single framework. The chemically coherent interface generates highly active oxygen sites, enabling faster CO conversion than conventional morphologies and surpassing physically mixed rods and cubes. Enhanced lattice oxygen reactivity is confirmed by facile redox cycling in in&#xa0;situ Raman and synchrotron-based ambient-pressure XPS, and fast lattice oxygen exchange in isotopic studies. As a support, nanomace amplifies activity across multiple reactions: Au-, Pd-, and Rh-loaded nanomace outperform commercial, rod, and cube CeO<sub>2</sub> by up to 14.4-fold in water&#xa0;gas shift, CH<sub>4</sub> combustion, and N<sub>2</sub>O decomposition. Molecular dynamics simulations reveal preferential lattice oxygen activation at the integrated interface. By establishing interface sites as uniquely reactive, nanomace demonstrates structural integration as a powerful strategy for next-generation redox catalysis.</p>

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Hierarchical ceria nanoarchitecture enabling accelerated lattice oxygen activation for efficient redox reactions

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年4月29日

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  • Seokhyun Choung,
  • Yunkyung Kim,
  • Myeong Gon Jang,
  • Gwang Hun Cho,
  • Dong Gwon Kang,
  • Taein Lee,
  • Doheon Lee,
  • Sehee Han,
  • Bohyeon Seo,
  • Wongyu Park,
  • Miyeon Kim,
  • Okkyun Seo,
  • Takeshi Watanabe,
  • Loku Singgappulige Rosantha Kumara,
  • Daiju Matsumura,
  • Tae Yong Kim,
  • Jun Hyuk Kim,
  • Jeongjin Kim,
  • Jeong Woo Han

摘要

Precisely engineered nanoarchitectures can unlock new catalytic active sites. We introduce nanomace, a ceria (CeO2) nanostructure integrating cubic and rod-like domains within a single framework. The chemically coherent interface generates highly active oxygen sites, enabling faster CO conversion than conventional morphologies and surpassing physically mixed rods and cubes. Enhanced lattice oxygen reactivity is confirmed by facile redox cycling in in situ Raman and synchrotron-based ambient-pressure XPS, and fast lattice oxygen exchange in isotopic studies. As a support, nanomace amplifies activity across multiple reactions: Au-, Pd-, and Rh-loaded nanomace outperform commercial, rod, and cube CeO2 by up to 14.4-fold in water gas shift, CH4 combustion, and N2O decomposition. Molecular dynamics simulations reveal preferential lattice oxygen activation at the integrated interface. By establishing interface sites as uniquely reactive, nanomace demonstrates structural integration as a powerful strategy for next-generation redox catalysis.