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Stable single platinum atoms trapped in sub-nanometer cavities in 12CaO·7Al2O3 for chemoselective hydrogenation of nitroarenes

Author

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  • Tian-Nan Ye

    (Tokyo Institute of Technology)

  • Zewen Xiao

    (Huazhong University of Science and Technology)

  • Jiang Li

    (Tokyo Institute of Technology)

  • Yutong Gong

    (Northwestern Polytechnical University)

  • Hitoshi Abe

    (High Energy Accelerator Research Organization
    The Graduate University for Advanced Studies)

  • Yasuhiro Niwa

    (High Energy Accelerator Research Organization)

  • Masato Sasase

    (Tokyo Institute of Technology)

  • Masaaki Kitano

    (Tokyo Institute of Technology)

  • Hideo Hosono

    (Tokyo Institute of Technology)

Abstract

Single-atom catalysts (SACs) have attracted significant attention because they exhibit unique catalytic performance due to their ideal structure. However, maintaining atomically dispersed metal under high temperature, while achieving high catalytic activity remains a formidable challenge. In this work, we stabilize single platinum atoms within sub-nanometer surface cavities in well-defined 12CaO·7Al2O3 (C12A7) crystals through theoretical prediction and experimental process. This approach utilizes the interaction of isolated metal anions with the positively charged surface cavities of C12A7, which allows for severe reduction conditions up to 600 °C. The resulting catalyst is stable and highly active toward the selective hydrogenation of nitroarenes with a much higher turnover frequency (up to 25772 h−1) than well-studied Pt-based catalysts. The high activity and selectivity result from the formation of stable trapped single Pt atoms, which leads to heterolytic cleavage of hydrogen molecules in a reaction that involves the nitro group being selectively adsorbed on C12A7 surface.

Suggested Citation

  • Tian-Nan Ye & Zewen Xiao & Jiang Li & Yutong Gong & Hitoshi Abe & Yasuhiro Niwa & Masato Sasase & Masaaki Kitano & Hideo Hosono, 2020. "Stable single platinum atoms trapped in sub-nanometer cavities in 12CaO·7Al2O3 for chemoselective hydrogenation of nitroarenes," Nature Communications, Nature, vol. 11(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-019-14216-9
    DOI: 10.1038/s41467-019-14216-9
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    Cited by:

    1. Wei Liu & Haisong Feng & Yusen Yang & Yiming Niu & Lei Wang & Pan Yin & Song Hong & Bingsen Zhang & Xin Zhang & Min Wei, 2022. "Highly-efficient RuNi single-atom alloy catalysts toward chemoselective hydrogenation of nitroarenes," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
    2. Zhongxin Chen & Jingting Song & Rongrong Zhang & Runlai Li & Qikun Hu & Pingping Wei & Shibo Xi & Xin Zhou & Phuc T. T. Nguyen & Hai M. Duong & Poh Seng Lee & Xiaoxu Zhao & Ming Joo Koh & Ning Yan & K, 2022. "Addressing the quantitative conversion bottleneck in single-atom catalysis," Nature Communications, Nature, vol. 13(1), pages 1-8, December.
    3. Hongqiang Jin & Peipei Li & Peixin Cui & Jinan Shi & Wu Zhou & Xiaohu Yu & Weiguo Song & Changyan Cao, 2022. "Unprecedentedly high activity and selectivity for hydrogenation of nitroarenes with single atomic Co1-N3P1 sites," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    4. Shuang Xiang & Lin Dong & Zhi-Qiang Wang & Xue Han & Luke L. Daemen & Jiong Li & Yongqiang Cheng & Yong Guo & Xiaohui Liu & Yongfeng Hu & Anibal J. Ramirez-Cuesta & Sihai Yang & Xue-Qing Gong & Yanqin, 2022. "A unique Co@CoO catalyst for hydrogenolysis of biomass-derived 5-hydroxymethylfurfural to 2,5-dimethylfuran," Nature Communications, Nature, vol. 13(1), pages 1-9, December.

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