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Enhancing polyol/sugar cascade oxidation to formic acid with defect rich MnO2 catalysts

Author

Listed:
  • Hao Yan

    (China University of Petroleum (East China)
    National University of Singapore)

  • Bowen Liu

    (University of Liverpool)

  • Xin Zhou

    (China University of Petroleum (East China)
    Ocean University of China)

  • Fanyu Meng

    (China University of Petroleum (East China))

  • Mingyue Zhao

    (China University of Petroleum (East China))

  • Yue Pan

    (China University of Petroleum (East China))

  • Jie Li

    (China University of Petroleum (East China))

  • Yining Wu

    (China University of Petroleum (East China))

  • Hui Zhao

    (China University of Petroleum (East China))

  • Yibin Liu

    (China University of Petroleum (East China))

  • Xiaobo Chen

    (China University of Petroleum (East China))

  • Lina Li

    (Chinese Academy of Sciences)

  • Xiang Feng

    (China University of Petroleum (East China))

  • De Chen

    (Norwegian University of Science and Technology)

  • Honghong Shan

    (China University of Petroleum (East China))

  • Chaohe Yang

    (China University of Petroleum (East China))

  • Ning Yan

    (National University of Singapore)

Abstract

Oxidation of renewable polyol/sugar into formic acid using molecular O2 over heterogeneous catalysts is still challenging due to the insufficient activation of both O2 and organic substrates on coordination-saturated metal oxides. In this study, we develop a defective MnO2 catalyst through a coordination number reduction strategy to enhance the aerobic oxidation of various polyols/sugars to formic acid. Compared to common MnO2, the tri-coordinated Mn in the defective MnO2 catalyst displays the electronic reconstruction of surface oxygen charge state and rich surface oxygen vacancies. These oxygen vacancies create more Mnδ+ Lewis acid site together with nearby oxygen as Lewis base sites. This combined structure behaves much like Frustrated Lewis pairs, serving to facilitate the activation of O2, as well as C–C and C–H bonds. As a result, the defective MnO2 catalyst shows high catalytic activity (turnover frequency: 113.5 h−1) and formic acid yield (>80%) comparable to noble metal catalysts for glycerol oxidation. The catalytic system is further extended to the oxidation of other polyols/sugars to formic acid with excellent catalytic performance.

Suggested Citation

  • Hao Yan & Bowen Liu & Xin Zhou & Fanyu Meng & Mingyue Zhao & Yue Pan & Jie Li & Yining Wu & Hui Zhao & Yibin Liu & Xiaobo Chen & Lina Li & Xiang Feng & De Chen & Honghong Shan & Chaohe Yang & Ning Yan, 2023. "Enhancing polyol/sugar cascade oxidation to formic acid with defect rich MnO2 catalysts," Nature Communications, Nature, vol. 14(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-40306-w
    DOI: 10.1038/s41467-023-40306-w
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    References listed on IDEAS

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    1. Zhe An & Zilong Zhang & Zeyu Huang & Hongbo Han & Binbin Song & Jian Zhang & Qi Ping & Yanru Zhu & Hongyan Song & Bin Wang & Lirong Zheng & Jing He, 2022. "Pt1 enhanced C-H activation synergistic with Ptn catalysis for glycerol cascade oxidation to glyceric acid," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    2. Huayu Gu & Xiao Liu & Xiufan Liu & Cancan Ling & Kai Wei & Guangming Zhan & Yanbing Guo & Lizhi Zhang, 2021. "Adjacent single-atom irons boosting molecular oxygen activation on MnO2," Nature Communications, Nature, vol. 12(1), pages 1-9, December.
    3. Sai Zhang & Zheng-Qing Huang & Yuanyuan Ma & Wei Gao & Jing Li & Fangxian Cao & Lin Li & Chun-Ran Chang & Yongquan Qu, 2017. "Solid frustrated-Lewis-pair catalysts constructed by regulations on surface defects of porous nanorods of CeO2," Nature Communications, Nature, vol. 8(1), pages 1-11, August.
    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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