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Gold catalysts containing interstitial carbon atoms boost hydrogenation activity

Author

Listed:
  • Yafei Sun

    (Shanghai Normal University)

  • Yueqiang Cao

    (East China University of Science and Technology)

  • Lili Wang

    (Shanghai Normal University)

  • Xiaotong Mu

    (Shanghai Normal University)

  • Qingfei Zhao

    (Shanghai Normal University)

  • Rui Si

    (Chinese Academy of Sciences)

  • Xiaojuan Zhu

    (Shanghai Normal University)

  • Shangjun Chen

    (Shanghai Normal University)

  • Bingsen Zhang

    (Chinese Academy of Sciences)

  • De Chen

    (Norwegian University of Science and Technology)

  • Ying Wan

    (Shanghai Normal University)

Abstract

Supported gold nanoparticles are emerging catalysts for heterogeneous catalytic reactions, including selective hydrogenation. The traditionally used supports such as silica do not favor the heterolytic dissociation of hydrogen on the surface of gold, thus limiting its hydrogenation activity. Here we use gold catalyst particles partially embedded in the pore walls of mesoporous carbon with carbon atoms occupying interstitial sites in the gold lattice. This catalyst allows improved electron transfer from carbon to gold and, when used for the chemoselective hydrogenation of 3-nitrostyrene, gives a three times higher turn-over frequency (TOF) than that for the well-established Au/TiO2 system. The d electron gain of Au is linearly related to the activation entropy and TOF. The catalyst is stable, and can be recycled ten times with negligible loss of both reaction rate and overall conversion. This strategy paves the way for optimizing noble metal catalysts to give an enhanced hydrogenation catalytic performance.

Suggested Citation

  • Yafei Sun & Yueqiang Cao & Lili Wang & Xiaotong Mu & Qingfei Zhao & Rui Si & Xiaojuan Zhu & Shangjun Chen & Bingsen Zhang & De Chen & Ying Wan, 2020. "Gold catalysts containing interstitial carbon atoms boost hydrogenation activity," Nature Communications, Nature, vol. 11(1), pages 1-9, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-18322-x
    DOI: 10.1038/s41467-020-18322-x
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