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June 3, 2026Fuel Processing Technology0 citationsOpen Access

Synergistic effect of surface hydroxyl anchoring and electronic metal-support interaction in Cu-ZnO-SrTiO3 catalysts for enhanced CO2 hydrogenation

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YLY LiuEast China University of Science and TechnologyXWXuguang WangMinistry of Education Science and TechnologyHLHuiling LiuEast China University of Science and Technology

Key Points

  • The research investigates how surface hydroxyl anchoring and electronic interactions enhance CO2 hydrogenation.
  • Analyzed the charge mediated anchoring mechanism to bind Cu²⁺ and Zn²⁺
  • Studied the effect of oxygen vacancies on catalyst structure
  • Compared catalytic activity using various oxygen vacancy densities.
  • Cu 0 step-edge sites enhanced H 2 adsorption, improving catalytic activity for methanol synthesis
  • Low-crystallinity SrTiO₃ with oxygen vacancies tuned the d-band center of Cu
  • Small Cu and ZnO particles were achieved through managing electron transfer.

Abstract

• The charge mediated anchoring mechanism at oxygen vacancies anchors Cu 2+ and Zn 2+ via electron transfer. • Oxygen vacancies induce highly dispersed small Cu with Cu 0 step-edge sites. and small ZnO particles. • Coordination-unsaturated Cu 0 step-edge sites serve as structural descriptors for the d-band center. • Upshifted d-band center enhances H 2 adsorption, boosting catalytic activity for methanol synthesis. • Low-crystallinity SrTiO₃ with rich oxygen vacancies offers a pathway to tune the d-band center of Cu. Dianhua Liu. Institution and address: East China University of Science and Technology, Shanghai 200,237, China.

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Cite This Study

Liu et al. (2026) studied this question.

synapsesocial.com/papers/6a1fc756dee9eb8c0dce835dhttps://doi.org/10.1016/j.fuproc.2026.108491
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