Abstract

Tuning the metal-support interaction is a general strategy of regulating the chemical state of catalytic active site for high-efficiency hydrogen production from ethanol steam reforming (ESR) reaction. In this work, a Co catalyst supported on the Si4Al2O2N6 solid solution of Si3N4 and Al2O3 (Co/Si4Al2O2N6) has been developed to effectively catalyze ESR reaction. Our results demonstrate that the Co/Si4Al2O2N6 catalyst exhibits remarkably improved performances as compared with the Co/Si3N4 and Co/Al2O3 catalysts. In the Co/Si4Al2O2N6-catalyzed ESR reaction, ethanol conversion of 97 % has been achieved with hydrogen yield reaching 73 %. Long-time catalytic experiment manifests the Co/Si4Al2O2N6 catalyst possesses excellent durability. X-ray photoelectron spectroscopy (XPS) studies reveal that the enhanced metal-support interaction (MSI) and charge transfer from Si4Al2O2N6 support to Co species in the Co/Si4Al2O2N6 catalyst confer lower valence state on the Co catalyst supported on Si4Al2O2N6, thus promoting the C–C bond cleavage capability, leading to high C1 product yield and boosting the hydrogen-production efficiency. The catalytic mechanism studies explored by in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) reveal that the Co/Si4Al2O2N6 exhibits a remarkable preference for C1 products over the Co/Si3N4 and Co/Al2O3 catalysts at low reaction temperature, thus resulting in high hydrogen-production efficiency with excellent catalytic durability.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.