Volume 44 Issue 8
Aug.  2016
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JIANG Jun-hui, CAO Yong-yong, NI Zhe-ming, ZHANG Lian-yang. Comparison of reaction mechanism of thiophene hydrodesulfurization on Au13 and Pt13 clusters[J]. Journal of Fuel Chemistry and Technology, 2016, 44(8): 961-969.
Citation: JIANG Jun-hui, CAO Yong-yong, NI Zhe-ming, ZHANG Lian-yang. Comparison of reaction mechanism of thiophene hydrodesulfurization on Au13 and Pt13 clusters[J]. Journal of Fuel Chemistry and Technology, 2016, 44(8): 961-969.

Comparison of reaction mechanism of thiophene hydrodesulfurization on Au13 and Pt13 clusters

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  • Corresponding author: Tel: +86-13858123256, E-mail: jchx@zjut.edu.cn
  • Received Date: 2016-03-15
  • Rev Recd Date: 2016-04-25
  • Available Online: 2021-01-23
  • Publish Date: 2016-08-10
  • The behaviors of thiophene adsorption and hydrodesulfurization on cubic octahedral M13 (M=Au, Pt) clusters were investigated by density functional theory. The results show that the adsorption energy of thiophene on Pt13 is higher than that on Au13; on the Au13 cluster, the Hol-tri site is most stable for the thiophene adsorption with ring, whereas on the Pt13 cluster, the Hol-quadr site is most stable. By the indirect desulfurization mechanism, the desulfurization is achieved probably via the cis-hydrogenation; the removal of C-S is the rate-determining step. By the direct desulfurization mechanism, the HS hydrogenation turns to be the rate-determining step. The desulfurization is most likely via the direct desulfurization mechanism, which exhibits much lower activation energy than the indirect desulfurization mechanism. The energy change for thiophene desulfurization on the Au13 cluster is exothermic, whereas on the Pt13 cluster it is endothermic; as a result, the hydrodesulfurization on Au13 is much easier than that on Pt13.
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