Promotion effect of epoxy group neighboring single-atom Cu site on acetylene hydrochlorination

• Published in: Chinese chemical letters 2024-06, Vol.35 (6), p.109508, Article 109508
• Main Authors: Peng, Junchen, Yin, Xue, Dong, Dandan, Guo, Zhongyuan, Wang, Qinqin, Liu, Minmin, He, Fei, Dai, Bin, Huang, Chaofeng
• Format: Article
• Language: English
• Subjects: Acetylene hydrochlorination; Epoxy group; Single-atom Cu catalyst; Synergistic dissociation
• ISSN: 1001-8417; 1878-5964
• DOI: 10.1016/j.cclet.2024.109508

Carbon materials have been used as the support for catalysts in the field of acetylene hydrochlorination, the influence of inevitable oxygen-containing moieties on the reaction is often ignored and the mechanism of the oxygen-doping structure remains ambiguous. Herein, we explored the effect of the oxygen-containing group (COC) in the support on the activity of single-atom dispersed Cu catalysts. By immersing the Cu single-atom catalyst in an alkaline solution, the epoxy species on the carbon support was cleaved to obtain a pure ether species while the Cu site was modified to a more electron-deficient state. The turnover frequency value of Cu/O-FLP catalyst with epoxy groups was 1.6-fold higher than that of alkaline treated catalyst. Our result indicated that the epoxy groups could assist adjacent single-atom Cu sites to synergistically promote the adsorption and cleavage of the reactant hydrogen chloride toward form COH and CuCl bonds, and reduce the reaction energy barrier. The presence of electron deficient Cu sites and ether species could induce competitive adsorption of the acetylene and hydrogen chloride, thereby reducing the activity of the catalyst. This study highlights the influence of surface oxygen species and the tunability of the support, providing the foundation for the fabrication of higher-activity Cu catalysts for acetylene hydrochlorination. [Display omitted] The epoxy groups assist Cu to promote adsorption and cleavage HCl, reduces the reaction energy barrier, and promotes the reaction.