Zhang Xueping, Zhang Qiang, Reng Jiacheng, Lin Yamei, Tang Yongxing, Liu Guigao, Wang Pengcheng, Lu Guo-Ping
School of Chemistry and Chemical Engineering, Nanjing University of Science & Technology, Xiaolingwei 200, Nanjing 210094, China.
School of Chemistry and Life Sciences, Suzhou University of Science and Technology, Suzhou 215009, China.
Nanomaterials (Basel). 2023 Jan 21;13(3):445. doi: 10.3390/nano13030445.
S-doping emerged as a promising approach to further improve the catalytic performance of carbon-based materials for organic synthesis. Herein, a facile and gram-scale strategy was developed using zeolitic imidazole frameworks (ZIFs) as a precursor for the fabrication of the ZIF-derived N, S co-doped carbon-supported zinc single-atom catalyst (CNS@Zn-AA) via the pyrolysis of S-doped ZIF-8, which was modified by aniline, ammonia and thiourea and prepared by one-pot ball milling at room temperature. This catalyst, in which Zn is dispersed as the single atom, displays superior activity in N-alkylation via the hydrogen-borrowing strategy (120 °C, turnover frequency (TOF) up to 8.4 h). S-doping significantly enhanced the catalytic activity of CNS@Zn-AA, as it increased the specific surface area and defects of this material and simultaneously increased the electron density of Zn sites in this catalyst. Furthermore, this catalyst had excellent stability and recyclability, and no obvious loss in activity after eight runs.
S掺杂作为一种有前景的方法,可进一步提高碳基材料在有机合成中的催化性能。在此,我们开发了一种简便的克级策略,以沸石咪唑框架(ZIFs)为前驱体,通过对经苯胺、氨和硫脲改性并在室温下一步球磨制备的S掺杂ZIF-8进行热解,制备ZIF衍生的N、S共掺杂碳负载锌单原子催化剂(CNS@Zn-AA)。这种锌以单原子形式分散的催化剂,在借氢策略的N-烷基化反应中表现出优异的活性(120℃,转换频率(TOF)高达8.4 h⁻¹)。S掺杂显著提高了CNS@Zn-AA的催化活性,因为它增加了该材料的比表面积和缺陷,同时提高了该催化剂中锌位点的电子密度。此外,该催化剂具有优异的稳定性和可回收性,八次循环后活性无明显损失。