文献类型：期刊文献

英文题名：Effect of Reflux Time on the Performance of the Cu/ZrO2 Catalyst for CO2 Hydrogenation to Methanol

作者：Dai, Wenhua[1];Meng, Xin[1];Xu, Bowen[1];Zhao, Rui[1];Jin, Daoming[1];Xu, Fan[1];Yang, Dandan[1];Xin, Zhong[1]

机构：[1]East China Univ Sci & Technol, Sch Chem Engn, Shanghai Key Lab Multiphase Mat Chem Engn, Shanghai 200237, Peoples R China

年份：2023

卷号：6

期号：18

起止页码：9417

外文期刊名：ACS APPLIED ENERGY MATERIALS

收录：;EI(收录号：20234314928101);WOS:【SCI-EXPANDED(收录号:WOS:001068495800001)】；

基金：This work was supported by the National Natural Science Foundation of China (grant numbers 21808064, 21808062, 21776091, and U1203293) and Shanghai "Double First-class" Supporting Special Funds.

语种：英文

外文关键词：CO2 hydrogenation; reflux; Cu/ZrO2 catalysts; basic site; oxygen vacancy

摘要：The hydrogenation of CO2 into methanol was investigated by means of the Cu/ZrO2 catalyst to analyze the effect of reflux time on catalytic performance. A series of high-activity Cu/ZrO2 catalysts were prepared by introducing the support pretreated with ammonia reflux. The effect of reflux time on the structure and performance of all catalysts was systematically studied. Combined with various characterizations such as X-ray diffraction (XRD), N-2 physisorption, temperature-programmed reduction by H2 (H2-TPR), temperature-programmed desorption of H-2 and CO2, X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM), it can be seen that the catalysts after reflux exhibited a stable amorphous structure with more medium and strong basic sites. Moreover, the proportion of defect oxygen and surface Cu+ species for Cu/ZrO2 catalysts increased, and the metal-support interaction was strengthened, which effectively increased active sites and promoted CO2 activation, and thus, the catalyst with stronger activity and better stability was obtained. The CO2 conversion dramatically increased by 4-5 times (from 5.4 to 22.1%) after reflux treatment, and the Cu/ZrO2-18h catalyst had the highest catalytic activity and a methanol space time yield of 394 g(MeOH) h-1 kg(cat)( -1) at 260 ?.