点击次数：

论文类型：期刊论文

发表时间：2018-07-01

发表刊物：JOURNAL OF CO2 UTILIZATION

卷号：26

页面范围：160-170

ISSN号：2212-9820

关键字：Carbon dioxide; Fe facet; Density functional theory; Adsorption; Dissociation; Hydrogenation

摘要：Periodic density functional theory (DFT) calculations were performed to investigate the facet effect on CO2 adsorption, dissociation and hydrogenation over Fe catalysts. The energetically most stable configurations of CO2 and H-2 adsorption over different Fe facets were identified from which we observed that CO2 adsorption on Fe(211) and Fe(111) is much stronger than other facets, indicating more sufficient activation of CO2 on these two surfaces. CO2 adsorption stability was found to be impacted by the surface coverage of H* on these Fe facets, showing that when surface H* coverage exceeds to certain percentage, CO2 adsorption is largely weakened whilst the electrons transfer from the Fe surface to CO2 becomes decreased. These results suggest that an appropriate H-2-CO2 co-adsorption equilibrium is important for effective activation of reactants. Based on the examination of CO2 dissociation and hydrogenation on these Fe facets, the Fe(111) is potentially the most active facet for CO2 conversion due to a lower barrier for HCOO* formation via CO2 hydrogenation while this facet is also catalytically more active for activating CO2. Fe(110) and Fe(100) exhibit more facile ability to dissociate CO2 to CO* while kinetically competitive formation of CO* and HCOO* was observed over Fe(211). The present work demonstrates that the facet of Fe catalysts can impact the molecular adsorption, activation and conversion path in CO2 hydrogenation and thus can alter the product selectivity.