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内蒙古自治区呼和浩特市赛罕区大学西街235号 邮编: 010021
作者机构:Key Laboratory of Materials PhysicsCentre for Environmental and Energy NanomaterialsAnhui Key Laboratory of Nanomaterials and NanotechnologyInstitute of Solid State PhysicsHefei Institutes of Physical ScienceChinese Academy of SciencesHefei 230031China University of Science and Technology of ChinaHefei 230026China Department of Energy and Petroleum EngineeringUniversity of Stavanger4036 StavangerNorway Centre for Clean Environment and EnergyGold Coast CampusGriffith UniversityQueensland 4222Australia
出 版 物:《Nano Research》 (纳米研究(英文版))
年 卷 期:2025年第18卷第2期
页 面:141-152页
核心收录:
学科分类:081704[工学-应用化学] 07[理学] 070304[理学-物理化学(含∶化学物理)] 08[工学] 0817[工学-化学工程与技术] 0703[理学-化学]
基 金:This work was financially supported by the National Natural Science Foundation of China(Nos.52072371 and 51871209) Key Technologies Research and Development Program of Anhui Province(No.202004a06020056) Special Foundation of President of HFIPS(No.YZJJ202102),HFIPS Director’s Fund(Nos.GGZX GTCX-2023-07 and YZJJ-GGZX-2022-01) HFIPS Director’s Fund(No.2023YZGH05)
主 题:green hydrogen N-doping dual active sites interface hydrogenation
摘 要:Utilization and storage are the two main themes of green *** hydrogen-involved system,development of highly active catalysts to achieve catalytic hydrogenation under mild conditions is a prerequisite for coupling with green hydrogen,so that green hydrogen with low outlet pressure can be directly used as a hydrogen *** achieve this aim,we developed a high active Co-CoOx@NC catalyst with metal/metal oxide induced by *** work function and Bader charge calculations reveal that N-doping can induce interfacial electrons rearrangement to form Co-CoOx interface on the surface of Co nanoparticles(NPs).The interface is the dual active sites,where Co plays a role in H_(2) dissociation and CoOx can enhance the adsorption and activation of aldehyde *** from traditional dissimilar metal/oxide interface,the Co-CoOx interface can effectively shorten hydrogen spillover distance and energy barrier,and thus exhibits high catalytic performance in hydrogenation of a variety of bio-derived aldehydes under aqueous-phase and mild reaction conditions that can couple with green hydrogen.