炔烃
选择性
催化作用
化学
活动站点
乙炔
乙烯
联轴节(管道)
光化学
氢
谱线
吸附
组合化学
结晶学
立体化学
二聚体
反应中间体
偶联反应
作者
Jingyun Jiang,Mengxian Yu,Chengxiang Shi,Zhen‐Feng Huang,Xiangwen Zhang,Lun Pan,Ruijie Gao,Jinlong Gong,Ji‐Jun Zou
摘要
Abstract Single‐site pairs are promising in achieving high selectivity and activity in alkyne semihydrogenation, but its applicability is limited by the insufficient activity because pair sites cannot adsorb and activate alkyne. Here, we couple single‐site Pd with Jahn–Teller active Cu atoms of Cu‐doped Fe 2 O 3 to construct a highly active and stable single‐site Pd‐Cu pairs. The Jahn–Teller active Cu possesses elongated axial orbitals, and the strong electronic coupling between Pd and Cu further contributes to their unoccupied axial d orbitals, which helps Pd‐Cu pair to cooperatively activate C 2 H 2 molecule, unlike ordinary single‐site pairs where only H 2 is activated. As a result, this catalyst exhibits state‐of‐the‐art performance, with > 99.99% conversion and 95.5% selectivity as well as excellent stability with negligible performance decay after 300‐h test in purifying acetylene of ethylene stream. Both in situ spectra and theoretical results indicate two H addition steps occur on Pd and Cu sites in sequence. This work opens an avenue for constructing highly efficient single‐site pairs for selective hydrogenation and beyond.
科研通智能强力驱动
Strongly Powered by AbleSci AI