Cao Xinxiang, Tong Ruijian, Tang Siye, Jang Ben W-L, Mirjalili Arash, Li Jiayi, Guo Xining, Zhang Jingyi, Hu Jiaxue, Meng Xin
Laboratory for Development & Application of Cold Plasma Technology, College of Chemistry and Chemical Engineering, Luoyang Normal University, Luoyang 471022, China.
School of Agriculture and Bioengineering, Heze University, Heze 274015, China.
Molecules. 2022 Sep 5;27(17):5736. doi: 10.3390/molecules27175736.
Novel zinc-palladium-porphyrin bimetal metal-organic framework (MOF) nanosheets were directly synthesized by coordination chelation between Zn(II) and Pd(II) tetra(4-carboxyphenyl)porphin (TCPP(Pd)) using a solvothermal method. Furthermore, a serial of carbon nanosheets supported Pd-Zn intermetallics (Pd-Zn-ins/CNS) with different Pd: Zn atomic ratios were obtained by one-step carbonization under different temperature using the prepared Zn-TCPP(Pd) MOF nanosheets as precursor. In the carbonization process, Pd-Zn-ins went through the transformation from PdZn (650 °C) to PdZn (~950 °C) then to PdZn/Pd (1000 °C) with the temperature increasing. The synthesized Pd-Zn-ins/CNS were further employed as catalysts for selective hydrogenation of acetylene. PdZn showed the best catalytic performance compared with other Pd-Zn intermetallic forms.
采用溶剂热法,通过锌(II)与四(4-羧基苯基)卟啉钯(II)(TCPP(Pd))之间的配位螯合直接合成了新型锌-钯-卟啉双金属金属有机框架(MOF)纳米片。此外,以制备的Zn-TCPP(Pd)MOF纳米片为前驱体,在不同温度下通过一步碳化获得了一系列具有不同钯:锌原子比的碳纳米片负载钯-锌金属间化合物(Pd-Zn-ins/CNS)。在碳化过程中,随着温度升高,Pd-Zn-ins经历了从PdZn(650℃)到PdZn(~950℃)再到PdZn/Pd(1000℃)的转变。合成的Pd-Zn-ins/CNS进一步用作乙炔选择性加氢的催化剂。与其他钯-锌金属间化合物形式相比,PdZn表现出最佳的催化性能。