催化作用
乙炔
纳米材料基催化剂
原子层沉积
材料科学
金属
合金
选择性
沉积(地质)
无机化学
化学工程
图层(电子)
化学
纳米技术
冶金
有机化学
古生物学
工程类
生物
沉积物
作者
Min Zhong,Jiafei Zhao,Yixin Fang,Danfeng Wu,Lina Zhang,Congcong Du,Sixu Liu,Shifeng Yang,Shaolong Wan,Ying‐Bing Jiang,Jianyu Huang,Haifeng Xiong
标识
DOI:10.1016/j.apcata.2023.119288
摘要
Supported Pd single-atom alloy (SAA) catalysts are selective in acetylene semi-hydrogenation. However, it is a challenge to prepare Pd SAA where Pd single atoms dispersed on the outmost surface of the catalysts because the Pd atoms on Pd SAA prepared by conventional impregnation distribute inside the alloyed particle or on the support surface after activation. In this work, we firstly synthesized Ni/SiO2 nanocatalysts by impregnation, followed by H2 reduction to generate metal Ni particles on SiO2. Subsequently, Pd single atoms are selectively deposited on the Ni particle surface by atomic layer deposition (ALD). The Pd species on the Pd1Ni/SiO2 prepared by ALD dispersed on the outmost surface of catalyst, presenting the improved catalytic performances in acetylene hydrogenation, as compared to a reference Pd1Ni/SiO2 catalyst prepared by impregnation. The Pd1Ni/SiO2 catalyst prepared by ALD with 5 cycles (0.04 wt. %Pd, 5c-Pd1Ni/SiO2) shows both superior hydrogenation activity (92 %) and selectivity (88 %) under mild temperature (80 °C) in the selective semi-hydrogenation of acetylene. Moreover, the specific activity of the 5c-Pd1Ni/SiO2 catalyst is the highest, as compared to the catalysts reported in literature. Therefore, we conclude that the metal single atoms on metal SAA catalyst prepared by ALD locate on the outmost surface of the catalyst, presenting the unusual catalytic performances in catalysis.
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