催化作用
苯甲醇
金属
金属有机骨架
苯甲醛
选择性
钯
化学
水溶液中的金属离子
酒精氧化
无机化学
材料科学
组合化学
有机化学
吸附
作者
Penghu Guo,Christian Froese,Qi Fu,Yen‐Ting Chen,Baoxiang Peng,Wolfgang Kleist,Roland A. Fischer,Martin Muhler,Yuemin Wang
标识
DOI:10.1021/acs.jpcc.8b05882
摘要
Metal–organic frameworks (MOFs) featuring isolated coordinatively unsaturated metal sites (CUS) have enormous potential as single-site catalysts. In particular, mixed-metal MOFs may exhibit unique catalytic properties compared to their monometallic counterparts. Herein, we report a thorough fundamental study on the mixed-metal CuPd-HKUST-1 ([Cu3–xPdx(BTC)2]n; BTC = 1,3,5-benzenetricarboxylate) including the two-step synthesis, characterization, and catalytic performance evaluation. The combined results from a multitechnique approach provide solid evidence that the chemical properties of HKUST-1 can be tuned via successful incorporation of Pd–CUS into the framework, leading to the formation of new Cu–Pd and/or Pd–Pd dimers. The introduction of Pd occurs exclusively at the metal nodes in a controlled manner while retaining the structural integrity. The incorporated Pd ions have an oxidation state of +2, whereas no PdO or metallic Pd nanoparticles embedded inside MOFs are detected. These mixed-metal CuPd-MOFs exhibit superior catalytic activity and selectivity for the aerobic oxidation of benzyl alcohol to benzaldehyde, and the doped Pd2+–CUS species are identified as isolated single-active sites.
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