Motif-mediated Au25(SPh)5(PPh3)ioX2 nanorods with conjugated electron delocalization

查看全文 作　　者：Kai [1,2]Zheng;Jiangwei [1]Zhang;Dan [3]Zhao;Yong [4]Yang;Zhimin [1,2]Li;Gao [1]Li

机构地区：[1]State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China;[2]University of Chinese Academy of Sciences, Beijing 100049, China;[3]Institute of Catalysis for Energy and Environment, College of Chemistry and Chemical Engineering, Shenyang Normal University, Shenyang 110034, China;[4]Department of Materials Science & Engineering, College of Engineering, Peking University, Beijing 100871, China

出　　处：《Nano Research》索引2019年第12卷第3期,共7页

基　　金：We thank the financial support by the National Natural Science Foundation of China (No. 21701168), Liaoning Natural Science Foundation (No. 20170540897),open project Foundation of State Key Laboratory of Physical Chemistry of Solid Surfaces, Xiamen University (No. 201709);Shanxi Province Hundred Talent Project;BL14B and BL17B beamline of National Facility for Protein Science in Shanghai, Shanghai Synchrotron Radiation Facility for providing the beam time. 摘　　要：We developed a general and effective strategy to afford rod-like [Au25(SPh)5(PPh3)10X2]X2 (X = Cl/Br) nanoclusters, capped by conjugated delocalized pπ electron mediated ligands. The detailed atomic structure of these materials was resolved by synchrotron radiation X-ray diffraction (SRXRD) combined with electrospray ionization mass spectrometry (ESI-MS) and UV–vis analyses. The Au17(SR)3(PPh3)6X2minimum asymmetric unit, with exposed Au atoms at the center, can serve as an important model to understand the transformation of homogold nanoclusters into alloy nanoclusters. The conjugated delocalized pπ electrons of the thiolate ligands can effectively tune the electronic properties of the Au25 kernel, as qualitatively evidenced by the energy gaps measured by UV–vis experiments and density functional theory (DFT) calculations. The delocalized electrons distinctly flow to the orbitals of the Au25 kernel via the S atoms of the aromatic thiolates. The ESI-MS analysis indicates that Au3 clusters are formed during the etching reactions, which provide an opportunity to gain insight into the intriguing conversion pathway of the Aun(PPh3)mXy precursor to the final Au25 nanorods. Finally, the thiophenol-protected Au25 nanorods, immobilized on activated carbon, show good catalytic activity in the aerobic oxidation of glucose to gluconic acid (74% glucose conversion and 100% selectivity for gluconic acid), much higher than that of the aliphatic Au25 analogue. The Au25(SPh)5(PPh3)10X2 catalyst yields a turnover frequency (TOF) of 13.5 s^–1, higher than that of commercial catalysts such as Pd/activated carbon (AC) and Pd-Bi/AC. The insight obtained from this study will support the development and design of efficient nanogold catalysts for special oxidation reactions. 关键词：gold clusters AU25 nanorod SYNCHROTRON radiation X-ray diffraction (SRXRD) AEROBIC oxidation

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Motif-mediated Au25(SPh)5(PPh3)ioX2 nanorods with conjugated electron delocalization

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