Catalysis by Metal Nanoparticles in a Plug-In Optofluidic Platform: Redox Reactions of p-Nitrobenzenethiol and p-Aminothiophenol

被引:43
作者
Zhang, Zhiyang [1 ,2 ,3 ]
Gerner, Ulrich [4 ]
Gerhardt, Renata F. [5 ]
Hoehn, Eva-Maria [5 ]
Belder, Detlev [5 ]
Kneipp, Janina [1 ,2 ,3 ]
机构
[1] Humboldt Univ, Dept Chem, Brook Taylor Str 2, D-12489 Berlin, Germany
[2] Humboldt Univ, Sch Analyt Sci Adlershof, Brook Taylor Str 2, D-12489 Berlin, Germany
[3] BAM Fed Inst Mat Res & Testing, Richard Willstatter Str 11, D-12489 Berlin, Germany
[4] Tech Univ Berlin, ZELMI, Str 17,Juni 135, D-10623 Berlin, Germany
[5] Univ Leipzig, Inst Analyt Chem, Dept Chem & Mineral, Linnestr 3, D-04103 Leipzig, Germany
关键词
heterogeneous catalysis; gaseous reactants; radicals; reusable; optofluidics; surface-enhanced Raman scattering (SERS); microfluidics; SURFACE-ENHANCED RAMAN; QUANTITATIVE SERS; SILVER; GOLD; AU; REDUCTION; SITU; AG; SCATTERING; MOLECULE;
D O I
10.1021/acscatal.8b00101
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The spectroscopic characterization by surface-enhanced Raman scattering (SERS) has shown great potential in studies of heterogeneous catalysis. We describe a plug-in multifunctional optofluidic platform that can be tailored to serve both as a variable catalyst material and for sensitive optical characterization of the respective reactions using SERS in microfluidic systems. The platform enables the characterization of reactions under a controlled gas atmosphere and does not present with limitations due to nanoparticle adsorption or memory effects. Spectra of the gold-catalyzed reduction of p-nitrothiophenol by sodium borohydride using the plug-in probe provide evidence that the borohydride is the direct source of hydrogen on the gold surface, and that a radical anion is formed as an intermediate. The in situ monitoring of the photoinduced dimerization of p-aminothiophenol indicates that the activation of oxygen is essential for the plasmon-catalyzed oxidation on gold nanoparticles and strongly supports the central role of metal oxide species.
引用
收藏
页码:2443 / +
页数:13
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