Plasmonic Temperature-Programmed Desorption

被引:8
|
作者
Murphy, Colin J. [1 ,2 ,3 ]
Nugroho, Ferry Anggoro Ardy [1 ]
Harelind, Hanna [2 ,3 ]
Hellberg, Lars [1 ]
Langhammer, Christoph [1 ]
机构
[1] Chalmers Univ Technol, Dept Phys, SE-41296 Gothenburg, Sweden
[2] Chalmers Univ Technol, Dept Chem & Chem Engn, SE-41296 Gothenburg, Sweden
[3] Chalmers Univ Technol, Competence Ctr Catalysis, SE-41296 Gothenburg, Sweden
基金
欧洲研究理事会;
关键词
temperature-programmed desorption; nanoparticles; metals; plasmonic sensing; molecules; adsorption; SURFACE; DEPENDENCE; RESONANCE; NANOPARTICLES; ADSORPTION; METHANOL; GOLD; SIZE; THERMODYNAMICS; CHEMISTRY;
D O I
10.1021/acs.nanolett.0c03733
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Temperature-programmed desorption (TPD) allows for the determination of the bonding strength and coverage of molecular mono- or multilayers on a surface and is widely used in surface science. In its traditional form using a mass spectrometric readout, this information is derived indirectly by analysis of resulting desorption peaks. This is problematic because the mass spectrometer signal not only originates from the sample surface but also potentially from other surfaces in the measurement chamber. As a complementary alternative, we introduce plasmonic TPD, which directly measures the surface coverage of molecular species adsorbed on metal nanoparticles at ultrahigh vacuum conditions. Using the examples of methanol and benzene on Au nanoparticle surfaces, the method can resolve all relevant features in the submonolayer and multilayer regimes. Furthermore, it enables the study of two types of nanoparticles simultaneously, which is challenging in a traditional TPD experiment, as we demonstrate specifically for Au and Ag.
引用
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页码:353 / 359
页数:7
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