Interface Science Using Ambient Pressure Hard X-ray Photoelectron Spectroscopy

被引:46
作者
Favaro, Marco [1 ]
Abdi, Fatwa Firdaus [1 ]
Crumlin, Ethan Jon [2 ]
Liu, Zhi [2 ,3 ]
van de Krol, Roel [1 ]
Starr, David Edward [1 ]
机构
[1] Helmholtz Zentrum Berlin Mat & Energie GmbH, Inst Solar Fuels, Hahn Meitner Pl 1, D-14109 Berlin, Germany
[2] Lawrence Berkeley Natl Lab, Adv Light Source, 1 Cyclotron Rd, Berkeley, CA 94720 USA
[3] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
来源
SURFACES | 2019年 / 2卷 / 01期
基金
中国国家自然科学基金;
关键词
in situ ambient pressure XPS; hard X rays; photoelectron simulations; solid; liquid interface; TiO2; APTES; ELECTRON-SPECTROSCOPY; SURFACE-CHEMISTRY; OPERANDO; RUTILE; MENISCUS; LIQUIDS; SPECTRA; ANGLE; TOOL; CO2;
D O I
10.3390/surfaces2010008
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 development of novel in situ/operando spectroscopic tools has provided the opportunity for a molecular level understanding of solid/liquid interfaces. Ambient pressure photoelectron spectroscopy using hard X-rays is an excellent interface characterization tool, due to its ability to interrogate simultaneously the chemical composition and built-in electrical potentials, in situ. In this work, we briefly describe the "dip and pull" method, which is currently used as a way to investigate in situ solid/liquid interfaces. By simulating photoelectron intensities from a functionalized TiO2 surface buried by a nanometric-thin layer of water, we obtain the optimal photon energy range that provides the greatest sensitivity to the interface. We also study the evolution of the functionalized TiO2 surface chemical composition and correlated band-bending with a change in the electrolyte pH from 7 to 14. Our results provide general information about the optimal experimental conditions for characterizing the solid/liquid interface using the "dip and pull" method, and the unique possibilities offered by this technique.
引用
收藏
页码:78 / 99
页数:22
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