Phosphonate monolayers on InAsSb and GaSb surfaces for mid-IR plasmonics

被引:13
作者
Bomers, Mario [1 ]
Mezy, Aude [2 ]
Cerutti, Laurent [1 ]
Barho, Franziska [1 ]
Flores, Fernando Gonzalez-Posada [1 ]
Tournie, Eric [1 ]
Taliercio, Thierry [1 ]
机构
[1] Univ Montpellier, CNRS, IES, Montpellier, France
[2] SiKEMIA, F-34095 Montpellier, France
关键词
Phosphonates; Native oxide layer; III-V semiconductor; Self-assembled monolayers; X-ray photoelectron spectroscopy; Plasmonic enhanced infrared spectroscopy; SELF-ASSEMBLED MONOLAYERS; RAY-PHOTOELECTRON-SPECTROSCOPY; ENHANCED INFRARED-ABSORPTION; GAAS-SURFACES; ADSORPTION; MOLECULES; PHOSPHATE; INDIUM; LAYERS; ACID;
D O I
10.1016/j.apsusc.2018.04.208
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
Stable functionalization of semiconductor surfaces is a prerequisite for all-semiconductor mid-IR biophotonics. This work demonstrates the adsorption of phosphonic acids on oxygen plasma activated GaSb and InAsSb surfaces. X-ray photoelectron spectroscopy shows that oxygen plasma treatment, used to activate the investigated III-V surfaces, increases the surface oxide layer beyond its native oxide thickness. Phosphonates with different terminal groups, either ethylene glycol or fluorinate carbon terminated groups, allow to modify the hydrophobicity of the surfaces and to protect the surfaces by an antifouling cover layer. Infrared spectroscopy indicates partial deprotonation of the phosphonic acid and thus phosphonate bonding to the surfaces. Adsorption of phosphonates on an all-semiconductor mid-IR plasmonic grating structure is detected by a shift and by a shape modulation of the plasmonic resonance peak. Compared with molecule adsorption on flat mirror-like layers a ten-fold signal enhancement is found. The adsorbed molecules are stable upon baking at 120 degrees C, ultrasonic cleaning with organic solvents and storage for several weeks at ambient conditions. These results show that stable functionalization of InAsSb and GaSb surfaces by phosphonate monolayers is possible. All-semiconductor enhanced plasmonic sensing in the mid-IR was demonstrated. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:241 / 249
页数:9
相关论文
共 41 条
[1]   Engineering mid-infrared nanoantennas for surface enhanced infrared absorption spectroscopy [J].
Adato, Ronen ;
Aksu, Serap ;
Altug, Hatice .
MATERIALS TODAY, 2015, 18 (08) :436-446
[2]  
[Anonymous], 2013, Surface Science Techniques, DOI DOI 10.1007/978-3-642-34243-1_1
[3]   Adsorption of organic phosphate as a means to bind biological molecules to GaAs surfaces [J].
Artzi, R ;
Daube, SS ;
Cohen, H ;
Naaman, R .
LANGMUIR, 2003, 19 (18) :7392-7398
[4]  
Barho F. B., 2017, NANOPHOTONICS, V7
[5]   All-semiconductor plasmonic gratings for biosensing applications in the mid-infrared spectral range [J].
Barho, Franziska B. ;
Gonzalez-Posada, Fernando ;
Milla-Rodrigo, Maria-Jose ;
Bomers, Mario ;
Cerutti, Laurent ;
Taliercio, Thierry .
OPTICS EXPRESS, 2016, 24 (14) :16175-16190
[6]   Spatially selective modification of PLLA surface: From hydrophobic to hydrophilic or to repellent [J].
Bastekova, Kristina ;
Guselnikova, Olga ;
Postnikov, Pavel ;
Elashnikov, Roman ;
Kunes, Martin ;
Kolska, Zdenka ;
Svorcik, Vaclav ;
Lyutakov, Oleksiy .
APPLIED SURFACE SCIENCE, 2017, 397 :226-234
[7]   Low-Loss Plasmonic Metamaterials [J].
Boltasseva, Alexandra ;
Atwater, Harry A. .
SCIENCE, 2011, 331 (6015) :290-291
[8]   Pedestal formation of all-semiconductor gratings through GaSb oxidation for mid-IR plasmonics [J].
Bomers, Mario ;
Barho, Franziska ;
Milla-Rodrigo, Maria Jose ;
Cerutti, Laurent ;
Arinero, Richard ;
Flores, Fernando Gonzalez-Posada ;
Tournie, Eric ;
Taliercio, Thierry .
JOURNAL OF PHYSICS D-APPLIED PHYSICS, 2018, 51 (01)
[9]   SILANIZATION OF SOLID SUBSTRATES - A STEP TOWARD REPRODUCIBILITY [J].
BRZOSKA, JB ;
BENAZOUZ, I ;
RONDELEZ, F .
LANGMUIR, 1994, 10 (11) :4367-4373
[10]   Adsorption of phenylphosphonic acid on GaAs (100) surfaces [J].
do Rego, AMB ;
Ferraria, AM ;
El Beghdadi, J ;
Debontridder, F ;
Brogueira, P ;
Naaman, R ;
Vilar, MR .
LANGMUIR, 2005, 21 (19) :8765-8773