TY - JOUR
T1 - Two-photon photoelectron emission microscopy for surface plasmon polaritons at the Au(111) surface decorated with alkanethiolate self-assembled monolayers
AU - Yamagiwa, Kana
AU - Shibuta, Masahiro
AU - Nakajima, Atsushi
N1 - Publisher Copyright:
© the Owner Societies 2017.
PY - 2017
Y1 - 2017
N2 - In this study, we have employed dual-color photoelectron emission microscopy (2P-PEEM) to visualize surface plasmon polaritons (SPPs) propagating along a chemically modified organic/metal interface of alkanethiolate self-assembled monolayers (Cn-SAMs; n is the number of alkyl carbon atoms) formed on Au(111). In dual-color 2P-PEEM, near-infrared photons around 900 nm generate SPPs at the Cn-SAMs/Au(111) interface, which interfere with the remaining light field. The resulting surface polarization beats are imaged as local distributions of 2P-photoelectrons probed by ultraviolet photons. Through dual-color 2P-PEEM for various alkyl chain lengths of Cn-SAMs, it is revealed that SPP properties are largely modified by an interfacial electronic state, particularly formed by the chemical interaction between surface Au atoms and adsorbate thiol molecules, thereby allowing the quantification of their group velocity at ∼0.86 times the speed of light. Since the SPP properties are controllable in terms of their height as organic dielectric layers, a bottom-up tailored technique using SAMs exhibits designer capability in adjusting the dielectric properties toward applications in surface plasmonic devices.
AB - In this study, we have employed dual-color photoelectron emission microscopy (2P-PEEM) to visualize surface plasmon polaritons (SPPs) propagating along a chemically modified organic/metal interface of alkanethiolate self-assembled monolayers (Cn-SAMs; n is the number of alkyl carbon atoms) formed on Au(111). In dual-color 2P-PEEM, near-infrared photons around 900 nm generate SPPs at the Cn-SAMs/Au(111) interface, which interfere with the remaining light field. The resulting surface polarization beats are imaged as local distributions of 2P-photoelectrons probed by ultraviolet photons. Through dual-color 2P-PEEM for various alkyl chain lengths of Cn-SAMs, it is revealed that SPP properties are largely modified by an interfacial electronic state, particularly formed by the chemical interaction between surface Au atoms and adsorbate thiol molecules, thereby allowing the quantification of their group velocity at ∼0.86 times the speed of light. Since the SPP properties are controllable in terms of their height as organic dielectric layers, a bottom-up tailored technique using SAMs exhibits designer capability in adjusting the dielectric properties toward applications in surface plasmonic devices.
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U2 - 10.1039/c7cp01693j
DO - 10.1039/c7cp01693j
M3 - Article
C2 - 28530270
AN - SCOPUS:85024393706
SN - 1463-9076
VL - 19
SP - 13455
EP - 13461
JO - Physical Chemistry Chemical Physics
JF - Physical Chemistry Chemical Physics
IS - 21
ER -