Oxidized porous silicon as a non-interfering support for luminescent dyes

2016 ◽  
Vol 3 (1) ◽  
Author(s):  
G. Santamaría-Juárez ◽  
E. Gómez-Barojas ◽  
E. Quiroga-González ◽  
E. Sánchez-Mora ◽  
J. A. Luna-López

AbstractThe objective of this work is to elucidate the possibility to passivate the surface states of porous Si (PSi) by thermal oxidation to be used as a passive host matrix. It is known that a large contribution to the Photoluminescence (PL) of PSi comes from defects at the surface. This PL could overlap the PL of guest materials making it difficult to identify the details of the PL spectrum of the guest. We report on an experimental study about the effect of thermal oxidation at low temperature on the PL of PSi and on the functionalization of oxidized PSi with fluorescein. The background PL is minimized allowing a better detection of fluorescein molecules adsorbed on oxidized PSi.

1994 ◽  
Vol 358 ◽  
Author(s):  
D. Stievenard ◽  
D. Deresmes

ABSTRACTPorous silicon is known to be sensitive to moisture. Using an aluminium-porous p+ silicon junction, we have realized a sensor which dc current increases up to two orders of magnitude in the presence of ammoniac. We have tested a series of various gases and we show that if the dipole moment of the molecule is zero, there is no effect on the dc current. To interpret quantitatively this phenomenon, we assume that the conductivity is governed by the width of a channel resulting from the partial depletion of silicon located between two pores. This depleted region is due to the charges trapped on surface states associated with the Si-SiO2 interface where SiO2 is the native silicon oxide. When some gas is adsorbed, we propose there is a passivation of the interface states (mainly dangling bonds), leading to a decrease of the depleted region, i.e. an increase of the width of the channel and thus an increase of the current. The adsorbed gas gives a dipole layer at the surface of the pore. This layer has no influence on the depleted region. It stabilizes electrons or holes at the porous Si surface, allowing a stable charge state of the dangling bonds.


1993 ◽  
Vol 298 ◽  
Author(s):  
Y. Kanemitsu ◽  
T. Matsumoto ◽  
T. Futagi ◽  
H. Mimura

AbstractWe have studied the origin of the visible photoluminescence (PL) from oxidized porous Si. The hydrogen–passivated surface of porous Si prepared by electrochemical etching is converted to stable silicon oxides by rapid–thermal–oxidization processes. At low oxidation temperature (Tox), the PL spectrum with a peak near 700 nm is observed. At high Tox above 800 °C, a strong blue PL is observed near 400 nm. We discuss the origin of blue and red PL by employing the results of ab initio electronic structure calculations of silicon–oxygen compounds.


1994 ◽  
Vol 358 ◽  
Author(s):  
V. Petrova-Koch ◽  
T. Muschik ◽  
G. Polisski ◽  
D. Kovalev

ABSTRACTThe visible and the infrared photoluminescence bands in porous Si have been studied at low temperature for two series of samples: one in which the size of the crystallites has been varied and another in which the degree of surface degradation has been changed. It is shown that the relation of the two bands can be explored for characterization of the porous Si bandstructure. The size- and the surface dependence of the valence band and of the conduction band related states is discussed. A model is proposed for explanation.


RSC Advances ◽  
2017 ◽  
Vol 7 (55) ◽  
pp. 34579-34583 ◽  
Author(s):  
Lu Gan ◽  
Haiping He ◽  
Qianqian Yu ◽  
Zhizhen Ye

Porous Si nanowires show anomalous luminescence quenching and improved sensing stability upon mild thermal oxidation.


2000 ◽  
Vol 638 ◽  
Author(s):  
Kazuo Goda ◽  
Ryuji Tanaka ◽  
Yukako Honda ◽  
Kazuhisa Inoue ◽  
Hideki Ohno

AbstractThe relationship between chemical states and optical properties for porous silicon (PS) under initial oxidation by heating at low temperatures (150, 200, 250 °C) in air was investigated using an infrared (IR) spectroscopy and photoluminescence (PL) measurements. The measurements in the IR region show that the IR absorption peaks for the Si-H stretching band (2050-2150 cm−1) change with appearance of the Si-O-Si-H stretching band (2100-2300 cm−1) when the thermal oxidation time is increased. On the other hand, the peak in the PL spectrum shows a blue shift from 820 nm to 710 nm with the oxidation time. The observed blue shift of the PL spectrum is due to the decrease in the initial PL peak intensity at 820 nm and the increase at 710 nm. Moreover, the peak intensities in the PL spectra at 820 nm and 710 nm have clear relationship to the amounts of the Si-H bonds and Si-O-Si-H bonds, respectively, as a function of the oxidation time.These results indicate that luminescence center (LC) for as-prepared PS is ascribed to complexes including Si-H bonds. Also the LC for oxidized PS under the oxidation process at low temperatures is ascribed to complexes including Si-O-Si-H bonds covering the inner surface of PS.


1987 ◽  
Vol 107 ◽  
Author(s):  
Sylvia S. Tsao

AbstractPorous silicon lends itself to a variety of applications due to its unique characteristics such as an interconnected pore network, large surface area, and dopant-dependent selectivity of formation. Although the best-known application of porous Si is for silicon-on-insulator (SOI) fabrication, the porous silicon technique also offers elegant approaches for silicon-on-conductor (SOC) fabrication.In this paper, we present an overview of porous Si techniques for both SOI and SOC applications. Possible limitations of the oxidized porous silicon process, for SOI in particular, are discussed. We also consider novel and multilayered structures which might be obtained using porous silicon.


1992 ◽  
Vol 283 ◽  
Author(s):  
S. Miyazakj ◽  
K. Shiba ◽  
K. Sakamoto ◽  
M. Hirose

ABSTRACTPhotoluminescence from porous silicon oxidized at 800 or 900°C in an N2 +O2 gas mixture has been investigated. The ideal passivation of the porous Si surface with thermally grown oxide results in stable, intense visible-light emission. The steady-state and time-resolved luminescence measured as functions of temperature and excitation power have indicated that a possible pathway for the light emission is the radiative recombination through localized states.


2011 ◽  
Vol 181-182 ◽  
pp. 374-377 ◽  
Author(s):  
Yuan Ming Huang ◽  
Qing Lan Ma ◽  
Bao Gai Zhai

Upon the 325 nm excitation from a helium-cadmium laser, the photoluminescence (PL) from aged porous silicon was investigated with fluorescence spectroscopy. Each PL spectrum of the aged porous silicon films contained two luminescent bands, one of the luminescent bands peaked at about 466.7 nm whereas the other luminescent band peaked at about 596.1 nm. The origin of the blue PL from aged porous silicon was discussed, and our results indicated that the blue photoluminescence of porous silicon films originated from the silicon oxide itself.


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