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Optical spectroscopy of silicon nanowires

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Đây là một bài báo khoa học về dây nano silic trong lĩnh vực nghiên cứu công nghệ nano dành cho những người nghiên cứu sâu về vật lý và khoa học vật liệu.Tài liệu có thể dùng tham khảo cho sinh viên các nghành vật lý và công nghệ có đam mê về khoa học

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Optical spectroscopy of silicon nanowires

a Department of Chemistry and Biochemistry, University of Texas, Welch 4.212, Austin, TX78712, USA

b Institute of Physics, University of Tsukuba, Tsukuba, Ibaraki 305, Japan Received 16 December 2002; in final form 13 March 2003

Abstract

Silicon nanowires (SiNWs) were prepared by laser ablation at high temperature and studied by electron microscopy and optical spectroscopy As-synthesized SiNWs are found orderly aligned on the silica substrates, exhibiting uniform shape with a silicon crystalline core and an amorphous silicon oxide sheath Asymmetrically broadened Raman spectral peaks downshifted from 520 cm1 were observed, which related to the confinement effects of optical phonon by nanowire boundaries The SiNWs showed strong photoluminescence (PL) bands peaked at 455 and 525 nm, which quenches rapidly with an increase in temperature and may arise from the defects surrounding the silicon nanowire crystalline core

Ó 2003 Elsevier Science B.V All rights reserved

Si nanowires (SiNWs) are expected to exhibit

potentially useful electrical, optical, mechanical,

and chemical properties due to their small

di-mensions, unique shapes, and high

surface-to-volume ratio The recent progress in large-scale

production of uniform and thin SiNWs has

at-tracted investigation interests of the quantum

confinement properties and potential applications

of SiNWs [1–6] Several researchers have reported

photoluminescence (PL) from the SiNWs of

as-grown and oxidized samples at room temperature

[5,6] They ascribed the observed red, green and

blue PL peaks at 816, 470 and 420 nm to the

quantum confinement effects and the recombina-tion emissions from the defect centers, respec-tively Since the studies of PL behavior at low temperature, and the temperature dependence are important to understand the mechanism of the luminescence, we will report in this Letter the optical spectroscopic properties of the SiNWs synthesized by laser ablation at high temperature, including the Raman scattering behavior and the temperature dependence of PL

The synthesis of the SiNWs was carried out by laser ablation of a mixed target of silicon powder (99.999 wt%) and nanosized iron powder (99.9 wt%) Typical molar ratio for Si to Fe was 0.95– 0.05 A quartz tube was mounted inside a high-temperature 50 cm tube furnace The target was placed in the center of the quartz tube, which was evacuated by a mechanical rotary pump to a pressure of 1 Pa High-purity argon was then

Chemical Physics Letters 372 (2003) 763–766

www.elsevier.com/locate/cplett

* Corresponding author Present address: Department of

Material Science and Engineering, Massachusetts Institute of

Technology, 77 Massachusetts Ave., #16-244, Cambridge, MA

02139, USA Fax: +6173243300.

E-mail address: jifa@mit.edu (J Qi).

0009-2614/03/$ - see front matter Ó 2003 Elsevier Science B.V All rights reserved.

doi:10.1016/S0009-2614(03)00504-9

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passed through the quartz tube at a flow rate of

50–100 standard cubic centimeters per second

(sccm) A pulsed XeCl excimer laser (308 nm, pulse

repetition 10 Hz, energy 170 mJ; Lambda Physik

product) was used to ablate the target for 3 h while

the furnace temperature was kept at 1200°C The

product was collected from the silica tube wall A

Hitachi H9000 and a JEOL 2010 transmission

electron microscopes (TEM) working at 200 kV

were used to characterize the products

Fig 1 shows the typical electron microscopic

image of the morphology of the SiNWs It was

observed that the product exemplified high purity

with a uniform diameter 20 nm and consisted of

most of the SiNWs aligning on the substrate Fig

2 shows a high resolution TEM (HRTEM) image

of a single SiNW with a diameter of about 18 nm

The (1 1 1) lattice fringes with the interplanar

spacing of 0.31 nm and the corresponding selected

area electron diffraction (SAED) patterns show the

SiNW consisted of a crystalline Si structure

Ad-ditionally, there is a thin amorphous silicon oxide

layer (about 3 nm) sheathing the crystalline core of

the SiNW The sheath of SiO2is determined by the

X-ray photon emission spectral measurements

The optical properties of SiNWs depend on

their nanosized crystallites and the surrounding

oxide layers Raman scattering spectra of SiNWs

were recorded on a Jasco NRS-1800 Raman

spectrometer in the back-scattering configuration, using a 514.5 nm line of Arþ laser at normal in-cidence The Raman scattered light was dispersed

by a triple-monochromator and recorded by a li-quid nitrogen-cooled CCD detector To avoid the laser-induced thermal effects, the exciting laser power was kept below 0.1 mW on the sample Fig 3 shows the Raman scattering spectra of the SiNWs and crystal silicon A very sharp and

Fig 1 A typical SEM image of the morphology of aligned

silicon nanowires of uniform diameter distribution on a silica

substrate.

Fig 2 A HRTEM image of a single SiNW Two-dimensional (1 1 1) lattice fringes can be seen, and a thin amorphous oxide layer surrounds the crystalline core The inset shows the cor-responding SAED pattern.

Fig 3 Raman spectra at room temperature of a single crys-talline silicon (thick solid line), SiNWs (dotted line) and the theoretical fitting results (thin solid line) The power output of laser at samples is about 70 W/cm 2

764 J Qi et al / Chemical Physics Letters 372 (2003) 763–766

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intense Raman line at 520 cm1with the full width

at half maximum (FWHM) of 4:7 cm1 was

wit-nessed in the Raman spectrum of crystal Si This

peak corresponds to the degenerate zone-center

optical phonon mode of crystal Si All SiNW

samples exhibit similar Raman spectral peaks

red-shifted from 520 cm1 and a small shoulder at

495 cm1 The main peak near 520 cm1

corre-sponds to the first-order optical phonon of

crys-talline Si The small broad peak at 495 cm1 was

attributed to the amorphous silicon that covers

SiNWs or distributed on the silica substrate, which

has a Raman structure between 400 and 550 cm1

peaked at 480 cm1[7] Asymmetrically broadened

and frequency downshifted line shapes are usually

observed in nanocrystalline and related to phonon

confinement effects by nanocrystallite boundaries,

hence the average crystallite size was estimated

according to the strong phonon confinement model

[8] The Raman intensity profile can be written as

IðxÞ ¼

Z 1

0

expðqD=2pÞ2dq3

ðx  xðqÞÞ2þ ðC0=2Þ2; ð1Þ

where xðqÞ is the phonon dispersion function, q is

the normalized phonon momentum, C0 is the

natural phonon linewidth of crystalline silicon,

and D is the size of crystal Eq (1) was used to fit

the Raman spectra The continuous line in Fig 3

shows the best-fit result, and the average crystal

size of nanowires D¼ 11:3 nm was obtained, as

shown in Fig 3 The good agreement in spectral

features between experimental and calculated

Ra-man spectra indicates that the identification of the

Raman peak of SiNW is correct However, the

diameters determined by Raman scattering

mea-surements were smaller than that obtained from

SEM and TEM observation The reasons for this

disparity are considered below First, only the

crystallite contributes to the main Raman

scat-tering peaks, our nanowires are capped by the

amorphous oxide layer and amorphous silicon,

their contributions to the Raman spectra were not

calculated Second, the existence of defects and

stresses in SiNWs can have a profound influence

on the Raman spectra of SiNWs

The PL measurements have been performed by

an experimental setup consisting of the excitation

source of a He–Cd laser (325 nm) and a 27.5 cm monochromator equipped with a liquid nitrogen cooled CCD detector In order to investigate the

PL as a function of temperature, samples were placed in a temperature-variable cryostat The PL spectra were measured at temperatures ranging from 10 to 300 K Fig 4 shows the PL spectra of SiNWs at different temperatures Two strong emission bands in the green and blue regions re-vealed peaking at 455 and 525 nm at low temper-ature, respectively The band that peaked at 455

nm is close to the observation results on the silica nanowires [5] that was ascribed to originate from the oxygen vacancies, while the band peaked at

525 nm is close to the results reported for as-grown silicon nanowires [6] According to theoretical prediction, visible light emission due to size con-finement can occur only when the mean size of the

Si crystalline is less than that of free exciton of silicon Therefore, these two peaks are not con-sidered to be due to the quantum confinement ef-fect Instead, Yu et al.Õs explanation that the green and blue PL emissions come from the radiative recombination from the defect centers in the over-coated silicon oxide layer and the interface be-tween crystalline core and amorphous sheath layer, such as oxygen vacancies [9], seems to agree with this observation

The inset curve in Fig 4 shows the integrated

PL intensity of SiNWs as a function of

tempera-Fig 4 PL spectra of SiNWs at different temperatures Inset is a temperature dependence of integrated PL intensity versus temperature The solid line shows the fit results.

J Qi et al / Chemical Physics Letters 372 (2003) 763–766 765

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ture The PL intensities decrease rapidly with an

increase of temperature The thermal quenching of

the luminescence is considered to originate from

the thermal ionization of electrons or holes

trap-ped on the defect centers in the sheath or interface

layer On the basis of two thermally activated

non-radiative recombination model, the temperature

dependence of the luminescence intensity can be

simply written by [10]

1þ CAexpðEA=kTÞ þ CBexpðEB=kTÞ;

ð2Þ

EA and EB are thermal activation energies of

cen-ters A and B, respectively, while CA and CB are

temperature-independent factors The fit result by

using Eq (2) presented by the solid line in the inset

of Fig 4 shows a good coincidence with the

ex-periment results The best-fit parameters are

EA ¼ 20 meV and EB¼ 104 meV, respectively The

EA value is very close to the binding energy of

excitons in silicon The related PL thermal

quenching process can be considered to be a

de-crease of luminescent carriers due to the thermally

induced exciton ionization in the SiNW EBmay be

related to the deep trap states The related PL

thermal quenching process can be considered in

terms of excited carriers that are trapped by the

defect levels and relaxed to the ground state

through a non-radiative process causing the

de-crease of luminescence with an inde-crease in

tem-perature Thus, the excitation process of the

observed luminescent centers in a SiNW is

con-sidered as light-created excited carriers in the

SiNW and the carriers are trapped at the defect

centers and relaxed to the ground state by

radia-tive and non-radiaradia-tive processes

In conclusion, SiNWs were synthesized by laser

ablation at high temperature The typical SiNW

exhibits a uniform shape of silicon crystallite sheathed by an amorphous silicon oxide layer A downshifted and broadened Raman spectral peak was observed, which is related to the confinement effects of optical phonons by the nanowire boundaries SiNWs emit green and blue light un-der ultraviolet photoexcitation The green and blue bands are related to the radiative recombi-nation of the defect centers in the outer oxide layer

of the SiNWs The luminescence quenches rapidly with an increase of temperature

Acknowledgements The authors would like to thank the Research Center for Advanced Carbon Materials, AIST, for use of the micro-Raman spectrometer instrument

References

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[3] Y.F Zhang, Y.H Zhang, N Wang, D.P Yu, C.S Lee,

I Bello, S.T Lee, Appl Phys Lett 72 (1998) 1835 [4] J Qi, Y Masumoto, Mater Res Bull 36 (2001) 1407 [5] D.P Yu, Q.L Hang, Y Ding, H.Z Zhang, Z.G Bai, J.J Wang, Y.H Zou, W Qian, G.C Xiong, S.Q Feng, Appl Phys Lett 73 (1998) 3076.

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[9] H Nishikawa, T Shiroyama, R Nakamura, Y Ohki, K Nagasawa, Y Hama, Phys Rev B 45 (1992) 586 [10] G Davies, Phys Rep 176 (1989) 83.

766 J Qi et al / Chemical Physics Letters 372 (2003) 763–766

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