Higher Crystalline Volume Yields from Excimer Laser Crystallization of Amorphous Silicon with an Asymmetrical Peak Pulse Profile

2007 ◽  
Vol 31 ◽  
pp. 185-188 ◽  
Author(s):  
A.A.D.T. Adikaari ◽  
N.K. Mudugamuwa ◽  
S.R.P. Silva

Excimer lasers have been utilized for the crystallization of hydrogenated amorphous silicon for electronic applications. These lasers typically operate in the ultraviolet and hence photons are absorbed by the silicon thin films within a few nanometres of the surface, melting and solidifying the silicon on a nanosecond timescale, often without affecting the underlying substrate. This technique enables the use of inexpensive substrates, such as glass, which are highly preferable for low cost, large-area electronic devices. The depth of crystallization becomes important for applications such as photovoltaics, which depends on a number of factors; with laser beam shape one of the most significant. A Gaussian beam profile has been reported to be best suited for controlled evolution of hydrogen during crystallization with minimum surface damage. Previous reports show the typical energy densities of crystallization, comparing the crystalline volume and surface roughness of the resultant films for different film thicknesses. We report significant reductions of laser energy densities for crystallization by modifying the Gaussian pulse profile, while retaining the controlled evolution of hydrogen from hydrogenated amorphous silicon films. An asymmetrical, shorter pulse profile retains the desirable gradual leading edge of the Gaussian pulse for controlled evaporation of hydrogen, while increasing the peak energy. The resultant films show increased surface roughness along with higher crystalline volumes, which may be beneficial for photovoltaics.

1994 ◽  
Vol 336 ◽  
Author(s):  
D.M. Tanenbaum ◽  
A. Laracuente ◽  
A.C. Gallagher

ABSTRACTA scanning tunneling microscope has been used to study the topology of the surface of device-quality, hydrogenated Amorphous silicon deposited by rf discharge from silane or “hot wire” CVD. The substrates were oxide-free single-crystal silicon or GaAs. Films studied were either grown in our laboratory and observed with no air exposure, or grown at other laboratories producing device-quality photovoltaic cells and viewed after air exposures of less than 30 Minutes. Thin films (10 nm) representing early growth stages appear significantly smoother than the thicker films. The topology of thick films (> 50 nm) has large variations over individual samples. While many regions can be characterized as “rolling hills”, atomically flat areas are sometimes observed nearby in our films. In most regions the observed slopes were 10% or less from the horizontal, but some steep-sided valleys, indicating incipient voids, are seen. Overall surface roughness measured on sub-Micron areas of our films is very inhomogeneous. Uniformity of the films grown off site was much better, although no atomically flat regions were observed, surface roughness can be estimated.


1993 ◽  
Vol 321 ◽  
Author(s):  
Nagarajan Sridhar ◽  
D. D. L. Chung ◽  
W. A. Anderson ◽  
L. P. Fu ◽  
A. Petrou

ABSTRACTHydrogenated amorphous silicon thick films deposited by dc glow discharge on molybdenum substrates were annealed by a pulsed Nd:glass laser. Mass spectrometry showed hydrogen remaining in all the laser annealed films. The amount of hydrogen remaining decreased with decreasing scan rate. The hydrogen evolved upon heating at 365 °C and mainly at 658 °C before laser annealing, but at 365, 575 (Mainly) and 645 °C after laser annealing, indicating weakening of the silicon-hydrogen bonding after laser annealing. The presence of hydrogen inhibited crystallization, as indicated by Raman scattering. The photo and dark conductivity of the film increased by one and three orders of magnitude respectively with increasing laser energy density up to 12 J/cm2 at a fixed scan rate. This Means that the photoresponse was decreased with laser annealing, in spite of the associated increase in crystallinity. This photoresponse decrease is attributed to the hydrogen evolution.


2000 ◽  
Vol 609 ◽  
Author(s):  
J. M. Shannon ◽  
E. G. Gerstner

ABSTRACTIt has been shown that useful current gains can be obtained in hot-electron device structures containing very thin chromium disilicide layers of nanometer dimensions in hydrogenated amorphous silicon [1]. The a-Si:H/a-CrSi2/a-Si:H device structure made using PECVD and sputtering techniques naturally forms a hot-electron transistor device where the electrons are emitted across a high potential barrier on one side of the silicide and are collected over a low barrier on the other. Recent results [2] have shown that current gains can be in excess of 40 in structures having a-CrSi2 bases ∼1 nm thick.Here we outline the relatively simple technology used to make these devices and examine their performance as phototransistors in which the photo-current is amplified by hot-electron transistor action. The speed of response can be maximised by operating the phototransistor with high electric field across the collector since it is the transit time of the photo-induced carriers that determines the response time. We show that these devices provide a useful new active element for large area amorphous silicon electronics.


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