Yadollah Gharayebi

Dr. Yadollah Gharayebi


Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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11 July 2012 in Discover Nano
Verified
Journal Article
Open access
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Arash DehzangiArash Dehzangi
Arash Dehzangi
AAA Makarimi Abdullah
A Makarimi Abdullah
FLFarhad Larki
Farhad Larki
SHSabar D Hutagalung
Sabar D Hutagalung
ESElias Saion
Elias Saion
YGYadollah Gharayebi
Yadollah Gharayebi
The junctionless nanowire transistor is a promising alternative for a new generation of nanotransistors. In this letter the atomic force microscopy nanolithography with two wet etching processes was implemented to fabricate simple structures as double gate and single gate junctionless silicon nanowire transistor on low doped p-type silicon-on-insulator wafer. The etching process was developed and optimized in the present work compared to our previous works. The output, transfer characteristics and drain conductance of both structures were compared. The trend for both devices found to be the same but differences in subthreshold swing, ‘on/off’ ratio, and threshold voltage were observed. The devices are ‘on’ state when performing as the pinch off devices. The positive gate voltage shows pinch off effect, while the negative gate voltage was unable to make a significant effect on drain current. The charge transmission in devices is also investigated in simple model according to a junctionless transistor principal.

5 August 2011 in Molecules
Verified
Journal Article
Open access
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HJHossein Jahangirian
Hossein Jahangirian
JHJelas Haron
Jelas Haron
NYNor Azah Yusof
Nor Azah Yusof
SSSidik Silong
Sidik Silong
AKAnuar Kassim
Anuar Kassim
YGYadollah Gharayebi
Yadollah Gharayebi
Fatty hydroxamic acid derivatives were synthesized using Lipozyme TL IM catalyst at biphasic medium as the palm kernel oil was dissolved in hexane and hydroxylamine derivatives were dissolved in water: (1) N-methyl fatty hydroxamic acids (MFHAs); (2) N-isopropyl fatty hydroxamic acids (IPFHAs) and (3) N-benzyl fatty hydroxamic acids (BFHAs) were synthesized by reaction of palm kernel oil and N-methyl hydroxylamine (N-MHA), N-isopropyl hydroxylamine (N-IPHA) and N-benzyl hydroxylamine (N-BHA), respectively. Finally, after separation the products were characterized by color testing, elemental analysis, FT-IR and 1H-NMR spectroscopy. For achieving the highest conversion percentage of product the optimum molar ratio of reactants was obtained by changing the ratio of reactants while other reaction parameters were kept constant. For synthesis of MFHAs the optimum mol ratio of N-MHA/palm kernel oil = 6/1 and the highest conversion was 77.8%, for synthesis of IPFHAs the optimum mol ratio of N-IPHA/palm kernel oil = 7/1 and the highest conversion was 65.4% and for synthesis of BFHAs the optimum mol ratio of N-BHA/palm kernel oil = 7/1 and the highest conversion was 61.7%.

13 July 2013 in Research on Chemical Intermediates
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Journal Article
Closed access
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MAM. B. Ahmad
M. B. Ahmad
YGYadollah Gharayebi
Yadollah Gharayebi
MSM. S. Salit
M. S. Salit
MHMohd Zobir Bin Hussien
Mohd Zobir Bin Hussien
KSK. Shameli
K. Shameli
KBKasra Behzad
Kasra Behzad