Controlling the direct growth of graphene on an insulating substrate by the solid phase reaction of a polymer layer

RSC Advances ◽  
2014 ◽  
Vol 4 (72) ◽  
pp. 38450-38454 ◽  
Author(s):  
Golap Kalita ◽  
Takatoshi Sugiura ◽  
Yuji Wakamatsu ◽  
Ryo Hirano ◽  
Masaki Tanemura
Keyword(s):  
Thin Film ◽  
Polyvinyl Alcohol ◽  
Growth Process ◽  
Solid Phase ◽  
Polymer Layer ◽  
Solid Phase Reaction ◽  
Phase Reaction ◽  
Graphene Growth ◽  
Direct Growth

Controllable direct graphene growth process on an insulating substrate (SiO2/Si and sapphire) by the solid phase reaction of polymer (polyvinyl alcohol) thin film.

scholarly journals A TEM STUDY OF Pd-Si THIN FILM SOLID-PHASE REACTION

1986 ◽  
Vol 35 (7) ◽  
pp. 965
Author(s):  
ZHANG JING ◽  
LIU AN-SHENG ◽  
WU ZI-QIN ◽  
GUO KE-XIN
Keyword(s):  
Thin Film ◽  
Solid Phase ◽  
Solid Phase Reaction ◽  
Phase Reaction ◽  
Si Thin Film

scholarly journals Red Carbon: a Carbon-Oxygen-based covalent semiconductor for selective amine sensing

2021 ◽  
Author(s):  
Paolo Giusto ◽  
Daniel Cruz ◽  
Yael Rodriguez ◽  
Regina Rothe ◽  
Nadezda Tarakina
Keyword(s):  
Thin Film ◽  
Organic Semiconductor ◽  
Solid Phase ◽  
Carbon Films ◽  
Semiconductor Materials ◽  
Solid Phase Reaction ◽  
Phase Reaction ◽  
Sensing Applications ◽  
Organic Semiconductor Materials ◽  
Thin Carbon

The requirements for organic semiconductor materials and new methods for their synthesis at low temperature have risen over the last decades, especially due to concerns of sustainability. Herein, we present an innovative method for the synthesis of a so-called “red carbon” thin film, being composed of carbon and oxygen, only. This material was already described by Kappe and Ziegler at the beginning of the 20th century, but now can complement the current research on covalent organic semiconductor materials. The herein described red carbon can be homogeneous deposited on glass substrates as thin ilms which reveal a highly ordered structure. The films are highly reactive towards amines and were employed as amine vapor sensors for a scope of analogous amines. The gas-to-solid phase reaction causes a significant change of the films optical properties in all cases, blue-shifting the bandgap and the photoluminescence spectra from the red to the near UV range. The irreversible chemical reaction between the thin film and the vapor was also exploited for the preparation of nitrogen containing thin carbon films. We expect the herein presented red carbon material is of interest not only for sensing applications, but also in optoelectronics.

Kinetic shape formation during Gd thin film and Si(100) solid phase reaction

1999 ◽  
Vol 74 (12) ◽  
pp. 1672-1674 ◽  
Author(s):  
G. L. Molnár ◽  
G. Petö ◽  
Z. Vértesy ◽  
E. Zsoldos
Keyword(s):  
Thin Film ◽  
Solid Phase ◽  
Solid Phase Reaction ◽  
Phase Reaction ◽  
Shape Formation

Solid-Phase Reaction of Ni with Amorphous SiGe Thin Film on SiO2

1997 ◽  
Vol 36 (Part 2, No. 12B) ◽  
pp. L1637-L1640 ◽  
Author(s):  
Zhonghe Jin ◽  
Gururaj A. Bhat ◽  
Milton Yeung ◽  
Hoi S. Kwok ◽  
Man Wong
Keyword(s):  
Thin Film ◽  
Solid Phase ◽  
Solid Phase Reaction ◽  
Phase Reaction

Thickness Dependent Phase Formation in Fe Thin Film and Si Substrate Solid Phase Reaction

1995 ◽  
Vol 402 ◽  
Author(s):  
G Y. Molnár ◽  
G. Pető ◽  
E. Zsoldos ◽  
Z. E. Horváth ◽  
N. Q. Khánh
Keyword(s):  
Thin Film ◽  
Film Thickness ◽  
Phase Formation ◽  
Solid Phase ◽  
Iron Film ◽  
Solid Phase Reaction ◽  
Phase Reaction ◽  
Si Substrate ◽  
Transmission Electron ◽  
Initial Iron

AbstractThe solid phase reaction of Fe thin films with (111) Si substrate was investigated at constant annealing temperature and time (700°C, 7 minutes) as a function of the initial iron film thickness (from 5 nm to 27.5 um in 2.5 nm steps). The formed phases were analysed by X-ray diffraction, Rutherford backscattering and transmission electron microscopy and optical microscopy.After annealing FeSi phase was detected in the thinner samples. Samples with Fe layers thicker than 12.5 nm contained a β-FeSi2 phase. This special phase sequence was explained with the help of a nucleation controlled phase formation model, taking into consideration the critical radius of nuclei of the new phase. The advantages of using the film thickness as a variable during investigation of solid phase thin film reactions and the probable substrate effects are also discussed.

Solid phase reaction in Ti(thin film)/Si(substrate) with Mo interlayer: SXES and PEEM study

2004 ◽  
Vol 464-465 ◽  
pp. 107-111 ◽  
Author(s):  
J. Labis ◽  
H. Namatame ◽  
M. Taniguchi ◽  
C. Kamezawa ◽  
M. Hirai ◽  
...  
Keyword(s):  
Thin Film ◽  
Solid Phase ◽  
Solid Phase Reaction ◽  
Phase Reaction ◽  
Si Substrate

scholarly journals Fe3O4@C Nanoparticles Synthesized by In Situ Solid-Phase Method for Removal of Methylene Blue

Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 330
Author(s):  
Hengli Xiang ◽  
Genkuan Ren ◽  
Yanjun Zhong ◽  
Dehua Xu ◽  
Zhiye Zhang ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Solid Phase ◽  
Raw Materials ◽  
Phase Method ◽  
Maximum Adsorption Capacity ◽  
High Catalytic Activity ◽  
Solid Phase Reaction ◽  
Phase Reaction ◽  
High Concentrations

Fe3O4@C nanoparticles were prepared by an in situ, solid-phase reaction, without any precursor, using FeSO4, FeS2, and PVP K30 as raw materials. The nanoparticles were utilized to decolorize high concentrations methylene blue (MB). The results indicated that the maximum adsorption capacity of the Fe3O4@C nanoparticles was 18.52 mg/g, and that the adsorption process was exothermic. Additionally, by employing H2O2 as the initiator of a Fenton-like reaction, the removal efficiency of 100 mg/L MB reached ~99% with Fe3O4@C nanoparticles, while that of MB was only ~34% using pure Fe3O4 nanoparticles. The mechanism of H2O2 activated on the Fe3O4@C nanoparticles and the possible degradation pathways of MB are discussed. The Fe3O4@C nanoparticles retained high catalytic activity after five usage cycles. This work describes a facile method for producing Fe3O4@C nanoparticles with excellent catalytic reactivity, and therefore, represents a promising approach for the industrial production of Fe3O4@C nanoparticles for the treatment of high concentrations of dyes in wastewater.

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