Phase Transitions in Thin Block Copolymer Films

MRS Bulletin ◽  
2010 ◽  
Vol 35 (6) ◽  
pp. 457-465 ◽  
Author(s):  
Edward J. Kramer

AbstractDavid Turnbull's experiments and theoretical insights paved the way for much of our modern understanding of phase transitions in materials. In recognition of his contributions, this lecture will concentrate on phase transitions in a material system not considered by Turnbull, thin diblock copolymer films. Well-ordered block copolymer films are attracting increasing interest as we attempt to extend photolithography to smaller dimensions. In the case of diblock copolymer spheres, an ordered monolayer is hexagonal, but the ordered bulk is body-centered cubic (bcc). There is no hexagonal plane in the bcc structure, so a phase transition must occur as n, the number of layers of spheres in the film, increases. How this phase transition occurs with nand how it can be manipulated is the subject of the first part of my presentation. In the second part of the talk, I show that monolayers of diblock copolymer spheres and cylinders undergo order-to-disorder transitions that differ greatly from those of the bulk. These ordered 2D monolayers are susceptible to phonon-generated disorder as well as to thermal generation of defects, such as dislocations, which, while they are line defects in 3D, are point defects in 2D. The results are compared to the theories of melting of 2D crystals (spheres) and of 2D smectic liquid crystals (cylinders), a comparison that will allow us to understand most, but not all, of the features of these order-disorder transitions that occur as the temperature is increased.

Nanoscale ◽  
2013 ◽  
Vol 5 (10) ◽  
pp. 4351 ◽  
Author(s):  
Ara Jo ◽  
Gil Ho Gu ◽  
Hong Chul Moon ◽  
Sung Hyun Han ◽  
Sang Ho Oh ◽  
...  

2006 ◽  
Vol 39 (8) ◽  
pp. 3024-3037 ◽  
Author(s):  
K. S. Lyakhova ◽  
A. V. Zvelindovsky ◽  
G. J. A. Sevink

2009 ◽  
Vol 42 (4) ◽  
pp. 1017-1023 ◽  
Author(s):  
Jung Hyun Park ◽  
Yujie Sun ◽  
Yale E. Goldman ◽  
Russell J. Composto

2013 ◽  
Vol 684 ◽  
pp. 94-98 ◽  
Author(s):  
Ling Zhou ◽  
Yong Liu ◽  
Bing Hua Sun

Structure transitions induced by selective solvents in diblock copolymer films are investigated by density functional theory. By changing the selectivity and the packing fraction of selective solvents, the disorder-lamellar transition, the position switched lamellar phase transitions and the reentrant transitions are observed. Phase diagrams are constructed to clarify these effects. The results provide an effective way to control the transitions between the different microstructures.


2005 ◽  
Vol 17 (21) ◽  
pp. 2618-2622 ◽  
Author(s):  
B. J. Kim ◽  
J. J. Chiu ◽  
G.-R. Yi ◽  
D. J. Pine ◽  
E. J. Kramer

Soft Matter ◽  
2020 ◽  
Vol 16 (12) ◽  
pp. 3005-3014
Author(s):  
Boris Rasin ◽  
Benjamin J. Lindsay ◽  
Xingchen Ye ◽  
Jeffrey S. Meth ◽  
Christopher B. Murray ◽  
...  

Nanorods bridge vertical cylinders in vertical cylinder diblock copolymer films.


Author(s):  
L. T. Pawlicki ◽  
R. M. Siegoczyński ◽  
S. Ptasznik ◽  
K. Marszałek

AbstractThe main purpose of the experiment was a thermodynamic research with use of the electric methods chosen. The substance examined was olive oil. The paper presents the resistance, capacitive reactance, relative permittivity and resistivity of olive. Compression was applied with two mean velocities up to 450 MPa. The results were shown as functions of pressure and time and depicted on the impedance phase diagram. The three first order phase transitions have been detected. All the changes in material parameters were observed during phase transitions. The material parameters measured turned out to be the much more sensitive long-time phase transition factors than temperature. The values of material parameters and their dependence on pressure and time were compared with the molecular structure, arrangement of molecules and interactions between them. Knowledge about olive oil parameters change with pressure and its phase transitions is very important for olive oil production and conservation.


2017 ◽  
Vol 19 (39) ◽  
pp. 26645-26650 ◽  
Author(s):  
Qingxin Zeng ◽  
Chuang Yao ◽  
Kai Wang ◽  
Chang Q. Sun ◽  
Bo Zou

H–O bond energy governs the PCx for Na/H2O liquid–VI–VII phase transition. Solute concentration affects the path of phase transitions differently with the solute type. Solute–solute interaction lessens the PC2 sensitivity to compression. The PC1 goes along the liquid–VI boundary till the triple phase joint.


2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Đorđe Dangić ◽  
Olle Hellman ◽  
Stephen Fahy ◽  
Ivana Savić

AbstractThe proximity to structural phase transitions in IV-VI thermoelectric materials is one of the main reasons for their large phonon anharmonicity and intrinsically low lattice thermal conductivity κ. However, the κ of GeTe increases at the ferroelectric phase transition near 700 K. Using first-principles calculations with the temperature dependent effective potential method, we show that this rise in κ is the consequence of negative thermal expansion in the rhombohedral phase and increase in the phonon lifetimes in the high-symmetry phase. Strong anharmonicity near the phase transition induces non-Lorentzian shapes of the phonon power spectra. To account for these effects, we implement a method of calculating κ based on the Green-Kubo approach and find that the Boltzmann transport equation underestimates κ near the phase transition. Our findings elucidate the influence of structural phase transitions on κ and provide guidance for design of better thermoelectric materials.


RSC Advances ◽  
2021 ◽  
Vol 11 (29) ◽  
pp. 17622-17629
Author(s):  
Ae Ran Lim

We studied the thermal behavior and structural dynamics of [NH3(CH2)3NH3]CdBr4 near phase transition temperatures.


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