scholarly journals Influence of Hydrogen Bonding on the Surface Diffusion of Molecular Glasses: Comparison of Three Triazines

2017 ◽  
Vol 121 (29) ◽  
pp. 7221-7227 ◽  
Author(s):  
Yinshan Chen ◽  
Men Zhu ◽  
Audrey Laventure ◽  
Olivier Lebel ◽  
M. D. Ediger ◽  
...  
2016 ◽  
Vol 120 (32) ◽  
pp. 8007-8015 ◽  
Author(s):  
Yinshan Chen ◽  
Wei Zhang ◽  
Lian Yu

CrystEngComm ◽  
2019 ◽  
Vol 21 (11) ◽  
pp. 1734-1741 ◽  
Author(s):  
Audrey Laventure ◽  
Dominic Lauzon ◽  
Christian Pellerin ◽  
Olivier Lebel

Hydrogen bonding is a key element in crystal engineering to direct crystal packing. Here, hydrogen bonding with molecular glasses is rather exploited to thwart crystallization.


2017 ◽  
Vol 19 (44) ◽  
pp. 29905-29912 ◽  
Author(s):  
K. L. Ngai ◽  
Marian Paluch ◽  
Cristian Rodríguez-Tinoco

The primitive/JG relaxation explains the same surface diffusion coefficient in ordinary, ultrastable and thin film glasses of OTP and TPD.


2016 ◽  
Vol 18 (3) ◽  
pp. 1681-1692 ◽  
Author(s):  
Audrey Laventure ◽  
Guillaume De Grandpré ◽  
Armand Soldera ◽  
Olivier Lebel ◽  
Christian Pellerin

Mexylaminotriazine derivatives form molecular glasses with outstanding glass-forming ability (GFA), glass kinetic stability (GS), and tunable glass transition temperature. This work establishes key molecular parameters for efficient glass engineering.


Soft Matter ◽  
2016 ◽  
Vol 12 (44) ◽  
pp. 9115-9120 ◽  
Author(s):  
Yue Zhang ◽  
Richard Potter ◽  
William Zhang ◽  
Zahra Fakhraai

2017 ◽  
Vol 114 (19) ◽  
pp. 4915-4919 ◽  
Author(s):  
Yue Zhang ◽  
Zahra Fakhraai

Tobacco mosaic virus is used as a probe to measure surface diffusion of ultrathin films of N,N′-Bis(3-methylphenyl)-N,N′-diphenylbenzidine (TPD) (12 nm <h< 53 nm, where h is the film thickness) at various temperatures below the glass transition temperature, 𝐓𝐠, of all films. As the film thickness is decreased, 𝐓𝐠 decreases rapidly and the average film dynamics are enhanced by 6–14 orders of magnitude. We show that the surface diffusion is invariant of the film thickness decrease and the resulting enhanced overall mobility. The values of the surface diffusion coefficient and its temperature dependence are invariant of film thickness and are the same as the corresponding bulk values (h=400 nm). For the thinnest films (h<20 nm), the effective activation energy for rearrangement (temperature dependence of relaxation times) becomes smaller than the activation energy for surface diffusion. These results suggest that the fast surface diffusion is decoupled from film relaxation dynamics and is a solely free surface property.


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