Solvent-assisted crystallization of two-dimensional Ruddlesden–Popper perovskite

2021 ◽  
Vol 57 (81) ◽  
pp. 10552-10555
Author(s):  
Yingjie Su ◽  
Cai Xu ◽  
Liguo Gao ◽  
Guoying Wei ◽  
Tingli Ma

A solvent-assisted method for preparing two-dimensional perovskite films was proposed to accurately control the top-down crystallization process of two-dimensional perovskites.

2021 ◽  
Author(s):  
Qizhi Xu ◽  
Boyuan Zhang ◽  
Yihang Zeng ◽  
Amirali Zangiabadi ◽  
Hongwei Ni ◽  
...  

Ultrathin porous films held together by non-covalent van der Waals interactions was obtained by a top-down approach, which is then utilized as channel material in a two-dimensional planar field-effect transistor device through easy stamp transfer.


2009 ◽  
Vol 20 (12) ◽  
pp. 2183-2191 ◽  
Author(s):  
Ji Eun Lee ◽  
John F. Kellie ◽  
John C. Tran ◽  
Jeremiah D. Tipton ◽  
Adam D. Catherman ◽  
...  

Author(s):  
Yuejuan Wan ◽  
Zejian Zhang ◽  
Haichao Liu ◽  
Jiadong Zhou ◽  
Liqun Liu ◽  
...  

The sheet-liked organic semiconductor crystals with two-dimensional (2D) packed structures play an essential role in practical applications of high-property optoelectronic devices. Here, we reported a practical example in combination with...


Crystals ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 655 ◽  
Author(s):  
Anna Drzewicz ◽  
Ewa Juszyńska-Gałązka ◽  
Wojciech Zając ◽  
Przemysław Kula

Vibrational dynamics in the glass transition and the cold crystallization process of (S)-4′-(1-methyloctyloxycarbonyl) biphenyl-4-yl 4-[7-(2,2,3,3,4,4,4-heptafluorobutoxy) heptyl-1-oxy]-benzoate (3F7HPhH7) was studied by Fourier transform infrared spectroscopy (FTIR) during cooling/heating experimental runs. The measured spectra processing was supported by quantum chemical density functional theory (DFT) calculations (frequency assignments). The perturbation-correlation moving window two-dimensional analysis (PCMW2D) was performed to examine how the height of individual absorption bands change under with temperature. Two-dimensional correlation analysis (2D-COS) was used to detect freezing-in or activation of the stochastic movements during the vitrification and the cold crystallization processes. Upon cooling, the vitrification process involves freezing-in of the stochastic movements of ester groups. Upon heating, as the cold crystallization process begins, the first to respond are the vibrations of the C–O–C and C=O groups in the rigid core.


2016 ◽  
Vol 4 (3) ◽  
pp. 1020-1027 ◽  
Author(s):  
M. Sygletou ◽  
P. Tzourmpakis ◽  
C. Petridis ◽  
D. Konios ◽  
C. Fotakis ◽  
...  

A novel top-down and universal optical technique for the effective decoration of two-dimensional (2D) nanosheets (NS), graphene oxide (GO), boron nitride (BN) and tungsten disulfide (WS2), with noble metallic nanoparticles (NPs) is reported.


1985 ◽  
Vol 50 ◽  
Author(s):  
A. D. Stalios ◽  
R. De Batist

AbstractThe crystallization behavior of a ferri-silicate α-waste glass was studied by means of several experimental techniques. The main crystal phase showed a plate-like morphology and was identified as a monoclinic pyroxene. The Johnson-Mehl-Avrami equation was used for the determination of the kinetic parameters of the process. Following both isothermal and non-isothermal techniques, the Avrami exponent, n, was found to be nearly one. The activation energy for crystal growth is Eg = 356 kJ mole−1. The crystallization process is governed by instantaneous nucleation and diffusion controlled two dimensional growth.


2013 ◽  
Vol 13 (11) ◽  
pp. 5551-5565 ◽  
Author(s):  
M. J. Newland ◽  
C. E. Reeves ◽  
D. E. Oram ◽  
J. C. Laube ◽  
W. T. Sturges ◽  
...  

Abstract. The atmospheric records of four halons, H-1211 (CBrClF2), H-1301 (CBrF3), H-2402 (CBrF2CBrF2) and H-1202 (CBr2F2), measured from air collected at Cape Grim, Tasmania, between 1978 and 2011, are reported. Mixing ratios of H-1211, H-2402 and H-1202 began to decline in the early to mid-2000s, but those of H-1301 continue to increase up to mid-2011. These trends are compared to those reported by NOAA (National Oceanic and Atmospheric Administration) and AGAGE (Advanced Global Atmospheric Experiment). The observations suggest that the contribution of the halons to total tropospheric bromine at Cape Grim has begun to decline from a peak in 2008 of about 8.1 ppt. An extrapolation of halon mixing ratios to 2060, based on reported banks and predicted release factors, shows this decline becoming more rapid in the coming decades, with a contribution to total tropospheric bromine of about 3 ppt in 2060. Top-down global annual emissions of the halons were derived using a two-dimensional atmospheric model. The emissions of all four have decreased since peaking in the late 1980s–mid-1990s, but this decline has slowed recently, particularly for H-1301 and H-2402 which have shown no decrease in emissions over the past five years. The UEA (University of East Anglia) top-down model-derived emissions are compared to those reported using a top-down approach by NOAA and AGAGE and the bottom-up estimates of HTOC (Halons Technical Options Committee). The implications of an alternative set of steady-state atmospheric lifetimes are discussed. Using a lifetime of 14 yr or less for H-1211 to calculate top-down emissions estimates would lead to small, or even negative, estimated banks given reported production data. Finally emissions of H-1202, a product of over-bromination during the production process of H-1211, have continued despite reported production of H-1211 ceasing in 2010. This raises questions as to the source of these H-1202 emissions.


1994 ◽  
Vol 361 ◽  
Author(s):  
James A. Voigt ◽  
B.A. Tuttle ◽  
T.J. Headley ◽  
D.L. Lamppa

ABSTRACTWe have characterized the pyrochlore-to-perovskite crystallization process in solution-derived Pb(Zr0.20Ti0.80)O3 thin films on (100) MgO single crystal substrates. It has been determined that the perovskite phase nucleated preferentially at the film/MgO interface out of a nanocrystalline (≈100Å grains) pyrochlore matrix. During the early stages of the pyrochlore-to-perovskite conversion process, perovskite growth proceeded nearly isotropically from the substrate to form hemispherically shaped grains. Deviations from isotropie growth were shown to result from a growth dependence based on the crystallographic orientation of a growing perovskite grain relative to the orientations of pyrochlore grains being transformed. The volume change that occurs during the pyrochlore-to-pervoskite transformation along with two-dimensional grain growth has been used to develop a mechanism for formation of porosity that commonly is concentrated in grain boundary regions.


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