Short-Range Migration of A-Site Cations Inhibit Photoinduced Phase Segregation in FAxMAyCs1–x–yPbI3–zBrz Single Crystals

Author(s):  
Kaiyu Wang ◽  
Qing Yao ◽  
Jie Zhang ◽  
Chenyu Shang ◽  
Changqian Li ◽  
...  
2021 ◽  
Vol 6 (3) ◽  
pp. 837-847
Author(s):  
Pronoy Nandi ◽  
Zijia Li ◽  
Younghoon Kim ◽  
Tae Kyu Ahn ◽  
Nam-Gyu Park ◽  
...  
Keyword(s):  

2009 ◽  
Vol 95 (17) ◽  
pp. 171907 ◽  
Author(s):  
Mianliang Huang ◽  
Thomas A. Lograsso

2001 ◽  
Vol 79 (12) ◽  
pp. 1786-1788 ◽  
Author(s):  
A. G. Schrott ◽  
J. A. Misewich ◽  
M. Copel ◽  
D. W. Abraham ◽  
Y. Zhang

2019 ◽  
Vol 58 (9) ◽  
pp. 2893-2898 ◽  
Author(s):  
Wenxin Mao ◽  
Christopher R. Hall ◽  
Anthony S. R. Chesman ◽  
Craig Forsyth ◽  
Yi‐Bing Cheng ◽  
...  

1988 ◽  
Vol 74 (2) ◽  
pp. 295-303 ◽  
Author(s):  
Andre´e Kahn ◽  
Tome´ Gbehi ◽  
Jeanine Thery ◽  
Jean-Jacques Legendre

2020 ◽  
Vol 235 (4-5) ◽  
pp. 117-125
Author(s):  
Myroslava Horiacha ◽  
Maximilian K. Reimann ◽  
Jutta Kösters ◽  
Vasyl‘ I. Zaremba ◽  
Rainer Pöttgen

AbstractThe quaternary gallium-rich intermetallic phases RE2Pt3Ga4In with RE = Y and Gd-Tm were synthesized by arc-melting of the elements and subsequent annealing. Small single crystals were obtained by high-frequency annealing of the samples in sealed tantalum ampoules. The polycrystalline samples were characterized through their X-ray powder patterns. The RE2Pt3Ga4In phases crystallize with a site ordering variant of the orthorhombic Y2Rh3Sn5 type, space group Cmc 21. The structures of Gd2Pt3Ga4In, Dy2Pt3Ga4.14In0.86, Er2Pt3Ga4.17In0.83 and Tm2Pt3Ga4.21In0.79 were refined from single-crystal X-ray diffraction data. The single crystals reveal small homogeneity ranges RE2Pt3Ga4±xIn1±x. The striking geometrical structural building units are slightly distorted trigonal prisms around the three crystallographically independent platinum atoms: Pt1@RE4Ga2, Pt2@RE2Ga4 and Pt3@RE2Ga2In2. Based on these prismatic building units, the RE2Pt3Ga4In structures can be described as intergrowth variants of TiNiSi and NdRh2Sn4 related structural slabs. Temperature dependent magnetic susceptibility studies of Gd2Pt3Ga4In and Tb2Pt3Ga4In show Curie-Weiss behavior and the experimental magnetic moments confirm stable trivalent gadolinium respectively terbium. Gd2Pt3Ga4In and Tb2Pt3Ga4In order antiferromagnetically at TN = 15.8(1) and 26.0(1) K. Magnetization curves at 3 K show field-induced spin reorientations.


2020 ◽  
Vol 22 (5) ◽  
pp. 3105-3111 ◽  
Author(s):  
Chao Wu ◽  
Daoyou Guo ◽  
Peigang Li ◽  
Shunli Wang ◽  
Aiping Liu ◽  
...  

Four types of organic cation-mixed single crystals were successfully synthesized by partially substituting A site cations to investigate the effect of organic cations on structure, optical features, thermal stability, and electrical transport properties.


2016 ◽  
Vol 52 (10) ◽  
pp. 2055-2058 ◽  
Author(s):  
Ivan Peran ◽  
Matthew D. Watson ◽  
Osman Bilsel ◽  
Daniel P. Raleigh

Selenomethionine is a short range quencher of p-cyanophenylalanine fluorescence and these residues provide a site-specific probe of protein helical structure.


Glycobiology ◽  
2020 ◽  
Author(s):  
Jonathon E Mohl ◽  
Thomas A Gerken ◽  
Ming-Ying Leung

Abstract Mucin-type O-glycosylation is one of the most common posttranslational modifications of proteins. The abnormal expression of various polypeptide GalNAc-transferases (GalNAc-Ts) which initiate and define sites of O-glycosylation are linked to many cancers and other diseases. Current O-glycosyation prediction programs utilize O-glycoproteomics data obtained without regard to the transferase isoform (s) responsible for the glycosylation. With 20 different GalNAc-Ts in humans, having an ability to predict and interpret O-glycosylation sites in terms of specific GalNAc-T isoforms is invaluable. To fill this gap, ISOGlyP (Isoform-Specific O-Glycosylation Prediction) has been developed. Using position-specific enhancement values generated based on GalNAc-T isoform-specific amino acid preferences, ISOGlyP predicts the propensity that a site would be glycosylated by a specific transferase. ISOGlyP gave an overall prediction accuracy of 70% against in vivo data, which is comparable to that of the NetOGlyc4.0 predictor. Additionally, ISOGlyP can identify the known effects of long- and short-range prior glycosylation and can generate potential peptide sequences selectively glycosylated by specific isoforms. ISOGlyP is freely available for use at ISOGlyP.utep.edu. The code is also available on GitHub (https://github.com/jonmohl/ISOGlyP).


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