scholarly journals Electronic properties of correlated metals in the vicinity of a charge-order transition: Optical spectroscopy ofα−(BEDT−TTF)2MHg(SCN)4(M=NH4, Rb, Tl)

2006 ◽  
Vol 74 (23) ◽  
Author(s):  
N. Drichko ◽  
M. Dressel ◽  
C. A. Kuntscher ◽  
A. Pashkin ◽  
A. Greco ◽  
...  
2012 ◽  
Vol 9 (5) ◽  
pp. 1161-1163 ◽  
Author(s):  
Mitsuharu Nagasawa ◽  
Tokiko Nagasawa ◽  
Koichi Ichimura ◽  
Kazushige Nomura

2020 ◽  
Vol 26 (S2) ◽  
pp. 2034-2035
Author(s):  
Noah Schnitzer ◽  
Elisabeth Bianco ◽  
Alemayehu Admasu ◽  
Jaewook Kim ◽  
Sang-Wook Cheong ◽  
...  

2012 ◽  
Vol 16 (02) ◽  
pp. 244-249 ◽  
Author(s):  
Thiago T. Tasso ◽  
Wania C. Moreira

Porphyrin and phthalocyanine macrocycles with ionic substituents can form mixed assemblies with interesting electronic properties for potential application on the development of new devices. This paper reports the synthesis, isolation and purification of heteroaggregate formed by cobalt(II) 4,4′,4″,4‴-tetrasulfophthalocyanine (CoTsPc) and cobalt(II) tetrakis(N-methyl-4-pyridyl)porphyrin (CoTMPyP), followed by its spectroscopic characterization. Spectroscopic titration, performed with a CoTsPc water/acetone solution, allowed the use of Job's method for determination of the heteroaggregates stoichiometry. The Job's plot revealed the formation of only one predominant heterocomplex in solution, containing two CoTsPc molecules in terminal positions and a central CoTMPyP one. For the first time, a method for isolation and purification of a mixed ionic array has been reported in the literature. The triad's electronic spectrum is quite different from the sum of the macrocycles isolated spectra, due to the overlap of their electronic densities and a charge transfer process between CoTsPc and CoTMPyP.


2018 ◽  
Vol 98 (23) ◽  
Author(s):  
Hitoshi Seo ◽  
Yasuhiro Tanaka ◽  
Sumio Ishihara

2002 ◽  
Vol 65 (17) ◽  
Author(s):  
R. Klingeler ◽  
J. Geck ◽  
R. Gross ◽  
L. Pinsard-Gaudart ◽  
A. Revcolevschi ◽  
...  

1999 ◽  
Vol 60 (12) ◽  
pp. R8417-R8421 ◽  
Author(s):  
Matthias Vojta ◽  
R. E. Hetzel ◽  
R. M. Noack

2004 ◽  
Vol 846 ◽  
Author(s):  
Marek Jura ◽  
Olivia F. Koentjoro ◽  
Paul R. Raithby ◽  
Emma L. Sharp ◽  
Paul J. Wilson

ABSTRACTA series of platinum(II) di-yne complexes with the general formula [PhPt(PR3)2-C≡C-X-C≡C-Pt(PR3)2Ph] where R = Et, nBu and X = a range of extended hetero-aromatic spacer groups, have been prepared by the coupling reaction between two molar equivalents of [PhPt(PR3)2Cl] and one molar equivalent of the terminal dialkyne, HC≡C-X-C≡CH, in the presence of CuI catalyst. The complexes have been characterised by IR, NMR and optical spectroscopy. These materials, which are precursors to related platinum(II) poly-yne polymers, have been specifically designed to be incorporated into metal-molecule-metal junctions in nanoelectronic devices.


2003 ◽  
Vol 17 (04n06) ◽  
pp. 799-804 ◽  
Author(s):  
A. PAOLONE ◽  
R. CANTELLI ◽  
G. ROUSSE ◽  
C. MASQUELIER ◽  
M. FERRETTI

We studied the charge order transition of LiMn 2 O 4 by means of anelastic spectroscopy, measuring the Young's modulus, E, and the elastic energy loss function, Q-1. Our measurements confirm the occurrence of a phase transition at 296 K on cooling, showing a large hysteresis on heating. Around the transition temperature the Young's modulus shape reveals that there is at least one elastic constant, possibly c44, decreasing lowering the temperature. Moreover the anelastic spectroscopy results confirm that the transformation is characterised by the coexistence of two phases in a narrow temperature range. The time constant of the transformation of the cubic into the orthorhombic phase sharply decreases lowering T from 296 to 290 K and then increases on further cooling to 289 K. The strong decrease of the time constant around 290 K can be related to the reduction of the c44 elastic constant.


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