Superconducting Parent Compound Pr2CuO4 Achieved by Special Post-Reduction

2011 ◽  
Vol 1309 ◽  
Author(s):  
Hideki Yamamoto ◽  
Osamu Matsumoto ◽  
Keitaro Yamagami ◽  
Michio Naito ◽  
Yoshiharu Krockenberger

ABSTRACTIt is commonly believed that the parent compounds of high-Tc cupratres are, universally, charge transfer insulators and triggered by Mott physics. In our experiments using metal-organic decomposition (MOD), however, accumulating evidences show that the parent compounds of “electron-doped” superconductors, RE2-xCexCuO4 [RE = rare earth ion] with x = 0, are not Mott insulators but superconductors [1-5]. They have a Tc of 30 K and crystallize in the Nd2CuO4 (T’) structure. Most likely, the sharp contradiction between our results and commonly achieved data originates from the complicated oxygen chemistry in these materials. The as-synthesized specimens contain a fair amount of impurity interstitial oxygen. Throughout the reduction process it is required to remove exclusively impurity oxygen while preserving regular oxygen site occupied in order to obtain superconductivity. With decreasing x the constraints of the reduction process are getting more tight. In this study, we systematically investigated the post-annealing process using MBE-grown T’-Pr2CuO4 films. The MBE films were reduced ex-situ in a tubular furnace following a specially designed 2-step process, as in the case of MOD films. The films were annealed at Ta = 700 - 850°C in a reducing atmosphere (PO2 = 2 x 10−5 − 2 x 10−3 atm) and finally reduced at a lower temperature Tred = 450 – 700°C under vacuum (< 10−4 Torr). The film properties systematically changed with Ta, PO2, and Tred. The optimized Tred varies from 475°C to 650°C mainly depending on Ta, since the microstructure and grain size of the films are determined by Ta. Optimal superconducting properties are Tc of 26 K, while ρ(300 K) = 250 μΩcm, and RRR ~ 10. We believe the combination of thin-film synthesis and specially designed post-reduction process enabled us to obtain nearly intact CuO2 planes. Samples prepared by above-mentioned method unveiled the intrinsic properties of the parent compounds, which are not triggered by Mott physics. This result also agrees with the recent calculation result indicating the parent compounds with T’ structure are not charge transfer insulators [6-8].

2020 ◽  
Vol 528 ◽  
pp. 147053 ◽  
Author(s):  
Siqi Wang ◽  
Fanqi Meng ◽  
Xuejiao Sun ◽  
Mingjun Bao ◽  
Jiawen Ren ◽  
...  

2021 ◽  
Vol 22 (9) ◽  
pp. 4803
Author(s):  
Eduardo Gomez ◽  
Ichiro Hisaki ◽  
Abderrazzak Douhal

Hydrogen-bonded organic frameworks (HOFs) are the focus of intense scientific research due their potential applications in science and technology. Here, we report on the synthesis, characterization, and photobehavior of a new HOF (T12F-1(124TCB)) based on a dehydrobenzoannulene derivative containing fluorine atoms (T12F-COOH). This HOF exhibits a 2D porous sheet, which is hexagonally networked via H-bonds between the carboxylic groups, and has an interlayers distance (4.3 Å) that is longer than that of a typical π–π interaction. The presence of the fluorine atoms in the DBA molecular units largely increases the emission quantum yield in DMF (0.33, T12F-COOH) when compared to the parent compound (0.02, T12-COOH). The time-resolved dynamics of T12F-COOH in DMF is governed by the emission from a locally excited state (S1, ~ 0.4 ns), a charge-transfer state (S1(CT), ~ 2 ns), and a room temperature emissive triplet state (T1, ~ 20 ns), in addition to a non-emissive triplet structure with a charge-transfer character (T1(CT), τ = 0.75 µs). We also report on the results using T12F-ester. Interestingly, FLIM experiments on single crystals unravel that the emission lifetimes of the crystalline HOF are almost twice those of the amorphous ones or the solid T12F-ester sample. This shows the relevance of the H-bonds in the photodynamics of the HOF and provides a strong basis for further development and study of HOFs based on DBAs for potential applications in photonics.


2003 ◽  
Vol 103 (2-3) ◽  
pp. 301-313 ◽  
Author(s):  
N. Guskos ◽  
G. Papadopoulos ◽  
J. Majszczyk ◽  
J. Typek ◽  
M. Wabia ◽  
...  

2018 ◽  
Vol 20 (40) ◽  
pp. 25772-25779 ◽  
Author(s):  
Pavel M. Usov ◽  
Chanel F. Leong ◽  
Bun Chan ◽  
Mikihiro Hayashi ◽  
Hiroshi Kitagawa ◽  
...  

Donor–Acceptor Metal–Organic Frameworks display redox and pressure dependent charge transfer properties.


2018 ◽  
Vol 9 (13) ◽  
pp. 3282-3289 ◽  
Author(s):  
S. Yamamoto ◽  
J. Pirillo ◽  
Y. Hijikata ◽  
Z. Zhang ◽  
K. Awaga

Using the “crystal sponge” approach, weak organic electron donor molecules were impregnated and evenly distributed in a crystal of a metal–organic framework (MOF), with the self-assembly of the donor–acceptor pairs with electron acceptor ligands. The nanopores of the MOF confined them and induced a charge transfer phenomenon, which would not occur between donor and acceptor molecules in a bulk scale.


2018 ◽  
Vol 20 (46) ◽  
pp. 29142-29151 ◽  
Author(s):  
Michael Adams ◽  
Nicolò Baroni ◽  
Michael Oldenburg ◽  
Felix Kraffert ◽  
Jan Behrends ◽  
...  

Upon prolonged illumination photoproducts are created in porphyrin-based metal–organic frameworks that limit the triplet exciton lifetime by charge-transfer quenching.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Saleh A. Ahmed ◽  
Damayanti Bagchi ◽  
Hanadi A. Katouah ◽  
Md. Nur Hasan ◽  
Hatem M. Altass ◽  
...  

AbstractIn this work, we have successfully synthesized a bimetallic (Zinc and Cobalt) Zeolitic Imidazolate Framework (Zn50Co50-ZIF), a class in a wider microporous Metal-Organic Framework (MOF) family. The synthesized nanostructures maintain both water stability like ZIF-8 (solely Zn containing) and charge transfer electronic band in the visible optical spectrum as ZIF-67 (solely Co containing). Crystal structure from XRD, high resolution transmission electron microscopy (HRTEM) followed by elemental mapping (EDAX) confirm structural stability and omnipresence of the metal atoms (Zn and Co) across the nanomaterial with equal proportion. Existence of charge transfer state consistent with ZIF67 and intact ultrafast excited state dynamics of the imidazolate moiety in both ZIF-8 and ZIF-67, is evidenced from steady state and time resolved optical spectroscopy. The thermal and aqueous stabilities of Zn50Co50-ZIF are found to be better than ZIF-67 but comparable to ZIF-8 as evidenced by solubility, scanning electron microscopy (SEM) and XRD studies of the material in water. We have evaluated the photoinduced ROS generation by the mixed ZIF employing dichloro-dihydro-fluorescein diacetate (DCFH-DA) assay. We have also explored the potentiality of the synthesized material for the alternate remediation of methicillin resistant Staphylococcus aureus (MRSA) infection through the photoinduced reactive oxygen species (ROS) generation and methylene blue (MB) degradation kinetics.


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