Structural and magnetic modulations of copper(ii) azido complexes: unexpected in situ reactions of mono-N-donor pyridine-based co-ligands

2016 ◽  
Vol 45 (4) ◽  
pp. 1514-1524 ◽  
Author(s):  
Jiong-Peng Zhao ◽  
Yabo Xie ◽  
Jian-Rong Li ◽  
Xian-He Bu

Hydrothermal reactions of azide anions, Cu(ii) ions, and fourmono-N-donor pyridine ligands lead to four new copper(ii) azides with different structures and magnetic properties, in which three co-ligands were generatedin situby decomposition, substitution, and oxidation reactions.

1990 ◽  
Vol 197 ◽  
Author(s):  
Serge Ricard ◽  
Robert H. Marchessault

ABSTRACTMagnetic paper handsheets with pigment loadings in the order of 10–30%, depending on the experimental conditions, have been made using the established “lumen-loading” technology. These sheets have bulk magnetic properties comparable with the computer floppy-disk products. In order to minimize the particle size of pigments and thereby explore a new level of optical and magnetic properties, in situ synthesis of pigment particles is a second approach. This chemistry starts with a carboxymethylcellulose substrate with ion-exchange properties for Fe(ll). The substrates, before and after oxidation reactions to produce ferrite particles, are characterized by: conductimetric titration, x-ray diffraction, thermogravimetric analysis, and magnetization determination. Electron microscopy and diffraction provide insight on the ferrite morphologicals. These specialty fibers allow exploration of new concepts in papermaking, information storage, security printing and paper handling.


Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 310
Author(s):  
Dohyeon Han ◽  
Doohwan Lee

Fine control of morphology and exposed crystal facets of porous γ-Al2O3 is of significant importance in many application areas such as functional nanomaterials and heterogeneous catalysts. Herein, a morphology controlled in situ synthesis of Al@Al2O3 core–shell architecture consisting of an Al metal core and a porous γ-Al2O3 shell is explored based on interfacial hydrothermal reactions of an Al metal substrate in aqueous solutions of inorganic anions. It was found that the morphology and structure of boehmite (γ-AlOOH) nano-crystallites grown at the Al-metal/solution interface exhibit significant dependence on temperature, type of inorganic anions (Cl−, NO3−, and SO42−), and acid–base environment of the synthesis solution. Different extents of the electrostatic interactions between the protonated hydroxyl groups on (010) and (001) facets of γ-AlOOH and the inorganic anions (Cl−, NO3−, SO42−) appear to result in the preferential growth of γ-AlOOH toward specific crystallographic directions due to the selective capping of the facets by adsorption of the anions. It is hypothesized that the unique Al@Al2O3 core–shell architecture with controlled morphology and exposed crystal-facets of the γ-Al2O3 shell can provide significant intrinsic catalytic properties with enhanced heat and mass transport to heterogeneous catalysts for applications in many thermochemical reaction processes. The direct fabrication of γ-Al2O3 nano-crystallites from Al metal substrate with in-situ modulation of their morphologies and structures into 1D, 2D, and 3D nano-architectures explored in this work is unique and can offer significant opportunities over the conventional methods.


Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 464
Author(s):  
Jie Yu ◽  
Angel Caravaca ◽  
Chantal Guillard ◽  
Philippe Vernoux ◽  
Liang Zhou ◽  
...  

Indoor toxic volatile organic compounds (VOCs) pollution is a serious threat to people’s health and toluene is a typical representative. In this study, we developed a composite photocatalyst of carbon nitride quantum dots (CNQDs) in situ-doped TiO2 inverse opal TiO2 IO for efficient degradation of toluene. The catalyst was fabricated using a sol-gel method with colloidal photonic crystals as the template. The as-prepared catalyst exhibited excellent photocatalytic performance for degradation of toluene. After 6 h of simulated sunlight irradiation, 93% of toluene can be converted into non-toxic products CO2 and H2O, while only 37% of toluene is degraded over commercial P25 in the same condition. This greatly enhanced photocatalytic activity results from two aspects: (i) the inverse opal structure enhances the light harvesting while providing adequate surface area for effective oxidation reactions; (ii) the incorporation of CNQDs in the framework of TiO2 increases visible light absorption and promotes the separation of photo-generated charges. Collectively, highly efficient photocatalytic degradation of toluene has been achieved. In addition, it can be expanded to efficient degradation of organic pollutants in liquid phase such as phenol and Rhodamine B. This study provides a green, energy saving solution for indoor toxic VOCs removal as well as for the treatment of organic wastewater.


2021 ◽  
Vol 203 ◽  
pp. 109538
Author(s):  
Boan Xu ◽  
Ping Jiang ◽  
Shaoning Geng ◽  
Yilin Wang ◽  
Jintian Zhao ◽  
...  

ChemSusChem ◽  
2021 ◽  
Author(s):  
Jifang Zhang ◽  
Wanbing Gong ◽  
Huajie Yin ◽  
Dongdong Wang ◽  
Yunxia Zhang ◽  
...  

Carbon ◽  
2013 ◽  
Vol 61 ◽  
pp. 647-649 ◽  
Author(s):  
Qingze Jiao ◽  
Liang Hao ◽  
Qingyan Shao ◽  
Yun Zhao

MRS Advances ◽  
2016 ◽  
Vol 1 (37) ◽  
pp. 2635-2640 ◽  
Author(s):  
Adele Moatti ◽  
Reza Bayati ◽  
Srinivasa Rao Singamaneni ◽  
Jagdish Narayan

ABSTRACTBi-epitaxial VO2 thin films with [011] out-of-plane orientation were integrated with Si(100) substrates through TiO2/TiN buffer layers. At the first step, TiN is grown epitaxially on Si(100), where a cube-on-cube epitaxy is achieved. Then, TiN was oxidized in-situ ending up having epitaxial r-TiO2. Finally, VO2 was deposited on top of TiO2. The alignment across the interfaces was stablished as VO2(011)║TiO2(110)║TiN(100)║Si(100) and VO2(110) /VO2(010)║TiO2(011)║TiN(112)║Si(112). The inter-planar spacing of VO2(010) and TiO2(011) equal to 2.26 and 2.50 Å, respectively. This results in a 9.78% tensile misfit strain in VO2(010) lattice which relaxes through 9/10 alteration domains with a frequency factor of 0.5, according to the domain matching epitaxy paradigm. Also, the inter-planar spacing of VO2(011) and TiO2(011) equals to 3.19 and 2.50 Å, respectively. This results in a 27.6% compressive misfit strain in VO2(011) lattice which relaxes through 3/4 alteration domains with a frequency factor of 0.57. We studied semiconductor to metal transition characteristics of VO2/TiO2/TiN/Si heterostructures and established a correlation between intrinsic defects and magnetic properties.


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