GdBa 2 Cu 3 O 7-X (Gd123) nanowires were synthesized using a modified sol-gel method, in the presence of an excellent surfactant, benzene tricarboxylic acid. The obtained results revealed that the decomposition of BaCO 3 and subsequent formation of the pure Gd123 phase complete after re-calcination process at 900 ºC. Structural study using Rietveld refinement of XRD and also electron diffraction patterns indicated an orthorhombic structure with Pmmm space group. It can be deduced that the shape and particle size of the products are greatly affected by the concentration of the surfactant. Magnetic susceptibility measurements showed clear diamagnetic behavior below the critical temperature of about 91.78 K in the nanowires, which is comparable to that in the bulk ones. Temperature dependence of the magnetic susceptibility was also found to be approximately insensitive to the strength of the applied magnetic field.Phase identification was carried out for the as-precipitated and heat treated samples by an X-ray diffraction (XRD) method with a Rigaku D-max C III, X-ray diffractometer using Ni-filtered Cu K α radiation. Scanning electron microscopy (SEM) images were obtained on Philips XL-30ESEM equipped with an energy dispersive X-ray spectroscopy. The compositional analysis was done by energy dispersive X-ray (EDS, Kevex, Delta Class I). The morphology of the as-precipitated and heat treated samples was observed with a transmission electron microscope (TEM) of Philips EM208 transmission electron microscope with an accelerating voltage of 200 kV. Fourier transform infrared (FT-IR) spectra were recorded on Shimadzu Varian 4300 spectrophotometer in KBr pellets.
Synthesis of Gd123 nanoparticlesAll the chemical reagents used in our experiments were of analytical grade, purchased from Aldrich Co. (with purify over 99%), and were used as received without further purification. A homogenous and light-blue solution with overall cation stoichiometry of Gd:Ba:Cu = 1:2:3 was obtained by dissolving the metal nitrates in polypropylene glycol. Polypropylene glycol (PPG) can play the role of a surfactant in the solution, too. 13/3 mmol benzene tricarboxylic acid (BTCA), in the mole ratio BTCA:Y= 13/3:1, was dissolved in 50 ml polypropylene glycol, and then the Gd123 solution was slowly added to that under vigorous stirring. The resulted light-blue viscous fluid was heated in the furnace at 300°C for about 1 h and cooled to room temperature. Finally, the obtained powder was calcined with a heating rate of 5 C/min up to 900˚C for 8 h, and then slowly cooled down to room temperature with a cooling rate of 2 C/min and crushed to a fine powder. Samples were re-calcined under the same conditions as the first calcination. The superconductivity phase formation process was completed with annealing treatment to 700˚C with a rate of 2˚C/min for 3 h and then cooling at the same conditions to room temperature. The optimum partial pressure was 0.5 bar during the entire thermal decomposition process 1051-8223 (c)