In this study, ITO nanoparticles (ITO-NPs) were reused from ITO target scraps to synthesize low cost ITO-NPs and to apply to make sputtering target for transparent conductive electrodes (TCEs). By controlling heat-treatment temperature as 980 °C, we achieved reused ITO-NPs having Brunauer, Emmett and Teller specific surface area (BET SSA) and average particle size 8.05 m2/g and 103.8 nm, respectively. The BET SSA decreases along with increasing heat-treatment temperature. The ITO-NPs were grown as round mound shape, and highly crystallized to (222) preferred orientations. Also, applying the reused ITO-NPs, we achieved an ITO target of which density was 99.6%. Using the ITO target, we achieved high quality TCE layer of which sheet resistance and optical transmittance at 550 nm were 29.5 Ω/sq. and 82.3%. Thus, it was confirmed that the reused ITO-NPs was feasible to sputtering target for TCEs layer.

In this study, iron oxide nanoparticles (FeOx NPs) were synthesized by using Fe solution recycled from NdFeB permanent magnet scrap. Furthermore, the effect of polyvinylpolypyrrolidone (PVP) as a surfactant on the characteristics of the FeOx NPs was investigated. Firstly, Fe solution was prepared by using 10% H2SO4 solution and Na2SO4 salt. In addition, three reducing agent solutions were prepared by dissolving PVP in 0.5 M NH4OH solution in distilled (D.I.) water with concentrations of 0 wt%, 1 wt%, and 2 wt%, respectively. Each reducing agent solution was added dropwise into the Fe solution to precipitate three precursors of FeOx NPs, and they were heat-treated at 400 °C to prepare three FeOx NPs samples, P0, P1, and P2. In X-ray diffractometer (XRD) analysis, diffraction peaks of P0 sample are consistent with the Fe3O4 with (311) preferred orientation. The XRD peak shifted from Fe3O4 to Fe2O3 structure as PVP concentration increased, and the crystal structure of P2 sample was transformed to Fe2O3 with (104) preferred orientation. Brunauer, Emmett, and Teller (BET) specific surface area increased in proportional to PVP concentration. HRTEM observation also supported the tendency; the particle size of the P0 sample was less than 40 nm, and particle size decreased as PVP concentration increased, leading to the particle size of the P2 sample being less than 20 nm in width. In addition, particle morphology started to be transformed from particle to rod shape as PVP concentration increased and, in the P2 sample, all the morphology of particles was transformed to a rod shape. Magnetic properties analysis revealed that the P0 sample exhibited the highest value of magnetic moment, 65.6 emu/g, and the magnetic moment was lowered in the P1 sample, and the P2 sample exhibited the lowest value of magnetic moment, 2.4 emu/g.