Martínez-Julián F, Ricart S, Pomar A, Col M, Abellán P, Sandiumenge F, Casanove M J, Obradors X, Puig T, Pastoriza-Santos I, Liz-Marzán L M
Institut de Ciència de Materials de Barcelona-CSIC, Campus de la UAB, Bellaterra 08193, Spain.
J Nanosci Nanotechnol. 2011 Apr;11(4):3245-55. doi: 10.1166/jnn.2011.3762.
We explore the feasibility of preparing YBa2CU3O7-Au (YBCO-Au) nanocomposite thin films by chemical solution deposition (CSD). Two approaches were used: (i) A standard in-situ methodology where Au metallorganic salts are added into the precursor solution of YBCO trifluoroacetate (TFA) salts and (ii) a novel approach where stable colloidal solutions of preformed gold nanoparticles (5-15 nm) were homogeneously mixed with TFA-YBCO solutions. A detailed analysis of the microstructure of the films showed that in both cases, there is a strong tendency of gold nanoparticles to migrate to the film surface. However the kinetics of this migration evidences important differences and in the case of preformed nanoparticles their size remains unchanged (a few nanometers) whereas for the in-situ nanocomposites gold ripening leads to large particles (hundreds of nanometers). The grown YBCO-Au films showed good superconducting characteristics (J(c) 2 MA/cm2 at 77 K) but the absence of Au inclusions inside the YBCO matrix explains the fact that no enhancement of vortex pinning was observed.
我们探讨了通过化学溶液沉积(CSD)制备YBa2CU3O7-Au(YBCO-Au)纳米复合薄膜的可行性。采用了两种方法:(i)一种标准的原位方法,即将金有机盐添加到YBCO三氟乙酸盐(TFA)的前驱体溶液中;(ii)一种新方法,即将预先形成的金纳米颗粒(5-15纳米)的稳定胶体溶液与TFA-YBCO溶液均匀混合。对薄膜微观结构的详细分析表明,在这两种情况下,金纳米颗粒都有强烈的迁移到薄膜表面的趋势。然而,这种迁移的动力学显示出重要的差异,对于预先形成的纳米颗粒,其尺寸保持不变(几纳米),而对于原位纳米复合材料,金的熟化导致形成大颗粒(数百纳米)。生长的YBCO-Au薄膜显示出良好的超导特性(在77 K时J(c)为2 MA/cm2),但YBCO基体中没有金夹杂物这一事实解释了未观察到涡旋钉扎增强的现象。