McNeill C R, Watts B, Swaraj S, Ade H, Thomsen L, Belcher W, Dastoor P C
Cavendish Laboratory, Department of Physics, University of Cambridge, J J Thomson Avenue, Cambridge CB3 0HE, UK.
Nanotechnology. 2008 Oct 22;19(42):424015. doi: 10.1088/0957-4484/19/42/424015. Epub 2008 Sep 25.
We investigate the influence of annealing on the morphology of intimately mixed blends of the conjugated polymers poly(9,9'-dioctylfluorene-co-bis-N,N'-(4-butylphenyl)-bis-N,N'-phenyl-1,4-phenylene-diamine) (PFB) and poly(9,9'-dioctylfluorene-co-benzothiadiazole) (F8BT) with scanning transmission x-ray microscopy (STXM). Through the use of a zone plate with theoretical Rayleigh resolution of 30 nm, we are able to resolve sub-100 nm bulk structure in these films. Surprisingly, for unannealed films spin-coated from chloroform we observe features with an average diameter of 85 nm. The high degree of photoluminescence quenching in these as-spun films (>95%) implies that there is significant intermixing within the 85 nm structures, indicating that a hierarchy of phase separation exists even on the length scale of less than 100 nm. With annealing up to 160 °C, close to the T(g) of the components, there is little change in the feature sizes observed by STXM, although an increase in variation of the composition is observed. With annealing above 160 °C the imaged features begin to evolve in size, increasing to 225 nm in extent, alongside large changes in composition with annealing to 200 °C. Comparing the evolution of morphology imaged by STXM with the change in photoluminescence quenching with annealing, we propose that phase separation first evolves via the evolution of relatively pure phases on the length scale of a few to tens of nanometres within the larger 85 nm structures. Once the length scale of compositional fluctuations exceeds 85 nm (for anneal temperatures above 160 °C) the hierarchy of phase separation is lost and the subsequent morphological evolution is readily imaged by STXM. Applying the results of an exciton diffusion and quenching model, we find good agreement between the size of the domains measured by STXM (above 180 °C) and the results of the model for an exciton diffusion length of 15 nm. The growth in domain size and towards purer structures has also been observed with resonant soft x-ray scattering.
我们利用扫描透射X射线显微镜(STXM)研究了退火对共轭聚合物聚(9,9'-二辛基芴-co-双-N,N'-(4-丁基苯基)-双-N,N'-苯基-1,4-苯二胺)(PFB)和聚(9,9'-二辛基芴-co-苯并噻二唑)(F8BT)紧密混合共混物形态的影响。通过使用理论瑞利分辨率为30 nm的波带片,我们能够分辨这些薄膜中小于100 nm的整体结构。令人惊讶的是,对于从氯仿旋涂的未退火薄膜,我们观察到平均直径为85 nm的特征。这些初纺薄膜中高度的光致发光猝灭(>95%)表明在85 nm结构内存在显著的相互混合,这表明即使在小于100 nm的长度尺度上也存在相分离层次结构。在高达160 °C(接近组分的玻璃化转变温度T(g))的退火条件下,STXM观察到的特征尺寸几乎没有变化,尽管观察到组成变化有所增加。在高于160 °C的退火条件下,成像特征的尺寸开始演变,在退火至200 °C时,尺寸增加到225 nm,同时组成也发生了很大变化。将STXM成像的形态演变与退火过程中光致发光猝灭的变化进行比较,我们提出相分离首先通过在较大的85 nm结构内几纳米到几十纳米的长度尺度上相对纯相的演变而发生。一旦组成波动的长度尺度超过85 nm(对于退火温度高于160 °C),相分离层次结构就会消失,随后的形态演变很容易被STXM成像。应用激子扩散和猝灭模型的结果,我们发现STXM测量的域尺寸(高于180 °C)与激子扩散长度为十五纳米的模型结果之间有很好的一致性。通过共振软X射线散射也观察到了域尺寸的增长和向更纯结构的转变。