Izumi Celly M S, Constantino Vera R L, Temperini Marcia L A
Departamento de Química Fundamental, Instituto de Química, Universidade de São Paulo, CP 26.077, CEP 05513-970, São Paulo, SP, Brazil.
J Nanosci Nanotechnol. 2008 Apr;8(4):1782-9.
In the present work, nanocomposites of polyaniline (PANI) and layered alpha-Zr(HPO4)2 x H2O (alpha-ZrP) were prepared using two different approaches: (i) the in situ aniline polymerization in the presence of the layered inorganic material and (ii) the layer-by-layer (LBL) assembly using an aqueous solution of the polycation emeraldine salt (ES-PANI) and a dispersion of exfoliated negative slabs of alpha-ZrP. These materials were characterized spectroscopically using mainly resonance Raman scattering at four exciting radiations and electronic absorption in the UV-VIS-NIR region. Structural and textural characterizations were carried out using powder X-ray diffraction (XRD) and scanning electron microscopy (SEM). The polymer obtained by the in situ aniline polymerization is located primarily in the external surface of the inorganic material although aniline monomers were intercalated between alpha-ZrP interlayer regions before oxidative polymerization. Through resonance Raman spectroscopy, it was observed that the formed polymer has semiquinone units (ES-PANI) and also azo bonds (-N=N-), showing that this method results in a polymer with a different structure from the usual "head-to-tail" ES-PANI. The LBL assembly of pre-formed ES-PANI and exfoliated alpha-ZrP particles produces homogeneous films with reproducible deposition from layer to layer, up to 20 bilayers. Resonance Raman (lambda0 = 632.8 nm) spectrum of PANI/ZrP LBL film shows an enhancement in the intensity of the polaronic band at 1333 cm(-1) (upsilonC-N*+) and the decrease of the band intensity at 1485 cm(-1) compared to bulk ES-PANI. Its UV-VIS-NIR spectrum presents an absorption tail in the NIR region assigned to delocalized free charge carrier. These spectroscopic features are characteristic of highly conductive secondary doped PANI suggesting that polymeric chains in PANI/ZrP LBL film have a more extended conformation than in bulk ES-PANI.
在本工作中,采用两种不同方法制备了聚苯胺(PANI)与层状α-Zr(HPO₄)₂·xH₂O(α-ZrP)的纳米复合材料:(i)在层状无机材料存在下原位苯胺聚合;(ii)使用聚阳离子翡翠盐(ES-PANI)水溶液和α-ZrP剥离负片分散体进行逐层(LBL)组装。主要通过在四种激发辐射下的共振拉曼散射以及紫外-可见-近红外区域的电子吸收对这些材料进行光谱表征。使用粉末X射线衍射(XRD)和扫描电子显微镜(SEM)进行结构和织构表征。尽管苯胺单体在氧化聚合之前插入到α-ZrP层间区域,但通过原位苯胺聚合得到的聚合物主要位于无机材料的外表面。通过共振拉曼光谱观察到,形成的聚合物具有半醌单元(ES-PANI)以及偶氮键(-N=N-),表明该方法得到的聚合物结构与通常的“头对尾”ES-PANI不同。预形成的ES-PANI与剥离的α-ZrP颗粒的LBL组装产生均匀的薄膜,可实现从一层到另一层的可重复沉积,直至20个双层。与本体ES-PANI相比,PANI/ZrP LBL膜的共振拉曼(λ₀ = 632.8 nm)光谱显示1333 cm⁻¹(υC-N⁺*)处极化子带强度增强,1485 cm⁻¹处带强度降低。其紫外-可见-近红外光谱在近红外区域呈现吸收尾,归因于离域自由电荷载流子。这些光谱特征是高导电性二次掺杂PANI的特征,表明PANI/ZrP LBL膜中的聚合物链比本体ES-PANI具有更伸展的构象。