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Comparative study of poly(4-vinylpyridine) and polylactic acid-block-poly(2-vinylpyridine) nanocomposites on structural, morphological and electrochemical properties

机译:聚(4-乙烯基吡啶)和聚乳酸嵌段-聚(2-乙烯基吡啶)纳米复合材料的结构,形态和电化学性质的比较研究

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摘要

Polymer-based nanocomposites have attracted a lot of attention for amperometric biosensor development due to their general physical and chemical properties including biocompatibility, film-forming ability, stability and different functional groups that can be bonded with other biomolecues. In this study, poly-4-vinlyridine homopolymer (P4VP) and polylactic acid-block-poly(2-vinylpyridine) block copolymer (PLA-b-P2VP) were used to hybridize with gold precursors (Au3+) based on the association between the nitrogen of the pyridine group of P4VP or P2VP block with gold precursors. P4VP/Au3+ and PLA-b-P2VP/Au3+ nanocomposites were prepared with ratio of gold to P2VP or P4VP (10:1). The Au3+ in both polymers was reduced to gold nanoparticles (AuNPs) via in-situ approach by using hydrazine. Fourier transform infrared spectroscopy (FTIR), ultraviolet-visible spectroscopy (UV-vis), transmission electron microscopy (TEM) and cyclic voltammetry (CV) were used to characterize the structural, morphological and electrochemical properties of the nanocomposites. The peak currents of P4VP/AuNPs and PLA-b-P2VP/AuNPs nanocomposites modified electrode were 6.685 nA and 69.432 nA, respectively, which are much lower than bare electrode (205.019 nA) due to the non-conductivity of P4VP and PLA-b-P2VP. In order to improve the electron transfer capability of electrode, graphene oxide (GO) was blended and electrochemically reduced to obtain P4VP/AuNPs/rGO and PLA-b-P2VP/AuNPs/rGO nanocomposites. After immobilization of these two nanocomposites on electrode through drop casting method, the peak currents of P4VP/AuNPs/rGO and PLA-b-P2VP/AuNPs/rGO nanocomposites modified electrode were 871.172 nA and 663.947 nA, respectively, which are much higher than bare electrode (205.019 nA) and shown good capability to accelerate electron transfer. Based on these characterizations, P4VP/AuNPs/rGO has potential as the nanocomposite to modify the electrode for enzymatic biosensor development.
机译:基于聚合物的纳米复合材料由于其一般的物理和化学特性(包括生物相容性,成膜能力,稳定性和可以与其他生物分子结合的不同官能团),已引起了安培生物传感器开发的广泛关注。在这项研究中,聚4-乙烯基吡啶均聚物(P4VP)和聚乳酸-嵌段-聚(2-乙烯基吡啶)嵌段共聚物(PLA-b-P2VP)用于与金前体(Au3 +)杂交,基于P4VP或P2VP的吡啶基团的氮原子被金前体封闭。以金与P2VP或P4VP的比例(10:1)制备P4VP / Au3 +和PLA-b-P2VP / Au3 +纳米复合材料。通过使用肼通过原位方法将两种聚合物中的Au3 +还原为金纳米颗粒(AuNPs)。傅立叶变换红外光谱(FTIR),紫外可见光谱(UV-vis),透射电子显微镜(TEM)和循环伏安法(CV)用于表征纳米复合材料的结构,形态和电化学性能。 P4VP / AuNPs和PLA-b-P2VP / AuNPs纳米复合修饰电极的峰值电流分别为6.685 nA和69.432 nA,由于P4VP和PLA-b的非导电性,其峰值电流远低于裸电极(205.019 nA)。 -P2VP。为了提高电极的电子转移能力,将氧化石墨烯(GO)共混并进行电化学还原,得到P4VP / AuNPs / rGO和PLA-b-P2VP / AuNPs / rGO纳米复合材料。通过滴铸法将这两种纳米复合材料固定在电极上后,P4VP / AuNPs / rGO和PLA-b-P2VP / AuNPs / rGO纳米复合材料修饰电极的峰值电流分别为871.172 nA和663.947 nA。电极(205.019 nA),并具有良好的加速电子传输的能力。基于这些特征,P4VP / AuNPs / rGO具有作为纳米复合材料的潜力,可以修饰用于酶促生物传感器开发的电极。

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