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首页> 外文期刊>Chemistry of Materials: A Publication of the American Chemistry Society >A General Approach To Study the Thermodynamics of Ligand Adsorption to Colloidal Surfaces Demonstrated by Means of Catechols Binding to Zinc Oxide Quantum Dots
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A General Approach To Study the Thermodynamics of Ligand Adsorption to Colloidal Surfaces Demonstrated by Means of Catechols Binding to Zinc Oxide Quantum Dots

机译:研究邻苯二酚与氧化锌量子点结合显示配体吸附到胶体表面的热力学的一般方法

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A general strategy to study the thermodynamics of ligand adsorption to colloidal surfaces was established. The versatility of our approach is demonstrated by means of catechols binding to ZnO quantum dots (QDs). First, isothermal titration calorimetry (ITC) was used to extract all relevant thermodynamic parameters, namely association constant, enthalpy, entropy, and free energy of ligand binding. Noteworthy, the determined Delta G of -20.3 +/- 0.4 kJ mol(-1) indicates a strong, reproducible, and exothermic interaction between the catechol anchor group and the oxide particle surface. To confirm the characterization of ligand binding by measuring the heat of adsorption, the free energy was cross-validated by mass-based adsorption isotherms. A combination of inductively coupled plasma optical emission spectroscopy (ICP-OES) and UV/vis spectroscopy was developed to quantitatively determine the mass of bound catechols with respect to the available particle surface. The association constant K was determined by a Langmuir fit to be 2618 M-1 which leads to Delta G = -19.50 kJ mol(-1) according to Delta G = -RTln K. To close the mass balance, analytical ultracentrifugation (AUC) was applied to detect the amount of the free, unbound catechol in solution. Finally, Raman spectroscopy and nuclear magnetic resonance spectroscopy (NMR) were performed to quantify the amount of remaining acetate from particle synthesis and to distinguish bound (chemisorbed) and unbound (physisorbed) catechol. Our results reveal that approximately 65 wt % of acetate is replaced, and physisorbed catechol will not affect the amount of remaining acetate on the ZnO surface. Moreover, no pronounced chemical shift peak as it would be expected for free catechol is observed by NMR at all. This indicates a highly dynamic adsorption-desorption equilibrium between the free and the physisorbed state of catechol on the particle surface. Our concept of combined analytics is seen to be a generally applicable strategy for particle-ligand interfacial studies. It gives detailed insight into thermodynamics, binding states, and ligand composition and is thus considered as an important step toward tailored colloidal surface properties.
机译:建立了研究配体吸附到胶体表面的热力学的一般策略。我们的方法的多功能性是通过儿茶酚与ZnO量子点(QD)的结合来证明的。首先,使用等温滴定热法(ITC)提取所有相关的热力学参数,即缔合常数,焓,熵和配体结合自由能。值得注意的是,确定的Delta G为-20.3 +/- 0.4 kJ mol(-1)表示邻苯二酚锚固基团和氧化物颗粒表面之间存在强烈的,可再现的放热相互作用。为了通过测量吸附热来确定配体结合的特征,通过基于质量的吸附等温线对自由能进行交叉验证。开发了电感耦合等离子体发射光谱(ICP-OES)和紫外/可见光谱的组合,以定量确定相对于可用粒子表面的邻苯二酚的质量。通过Langmuir拟合确定缔合常数K为2618 M-1,根据Delta G = -RTln K,得出Delta G = -19.50 kJ mol(-1)。要关闭质量平衡,请使用分析超速离心(AUC)用于检测溶液中游离的,未结合的邻苯二酚的量。最后,进行了拉曼光谱和核磁共振光谱(NMR),以量化颗粒合成过程中残留的乙酸盐量,并区分结合的(化学吸附的)和未结合的(物理吸附的)邻苯二酚。我们的结果表明,大约65 wt%的乙酸盐被替代了,而物理吸附的邻苯二酚不会影响ZnO表面上残留的乙酸盐的量。此外,完全没有通过NMR观察到明显的化学位移峰,如对游离儿茶酚所预期的那样。这表明在颗粒表面上邻苯二酚的游离状态和物理吸附状态之间具有高度动态的吸附-解吸平衡。我们的组合分析概念被认为是粒子-配体界面研究的普遍适用策略。它提供了对热力学,结合态和配体组成的详细了解,因此被认为是朝着定制的胶体表面性能迈出的重要一步。

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