Savchenko Pavel, Zelikovich Din, Elgavi Sinai Hadassah, Baer Roi, Mandler Daniel
Fritz Haber Research Center for Molecular Dynamics and Institute of Chemistry, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel.
Institute of Chemistry, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel.
J Am Chem Soc. 2024 Aug 14;146(32):22208-22219. doi: 10.1021/jacs.4c02524. Epub 2024 Jul 3.
Engineered metallic nanoparticles, which are found in numerous applications, are usually stabilized by organic ligands influencing their interfacial properties. We found that the ligands affect tremendously the electrochemical peak oxidation potentials of the nanoparticles. In this work, identical gold nanoparticles were ligand-exchanged and carefully analyzed to enable a precise and highly reproducible comparison. The peak potential difference between gold nanoparticles stabilized by various ligands, such as 2- and 4-mercaptobenzoic acid, can be as high as 71 mV, which is substantial in energetic terms. A detailed study supported by density functional theory (DFT) calculations aimed to determine the source of this interesting effect. The DFT simulations of the ligand adsorption modes on Au surfaces were used to calculate the redox potentials through the thermodynamic cycle method. The DFT results of the peak potential shift were in good agreement with the experimental results for a few ligands, but showed some discrepancy, which was attributed to kinetic effects. The kinetic rate constant of the oxidation of Au nanoparticles stabilized by 4-mercaptobenzoic acid was found to be twice as large as that of the Au nanoparticles stabilized by citrate, as calculated from Laviron's theory and the Tafel equation. Finally, these findings could be applied to some novel applications such as determining the distribution of nanoparticle population in a dispersion as well as monitoring the ligand exchange between nanoparticles.
工程金属纳米颗粒存在于众多应用中,通常由影响其界面性质的有机配体来稳定。我们发现配体对纳米颗粒的电化学峰氧化电位有极大影响。在这项工作中,对相同的金纳米颗粒进行配体交换并仔细分析,以实现精确且高度可重复的比较。由各种配体(如2 - 巯基苯甲酸和4 - 巯基苯甲酸)稳定的金纳米颗粒之间的峰电位差可高达71 mV,从能量角度来看这是相当可观的。一项由密度泛函理论(DFT)计算支持的详细研究旨在确定这种有趣效应的来源。通过热力学循环方法,利用配体在金表面吸附模式的DFT模拟来计算氧化还原电位。对于一些配体,峰电位移动的DFT结果与实验结果吻合良好,但也存在一些差异,这归因于动力学效应。根据拉维隆理论和塔菲尔方程计算得出,由4 - 巯基苯甲酸稳定的金纳米颗粒的氧化动力学速率常数是由柠檬酸盐稳定的金纳米颗粒的两倍。最后,这些发现可应用于一些新的应用中,如确定分散体中纳米颗粒群体的分布以及监测纳米颗粒之间的配体交换。