Lackinger Markus
Deutsches Museum, Museumsinsel 1, 80538, München, Germany.
Physics Department, Technical University of Munich, 85748, Garching, Germany.
Chemphyschem. 2024 Jun 3;25(11):e202400156. doi: 10.1002/cphc.202400156. Epub 2024 Mar 25.
The kinetics of coupling reactions on surfaces can be quantitatively studied in real time by X-ray Photoelectron Spectroscopy (XPS). From fitting experimental data, kinetic reaction parameters such as the rate constant's pre-exponential and activation energy can be deduced and compared to quantum chemical simulations. To elucidate the possibilities and limitations of this approach, we propose studies in which experimental data are first simulated and subsequently fitted. Knowing the exact kinetic parameters used in the simulation allows one to evaluate the accuracy of the fit result. Here, several experimental influences, such as the data point density and the addition of noise, are explored for a model reaction with first-order kinetics. The proposed procedure sheds light on the accuracy with which kinetic parameters can be derived and may also help in the design of future experiments.
表面耦合反应的动力学可以通过X射线光电子能谱(XPS)进行实时定量研究。通过拟合实验数据,可以推导动力学反应参数,如速率常数的指前因子和活化能,并与量子化学模拟结果进行比较。为了阐明这种方法的可能性和局限性,我们建议进行相关研究,即先对实验数据进行模拟,然后再进行拟合。知道模拟中使用的精确动力学参数,就可以评估拟合结果的准确性。在此,针对具有一级动力学的模型反应,探讨了几个实验影响因素,如数据点密度和噪声添加。所提出的程序揭示了推导动力学参数的准确性,也可能有助于未来实验的设计。