Lake William R, Meng Jinhui, Dawlaty Jahan M, Lian Tianquan, Hammes-Schiffer Sharon
Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States.
Department of Chemistry, Emory University, Atlanta, Georgia 30322, United States.
J Phys Chem Lett. 2024 Sep 5;15(35):9100-9104. doi: 10.1021/acs.jpclett.4c02183. Epub 2024 Aug 28.
A microscopic understanding of electric fields and molecular polarization at interfaces will aid in the design of electrocatalytic systems. Herein, variants of 4-mercaptobenzonitrile are designed to test different schemes for breaking the continuous conjugation between a gold electrode surface and a nitrile group. Periodic density functional theory calculations predict applied potential dependencies of the CN vibrational frequencies similar to those observed experimentally. The CN frequency response decreased more when the conjugation was broken between the benzene ring and the nitrile group than between the electrode and the benzene ring, highlighting molecular polarizability effects. The systems with continuous or broken conjugation are dominated by electro-inductive effects or through-space electrostatic effects, respectively. Analysis of the fractional charge transfer between the electrode and the molecule as well as the occupancy of the CN antibonding orbital provides further insights. Balancing the effects of molecular polarizability, electro-induction, and through-space electrostatics has broad implications for electrocatalyst design.
对界面处电场和分子极化的微观理解将有助于电催化系统的设计。在此,设计了4-巯基苯甲腈的变体,以测试打破金电极表面与腈基之间连续共轭的不同方案。周期性密度泛函理论计算预测了CN振动频率与实验观察到的类似的外加电势依赖性。当苯环与腈基之间的共轭被打破时,CN频率响应的下降比电极与苯环之间的共轭被打破时更多,突出了分子极化率效应。具有连续或断裂共轭的体系分别由电感应效应或空间静电效应主导。对电极与分子之间的分数电荷转移以及CN反键轨道的占据情况的分析提供了进一步的见解。平衡分子极化率、电感应和空间静电的影响对电催化剂设计具有广泛的意义。