Laurans Maxime, Trinh Kelly, Dalla Francesca Kevin, Izzet Guillaume, Alves Sandra, Derat Etienne, Humblot Vincent, Pluchery Olivier, Vuillaume Dominique, Lenfant Stéphane, Volatron Florence, Proust Anna
Sorbonne Université, CNRS, Institut Parisien de Chimie Moléculaire, IPCM, 4 Place Jussieu, F-75005 Paris, France.
Sorbonne Université, CNRS, Institut des Nanosciences de Paris, INSP, 4 Place Jussieu, F-75005 Paris, France.
ACS Appl Mater Interfaces. 2020 Oct 21;12(42):48109-48123. doi: 10.1021/acsami.0c12300. Epub 2020 Oct 6.
Immobilization of polyoxometalates (POMs) onto oxides is relevant to many applications in the fields of catalysis, energy conversion/storage, or molecular electronics. Optimization and understanding the molecule/oxide interface is crucial to rationally improve the performance of the final molecular materials. We herein describe the synthesis and covalent grafting of POM hybrids with remote carboxylic acid functions onto flat Si/SiO substrates. Special attention has been paid to the characterization of the molecular layer and to the description of the POM anchoring mode at the oxide interface through the use of various characterization techniques, including ellipsometry, AFM, XPS, and FTIR. Finally, electron transport properties were probed in a vertical junction configuration and energy level diagrams have been drawn and discussed in relation with the POM molecular electronic features inferred from cyclic-voltammetry, UV-visible absorption spectra, and theoretical calculations. The electronic properties of these POM-based molecular junctions are driven by the POM LUMO (d-orbitals) whatever the nature of the tether or the anchoring group.
将多金属氧酸盐(POMs)固定在氧化物上与催化、能量转换/存储或分子电子学等领域的许多应用相关。优化和理解分子/氧化物界面对于合理提高最终分子材料的性能至关重要。我们在此描述了具有远程羧酸功能的POM杂化物在平坦Si/SiO₂ 衬底上的合成和共价接枝。通过使用各种表征技术,包括椭偏仪、原子力显微镜、X射线光电子能谱和傅里叶变换红外光谱,特别关注了分子层的表征以及POM在氧化物界面处的锚定模式的描述。最后,在垂直结配置中探测了电子传输特性,并绘制了能级图,并结合从循环伏安法、紫外可见吸收光谱和理论计算推断出的POM分子电子特征进行了讨论。无论系链或锚定基团的性质如何,这些基于POM的分子结的电子性质都由POM的最低未占分子轨道(d轨道)驱动。