Li Tiexin, Peiris Chandramalika R, Aragonès Albert C, Hurtado Carlos, Kicic Anthony, Ciampi Simone, MacGregor Melanie, Darwish Tamim, Darwish Nadim
School of Molecular and Life Sciences, Curtin University, Bentley, Western Australia 6102, Australia.
Departament de Ciència de Materials i Química Física, Universitat de Barcelona, Marti i Franquès 1, 08028 Barcelona, Spain.
ACS Appl Mater Interfaces. 2023 Oct 11;15(40):47833-47844. doi: 10.1021/acsami.3c11598. Epub 2023 Sep 28.
In recent years, the hybrid silicon-molecular electronics technology has been gaining significant attention for applications in sensors, photovoltaics, power generation, and molecular electronics devices. However, Si-H surfaces, which are the platforms on which these devices are formed, are prone to oxidation, compromising the mechanical and electronic stability of the devices. Here, we show that when hydrogen is replaced by deuterium, the Si-D surface becomes significantly more resistant to oxidation when either positive or negative voltages are applied to the Si surface. Si-D surfaces are more resistant to oxidation, and their current-voltage characteristics are more stable than those measured on Si-H surfaces. At positive voltages, the Si-D stability appears to be related to the flat band potential of Si-D being more positive compared to Si-H surfaces, making Si-D surfaces less attractive to oxidizing OH ions. The limited oxidation of Si-D surfaces at negative potentials is interpreted by the frequencies of the Si-D bending modes being coupled to that of the bulk Si surface phonon modes, which would make the duration of the Si-D excited vibrational state significantly less than that of Si-H. The strong surface isotope effect has implications in the design of silicon-based sensing, molecular electronics, and power-generation devices and the interpretation of charge transfer across them.
近年来,混合硅分子电子技术在传感器、光伏、发电及分子电子器件等应用领域备受关注。然而,作为这些器件形成平台的硅氢键(Si-H)表面易于氧化,会损害器件的机械和电子稳定性。在此,我们表明,当氢被氘取代时,在硅表面施加正电压或负电压时,硅氘键(Si-D)表面对氧化的抗性显著增强。Si-D表面更耐氧化,其电流-电压特性比在Si-H表面测得的更稳定。在正电压下,Si-D的稳定性似乎与Si-D的平带电位比Si-H表面更正有关,这使得Si-D表面对氧化的氢氧根离子吸引力更小。Si-D表面在负电位下的有限氧化可通过Si-D弯曲模式的频率与体硅表面声子模式的频率耦合来解释,这将使Si-D激发振动状态的持续时间显著短于Si-H。这种强烈的表面同位素效应在硅基传感、分子电子学和发电器件的设计以及对其电荷转移的解释方面具有重要意义。