Yang Jijin, Ascrizzi Eleonora, Cattelan Mattia, Nalesso Marco, Cielo Leonardo, Matvija Peter, Sedona Francesco, Ferrari Anna Maria, Agnoli Stefano
Department of Chemical Sciences, University of Padova, Padova 35131, Italy.
Department of Chemistry, University of Torino, Torino 10125, Italy.
Nano Lett. 2024 Oct 9;24(40):12552-12559. doi: 10.1021/acs.nanolett.4c03521. Epub 2024 Sep 20.
The interaction of water with solid surfaces is crucial for a wide range of disciplines, including catalysis, environmental science, corrosion, geology, and biology. In this study, we present a combined experimental and theoretical investigation that elucidates the interaction of water with a model iron oxide surface under near ambient conditions (i.e., room temperature and water vapor in the mbar range). Our findings reveal that surface hydroxylation can be controlled at the nanoscale by the local properties of the oxide film, such as local rumpling and electrostatic potential. The iron oxide surface presents alternating hydrophilic and hydrophobic domains, creating after water exposure a hexagonal pattern with a pitch of approximately 3 nm, where the highly hydroxylated regions act as nucleation centers for nanoconfined water molecule clusters.
水与固体表面的相互作用对于包括催化、环境科学、腐蚀、地质学和生物学在内的广泛学科至关重要。在本研究中,我们进行了一项结合实验和理论的研究,阐明了在接近环境条件下(即室温以及毫巴范围内的水蒸气)水与模型氧化铁表面的相互作用。我们的研究结果表明,表面羟基化可以在纳米尺度上通过氧化膜的局部性质来控制,例如局部褶皱和静电势。氧化铁表面呈现出交替的亲水和疏水区域,在水暴露后形成间距约为3 nm的六边形图案,其中高度羟基化的区域充当纳米受限水分子簇的成核中心。