Quantification of solvation forces with amplitude modulation AFM

被引:0
|
作者
Benaglia, Simone [1 ,2 ]
Chiodini, Stefano [3 ]
机构
[1] Univ Manchester, Dept Phys & Astron, Manchester M13 9PL, England
[2] Univ Manchester, Natl Graphene Inst, Manchester M13 9PL, England
[3] Fdn Ist Italiano Tecnol, Ctr Nano Sci & Technol, Via R Rubattino 81, I-20134 Milan, Italy
关键词
Solid-liquid interfaces; Three-dimensional atomic force microscopy; Force reconstruction; HYDRATION STRUCTURES; WATER INTERFACES; MICROSCOPY; SURFACES; ELECTROLYTES; REPULSION; BINDING; LAYERS;
D O I
10.1016/j.jcis.2025.01.131
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hypothesis: Interfacial solvation forces arise from the organisation of liquid molecules near solid surfaces. They are crucial to fundamental phenomena, spanning materials science, molecular biology, and technological applications, yet their molecular details remain poorly understood. Achieving a complete understanding requires imaging techniques, such as three-dimensional atomic force microscopy (3D AFM), to provide atomically resolved images of solid-liquid interfaces (SLIs). However, converting 3D AFM data into accurate tip-sample forces remains challenging, as the process of translating observables into forces is not straightforward. Experiments/simulations: This study compares standard amplitude modulation AFM (AM-AFM) force reconstruction methods (FRMs) and identifies their limitations in reconstructing SLI forces. A novel numerical matrixbased FRM specifically designed for AM-AFM is then introduced, aiming to overcome the limitations and inaccuracies found in standard approaches. The new method is validated through simulations and experimental data obtained at the SLI of silicon oxide and water with 3D AFM. Findings: The proposed matrix-based FRM, differently from standard FRMs, can reconstruct the full SLI interaction at the atomic scale, with no loss of information deriving from the specific choice of AFM experimental parameters or the force functional form. This method unlocks the full spectrum of physical phenomena encoded in the tip-sample interaction at the SLI in AFM experiments, greatly advancing our understanding of interfacial properties and their effects on colloid science, including nanoparticle interactions and molecular self-assembly.
引用
收藏
页码:342 / 349
页数:8
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