Many self-assembly approaches of colloidal monolayers have flourished but with some shortages, such as complexity, time-consumption, parameter sensitivity, and high-cost. This paper presents a facile, rapid, well-controlled, and low-cost method to prepare monolayers by directly adding silica particle suspensions containing water and ethanol to different liquids. A detailed analysis of the self-assembly process was conducted. The particles dove into water firstly, then moved up under the effect of the buoyancy and the tension gradient. The tension gradient induced the Marangoni convection and the relative motion between the water and the particles. At last, the particles were adsorbed at the air-water interface to minimize the free energy. The quality of the monolayers depended on the addition of sodium dodecyl sulfonate or ethanol in the water subphase. An interfacial polymerization of ethyl 2-cyanoacrylate was used to determine the contact angles of the particles at different subphase surfaces. The value of the detachment energy was positively associated with the contact angle and the surface tension. When the detachment energy decreased to a certain value, some particles detached from the surface, leading to the formation of a quasi-double layer. We also observed that the content of ethanol in suspensions influenced the arrangement of particles.

Pulse number dependent evolution from nanodents to nanobumps has been studied on a bearing steel substrate, which was coated with a self-assembled monolayer of silica microspheres and repeatedly irradiated by an 800 nm femtosecond laser. Scanning electron microscope and atomic force microscope were employed to characterize nanopatterns, the dimensions of which were related to the laser pulse number and pulse fluences. The transformation depending on the number of laser pulses could be attributed to the changes of electric field distribution and material property after the impacts of multiple laser pulses, the process of which could be divided into three steps. First, the bottoms of silica microspheres were ablated because of the incubation effects from repeated irradiation. Second, strong plasmonic localization at the edges of the deep nanodents resulted in plasma-chemical reactions between ablated materials, which was confirmed by electromagnetic simulations. Third, recrystallized solid matter from ablated materials deposited in nanodents and then formed nanobumps, which was confirmed by transmission electron microscope and energy dispersive X-ray spectrometer analyses on their longitudinal sections.