Indian Institute of Technology Palakkad&nbsp;(IIT Palakkad or IIT PKD) is a public autonomous&nbsp;engineering&nbsp;and&nbsp;research&nbsp;institute located in&nbsp;Palakkad,&nbsp;Kerala. It was&nbsp;one of the five new&nbsp;IITs&nbsp;proposed in the&nbsp;2014 Union budget of India. The campus was inaugurated on 3 August 2015. The institute has 94 faculty, 978 students, and 63 non-teaching staffs.

IT Palakkad currently offers four-year Bachelor of Technology (B.Tech) and two years MS programmes in 8 different engineering disciplines including&nbsp;Computer Science, Electrical, Mechanical, Civil among others.

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IIT Palakkad

We have reported experimental studies on the self-assembly and degree of ordering of a binary mixture of soft colloids in monolayer deposits obtained by controlled evaporation. A sessile drop containing soft colloids is evaporated on a solid surface to achieve a loosely-packed two-dimensional deposit with a hexagonal arrangement. The soft microgel particles possess a hard core with a compliant corona, which plays a crucial role in retaining the crystallinity of the binary particle monolayer. The ordered arrangement of the binary mixture is observed even when the bulk diameter of one type of particle is 25% higher than the other, irrespective of their mixing ratio (1 : 3, 1 : 1, and 3 : 1). The microgel particles of both sizes are found to be homogeneously distributed throughout the deposit, completely suppressing the size-dependent particle segregation. Furthermore, in contrast to the self-assembly of bidisperse hard colloids, wherein the lattice distorts to accommodate particles of disparate sizes, in soft colloids, the particles deform at the interface to preserve the crystalline lattice. Moreover, unlike the gradual order-to-disorder transition observed in the deposits consisting of monodisperse microgel particles, the deposits of a binary mixture of microgels exhibit no noticeable trend. The areal disorder parameter, pair correlation function and the shape factor which quantifies the local ordering of particles in the deposit indicate the absence of a distinct order-to-disorder transition for the binary mixtures. © the Owner Societies 2021.

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Department of Physics

Physical Chemistry Chemical Physics

Evaporative self-assembly of the binary mixture of soft colloids

Hypothesis: Evaporating sessile drops containing surface active colloids is a promising route to self-assemble two-dimensional nanostructures. The standard protocol is to first self-assemble surface active nanoscale particles at the water-vapour interface and subsequently transfer it on to a solid surface. Colloidal monolayers with very few morphologies have been fabricated, exploiting this bottom-up self-assembly technique. However, the evaporation kinetics under controlled humidity conditions may dramatically alter the microstructure of self-assembled colloidal monolayers at the liquid–vapor interface and that on the solid surfaces, an aspect that has not been fully addressed in the prior studies. Experiments: To this end, we present an experimental study of evaporation driven self-assembly of soft poly(N-isopropylacrylamide) (pNIPAM) microgel particles loaded in a sessile drop. The surface-active microgel particles spontaneously populate the water-vapour interface facilitating the suppression of the coffee-ring effect and the formation of monolayer stains. The role of evaporation kinetics under controlled humidity conditions on the colloid's microstructure adsorbed to the solvent-air interface and on the morphology of the colloidal monolayer transferred onto the solid surface are studied in detail. Findings: The formation of particle-free and particle-rich regions at the water–vapor interface is observed for sessile drops evaporated under saturated humidity conditions. We show that the evaporation induced shrinkage of the interface area and the enhancement of the areal density of microgel particles adsorbed onto the interface leads to a restructuring of the particle-laden interface. The rearrangement of microgel particles along the water–vapor interface resembling the de-wetting assisted patterns is transferred to the solid substrate upon complete evaporation of the solvent. The microgel particles in the deposit assemble into domains with enhanced crystalline order. The evolution of Voronoi entropy across the monolayer deposit patterns obtained by the standard and slow evaporation routes are presented. © 2020 Elsevier Inc.

Journal of Colloid and Interface Science

Colloidal monolayers with cell-like tessellations via interface assisted evaporative assembly

Effect of Fe doping on the structure, optical and thermoelectric properties of SrTi 0.8 Sn 0.2 O 3 sample has been investigated. The SrTi 0.8−x Sn 0.2 Fe x O 3 (x = 0, 0.1, 0.3) samples are fabricated using solid-state synthesis route. It is observed that Fe doping helps in reducing the densification temperature of SrTi 0.8 Sn 0.2 O 3 during spark plasma sintering. Precipitation of Sn has been observed in SrTi 0.8−x Sn 0.2 Fe x O 3 (x = 0, 0.1) samples while the SrTi 0.8−x Sn 0.2 Fe x O 3 (x = 0.3) sample is of purely single cubic perovskite phase. All the samples consist of nanocrystalline grains and the grain size varies between 150 to 200 nm. Fourier transform infrared spectroscopy (FTIR) analysis reveals the distortion of TiO 6 octahedra due to the increase in Fe content. Raman spectroscopy analysis has shown that perovskite cubic structure is stable from room temperature to 873 K. From thermophysical measurements, it is shown that the Fermi band gap reduces from 2.87 to 0.66 eV with increase in Fe in the investigated samples. The Seebeck co-efficient is found to change the sign from n–type to p-type with the increase of Fe concentration in SrTi 0.8 Sn 0.2 O 3 which is an interesting observation to obtain p-type SrTiO 3 based thermoelectric materials. The optical and thermoelectric properties show that Fe doping improves the thermoelectric properties of SrTi 0.8 Sn 0.2 O 3 ceramics by altering the Seebeck coefficient and thermal conductivity. © 2019 IOP Publishing Ltd.

Materials Research Express

Tuning the optical and thermoelectric properties of SrTi 0.8− x Sn 0.2 Fe x O 3

We show that loosely packed homogeneous monolayers of soft colloidal particles can be fabricated via simple evaporative drying of aqueous dispersion containing colloidal particles. Owing to the inherent amphiphilicity of the soft microgels, they are preferentially adsorbed onto the water-vapor interface of the drying droplet, resulting in a uniform deposition of the particles throughout the fluid-substrate contact area. Distinct order-to-disorder transition is also identified within the dried deposits on changing spatial locations from edge to center of the circular stain. Such monolayer deposits exhibit vibrant colors on irradiating with white light due to interference. © 2019 Author(s).

AIP Conference Proceedings

Order-to-disorder transition in colored microgel monolayers

The variation in the concentration of surfactant molecules along the air-water interface of a drying sessile drop containing colloidal particle-surfactant mixtures is known to inhibit the formation of coffee stains. This also leads to the formation of particulate deposits with a region almost deprived of the particles, often called the depletion zone. The molecular size of the surface-active species used in such experiments poses limitations on the direct visualization of the build-up of surfactant molecules at the interface and how it correlates with the nucleation and growth kinetics of the depletion zone. We report a quantitative analysis of the origin and evolution of the depletion zone that forms in a drying sessile drop. By evaporating an aqueous sessile droplet containing a mixture of surface-active poly(N-isopropylacrylamide) (pNIPAM) microgels and polystyrene (PS) colloids, we establish that the concentration fluctuations of the PS particles along the air-water interface trigger a surface tension driven Marangoni flow along the interface. As a result of this, a depletion zone forms within the particulate deposit, which is analogous to the depletion zones observed for dried drops of particle- surfactant mixtures. The critical time at which the depletion zone forms correlates to the time at which surface tension-driven stress along the interface is maximum. Moreover, we show that the increase in the initial concentration of PS particles results in a decrease in the critical time. By using in situ video microscopy, we established that the rate at which the depletion zone grows is non-linear in time. The growth rate of the depletion zones for drops containing different concentrations of PS particles collapses into a master curve upon scaling with concentration and radius of the drop. © 2019 The Royal Society of Chemistry.

Soft Matter

On the origin and evolution of the depletion zone in coffee stains

We investigate the evaporation-driven pattern formation in drying drops containing mixtures of polystyrene and soft microgel particles. The well-known coffee-rings that form when drops containing polystyrene particles are dried can be completely undone in the presence of a small quantity of soft colloids. The addition of soft colloids facilitates the adsorption of polystyrene particles to the water-vapor interface leading to a steep increase in their concentration and also imparts viscoelasticity to the interface. Time-resolved video microscopy is used to conclusively show the formation of a gel-like particle-laden interface. The mean square displacement of the polystyrene particles adsorbed to the interface confirms their immobile nature at the interface. This viscoelastic interface almost prevents the bulk flow-assisted migration of polystyrene particles toward the drop edge, leading to the suppression of coffee-ring effect and the formation of uniform particulate deposits. Copyright © 2018 American Chemical Society.

Langmuir

Viscoelastic Particle-Laden Interface Inhibits Coffee-Ring Formation

We report a complete suppression of the coffee-ring effect resulting in the formation of loosely packed two-dimensional particle monolayers by controlled evaporation of sessile drops containing soft microgel particles. These particulate deposits show gradual order-to-disorder transitions that are not abrupt like deposits of hard colloids. The areal coverage of the monolayer deposits can also be precisely controlled by tuning the particle concentration. The preferential adsorption of soft-microgel particles to the water-vapor interface, and their radial flow along the interface towards the drop edge facilitates the creation of the novel monolayer deposits. © 2017 The Royal Society of Chemistry.