6 research outputs found
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Towards Real-Time Oxygen Sensing: From Nanomaterials to Plasma
A significantly large scope is available for the scientific and engineering developments of high-throughput ultra-high sensitive oxygen sensors. We give a perspective of oxygen sensing for two physical states of matters—solid-state nanomaterials and plasma. From single-molecule experiments to material selection, we reviewed various aspects of sensing, such as capacitance, photophysics, electron mobility, response time, and a yearly progress. Towards miniaturization, we have highlighted the benefit of lab-on-chip-based devices and showed exemplary measurements of fast real-time oxygen sensing. From the physical–chemistry perspective, plasma holds a strong potential in the application of oxygen sensing. We investigated the current state-of-the-art of electron density, temperature, and design issues of plasma systems. We also show numerical aspects of a low-cost approach towards developing plasma-based oxygen sensor from household candle flame. In this perspective, we give an opinion about a diverse range of scientific insight together, identify the short comings, and open the path for new physical–chemistry device developments of oxygen sensor along with providing a guideline for innovators in oxygen sensing
Towards Real-Time Oxygen Sensing: From Nanomaterials to Plasma
A significantly large scope is available for the scientific and engineering developments of high-throughput ultra-high sensitive oxygen sensors. We give a perspective of oxygen sensing for two physical states of matters—solid-state nanomaterials and plasma. From single-molecule experiments to material selection, we reviewed various aspects of sensing, such as capacitance, photophysics, electron mobility, response time, and a yearly progress. Towards miniaturization, we have highlighted the benefit of lab-on-chip-based devices and showed exemplary measurements of fast real-time oxygen sensing. From the physical–chemistry perspective, plasma holds a strong potential in the application of oxygen sensing. We investigated the current state-of-the-art of electron density, temperature, and design issues of plasma systems. We also show numerical aspects of a low-cost approach towards developing plasma-based oxygen sensor from household candle flame. In this perspective, we give an opinion about a diverse range of scientific insight together, identify the short comings, and open the path for new physical–chemistry device developments of oxygen sensor along with providing a guideline for innovators in oxygen sensing
Self-driven flow and chaos at liquid-gas nanofluidic interface
We report a novel flow dynamics at the interface of liquid and gas through
nanofluidic pores without applying any external driving force. Rayleigh-Taylor
instability of water and air in sub-100 nanometer fluidic pores in a micrometre
square domain of water and air are studied. We analyse it in the context of
parameters, such as applied pressure, position to pore size ratio of the
nanofluidic pore, gravity, and density. Our research also verifies the flow
velocity equation with the simulation results and discuss the mass transfer
efficiency of such flow structures. This is the first report on a self-driven
switching mechanism of nanofluidic flow from ON to OFF or vice versa. A highly
nonlinear complex nature of fluid dynamics is observed in nanometric
length-scale, which is also one of the first studies in room temperature.
Self-driven nanofluidics will have a large positive impact on biosensors,
healthcare, net-zero sustainable energy production, and fundamental physic of
fluid dynamics
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Active Solid-State Nanopores: Self-Driven Flows/Chaos at the Liquid-Gas Nanofluidic Interface.
Publication status: PublishedHere, we present a comprehensive study of self-driven flow dynamics at the liquid-gas interface within nanofluidic pores in the absence of external driving forces. The investigation focuses on the Rayleigh-Taylor instability phenomena that occur in sub-100 nm scale fluidic pores interfacing between 2 μm scale water and air reservoir. We obtain a flow velocity equation, and we validate it using simulations, concentrating on the mass transfer efficiency of these flow structures. Furthermore, we introduce the concept─"active solid-state nanopore"─that exhibits a self-driven flow switching behavior, transitioning between active and passive states without the need for mechanical components. We found a unique state of chaos at the nanoscale resembling the chaotic motion of fluid. This study contributes to the preliminary understanding of fluid dynamics at the classical-quantum interface. Implications of self-driven nanofluidics extend across diverse fields from biosensing and healthcare applications to advancing net-zero sustainable energy production and contributing to the fundamental understanding of fluid dynamics in confined spaces
Nanometric chemical decomposition of infertile Himalayan soils from Uttarakhand
We present the nanometric chemical decomposition of Himalayan agricultural soils. The motivation to use this state-of-the-art material characterisation in the soil is to reduce the testing cost while increasing the efficiency of the characterisation. In India, a bulk volume of soil is still required for the characterisation of agricultural soil. The fertility of micronutrient contents and crop supply capacity vary greatly depending on soil types, crop types, ecology, and agroclimatic variability. Since total levels of micronutrients are rarely predictive of the availability of a nutrient to plants, knowledge of the differences in soil micronutrients that are available to plants is essential for the sensible management of micronutrient fertility and toxicity. In the state of Uttarakhand, low levels of micro-nutrients in the soil are frighteningly common, and this issue is made worse by the fact that many current cultivars of important crops are extremely vulnerable to low mineral levels. These baseline results are to be used to inform local farmers about the potential remedies, costs, and consequential benefits and durability. We intend not to present a generalized or generalized solution. Therefore, we limit our soil sample collections to five arc minutes (8.6 square kilometers) and document variations and heterogeneity in the chemical components of the soil. In this study, we used scanning electron microscopy to chemically deconstruct the barren Himalayan soils from Uttarakhand. Aluminium, carbon, oxygen, and silicon were identified as the primary elements that contributed more than 5% of the total weight and atomic percentage. Other elements include less than 4% of iron, titanium, nitrogen, sodium, magnesium, chloride, phosphorus, sulfur, potassium, and calcium