Publications by authors named "Sanjit Manohar Majhi"

Article Synopsis
  • MXenes are emerging materials with unique properties that make them suitable for biosensing applications in health and environmental monitoring.
  • The review covers various biosensor types—electrochemical, enzymatic, optical, and fluorescent—detailing how MXenes enhance their performance and sensitivity.
  • It highlights applications in wearable technology and VOC detection, while also discussing future challenges and advancements in MXene-based biosensor development.
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High-performance, room temperature-based novel sensing materials are one of the frontier research topics in the gas sensing field, and MXenes, a family of emerging 2D layered materials, has gained widespread attention due to their distinctive properties. In this work, we propose a chemiresistive gas sensor made from VCT MXene-derived, urchin-like VO hybrid materials (VC/VO MXene) for gas sensing applications at room temperature. The as-prepared sensor exhibited high performance when used as the sensing material for acetone detection at room temperature.

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The development of gas sensing devices to detect environmentally toxic, hazardous, and volatile organic compounds (VOCs) has witnessed a surge of immense interest over the past few decades, motivated mainly by the significant progress in technological advancements in the gas sensing field. A great deal of research has been dedicated to developing robust, cost-effective, and miniaturized gas sensing platforms with high efficiency. Compared to conventional metal-oxide based gas sensing materials, metal-organic frameworks (MOFs) have garnered tremendous attention in a variety of fields, including the gas sensing field, due to their fascinating features such as high adsorption sites for gas molecules, high porosity, tunable morphologies, structural diversities, and ability of room temperature (RT) sensing.

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This review presents the results of cutting-edge research on chemiresistive gas sensors in Korea with a focus on the research activities of the laboratories of Professors Sang Sub Kim and Hyoun Woo Kim. The advances in the synthesis techniques and various strategies to enhance the gas-sensing performances of metal-oxide-, sulfide-, and polymer-based nanomaterials are described. In particular, the gas-sensing characteristics of different types of sensors reported in recent years, including core-shell, self-heated, irradiated, flexible, Si-based, glass, and metal-organic framework sensors, have been reviewed.

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Reduced graphene oxide (rGO) is a reduced form of graphene oxide used extensively in gas sensing applications. On the other hand, in its pristine form, graphene has shortages and is generally utilized in combination with other metal oxides to improve gas sensing capabilities. There are different ways of adding rGO to different metal oxides with various morphologies.

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The ongoing need to detect and monitor hazardous, volatile, and flammable gases has led to the use of gas sensors in several fields to improve safety and health issues. Conductometric type gas sensors, which have considerable advantages over other gas sensors, have thrived in numerous gas sensing fields. The ever-present key challenges and requirements of these sensors are to achieve excellent performance, including high sensitivity, good selectivity, low working temperature, and durability.

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With the tremendous advances in technology, gas-sensing devices are being popularly used in many distinct areas, including indoor environments, industries, aviation, and detectors for various toxic domestic gases and vapors. Even though the most popular type of gas sensor, namely, resistive-based gas sensors, have many advantages over other types of gas sensors, their high working temperatures lead to high energy consumption, thereby limiting their practical applications, especially in mobile and portable devices. As possible ways to deal with the high-power consumption of resistance-based sensors, different strategies such as self-heating, MEMS technology, and room-temperature operation using especial morphologies, have been introduced in recent years.

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Vertically oriented zinc oxide (ZnO) nanomaterials, such as nanorods (NRs), nanowires (NWs), nanotubes (NTs), nanoneedles (NNs), and nanosheets (NSs), are highly ordered architectures that provide remarkable properties for sensors. Furthermore, these nanostructures have fascinating features, including high surface-area-to-volume ratios, high charge carrier concentrations, and many surface-active sites. These features make vertically oriented ZnO nanomaterials exciting candidates for gas sensor fabrication.

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ZnFeO was fabricated by a simple solution-combustion method. The structural, optical and electronic properties are investigated by XRD, TEM, FESEM, UV-vis DRS, PL, FTIR and photocurrent measurements. The photocatalytic activity of the prepared material is studied with regard to the degradation of rhodamine B (Rh B) and Congo red under solar irradiation.

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We successfully prepared Au@ZnO core-shell nanoparticles (CSNPs) by a facile low-temperature solution route and studied its gas-sensing properties. The obtained Au@ZnO CSNPs were carefully characterized by X-ray diffraction, transmission electron microscopy (TEM), high-resolution TEM, and UV-visible spectroscopy. Mostly spherical-shaped Au@ZnO CSNPs were formed by 10-15 nm Au NPs in the center and by 40-45 nm smooth ZnO shell outside.

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In this work, Au@Cu2O core-shell nanoparticles (NPs) were synthesized by simple solution route and applied for CO sensing applications. Au@Cu2O core-shell NPs were formed by the deposition of 30-60 nm Cu2O shell layer on Au nanorods (NRs) having 10-15 nm width and 40-60 nm length. The morphology of Au@Cu2O core-shell NPs was tuned from brick to spherical shape by tuning the pH of the solution.

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Au@Cu2O core-shell nanoparticles (NPs) were synthesized by a solution method at room temperature and applied for gas sensor applications. Transmission electron microscopy (TEM) images showed the formation of Au@Cu2O core-shell NPs, where 12-15 nm Au NPs were covered with 60-30 nm Cu2O shell layers. The surface plasmon resonance (SPR) peak of Au NPs was red-shifted (520-598 nm) after Cu2O shell formation.

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