Faculty Publications

Now showing 1 - 3 of 3

Defects Enriched p-type Zinc Stannate for Selective Detection of ppb-Level NO2 Gas at Ambient Temperature
(American Chemical Society, 2024) Pawar, N.; Nath, V.G.; Rodney, J.D.; Joshi, S.; Subramanian, A.; Udayashankar, N.K.
In this study, we explore the synthesis and gas-sensing capabilities of zinc stannate (Zn2SnO4) in three morphologies─spherical nanoparticles, urchins, and octahedrons─aiming to investigate the influence of morphology on sensing properties. The fabricated devices exhibit a significant resistance decrease upon exposure to NO2 at room temperature (24 °C), indicating p-type sensing behavior. Among these morphologies, the spherical nanoparticle-based sensor exhibits the highest sensor response of 57% to 6 ppm of NO2, outperforming urchins and octahedrons by approximately 1.2 and 4.1 times, respectively. This superior performance, with response and recovery times of 6.3 s and 224 s, is attributed to enhanced redox reactions from a larger surface area and a higher proportion of oxygen interstitials. The spherical nanoparticle-based sensor also demonstrates exceptional selectivity for NO2 over SO2, CO, NH3, and CH4, with a detection limit of 200 ppb. Furthermore, the sensor exhibits excellent reversibility with only 2% variation across 20 consecutive test cycles and demonstrates remarkable long-term stability, with a performance fluctuation of approximately 2.3% over 63 days without significant degradation. © 2024 American Chemical Society.
Assessment on the effectiveness of chemical admixture in processed laterite and copper slag based geopolymer mortar
(Elsevier Ltd, 2025) Clement, D.; C, R.; Singh, S.K.; Tiwari, M.
Geopolymer-based cementitious materials known for their robust durability and lower environmental impact make them an ideal choice for sustainable construction. The main focus of this study is to understand the influence of chemical admixtures which plays a pivotal role in improving the properties of geopolymer mortar (GM). This research integrates various chemical admixtures, including calcium chloride, sodium sulphate, sodium hexametaphosphate, and MasterGlenium SKY 8233 (SKY) which falls under the category of either accelerators, retarders, or superplasticisers. Assessments were conducted on the fresh and hardened states of flyash-based GM mixes with varying proportion of river sand (RS), laterite soil (LS) and copper slag (CS), encompassing flowability, setting times, compressive strength, durability study in aggressive environmental conditions and microstructural analyses after 56 days of ambient curing. Findings reveal that calcium chloride and sodium sulphate efficiently decrease the initial and final setting times of the geopolymer paste, highlighting their roles as accelerators, with calcium chloride showing greater efficacy than sodium sulphate. On the other hand, sodium hexametaphosphate serves as a retarder, substantially extending the initial setting time of the geopolymer paste. Introducing the modified polycarboxylic ether (PCE) based superplasticiser SKY into the mortar matrix caused the initial setting time to be extended and resulted in a slight drop in compressive strength compared to the other mixes. Durability tests confirmed the superior resistance of GM mixes to harsh environments like acid, sulphate, and marine water exposure. These findings highlight the potential for tailoring geopolymer blends to achieve desired properties under ambient curing conditions using chemical admixtures. © 2025 Elsevier Ltd
Rotational Flexibility in Dication Drives Ambient Temperature Ferroelectricity in an Organic–Inorganic Hybrid Halide
(John Wiley and Sons Inc, 2025) Hassan, N.; Panday, R.; Chandru, P.G.; Ananthram, K.S.; Jose, T.M.; Bhoi, U.; Sieradzki, A.; Zar?ba, J.K.; Boomishankar, R.; Tarafder, K.; Ballav, N.
Organic–inorganic hybrid halides (OIHHs) have gained attention as potential ferroelectric materials due to structure-property synergy of the organic and inorganic constituents. This study introduces an unusual Ag(I)-based ternary OIHH, (4,4?-bpy)Ag2Br4, featuring rotational flexibility in the organic dication to induce asymmetry into the structure. The compound crystallizes in a monoclinic crystal system with a non-centrosymmetric polar P21 space group at room-temperature and undergoes a structural phase transition to a centrosymmetric phase (P21/c) at Curie temperature (Tc) of 330 K which was further supported by differential scanning calorimetry (DSC), second harmonic generation (SHG) signals, dielectric anomaly, current-voltage (I–V) profiles, and X-ray photoelectron spectroscopy (XPS) data. Ferroelectricity is confirmed through polarization–electric field (P–E) hysteresis loops and piezoresponse force microscopy (PFM), exhibiting switchable polar domains. Density functional theory (DFT) calculations revealed electronic structures of the ferroelectric and paraelectric phases, identified the (?-AgBr2)nn? inorganic anionic chain contributing to the net polarization, and in general, complemented the experimental results. Comparative studies with structurally analogous Ag(I)-based OIHHs lacking dication rotational freedom endorse the critical role of organic flexibility in driving ferroelectricity. This study provides insights into the role of organic dications in controlling ferroelectric behavior and offers a promising pathway for developing coinage metal-based OIHH ferroelectric materials. © 2025 Wiley-VCH GmbH.

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