Sensor Material Research Articles

Rational Design of 3D Polymer Corona Interfaces of Single-Walled Carbon Nanotubes for Receptor-Free Virus Recognition.

Facing the escalating threat of viruses worldwide, the development of efficient sensor elements for rapid virus detection has never been more critical. Traditional point-of-care (POC) sensors struggle due to their reliance on fragile biological receptors and limited adaptability to viral strains. In this study, we introduce a nanosensor design for receptor-free virus recognitions using near-infrared (NIR) fluorescent single-walled carbon nanotubes (SWCNTs) functionalized with a poly(ethylene glycol) (PEG)-phospholipid (PEG-lipid) array. Three-dimensional (3D) corona interfaces of the nanosensor array enable selective and sensitive detection of diverse viruses, including Ebola, Lassa, H3N2, H1N1, Middle East respiratory syndrome (MERS), severe acute respiratory syndrome coronavirus 1 (SARS-CoV-1), and SARS-CoV-2, even without any biological receptors. The PEG-lipid components, designed considering chain length, fatty acid saturation, molecular weight, and end-group moieties, allow for precise quantification of viral recognition abilities. High-throughput automated screening of the array demonstrates how the physicochemical properties of the PEG-lipid/SWCNT 3D corona interfaces correlate with viral detection efficiency. Utilizing molecular dynamics and AutoDock simulations, we investigated the impact of PEG-lipid components on 3D corona interface formation, such as surface coverage and hydrodynamic radius and specific molecular interactions based on chemical potentials. Our findings not only enhance detection specificity across various antigens but also accelerate the development of sensor materials for promptly identifying and responding to emerging antigen threats.

Natural honey (Mellifera) assisted combustion synthesis of ZnO, Ag-ZnO and Fe-ZnO nanoparticles for ethanol gas sensor applications

Biogenic combustion with Mellifera (Honey) capping produced ZnO, Ag-doped ZnO, and Fe-doped ZnO nanoparticles. The phase and crystal structure of metal oxide nanoparticles (MONPs) have been recorded through XRD spectrum. It confirms that the prepared metal oxides are within the nanoscale range. The average crystallite size of Fe-doped ZnO is 8.8 nm, smaller than ZnO and Ag-doped nanoparticles. The vibrational spectra of ZnO, Ag-doped ZnO, and Fe-doped ZnO nanoparticles confirm functional group stretching vibrational modes. The exterior surface morphology of all metal oxide nanoparticles was captured by FESEM. Metal oxide nanoparticle compositional analysis shows elemental presence, atomic, and weight %. The optical properties of metal oxide nanoparticles have been examined using UV–vis spectroscopy. The band gap energy of ZnO nanoparticles reduced from 2.68 eV to 1.74 eV under Fe doing and increased to 2.9 eV under Ag doing. Metal oxide thermal stability is also being investigated to determine how it affects ZnO nanoparticles. Fe-doped ZnO nanoparticles have greater sensor properties than other metal oxides due to their tiny size, band gap, and stability. Gas sensor behaviour of three metal oxide nanoparticles was examined in various accepts. It proves Fe-doped ZnO is a promising gas sensor material.

Bromine‐Enhanced Organic Materials for X‐ray Sensors: Unveiling the Potential of Small Molecules and Polymers through Material Design and Film Fabrication

AbstractOrganic X‐ray sensors are a promising new class of detectors with the potential to revolutionize medical imaging, security screening, and other applications. However, the development of high‐performance organic X‐ray sensors is challenged by low sensitivity. This paper reports on the development of nine X‐ray sensors based on new organic materials. It is demonstrated that the incorporation of bromine atoms into the sidechains of carbazolyl‐containing organic molecules significantly enhances their X‐ray sensitivity. This research suggests that incorporating a variety of high‐atomic‐number chemical elements into well‐established organic semiconductors is a promising strategy for designing efficient X‐ray sensor materials.

Spider silk biological material for Q-switched temperature sensor

Abstract A temperature sensor using compact design and highly sensitivity of side polished fiber and fiber Bragg grating as the sensing elements, Q-switched pulse fiber laser source with spider silk as a saturable absorber is proposed and demonstrated. Spider silk sample was gently collected from a live spider, specifically, the jumping spider of Plexippus sp. which then incorporated within the laser cavity by deposited the silk onto the surface of the fiber ferrule to facilitate the generation of Q-switched pulse fiber laser. The temperature variations were detected by monitoring the pulse train and radio frequency shift from the oscilloscope. The performance of the side polished fiber sensor probe shows a sensitivity of 0.1522 kHz/°C, with 0.9479 coefficient of determination value as the temperature increased from -0.5 °C to +3.1 °C. Besides, a linear temperature re-sponse in the range of 25 °C – 55 °C with a sensitivity of 0.0423 kHz/°C, and a linear correlation coefficient of 0.951 was experimentally achieved for a fiber Bragg grating device. The spider silk as a saturable absorber material is compatible with fiber optic interconnection and the temperature sensing characteristics were successfully demonstrated. The sensor's straight-forward design further enhances its desirability as a sensor for temperature monitoring, including in the field of biological treatments, consumer electronics, detection of chemical analytes, and medical diagnosis.

Morphologically tailored NiMn2O4nanocubic material for high energy-power density asymmetric supercapacitor and non-enzymatic H2O2 sensing

Developing an advanced material for energy storage and sensors is considered a key solution to meet future energy demands and economic challenges. The inverse spinel-structured NiMn2O4 emerges as a promising electrode material for next-gen energy storage due to its notable power capability, high energy density, and excellent cyclic stability. Nanostructuring enhances features not achievable in bulk materials, with a mixed morphology of nano-cubic and nanoflakes optimizing surface-to-volume ratio for effective use in energy storage devices. The addition of PVP as a surfactant, transforms the diffusion-controlled behavior to a capacitive mechanism, enhancing energy density and cyclic stability. Electrodes exhibit a specific capacitance of 816 F g−1 at 1 A g−1 and stable cyclic behavior over 5000 cycles in 1 M KOH. The constructed ASC device shows 96% cyclic stability over 10,000 cycles, maintaining an energy density of 8.8 Wh kg−1 at 6400 W kg−1 and reaching a maximum of 36.55 Wh kg−1 at 400 W kg−1. Electronic structural characteristics explained through density functional theory (DFT) contribute insights. Furthermore, the non-enzymatic NiMn4/GCE H2O2 sensor demonstrates high sensitivity, a low detection limit, and remarkable selectivity against various biological interferences across a broad concentration range.

Prediction of hydrogel swelling states using machine learning methods

AbstractIn the field of material informatics, artificial neural networks (ANNs) contribute to the investigation of the processing‐structure‐properties‐performance relationship of materials. This inspires us to leverage the capabilities of ANNs to decode properties of hydrogels, thereby customizing these active materials for sensors or actuators. In the current work, we introduce an approach to predict discrete swelling states of temperature‐responsive hydrogels, especially PNIPAAm, based on their synthesis parameters, utilizing ANN models. To build the database, we analyze literature on temperature‐responsive hydrogels and compile essential synthesis parameters. The corresponding data points related to these synthesis parameters are then extracted. We propose different variants of ANN models and compare their accuracy on the acquired dataset. The selected model can predict the swelling states of hydrogel samples within the test dataset with relative prediction error of 0.11. This approach is applied to predict the expected properties. Subsequently, the hydrogels can be synthesized, and their properties can be experimentally verified. Our approach can be extended to other types of hydrogels and in the prediction of additional properties. The identified synthesis parameters serve as a valuable foundation for the expansion of the database with further literature resources. An enriched database will enhance the performance of the data‐driven model, thereby improving its predictive capabilities.

Porous flexible piezoresistive sensor using liquid metal for low pressure detection

Gallium-based liquid metals with the superiority of exceptional metallic conductivity, fluidity at room temperature, and nontoxicity are showing promising perspectives in flexible sensors and electronics. However, the limited particle size that serves as one of the intrinsic properties of the materials may induce poor charge transfer, thus further weakening their application performance. This paper presents a flexible pressure sensor using a simple and low-cost method of integrating gallium-based liquid metal and multi-walled carbon nanotubes (MWCNTs), which have the merit of forming numerous conductive pathways due to the exceptional aspect ratio. Meanwhile, liquid metal particles can deform flexibly under pressure, which enables them to serve as conductive links between the nanotubes, greatly strengthening the inner conductive network, and thus exhibiting a desirable piezoresistive performance when functioning as sensor material. Benefitting from the proposed porous structure, the developed sensor shows excellent mechanical softness which is a critical merit in detecting low pressure. Our experimental results indicate that the sensor has a fast response/recovery time of 400/1200 ms and high sensitivity of signal output (normalized resistance change of 84 %) under a low pressure (2.4 kPa). Our proposed design and sensor prototype exhibit significant potential in human motion detection including the counting of walking steps as a demonstration of the application.

Rod-Like MnMoO4 with Excellent Electrochemical Performance as Sensing Material to Detect Triethylamine

MnMoO4 has excellent electrochemical properties and is widely used in the field of electrochemistry. In this study, MnMoO4 with rod-like structure was successfully prepared by simple solvothermal method and used as sensitive material for gas sensors. The gas sensing performance shows that the response of MnMoO4-based sensor to 50 ppm triethylamine is 224.2, which is 2.3 times higher than that of pure MoO3. That reason why MnMoO4 exhibits better sensitivity is that the increase of oxygen vacancy content gives the surface of MnMoO4 material abundant active sites. In addition, its large baseline resistance is also conducive to the improvement of gas sensitivity. These factors make the MnMoO4-based sensor exhibit high response to triethylamine. What’s more, the sensor also has excellent selectivity, satisfactory repeatability, and long-term stability to triethylamine under chemical sensitization and synergistic action. This work provides a new thinking for the application of MnMoO4 in gas sensors.

Quantum-level investigation of air decomposed pollutants gas sensor (Pd-modified g-C3N4) influenced by micro-water content.

In the electrical industry, there are many hazardous gases that pollute the environment and even jeopardize human health, so timely detection and effective control of these hazardous gases is of great significance. In this work, the gas-sensitive properties of Pd-modified g-C3N4 interface for each hazardous gas molecule were investigated from a microscopic viewpoint, taking the hazardous gases (CO, NOx) that may be generated in the power industry as the detection target. Then, the performance of Pd-modifiedg-C3N4 was evaluated for practical applications as a gas sensor material. Novelly, an unconventional means was designed to briefly predict the effect of humidity on the adsorption properties of this sensor material. The final results found that Pd-modified g-C3N4 is most suitable as a potential gas-sensitizing material for NO2 gas sensors, followed by CO. Interestingly, Pd-modified g-C3N4 is less suitable as a potential gas-sensitizing material for NO gas sensors, but has the potential to be used as a NO cleaner (adsorbent). Unconventional simulation explorations of humidity effects show that in practical applications Pd-modified g-C3N4 remains a promising material for gas sensing in specific humidity environments. This work reveals the origin of the excellent properties of Pd-modified g-C3N4 as a gas sensor material and provides new ideas for the detection and treatment of these three hazardous gases.

Synthesis and Characterization of PVA/PANI Nanofiber as Active Material for Humidity Sensors

PANI is a nanostructure conductive polymer that has been widely researched by making nanofibers using electrospinning, by adding PVA as a non-conductive material. In this research, we have successfully synthesized PVA/PANI nanofiber using the electrospinning method and applied it as a humidity sensor. The oxidation polymerization method was conducted to produce polyaniline (PANI) powder. PVA was used as a non-conductive polymer to carry PANI. PANI is blended with 10 % PVA to produce nanofiber PVA/PANI. The results of the synthesis of PVA/PANI nanofibers using the electrospinning method have been characterized by FTIR and EDX to identify the functional groups and elements of PVA/PANI. The FTIR results confirmed that for the PVA nanofiber samples, the type of polyvinyl alcohol bond has been identified according to the reference. The EDX results show the elements C, O and N. The element nitrogen (N) is the characteristic element of polyaniline (C6H5(NH)2)n. The optical Microscope and Scanning Electron Microscope show that the electrospinning method has succeeded in synthesizing PVA/PANI nanofibers with a fiber size of around 0.313 mm. The porosity of PVA/PANI is around 55 %, which is related to the ability of PVA/PANI sensitivity to detect humidity. These results are demonstrated by measurements using a Four-Point Probe (FPP), with the humidity value varying from 64 - 80 %. The results show that variations of PANI powder content improve the sensitivity performance of PVA/PANI nanofibers. This method can optimize PVA/PANI nanofiber as a humidity sensor, increase conductivity flexibility, make it easier and enhance the PANI to use as an active sensor. HIGHLIGHTS The active material for the sensor is polyaniline-based. Polyaniline oxidation polymerization using a method with solid acid doping, which can increase the conductivity of polyaniline (PANI). The formation of PANI nanofibers increases the sensing activities’ effectiveness. Polyvinyl alcohol (PVA) is used as a carrier to facilitate the synthesis process by electrospinning. GRAPHICAL ABSTRACT

Etching of quartz crystals in liquid phase environment: A review

Quartz crystals are the most widely used material in resonant sensors, owing to their excellent piezoelectric and mechanical properties. With the development of portable and wearable devices, higher processing efficiency and geometrical precision are required. Wet etching has been proven to be the most efficient etching method for large-scale production of quartz devices, and many wet etching approaches have been developed over the years. However, until now, there has been no systematic review of quartz crystal etching in liquid phase environments. Therefore, this article provides a comprehensive review of the development of wet etching processes and the achievements of the latest research in this field, covering conventional wet etching, additive etching, laser-induced backside wet etching, electrochemical etching, and electrochemical discharge machining. For each technique, a brief overview of its characteristics is provided, associated problems are described, and possible solutions are discussed. This review should provide an essential reference and guidance for the future development of processing strategies for the manufacture of quartz crystal devices.

In-situ forming ultra-mechanically sensitive materials for high-sensitivity stretchable fiber strain sensors.

Fiber electronics with flexible and weavable features can be easily integrated into textiles for wearable applications. However, due to small sizes and curved surfaces of fiber materials, it remains challenging to load robust active layers, thus hindering production of high-sensitivity fiber strain sensors. Herein, functional sensing materials are firmly anchored on the fiber surface in-situ through a hydrolytic condensation process. The anchoring sensing layer with robust interfacial adhesion is ultra-mechanically sensitive, which significantly improves the sensitivity of strain sensors due to the easy generation of microcracks during stretching. The resulting stretchable fiber sensors simultaneously possess an ultra-low strain detection limit of 0.05%, a high stretchability of 100%, and a high gauge factor of 433.6, giving 254-folds enhancement in sensitivity. Additionally, these fiber sensors are soft and lightweight, enabling them to be attached onto skin or woven into clothes for recording physiological signals, e.g. pulse wave velocity has been effectively obtained by them. As a demonstration, a fiber sensor-based wearable smart healthcare system is designed to monitor and transmit health status for timely intervention. This work presents an effective strategy for developing high-performance fiber strain sensors as well as other stretchable electronic devices.

Adsorption of toxic gases by Janus MoSeTe monolayers doped with transition metals and surface defects: A first-principles study

In recent years, two-dimensional TMDs materials have been proved to be high-performance gas sensor materials. Janus material is a member of the TMD family, and its gas sensing performance research is particularly important. Gas sensing mechanism of toxic gases on transition metal dichalcogenides based Janus MoSeTe monolayers is investigated using the density functional theory. Six transition metals are considered to modify the MoSeTe surface, by comparing the adsorption energies of the transition metal on both sides of the MoSeTe monolayer, it is found that the transition metal doping is more stable on the Se side. The MoSeTe surface is activated by transition metal modification, and the gas behavior is improved by transition metal modification, it is found that Ir-MoSeTe had the best sensing performance for NO2, Os-MoSeTe had the best sensing performance for CO, and Ru-MoSeTe had the best sensing performance for H2S, NO, and SO2. After that, we explain the adsorption mechanism of gas molecules by calculating the band structure, state density, differential charge density and work function of the adsorption structure, and the recovery time explain the reuse performance of the sensor. The results show that transition metal doped MoSeTe is a promising toxic gas sensor, which provides a theoretical basis for the development of new gas sensors.

Recyclable and mechanically tough nanocellulose reinforced natural rubber composite conductive elastomers for flexible multifunctional sensor

The development of flexible wearable multifunctional electronics has gained great attention in the field of human motion monitoring. However, developing mechanically tough, highly stretchable, and recyclable composite conductive materials for application in multifunctional sensors remained great challenges. In this work, a mechanically tough, highly stretchable, and recyclable composite conductive elastomer with the dynamic physical-chemical dual-crosslinking network was fabricated by the combination of multiple hydrogen bonds and dynamic ester bonds. To prepare the proposed composite elastomers, the polyaniline-modified carboxylate cellulose nanocrystals (C-CNC@PANI) were used as both conductive filler to yield high conductivity of 15.08 mS/m, and mechanical reinforcement to construct the dynamic dual-crosslinking network with epoxidized natural rubber latex to realize the high mechanical strength (8.65 MPa) and toughness (29.57 MJ/m3). Meanwhile, the construction of dynamic dual-crosslinking network endowed the elastomer with satisfactory recyclability. Based on these features, the composite conductive elastomers were used as strain sensors, and electrode material for assembling flexible and recyclable self-powered sensors for monitoring human motions. Importantly, the composite conductive elastomers maintained reliable sensing and energy harvesting performance even after multiple recycling process. This study provides a new strategy for the preparation of recyclable, mechanically tough composite conductive materials for wearable sensors.

Mining Metal‐Biomolecular Framework/PANI Composite CO Sensor: Material Synthesis, Gas Sensing Performance and Mechanism

AbstractIn addressing the issue of poor gas sensitivity in semiconductor CO sensor materials used in mining, such as pure PANI. This study utilized an ice‐water bath in combination with an in‐situ polymerization method to synthesize a new composite material consisting of Cu(II)‐racemic glutamate nanofibers and PANI. The morphology, structure, and chemical bonds of the composite material were analyzed using scanning electron microscopy‐energy dispersive spectroscopy (SEM‐EDS) and spectral analysis. The material's ability to detect CO (100–500 ppm) at room temperature was investigated, revealing a response value of up to 6.8 % for 400 ppm CO detection when the composite material was deposited on a ceramic interdigital electrode. The material exhibited good selectivity and responsiveness to CO detection at room temperature, attributed to the heterojunction formed between Cu(II)‐racemic glutamate nanofibers and PANI, which enhanced carrier migration. Consequently, the Cu(II)‐racemic glutamate nanofiber/PANI composite(Cu(II)‐RGlu/PANI) material shows promise as a high‐performance sensing material for CO detection at room temperature and as a low‐power, integrable sensor material for underground coal mines. This research contributes to the development of a theoretical framework for such applications.

Nanosized tin dioxide based semiconductor materials for creation of gas sensors

Nanosized initial semiconductor tin dioxide based material was synthesized by a sol-gel technique and characterized by XRD, IR-spectroscopy, DTA-DTG and TEM methods. Nanosized SnO2-based sensor materials were prepared using the pastes with different quantities of tin dioxide and carboxymethyl cellulose and formatted at various temperatures. It was found that the compositions of the pastes significantly affect the characteristics of the sensors obtained on their base. The characteristics of the sensors of different compositions were explained by necessity of the presence of sufficient number of contacts between the nanoparticles of the sensor material, which ensure the electrical conductivities of the sensors.

Specific temperature-modulated crab shell-derived porous carbon as a typical recycling material for nitrofurazone electrochemical sensor

Nitrofurazone (NFZ), a nitroimidazole antibiotic, can cause serious toxicity when overused, its quantification is crucial for human health. Herein, crab shell waste is converted into porous biochar at a high temperature, which can be employed for the establishment of an electrochemical sensor for the quantitative detection of NFZ. The morphological and structural properties of the crab shell carbon at different temperatures were characterized by SEM, XRD, FT-IR and N2 adsorption-desorption analyses. The crab shell carbon prepared at 500 °C (C-CS-500) and 700 °C (C-CS-700) is calcite-based and contains micro-fibrillar similar to chitin structure, while the crab shell carbon prepared at 900 °C (C-CS-900) is lime-based and lacks the similar structure. And the synergistic influence of calcite-based composition and micro-fibrillar structure of crab shell carbon offered strong electron-transport properties and a large electrode active at a higher carbonized temperature. The electrochemical signals demonstrated that the crab shell carbon prepared at 700 °C provided enhanced sensing capability for rapid NFZ detection with a wide linear range of 0.40–80 μM, a high sensitivity of 0.55 μA μM−1 and a low detection limit of 0.11 μM (S/N = 3), as compared to the crab shell carbon prepared at 500 °C and 900 °C. In addition, the sensor can also be utilized to quantify nitrofurazone in the real drug (compound cod liver oil ointment) with satisfactory recovery.

Environmentally friendly use of silver nanoparticles prepared with Anchusa azurea flower to detect mercury (II) ions

ABSTRACT In this study, the extract obtained from the flowers of the Anchusa azurea (AA) plant was mixed with silver nitrate to obtain silver nanoparticles. The ion sensing ability of the obtained bio-sourced silver nanoparticles in aqueous solutions was investigated and the presence of Hg2+ ions was determined colorimetrically. Silver nanoparticles (AgNPs) prepared on Green Chemistry method, which is both an environmentally friendly and cost-effective synthesis technique, were characterised using different analytical tools. The mean particle size of AA-AgNPs from transmission electron microscopy (TEM) images was determined to be 22 nm in diameter. XRD measurements showed that the crystallite sizes of the synthesised AgNPs were in the face-centred cubic crystal structure with an average size of 22 nm, which is consistent with TEM results. AA-AgNPs showed absorption at 435 nm, indicating that AgNPs exhibit a strong surface plasmon resonance (SPR) and play a role in stabilisation. AgNPs synthesised with Anchusa azurea flowers were observed using UV-vis spectroscopy to selectively and sensitively detect mercury ions (Hg2+). When Hg2+ in aqueous solution was added to the AgNPs, the overall absorbance dramatically decreased and the colour changed from yellow to colourless. This study shows that AA-AgNPs can be used as a cost-effective material in optical sensors for colorimetric determinations.

Evaluating the effect of unidirectional loading on the piezoresistive characteristics of carbon nanoparticles

The piezoresistive effect of materials can be adopted for a plethora of sensing applications, including force sensors, structural health monitoring, motion detection in fabrics and wearable, etc. Although metals are the most widely adopted material for sensors due to their reliability and affordability, they are significantly affected by temperature. This work examines the piezoresistive performance of carbon nanoparticle (CNP) bulk powders and discusses their potential applications based on strain-induced changes in their resistance and displacement. The experimental results are correlated with the characteristics of the nanoparticles, namely, dimensionality and structure. This report comprehensively characterizes the piezoresistive behavior of carbon black (CB), onion-like carbon (OLC), carbon nanohorns (CNH), carbon nanotubes (CNT), dispersed carbon nanotubes (CNT-D), graphite flakes (GF), and graphene nanoplatelets (GNP). The characterization includes assessment of the ohmic range, load-dependent electrical resistance and displacement tracking, a modified gauge factor for bulk powders, and morphological evaluation of the CNP. Two-dimensional nanostructures exhibit promising results for low loads due to their constant compression-to-displacement relationship. Additionally, GF could also be used for high load applications. OLC’s compression-to-displacement relationship fluctuates, however, for high load it tends to stabilize. CNH could be applicable for both low and high loading conditions since its compression-to-displacement relationship fluctuates in the mid-load range. CB and CNT show the most promising results, as demonstrated by their linear load-resistance curves (logarithmic scale) and constant compression-to-displacement relationship. The dispersion process for CNT is unnecessary, as smaller agglomerates cause fluctuations in their compression-to-displacement relationship with negligible influence on its electrical performance.

Molecular receptors integrated bimodal porous polymer scaffolds as portable solid-state optical ion-sensors and extractors for the selective capturing of ultra-trace toxic copper ions

BackgroundEnvironmental contamination by heavy metal ions has caused growing ecological and public health concerns. In this line, monitoring of copper toxicity gains importance due to its application in industrial, agricultural, domestic, medical and technological sectors. Although noteworthy breakthroughs were made, critical issues, such as portability, the need for well-trained personnel, costly/complex instrumentations, long response time, and the introduction of secondary contaminants, required attention. Hence, developing a low-cost, user-friendly, real-time, portable analytical platform for rapid and on-site analysis remained imperative. Solid-state colorimetric sensors have gained widespread popularity due to their low cost, ease of use, and brilliant sensitivity/selectivity. ResultsWe have successfully unfolded an ultra-portable azomethine-infused structurally interwoven polymer monolith as the solid-state chromatic sensor for the quantitative naked-eye detection of ultra-trace Cu2+ in industrial/environmental samples. For the sensor fabrication, non-hygroscopic conjugated Schiff-base receptors, namely N-(1E,2E)-3-(4-dimethylamino)phenyl)allylidene)-3-nitrobenzohydrazide (DPAN) and 2,3-bis(((1E,2E)-3-(4-dimethylamino)phenyl)allylidene)amino)malononitrile (DPAM) were synthesized in-house and voluminously immobilized onto a crack-free porous poly(4VP-co-EGDMA) monolith framework. The topological structure and functionalities of the porous polymer monolith and chromatic sensor materials were examined using various surface analytical and microscopic techniques. The excellent surface area and intriguing interlaced porosity features of the tailor-made polymer monolith facilitated the voluminous anchoring of the chromatic receptors for the selective/sensitive targeting of Cu2+. The DPAN and DPAM receptor-loaded poly(4VP-co-EGDMA) sensors exhibited a linear range of 0–150 μg/L, with the limit of detection of 0.11 and 0.13 μg/L for Cu2+, respectively. The sensors manifested Cu2+ specificity amidst concomitant matrix ions to highlight the relevance of the proposed solid-state sensor. SignificanceThe sensor materials offered a reliable approach for detecting and quantifying environmentally toxic and industrially pertinent Cu2+ from aqueous samples, with the prospect of large-scale production, owing to the sensor's integrated compact design that can be reused for repeated real-time surveillance. The sensor's ability to sense/trap traces of toxic Cu2+ can provide an early warning about the growing toxicity in a particular resource, thereby providing an opportunity to initiate remediation protocols for speedy decontamination.