This study reports, for the first time, the utilization of two-dimensional (2D) tellurium (Te) nanosheets for the efficient nonenzymatic detection of hydrogen peroxide (H2O2). H2O2 acts as a pivotal biomarker with widespread applications across environmental, biological, industrial, and food processing domains. However, an excessive accumulation of H2O2 in the body poses a severe threat to human life. Consequently, the imperative need for a selective, sensitive, and cost-effective sensing platform for H2O2 detection has gained paramount significance. Employing a low-cost and straightforward hydrothermal method, Te nanosheets were synthesized to address the escalating demand for a reliable detection platform. The as-synthesized Te nanosheets are characterized through Raman spectroscopy and atomic force microscopy techniques. The electrochemical performance of the Te nanosheets integrated onto a glassy carbon (Te-GC) electrode was thoroughly investigated using cyclic voltammetry, differential pulse voltammetry, and chronoamperometry. The experiments were designed to evaluate the response of the Te-GC electrode in the presence and absence of H2O2, alongside its performance in the detection of other pertinent interfering analytes. The sensor shows a limit of detection of 0.47 µM and a sensitivity of 27.2 µA µM−1 cm−2 towards H2O2. The outcomes of this study demonstrate the efficacy of Te nanosheets as a promising material for nonenzymatic H2O2 detection in urine samples. The simplicity and cost-effectiveness of the hydrothermal synthesis process, coupled with the notable electrochemical performance of the Te/GC electrode, highlight the potential of Te nanosheets in the development of a robust sensing platform. This research contributes to the ongoing efforts to enhance our capabilities in monitoring and detecting H2O2, fostering advancements in environmental, biomedical, and industrial applications.
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Free, publicly-accessible full text available March 26, 2025
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Bottlebrush polymers are complex macromolecules with tunable physical properties dependent on the chemistry and architecture of both the side chains and the backbone. Prior work has demonstrated that bottlebrush polymer additives can be used to control the interfacial properties of blends with linear polymers but has not specifically addressed the effects of bottlebrush side chain microstructures. Here, using a combination of experiments and self-consistent field theory (SCFT) simulations, we investigated the effects of side chain microstructures by comparing the segregation of bottlebrush additives having random copolymer side chains with bottlebrush additives having a mixture of two different homopolymer side chain chemistries. Specifically, we synthesized bottlebrush polymers with either poly(styrene- ran -methyl methacrylate) side chains or with a mixture of polystyrene (PS) and poly(methyl methacrylate) (PMMA) side chains. The bottlebrush additives were matched in terms of PS and PMMA compositions, and they were blended with linear PS or PMMA chains that ranged in length from shorter to longer than the bottlebrush side chains. Experiments revealed similar behaviors of the two types of bottlebrushes, with a slight preference for mixed side-chain bottlebrushes at the film surface. SCFT simulations were qualitatively consistent with experimental observations, predicting only slight differences in the segregation of bottlebrush additives driven by side chain microstructures. Specifically, these slight differences were driven by the chemistries of the bottlebrush polymer joints and side chain end-groups, which were entropically repelled and attracted to interfaces, respectively. Using SCFT, we also demonstrated that the interfacial behaviors were dominated by entropic effects with high molecular weight linear polymers, leading to enrichment of bottlebrush near interfaces. Surprisingly, the SCFT simulations showed that the chemistry of the joints connecting the bottlebrush backbones and side chains played a more significant role compared with the side chain end groups in affecting differences in surface excess of bottlebrushes with random and mixed side chains. This work provides new insights into the effects of side chain microstructure on segregation of bottlebrush polymer additives.more » « less
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Analytical and semianalytical expressions for the surface tension of dielectric–air interfaces are presented after considering local and nonlocal dielectric effects near interfaces. It is shown that the nonlocal effects of dielectrics are significant for highly polar dielectric fluids such as water. Far from the interface, nonlocal dielectric effects are shown to cause not only the oscillatory potential of the mean force but also a reversal of sign at intermediate distances.more » « less