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Driven by the need to investigate enhanced biosensing properties alongside the development of low-toxicity, economical, eco-friendly, and sustainable materials, this work explores the functionalization of biochara carbon-based materialand its subsequent anchoring onto the working electrode for the detection of cardiac troponin T (cTnT). Here, we discuss the interaction between biochar and glutaraldehyde at various concentrations, aiming to elucidate the relationship between the formation of full acetals and hemiacetals. It first allows an understanding of the cross-link reactions between glutaraldehyde and biochar and then better anchoring with the Cystamine-Au working electrode of a printed circuit board (PCB). These aspects improve the biosensor's stability and the cTnT antibody's specific adsorption. Electrochemical, AFM, Fluorescence Confocal, SEM, and FTIR analyses were employed to identify the optimal glutaraldehyde concentration that maximizes hemiacetal group formation, critical for stability to the electrode and the specific adsorption of the antibody. The resulting label-free, direct electrochemical cTnT immunosensor showed high sensitivity and selectivity, with a detection capacity of 0.01-5.00 ng·mL and a Limit of Detection (LOD) of 0.003 ng·mL, as determined by cyclic voltammetry. An additional advantage is the reusability of the PCB, which can be recycled at least twice by replacing the biochar layer on the working electrode, assigning an environmentally friendly characteristic to the immunoassay.
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http://dx.doi.org/10.1021/acsomega.5c02113 | DOI Listing |
Nanoscale
September 2025
College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, Jiangsu, China.
Proton exchange membrane water electrolysis (PEMWE) is regarded as the most promising technique for the sustainable production of green hydrogen due to its multiple advantages such as high working current density and high hydrogen purity. However, the anodic oxygen evolution reaction (OER) has a significant impact on the overall efficiency of the electrolytic water reaction due to its sluggish kinetics, which has prompted the search for catalysts possessing both high activity and durability. Iridium oxide exhibits excellent stability under acidic conditions but has poor catalytic activity, leading to its inability to meet the strict requirements of large-scale industrial applications.
View Article and Find Full Text PDFLangmuir
September 2025
Key Laboratory of Colloid and Interface Chemistry of the Education Ministry of China, Shandong University, Jinan 250100, China.
In this paper, a phosphate buffer (0.10 M, pH 7.5)--hexadecane bicontinuous microemulsion (BME) stabilized by the nonionic surfactant CE was for the first time used as the medium to investigate its effect on the electrochemical behavior of the cobaltocene redox couple ( (III)/ (II)) as electron mediator and the -mediated electroreduction of coenzyme NAD.
View Article and Find Full Text PDFACS Electrochem
September 2025
Department of Chemistry, University of Warwick, Coventry CV4 7AL, United Kingdom.
The surface structure of an electrocatalyst plays a crucial role in determining the activity. As a model system, gold has been widely investigated as an electro-oxidation catalyst, although there has been much less research on the oxygen evolution reaction (OER) in the potential region of gold oxidation. Here, we combine voltammetric scanning electrochemical cell microscopy (SECCM) and electron backscatter diffraction (EBSD), at different spatial and angular resolutions, respectively, to correlate the local crystallographic structure of polycrystalline goldfocusing on grains close to (113), (011), (114), and (111) orientationswith the electrocatalytic behavior for the OER.
View Article and Find Full Text PDFACS Electrochem
September 2025
Liquid Sunlight Alliance, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.
Reaction rate coefficients for electron-transfer processes at the electrode-electrolyte interface are commonly estimated by using the Butler-Volmer equation, but their values are inaccurate beyond a few tenths of volts of overpotential. The Marcus-Hush-Chidsey (MHC) formalism yields correct asymptotic behavior of the rate coefficients vs applied overpotential but has complex dependencies on the redox system's intrinsic parameters, which can be difficult to model or measure. In this work, we bridge the two kinetics formalisms to estimate the reorganization energy, one of the important parameters for the MHC formalism, and investigate its dependence on other intrinsic parameters such as activation barriers, electronic coupling strength, and the density of states of the electrode surface.
View Article and Find Full Text PDFBeilstein J Nanotechnol
August 2025
Department of Physics & Engineering Physics, Morgan State University, Baltimore, MD 21251, USA.
Nanoscale biosensors have gained attention in recent years due to their unique characteristics and size. Manufacturing steps, cost, and other shortcomings limit the widespread use and commercialization of nanoscale electrodes. In this work, a nano-size electrode fabricated by directed electrochemical nanowire assembly and parylene-C insulation is introduced.
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