Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

A highly sensitive fluorescence sensor for monitoring low concentrations of hydrogen peroxide was designed. The sensor employs the commercially available palladium or platinum metal on activated charcoal as catalysts to decompose hydrogen peroxide into water and molecular oxygen. The produced oxygen concentration can be measured in real time using an oxygen-sensitive layer doped with photostable oxygen probes. The sensor exhibits high sensitivity that is able to measure hydrogen peroxide concentration down to 20 ppb and can measure hydrogen peroxide concentration in the range of 0.1-100 ppm and 0.02-100 ppm, respectively. The response is fully reversible and the typical response time is less than one minute, which makes it suitable to continuously measure hydrogen peroxide over a long duration. Due to the excellent batch-to-batch consistency of palladium or platinum metal on activated charcoal, the sensor can be massively produced with good reproducibility and affordable price, which holds great potential for constructing sensors for industrial and practical applications.

Download full-text PDF

Source
http://dx.doi.org/10.1039/d4an00975dDOI Listing

Publication Analysis

Top Keywords

hydrogen peroxide
24
measure hydrogen
12
highly sensitive
8
fluorescence sensor
8
palladium platinum
8
platinum metal
8
metal activated
8
activated charcoal
8
peroxide concentration
8
hydrogen
6

Similar Publications

The oxygen reduction reaction (ORR) is critical to energy conversion technologies and requires efficient catalysts for superior performance. Herein, nitrogen-doped carbide-derived carbon (N-CDC) catalysts are prepared using novel engineered molecular architectures based on polymer-derived ceramic technology. The obtained catalyst materials show a surface N concentration of >5 wt % and a hierarchically porous structure, resulting in a specific surface area of over 2000 m g.

View Article and Find Full Text PDF

Characterization, photocatalysis, antimicrobial and antioxidant activities of manganese oxide nanoparticles green synthesis using seed extract.

Int J Phytoremediation

September 2025

Innovative Food Technologies Development Application and Research Center, Gölköy Campus Bolu, Bioenvironment and Green Synthesis Research Group, Bolu Abant İzzet Baysal University, Bolu, Türkiye.

This study presents an eco-friendly approach for the green synthesis of manganese oxide nanoparticles (MnONPs) using () (einkorn wheat) seed extract as a reducing and stabilizing agent. The synthesized MnONPs were characterized by UV-Vis, XRD, FTIR, SEM-EDX, BET, and zeta potential analyses, which confirmed their crystalline nature, spherical morphology, and mesoporous structure with a surface area of 41.50 m/g.

View Article and Find Full Text PDF

Chemodynamic therapy (CDT), leveraging Fenton reactions to generate hydroxyl radicals (•OH) from intracellular hydrogen peroxide (HO), offers a promising cancer treatment strategy due to its high specificity and low systemic toxicity. However, the targeted delivery of •OH-producing prodrugs using covalent organic frameworks (COFs) remains a significant challenge. Here, we report a mitochondria-targeted COF-based nano prodrug, COF-31@P, designed for enhanced CDT efficacy.

View Article and Find Full Text PDF

Hydrogen Radical Mediated Concerted Electron-Proton Transfer in 1D Sulfone-based Covalent Organic Framework for Boosting Photosynthesis of HO.

Angew Chem Int Ed Engl

September 2025

College of Smart Materials and Future Energy, Fudan University, Songhu Road 2005, Shanghai, 200438, P.R. China.

Solar-driven photocatalytic oxygen reduction reaction using covalent organic frameworks (COFs) offers a promising approach for sustainable hydrogen peroxide (HO) production. Despite their advantages, the reported COFs-based photocatalysts suffer insufficient photocatalytic HO efficiency due to the mismatched electron-proton dynamics. Herein, we report three one-dimensional (1D) COF photocatalysts for efficient HO production via the hydrogen radical (H•) mediated concerted electron-proton transfer (CEPT) process.

View Article and Find Full Text PDF

Mechanical stimuli have been shown to dynamically alter solid-liquid interfaces and induce electron transfer, enabling catalytic reactions, most notably contact-electro-catalysis (CEC). However, the underlying mechanism of charge transfer at solid-liquid interfaces under mechanical stimulation remains unclear, particularly at semiconductor-liquid interfaces. To date, rare studies have reported on the catalytic activity of semiconductor-liquid interfaces under mechanical stimulation.

View Article and Find Full Text PDF