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In situ synthesis of RGO and CNT-templated diamond-shaped Fe-based metal-organic frameworks: Exploring their remarkable photocatalytic and antioxidant properties.

Authors :
Kumar, Sunil
Siddharth
Ahlawat, Rachna
Rani, Gita
Devi, Jai
Kamboj, Ajay
Source :
Inorganic Chemistry Communications. Jan2025, Vol. 171, pN.PAG-N.PAG. 1p.
Publication Year :
2025

Abstract

[Display omitted] • RGO and CNT-doped-based MOFs with diamond-like structure were fabricated. • The band gap was 2.62 eV at 474 nm for RGO@MIL-53 and 2.33 eV at 531 nm for CNT@MIL-53. • The photocatalytic degradation efficiency against AB10 dye is 88.15% for RGO@MIL-53 and 98.42% for CNT@MIL-53. • DPPH assay showed EC50 at 183.89 with 77.81 % inhabitation for RGO@MIL-53 and 153.59 with 92% for CNT@MIL-53. This research examines the antioxidant and photocatalytic capabilities of diamond-shaped RGO and CNT-doped Fe-based Metal-Organic Frameworks (MOFs), utilizing MIL-53 as the structural framework. A solvothermal method was used for the synthesis of diamond-shaped RGO and CNT-doped MOFs. MOFs structural properties were characterized using FTIR, Raman spectroscopy, FE-SEM, XPS, and p-XRD methods. UV–visible spectroscopy was utilized to analyze the photocatalytic performance and band gap measured as 2.62 eV at 474 nm for RGO-doped MOF and 2.33 eV at 531 nm for CNT-doped MOFs. Amido black 10B (AB10) dye was used to assess the sample's photocatalytic efficacy in the presence and absence of H 2 O 2. After 40 min of sunshine exposure, the RGO-doped MOFs-H 2 O 2 combination revealed 88.15 % photocatalytic degradation capability, while the CNT-doped MOFs demonstrated 98.42 %. To determine the antioxidant activity of the material, a DPPH test was performed. At 400 μg/ml, RGO-doped MOFs showed an EC50 value of 183.89 and 77.81 % inhibition, while CNT-doped MOFs showed 153.59 and 92 % inhibition. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13877003
Volume :
171
Database :
Academic Search Index
Journal :
Inorganic Chemistry Communications
Publication Type :
Academic Journal
Accession number :
181543489
Full Text :
https://doi.org/10.1016/j.inoche.2024.113589