@article{Ye2026, 
author = {Gan Ye and Ruodi Huang and Hongbo Wang and Hao Chen and Jun Zhou and Qiuli Zhang and Jin Wang},
title = {Activating oxidative desulfurization and acetalization performance over metal-organic frameworks by introducing Fe single-atom under solvent-free conditions},
year = {2026},
journal = {Nano Research},
volume = {19},
number = {3},
pages = {94908154},
keywords = {metal-organic frameworks, acetalization, single-atom catalysts, solvent-free, oxidative desulfurization},
url = {https://www.sciopen.com/article/10.26599/NR.2025.94908154},
doi = {10.26599/NR.2025.94908154},
abstract = {The utilization of green synthesis techniques for the fabrication of multipurpose single-atom catalysts offers new opportunity to enable a single catalyst to be employed in multiple target applications. Herein, we show a one-pot green strategy for in-situ anchoring of Fe single atom (Fe1) onto the Zr-oxo clusters of UiO-66(Zr) via the formation of Fe–O–Zr bonds without the use of any solvent. The introduction of Fe1 endows the UiO-66(Zr) supporter with significantly enhanced catalytic performance in oxidative desulfurization (ODS) and acetalization reactions. 1000 ppm sulfur of thioanisole, dibenzothiophene or 4,6-dimethyldibenzothiophene can be completely removed within 12, 15, or 20 min at 40 °C during the ODS reaction, and 11.2 mmol benzaldehyde is converted to (dimethoxymethyl)benzene within 2 min at 25 °C during the acetalization reaction. The turnover frequency values over Fe1/UiO-66(Zr) reach 545.0 h−1 at 40 °C for ODS (29.3 and 362.3 times higher than FeCl3 and UiO-66(Zr) supporter), and 2829 h−1 at 25 °C for acetalization, exceeding most reported catalysts. Density functional theory calculations confirm that the anchored Fe1 in Fe1/UiO-66(Zr) not only exhibits an exceptionally strong adsorption capacity for H2O2 but also facilitates the decomposition of absorbed H2O2 into ·OH radicals, which plays a critical role in determining the reaction efficiency. This work provides a sustainable one-pot green approach for decorating multi-purpose single-atom catalysts (SACs) on metal-organic frameworks to enhance their redox and acid catalytic activities for diverse reactions.}
}