Li, Rong-Jian, Lewis, Richard J., Morgan, David J. ![]() ![]() ![]() ![]() |
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Abstract
Harnessing the in situ generation of hydrogen peroxide (H2O2) and associated reactive oxygen species (ROS) from molecular hydrogen (H2) and oxygen (O2) offers a powerful and sustainable alternative to conventional oxidative treatments for water purification. In this contribution, we explore the potential of AuPdFe‐based catalysts to achieve the in situ, oxidative degradation of phenol, a widely studied representative organic pollutant. By finely tuning the AuPd/Fe ratio, it is possible to balance H2O2 synthesis with Fe‐mediated ROS generation, achieving efficient phenol degradation and high selectivity toward deeply oxidized products. The optimized catalyst formulation outperforms its bimetallic counterpart by a factor of 10 in conversion efficiency. However, this enhanced activity comes at a cost, with the formation of strongly oxidized species such as formic, oxalic, and malonic acids resulting in the leaching of the active metal components, highlighting a critical trade‐off between catalytic performance and long‐term stability, particularly in the presence of highly concentrated chelating agents.
Item Type: | Article |
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Date Type: | Published Online |
Status: | In Press |
Schools: | Research Institutes & Centres > Cardiff Catalysis Institute (CCI) Schools > Chemistry |
Additional Information: | License information from Publisher: LICENSE 1: URL: http://creativecommons.org/licenses/by/4.0/ |
Publisher: | Wiley |
ISSN: | 1867-3880 |
Date of First Compliant Deposit: | 24 September 2025 |
Date of Acceptance: | 9 September 2025 |
Last Modified: | 02 Oct 2025 08:11 |
URI: | https://orca.cardiff.ac.uk/id/eprint/181303 |
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