pH-Independent Production of Hydroxyl Radical from Atomic H*-Mediated Electrocatalytic H₂O₂ Reduction: A Green Fenton Process without Byproducts
2020
Zeng, Huabin | Zhang, Gong | Ji, Qinghua | Liu, Huijuan | Hua, Xin | Xia, Hailun | Sillanpää, Mika | Qu, Jiuhui
Hydroxyl radical (•OH) can hydroxylate or dehydrogenate organics without forming extra products and is thereby expediently applied in extensive domains. Although it can be efficiently produced through single-electron transfer from transition-metal-containing activators to hydrogen peroxide (H₂O₂), narrow applicable pH range, strict activator/H₂O₂ ratio requirement, and byproducts that are formed in the mixture with the background matrix necessitate the need for additional energy-intensive up/downstream treatments. Here, we show a green Fenton process in an electrochemical cell, where the electro-generated atomic H* on a Pd/graphite cathode enables the efficient conversion of H₂O₂ into •OH and subsequent degradation of organic pollutants (80% efficiency). Operando liquid time-of-fight secondary ion mass spectrometry verified that H₂O₂ activation takes place through a transition state of the Pd–H*–H₂O₂ adduct with a low reaction energy barrier of 0.92 eV, whereby the lone electron in atomic H* can readily cleave the peroxide bridge, with •OH and H₂O as products (ΔGᵣ = −1.344 eV). Using H⁺ or H₂O as the resource, we demonstrate that the well-directed output of H* determines the pH-independent production of •OH for stable conversion of organic contaminants in wider pH ranges (3–12). The research pioneers a novel path for eliminating the restrictions that are historically challenging in the traditional Fenton process.
Afficher plus [+] Moins [-]Mots clés AGROVOC
Informations bibliographiques
Cette notice bibliographique a été fournie par National Agricultural Library
Découvrez la collection de ce fournisseur de données dans AGRIS