Advanced oxidation processes based on nonradical oxidation pathways have become promising pollutant removal methods because of their selectivity and adaptability. In this study, three ceria with different morphologies were synthesized: plate (p-CeO2), rod (r-CeO2), and cubic (c-CeO2). p-CeO2 was observed to have the highest activity for hydrogen peroxide (H2O2) decomposition. Cu doping further improved the catalytic activity of p-CeO2 for H2O2 decomposition compared to other metals, such as Mn, Co, Cu, and Zn. The plate copper-ceria material (p-Cu/CeO2-3) activated the H2O2 and completely degraded amino-G acids (10 mg L–1) within 90 min under optimal conditions (0.3 g L–1p-Cu/CeO2-3, 5 mM H2O2). Through a comprehensive study of the scavenging and pretreatment experiment, electron paramagnetic resonance (EPR), and in situ Raman spectroscopy, it was proven that the catalytic oxidation of amino-G acid on p-Cu/CeO2-3 was mainly mediated by an electron transfer mechanism·H2O2 can be absorbed on the surface of p-Cu/CeO2-3 to form the Ce-hydrogen peroxide surface complex (Ce(III)− •OOH), which can act as an electron acceptor when the amino G acid is in close proximity to the complex. In addition, p-Cu/CeO2-3 showed excellent catalytic performance over a wide pH range (3−9). This study provides a new system for the degradation of amino-G acid through electron transfer pathways.
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