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In relation to this article, we declare that there is no conflict of interest.
Publication history
Received January 28, 2026
Accepted April 24, 2026
Available online August 25, 2026
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Most Cited

Tetrabromobisphenol A Degradation by a Photoelectrocatalytic System with a Carbon Layer-Protected Cuprous Oxide Cathode: Performance and Promoting Mechanism

tate Key Laboratory of Urban-Rural Water Resources and Environment, Harbin Institute of Technology 1School of Marine Science and Technology, Harbin Institute of Technology
yuhongjia@hit.edu.cn, lizhipengcn@hit.edu.cn
Korean Journal of Chemical Engineering, August 2026, 43(10), 2735-2751(17)
https://doi.org/10.1007/s11814-026-00733-z

Abstract

Tetrabromobisphenol A (TBBPA), as the most widely used brominated flame retardant, was characterized by its recalcitrance

to degradation and bioaccumulation. To address this limitation, a carbon layer-protected Cu2O (C-Cu2O/Cu) cathode 

was fabricated via in-situ chemical oxidation and calcination followed by glucose impregnation-carbonization, which was 

subsequently coupled with silver-loaded TiO2 (Ag-TiO2/Ti) anode prepared by anodic oxidation and photodeposition to 

construct an efficient photoelectrocatalytic (PEC) system. By optimizing preparation parameters such as impregnation 

concentration and calcination temperature, the photocurrent density of the C-Cu2O/Cu cathode was enhanced to 2.6 times 

higher than that of Cu2O/Cu, and it maintained stable performance during 1200 s of light on/off cycles, contrasting with 

the rapid decay of Cu2O/Cu. Within the PEC system, the C-Cu2O/Cu photocathode achieved a TBBPA degradation efficiency

of 97.1%, significantly surpassing the 87.2% of Cu2O/Cu. Systematic investigation of various applied voltages, 

pH levels, and electrolyte concentrations revealed that the optimal operating parameters were a 1.5 V bias, pH 9.5 and 

0.05 mol/L Na2SO4. Radical trapping experiments confirmed that hydroxyl radicals (·OH) and superoxide radicals (·O2

served as the primary reactive species, while GC–MS analysis elucidated the degradation pathway involving debromination,

ring cleavage, and mineralization. This study provided a novel strategy for enhancing the stability of Cu2O photoelectrodes

and achieving efficient degradation of persistent organic pollutants with the PEC system.

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