TY - JOUR
T1 - Advanced anode design for the electrochemical degradation of refractory organic pollutants——from materials engineering to mechanistic insights
AU - Liu, Xu
AU - Zhang, Luping
AU - Zhang, Zekun
AU - He, Xixue
AU - Jing, Xiaosheng
AU - Wang, Xue
AU - Li, Qiao
AU - Xu, Hao
AU - Yan, Wei
AU - Qiao, Zhihua
N1 - Publisher Copyright:
© 2026 Elsevier B.V.
PY - 2026/8/30
Y1 - 2026/8/30
N2 - Electrocatalytic advanced oxidation processes (EAOPs) are premier technologies for the deep mineralization of recalcitrant organic pollutants (ROPs) due to their clean operation and efficient in situ generation of reactive radicals. However, the development of core anode materials remains constrained by the “activity-stability-cost” ternary paradox. “Active” anodes, such as RuO2, offer stability but suffer from severe oxygen evolution side reactions that limit mineralization efficiency; conversely, “non-active” anodes like boron-doped diamond (BDD) achieve superior mineralization but face prohibitive costs and scalability challenges. This paper establishes a key performance indicator (KPI) system for ideal anodes and systematically reviews advanced design strategies to overcome these bottlenecks across three dimensions. At the atomic scale, electronic structures are regulated via elemental doping and defect engineering to optimize intrinsic activity. At the nanoscale, heterojunctions and functional interlayers are constructed to resolve the trade-off between conductivity and stability. At the macroscale, three-dimensional porous electrodes and flow-through reactors are developed to enhance mass transfer efficiency. Furthermore, we explore the critical roles of in situ spectroscopic characterization, density functional theory (DFT), and machine learning (ML) in elucidating reaction mechanisms and facilitating material reverse design. Finally, the review addresses challenges regarding matrix effects, standardize lifetime assessment, and engineering scale-up, aiming to propel anode development from traditional trial-and-error approaches toward data-driven rational design.
AB - Electrocatalytic advanced oxidation processes (EAOPs) are premier technologies for the deep mineralization of recalcitrant organic pollutants (ROPs) due to their clean operation and efficient in situ generation of reactive radicals. However, the development of core anode materials remains constrained by the “activity-stability-cost” ternary paradox. “Active” anodes, such as RuO2, offer stability but suffer from severe oxygen evolution side reactions that limit mineralization efficiency; conversely, “non-active” anodes like boron-doped diamond (BDD) achieve superior mineralization but face prohibitive costs and scalability challenges. This paper establishes a key performance indicator (KPI) system for ideal anodes and systematically reviews advanced design strategies to overcome these bottlenecks across three dimensions. At the atomic scale, electronic structures are regulated via elemental doping and defect engineering to optimize intrinsic activity. At the nanoscale, heterojunctions and functional interlayers are constructed to resolve the trade-off between conductivity and stability. At the macroscale, three-dimensional porous electrodes and flow-through reactors are developed to enhance mass transfer efficiency. Furthermore, we explore the critical roles of in situ spectroscopic characterization, density functional theory (DFT), and machine learning (ML) in elucidating reaction mechanisms and facilitating material reverse design. Finally, the review addresses challenges regarding matrix effects, standardize lifetime assessment, and engineering scale-up, aiming to propel anode development from traditional trial-and-error approaches toward data-driven rational design.
KW - Anode materials
KW - Electrocatalytic oxidation
KW - Rational design
KW - Refractory organic pollutants (ROPs)
KW - Ternary paradox
UR - https://www.scopus.com/pages/publications/105037179890
U2 - 10.1016/j.seppur.2026.138236
DO - 10.1016/j.seppur.2026.138236
M3 - 文献综述
AN - SCOPUS:105037179890
SN - 1383-5866
VL - 398
JO - Separation and Purification Technology
JF - Separation and Purification Technology
M1 - 138236
ER -