생태융합환경공학연구실

논문 초록 (Abstract)

Antibiotic- resistant bacteria (ARB) and antibiotic resistance genes (ARGs) persist in wastewater as chemically stable contami nants that evade conventional treatment, driving a global health crisis. Photocatalysis offers a promising route to simultaneously inactivate ARB and degrade ARGs. However, its practical implementation stays hindered by fundamental gaps in understanding how material interfaces control their fate. This review critically analyzes the interfacial battlefield, where surface chemistry, charge dynamics, and nanoconfinement determine the efficiency and mechanism of resistance destruction. We establish a quan titative reaction–diffusion framework that reveals why photocatalytic degradation is governed not by bulk- phase kinetics but by coupled transport–adsorption–reaction processes at the nanoscale interface. Through Damköhler analysis, we demonstrate that short- lived reactive oxygen species (ROS, ●OH diffusion < 10 nm) impose transport- limited regimes where adsorption and nano confinement become as critical as charge separation. We evaluate the dual target challenge: ARB as complex, multi- layered cellu lar structures requiring membrane disruption, and ARGs as persistent polyelectrolytes demanding complete mineralization. By examining how ROS with distinct lifetimes and diffusion distances operate at material interfaces, we establish that adsorption and nanoconfinement are as critical as charge separation. The review synthesizes recent advances in doping, heterojunction engineering (Z- scheme, S- scheme), defect creation, and carbon- based mediators through the cohesive perspective of interfacial design. Key gaps include unverified eARG mineralization, matrix scavenging, catalyst fouling and regeneration, biofilm and dormant cell formation after sublethal treatment, and insufficient life assessment. A roadmap is proposed toward selective, re generable, matrix- tolerant and sustainability guided photocatalytic systems for antibiotic- resistance control.