Waterborne pathogens in drinking water remains a prominent cause of morbidity and mortality in developing rural areas. Electrochlorination offers a promising alternative for decentralized water disinfection, but its efficiency was strongly restrained by the low Cl- concentrations in natural waters. Herein, we proposed a Magnéli Ti4O7 nanowire-assisted electrochemical approach via forming locally enhanced electric field over nanowire tips for reinforcing electroporation, and via forming locally enhanced charge density for promoting Cl- enrichment and subsequent electrochlorination on anodic nanowire tips. Ti4O7 nanowires induced the enhancement of electric field by 4 orders of magnitude and Cl- concentration by ∼3 orders of magnitude at nanowire tips, and promoted ∼3 times more active chlorine generation at a voltage of 3.0 V compared with non-nanostructured one. Synergistic electroporation and electrochlorination on nanowires enabled rapid and efficient disinfection with hydraulic retention time of ∼36 s and energy consumption below ∼5 J/L/log for inactivation of various gram-positive/negative bacteria and phage MS2. Analyses of cell morphology and membrane integrity revealed that electroporation-induced cell pores provided diffusion channels of reactive chlorine species for oxidative damage of cell structures, resulting in ∼1.5–4.5 times lower energy consumption than the thin-film, nanoparticle, and nanorod ones. The excellent operation stability for tap water with significant bacterial inactivation and active chlorine generation demonstrated its great application potential for decentralized water disinfection.
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