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Bridging oxygen adsorption and activation by Ag single-atom/cluster hybrid for efficient photocatalytic sterilization

Journal 2026 · IF 9.6 · 发表于 2026 年 9 月 3 日
作者: Yaliu Jian,Wenyuan Pan,Tengfei Chen,Jinwei Luo,Hongtian Mi,CuiPing Guo,Xiangdong Xue,Mingyang Chen,Wenjun Dong
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摘要

A two-step anchoring-reduction strategy controllably converts Ag 1 to Ag ACs , yielding an electronically coupled hybrid. • Coordinatively unsaturated Ag ACs sites adsorb O 2 , while adjacent Ag 1 donors raise their Fermi level above the O 2 LUMO.The elevated Fermi level enables spontaneous electron injection, O–O bond elongation, and enhanced •O 2 – generation. • Ag ACs+1 /CNs inactivates >99.9% of E. coli and S. aureus within 1.5 h under visible light at 2 μg/mL. Oxygen adsorption and activation are pivotal steps that drive the reactive oxygen species (ROS) cascade and fundamentally govern the efficacy of photocatalytic antibacterial processes. However, reconciling the distinct electronic requirements for O 2 capture and subsequent activation at a unified catalytic site remains a significant challenge. Herein, we report a hybrid-state catalyst (Ag ACs+1 /CNs), fabricated by anchoring silver single atoms (Ag 1 ) onto carbon nitride and subsequently converting part of the Ag 1 into atomically precise silver clusters (Ag ACs ). In this architecture, the coordinatively unsaturated edge Ag atoms of Ag ACs serve as oxygen adsorption sites. Simultaneously, neighboring Ag 1 sites act as electron donors, which is proposed to elevate the Fermi level of Ag ACs above the lowest unoccupied molecular orbital (LUMO) of O 2 . This elevated Fermi level promotes oxygen activation by enabling spontaneous electron injection from Ag ACs into O 2 , elongating the O O bond, and thereby facilitating the formation of superoxide radicals (•O 2 − ). As a result, Ag ACs+1 /CNs demonstrate exceptional bactericidal activity under visible light irradiation at a low concentration of 2 μg/mL, achieving over 99.9% inactivation of both E. coli and S. aureus within 1.5 h. This work presents a design paradigm for hybrid single-atom/cluster catalysts, which provides an integrated strategy to synergistically enhance adsorption and activation at unified active sites. Download: Download high-res image (180KB) Download: Download full-size image