Citation:
Yanyan Zhao, Jing Zhang, Xiaolong Li, Hailun Su, Lin Yang, Jianjun Zhang. TiO2/Py-HOF S型异质结中的超快电荷转移用于高效光催化产H2O2及灭菌[J]. Acta Physico-Chimica Sinica,
;2026, 42(11): 100370.
doi:
10.1016/j.actphy.2026.100370
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氢键有机框架(HOFs)在光催化领域具有巨大的应用潜力。然而,其在光催化产H2O2及抗菌活性中的实际应用仍受限于固有的低效电子-空穴分离及结构稳定性不足。本研究以1,3,6,8-四(对苯甲酸)芘(H4TBAPy)为前驱体,通过自组装法制备了Py-HOF光催化剂,并采用原位合成策略合理构建了二氧化钛/氢键有机框架(TiO2/Py-HOF, T/Py-HOF)S型异质结。由于H4TBAPy的强氢键和π-π相互作用,T/Py-HOF S型异质结展现出优异的稳定性。此外,原位光照光电子能谱(ISXPS)、飞秒瞬态吸收光谱(fs-TAS)及密度泛函理论计算(DFT)验证了T/Py-HOF异质结中的S型载流子迁移机制。得益于T/Py-HOF S型光催化剂的超快电荷转移和优异氧化还原能力,最优配比的T/Py-HOF-5%实现了1890 μmol g-1 h-1的显著H2O2产率,分别较纯TiO2和裸Py-HOF提升约15.24倍和6.19倍,同时保持优异的稳定性。进一步地,T/Py-HOF异质结对大肠杆菌(E. coli)展现出卓越的光催化灭菌活性,在90 min光照后实现近100%的细菌灭活。综上,本研究为设计能源与环境应用中基于HOF的高效S型光催化剂提供了新见解。
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