光催化
质子化
分子内力
亚胺
光化学
质子
分子
部分
化学
电子
密度泛函理论
电子受体
材料科学
腙
化学物理
纳米技术
计算化学
催化作用
有机化学
物理
离子
量子力学
作者
Menghao Li,Zhiqiang Yang,Hui Hui,Yan Wang,Bing Yang,Zhiquan Zhang,Ying‐Wei Yang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-04-28
卷期号:25 (18): 7524-7532
标识
DOI:10.1021/acs.nanolett.5c01273
摘要
Smart materials that adapt to environmental stimuli have massive technological potential. Translating well-established molecular-level responsiveness to macroscopic systems, particularly complex systems for photocatalysis, remains a significant hurdle. Herein, we introduce a new approach using a hydrazone-linked pillararene microsphere (NP5-TF-HPM) as a smart stimuli-responsive photocatalyst. NP5-TF-HPM showcases unique proton responsiveness owing to electron-rich cavities, resulting in a proton-induced structural rearrangement from the enol-imine to keto-amine form. Experiments and density functional theory calculations reveal that pillararenes in the protonated framework function as activity amplifiers. These molecules donate π-electrons from their cavities to another building unit, not only shifting the framework's conduction band to a more negative potential, which enhances its electron-donating capability, but also inducing a nonuniform charge distribution in the donor-acceptor moiety, thereby resulting in an intramolecular built-in electric field. Consequently, protonated HPM exhibits amplified photo-oxidation activity, efficiently catalyzing sulfide photo-oxidation with high conversions (up to 99%).
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