Enhanced photocatalytic degradation activity of titanium dioxide by adsorbing aromatic amines through N-bonding

Shivam Patel , Sagnik Mukherjee , Mahesh Neem , Subhadip Neogi , K.L. Ameta , Arvnabh Mishra , M.P. Deshpande , Manish Kumar Mishra
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Abstract

Narrowing the wide band gap of TiO2 (∼3.2 eV) to enhance its visible light efficiency is crucial for advancing photocatalytic degradation of organic pollutants in industrial wastewater. In this study, we achieved band gap reduction and slowed recombination rates by adsorbing some aromatic amines, like aniline and its electron-donating derivatives, onto TiO2. The predominantly present N-bonded amine species reduced the band gap and decelerated charge carriers’ recombination, enhancing photocatalytic degradation under visible light. In contrast, the amine with electron-withdrawing group is adsorbed as only H-bonded species, which showed no improvement in photocatalytic activity, performing similarly to pristine TiO2. This surface modification strategy offers potential for creating visible light-driven photocatalysts for effective degradation of organic pollutants in water.
通过 N 键吸附芳香胺增强二氧化钛的光催化降解活性
缩小二氧化钛的宽带隙(3.2 eV)以提高其可见光效率,对于推进工业废水中有机污染物的光催化降解至关重要。在本研究中,我们通过在 TiO2 上吸附一些芳香胺(如苯胺及其电子捐赠衍生物),实现了带隙的减小和重组速率的减慢。以 N 键为主的胺类降低了带隙,减缓了电荷载流子的重组,从而增强了在可见光下的光催化降解能力。与此相反,带有电子抽离基团的胺只以 H 键形式被吸附,光催化活性没有得到改善,与原始二氧化钛的性能相似。这种表面改性策略为制造可见光驱动的光催化剂提供了潜力,可有效降解水中的有机污染物。
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