材料科学
纳米复合材料
机制(生物学)
碳纤维
纳米技术
纳米颗粒
化学工程
复合材料
复合数
哲学
认识论
工程类
作者
Ruyan Xie,Shuzhe Zhang,Yanhua Song,Qian Zhang,Shihou Sheng,Haifeng Zou
标识
DOI:10.1002/adfm.202411155
摘要
Abstract The optical properties of quantum dots are significantly influenced by photoactivation. However, the progress in the development of photoactivation carbon dot (CDs) is still stagnant. Herein, a method for preparing photoactivated CDs/NiFe 2 O 4 by introducing affluent defects onto the surface of CDs through modification with NiFe 2 O 4 , extremely filling the gap of photoactivated CDs is proposed. Interestingly, a fantastic fluorescence detection strategy in a unique “OFF‐ON‐OFF” mode, combined with Ag + ‐assisted fluorescence enhancement, to establish a dual‐channel regulation mechanism for ultra‐sensitive detection of Hg 2+ is first proposed. By increasing surface traps and non‐radiative recombination, defect‐induced manipulation on the surface of CDs creates favorable conditions for enhancing photoactivation capacity. Unexpectedly, the CDs/NiFe 2 O 4 shows a 25‐fold enhancement in fluorescence intensity after exposure to UV‐lamp. Compared to CDs/NiFe 2 O 4 , Ag + ‐assisted photoactivation CDs/NiFe 2 O 4 exhibits superior selectivity and sensitivity for Hg 2+ detection, with low detection limits of 0.7 nM. Moreover, TiO 2 @CDs/NiFe 2 O 4 catalyst is successfully prepared by anchoring CDs/NiFe 2 O 4 onto the surface of TiO 2 , which demonstrates efficient degradation of tetracycline within 90 min under visible light irradiation, with a degradation rate of 98.3%. This work first provides a novel defects modification strategy for developing highly active photoactivated CDs technology that is significant for future environmentally sensitive applications.
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