Surface Defects‐Induced Photoactivation of Carbon Dots‐NiFe2O4 Nanocomposite: Synthesis, Mechanism and Applications

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
出处
期刊:Advanced Functional Materials [Wiley]
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.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Hulda完成签到,获得积分10
刚刚
111完成签到,获得积分10
1秒前
张同学要谦虚完成签到,获得积分10
1秒前
2秒前
斯文败类应助keplek采纳,获得10
3秒前
3秒前
今后应助JunHan采纳,获得10
3秒前
3秒前
4秒前
4秒前
Weining发布了新的文献求助10
5秒前
5秒前
徐徐徐关注了科研通微信公众号
5秒前
上官若男应助合适的凝安采纳,获得10
5秒前
wanci应助mmqq采纳,获得10
5秒前
transition完成签到,获得积分10
6秒前
小马甲应助小飞飞采纳,获得10
7秒前
隐形曼青应助专注乐巧采纳,获得10
7秒前
8秒前
8秒前
8秒前
5007zsx完成签到,获得积分10
9秒前
zjy发布了新的文献求助10
9秒前
9秒前
9秒前
科目三应助科研通管家采纳,获得10
10秒前
李爱国应助科研通管家采纳,获得10
10秒前
寻道图强应助科研通管家采纳,获得50
10秒前
10秒前
Akim应助科研通管家采纳,获得10
10秒前
SciGPT应助科研通管家采纳,获得10
10秒前
FashionBoy应助科研通管家采纳,获得10
10秒前
Akim应助科研通管家采纳,获得10
10秒前
10秒前
11秒前
11秒前
科研通AI2S应助wby采纳,获得10
11秒前
姬霓太美完成签到,获得积分10
11秒前
GY完成签到,获得积分20
12秒前
ai zs发布了新的文献求助10
13秒前
高分求助中
Sustainability in Tides Chemistry 2800
The Young builders of New china : the visit of the delegation of the WFDY to the Chinese People's Republic 1000
юрские динозавры восточного забайкалья 800
Foreign Policy of the French Second Empire: A Bibliography 500
Chen Hansheng: China’s Last Romantic Revolutionary 500
XAFS for Everyone 500
Classics in Total Synthesis IV 400
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3144560
求助须知:如何正确求助?哪些是违规求助? 2796059
关于积分的说明 7817719
捐赠科研通 2452134
什么是DOI,文献DOI怎么找? 1304892
科研通“疑难数据库(出版商)”最低求助积分说明 627331
版权声明 601432