The Confined Interlayer Growth of Ultrathin Two-Dimensional Fe3O4 Nanosheets with Enriched Oxygen Vacancies for Peroxymonosulfate Activation

催化作用 电子转移 化学工程 氧化还原 氧气 石墨烯 透射电子显微镜 单层 猝灭(荧光) 光化学 化学 材料科学 X射线光电子能谱 纳米技术 无机化学 有机化学 荧光 物理 工程类 量子力学
作者
Weixue Wang,Yang Liu,Yifan Yue,Huihui Wang,Gong Cheng,Chunyang Gao,Chunlin Chen,Yuejie Ai,Zhe Chen,Xiangke Wang
出处
期刊:ACS Catalysis [American Chemical Society]
卷期号:11 (17): 11256-11265 被引量:207
标识
DOI:10.1021/acscatal.1c03331
摘要

Developing iron-based catalysts with superior activity and stability is a long-term goal for peroxymonosulfate (PMS) activation in advanced oxidation processes. Combining the confined interlayer growth strategy with melt infiltration under dry-chemical conditions, we successfully synthesized ultrathin 2D Fe3O4 nanosheets with a monolayer thickness of about 1 nm. Atomic force microscopy, CS-corrected high-resolution transmission electron microscopy, X-ray photoelectron spectroscopy, X-ray absorption fine structure, etc. jointly revealed that the 2D Fe3O4 nanosheets possessed special graphene-like morphology and enriched oxygen vacancies. As highly efficient AOP catalysts, a series of refractory organic pollutants, including phenolic compounds, antibiotics, and pharmaceuticals, were degraded and mineralized effectively via the activation of PMS. On the basis of radical quenching experiments, electrochemical analysis, and theory calculations, the radical generation (·OH and SO4·–) and mediated electron transfer were verified to be key mechanisms in the reaction. The oxygen vacancy-rich ultrathin 2D Fe3O4 mediated the electron transfer between pollutions and oxidants, prompted the redox cycle of Fe3O4, and remarkably lowered the energy barrier for interfacial charge transfer. This work could generate 2D metal oxides nanosheets with sufficient oxygen vacancies in a large scale, leading the insight for boosting the activity of iron-based catalysts.
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
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
ASH应助科研通管家采纳,获得10
1秒前
隐形曼青应助科研通管家采纳,获得10
2秒前
搜集达人应助科研通管家采纳,获得10
2秒前
汉堡包应助科研通管家采纳,获得10
2秒前
Astraeus应助科研通管家采纳,获得10
2秒前
白石人家应助jiabaoyu采纳,获得10
2秒前
东方元语应助科研通管家采纳,获得20
2秒前
东方元语应助科研通管家采纳,获得20
2秒前
李爱国应助科研通管家采纳,获得10
3秒前
慕青应助科研通管家采纳,获得10
3秒前
沐沐汐完成签到 ,获得积分10
3秒前
大模型应助科研通管家采纳,获得10
3秒前
NN应助科研通管家采纳,获得10
3秒前
李孟林应助科研通管家采纳,获得10
3秒前
烟花应助科研通管家采纳,获得10
3秒前
Judy发布了新的文献求助20
4秒前
4秒前
ASH应助科研通管家采纳,获得10
4秒前
4秒前
4秒前
星辰大海应助科研通管家采纳,获得10
4秒前
4秒前
molihuakai应助科研通管家采纳,获得10
4秒前
JamesPei应助科研通管家采纳,获得10
5秒前
5秒前
Pursue完成签到,获得积分10
5秒前
陈少华完成签到 ,获得积分10
6秒前
高大的未来完成签到,获得积分10
6秒前
Clara完成签到,获得积分10
6秒前
6秒前
TOM完成签到,获得积分10
7秒前
科目三应助川川采纳,获得10
7秒前
秋月白完成签到,获得积分10
7秒前
7秒前
dddd完成签到,获得积分10
8秒前
科研通AI6.2应助千鸟采纳,获得10
8秒前
qiqi发布了新的文献求助50
11秒前
晴枫3648完成签到,获得积分10
11秒前
11秒前
无机完成签到,获得积分10
12秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Reducing Compassion Fatigue, Secondary Traumatic Stress and Burnout 600
Comparative Elite Sport Development Systems, Structures and Public Policy 600
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Auslegungsgeschichte 500
Cosmos as Art Object: Studies in Plato's Timaeus and Other Dialogues 500
What is the Future of Psychotherapy in Digital Age? Technology, AI Bots, and Psychotherapy after Covid 444
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7636161
求助须知:如何正确求助?哪些是违规求助? 9210032
关于积分的说明 19754351
捐赠科研通 7203824
什么是DOI,文献DOI怎么找? 3275358
关于科研通互助平台的介绍 2437186
邀请新用户注册赠送积分活动 2272470