2D MOF/COF Heterojunction for Efficient Photothermal Synergistic Catalysis of CO 2 Reduction

光热治疗 材料科学 催化作用 异质结 光热效应 光催化 纳米技术 载流子 连接器 二氧化碳电化学还原 还原(数学) 化学工程 能量转换效率 协同催化 共轭体系 金属 科技与社会 金属有机骨架 有效核电荷 表面电荷
作者
Nan nan Zhang,Yan Sun,Xin-Ran Liu,Rong Yin,Ya Wang,Shuang-yu Wang,Jin Zhi-wei,Gui-ling Zhang,Hong Dong,Feng Ming Zhang
出处
期刊:Advanced Functional Materials [Wiley]
标识
DOI:10.1002/adfm.202523743
摘要

Abstract Photothermal synergistic catalysis of carbon dioxide (CO 2 ) reduction by combining the advantages of photocatalysis and thermocatalysis is an effective strategy for enhancing the efficiency of solar‐to‐fuel conversion. However, it is still a great challenge to integrate the high photothermal effect and charge separation efficiency simultaneously in one system. Herein, a type of bonded 2D Metal organic framework (MOF)/Covalent organic framework (COF) heterostructure with the same linker is constructed for efficient photothermal synergistic catalysis of CO 2 reduction. In this system, an S‐scheme heterojunction interface is formed between the MOF (CAT‐1) and COF‐316 through planar conjugated molecules, which facilitates the separation of photogenerated charge carriers. CAT‐1 serves as a photoinduced self‐heating component and simultaneously provides active metal sites for CO 2 reduction, enabling efficient photothermal conversion under visible‐near‐infrared light. As a result, a series of CAT‐1/COF‐316 composites delivered enhanced photothermal catalytic activity for CO 2 reduction without adding additional photosensitizers, with the optimal CO production rate of 263.63 µmol g −1 h −1 . Detailed control experiments and density functional theory (DFT) calculations confirm that the superior photothermal catalytic CO 2 reduction performance of CAT‐1/COF‐316 is attributed to the synergistic effect of photo‐thermal processes and highly improved charge separation. The present work provides a potential strategy for developing highly‐efficient photothermal catalysts in artificial photosynthesis.
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
prefectmi完成签到,获得积分10
1秒前
2秒前
舒服的幻梅完成签到 ,获得积分10
2秒前
隐形以蓝完成签到,获得积分10
3秒前
ash完成签到,获得积分10
3秒前
奋斗若风完成签到,获得积分10
3秒前
4秒前
发呆员发布了新的文献求助10
4秒前
简单幸福完成签到 ,获得积分10
4秒前
风笛完成签到,获得积分10
4秒前
5秒前
华仔应助小新采纳,获得10
6秒前
严念桃完成签到,获得积分10
6秒前
嘎发完成签到,获得积分10
7秒前
江枫完成签到,获得积分10
7秒前
Miya完成签到,获得积分10
8秒前
8秒前
8秒前
8秒前
石榴完成签到,获得积分10
9秒前
小虫子完成签到,获得积分10
9秒前
Fuckacdemic完成签到,获得积分10
9秒前
贪玩的秋柔应助B_lue采纳,获得10
9秒前
正经大善人完成签到,获得积分10
10秒前
Ya_Yen完成签到,获得积分10
10秒前
靓丽的悒完成签到 ,获得积分10
10秒前
严念桃发布了新的文献求助50
10秒前
11秒前
zzzxiangyi完成签到,获得积分10
11秒前
rong完成签到,获得积分10
11秒前
共享精神应助ahhh采纳,获得10
11秒前
沉静的浩然完成签到,获得积分10
12秒前
12秒前
无限丸子发布了新的文献求助10
12秒前
ZMH完成签到,获得积分10
12秒前
等待谷南完成签到,获得积分10
13秒前
科研小白发布了新的文献求助10
13秒前
13秒前
罗勍完成签到,获得积分10
13秒前
Ava应助发呆员采纳,获得10
14秒前
高分求助中
Adhesion Science: Principles & Practice 1234
Signals, Systems, and Signal Processing 610
Burger's Medicinal Chemistry and Drug Discovery 400
A Step-by-Step Guide to Qualitative Data Coding 2nd Edition 400
Impact of Storage Orientation and Duration on Prefilled Syringe Performance: Break-Loose and Glide Forces, and Injection Time Across Multiple Time Points 360
Programming for Chemical Engineers Using C, C++, and MATLAB 300
Upland Kenya wild flowers and ferns: a flora of the flowers, ferns, grasses, and sedges of highland Kenya 300
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 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6664070
求助须知:如何正确求助?哪些是违规求助? 8413933
关于积分的说明 17985470
捐赠科研通 5869018
什么是DOI,文献DOI怎么找? 2975322
邀请新用户注册赠送积分活动 1951216
关于科研通互助平台的介绍 1877565