A Promoted Charge Separation/Transfer System from Cu Single Atoms and C(3)N(4)Layers for Efficient Photocatalysis | |
Xiao, XD; Gao, YT; Zhang, LP; Zhang, JC; Zhang, Q; Li, Q; Bao, HL; Zhou, J; Miao, S; Chen, N | |
刊名 | ADVANCED MATERIALS |
2020 | |
卷号 | 32期号:33页码:- |
关键词 | CARBON NITRIDE HYDROGEN EVOLUTION BENZENE PHENOL NANOSTRUCTURE OXIDATION CATALYST INSIGHT G-C3N4 WATER |
ISSN号 | 0935-9648 |
DOI | 10.1002/adma.202003082 |
文献子类 | 期刊论文 |
英文摘要 | Establishing highly effective charge transfer channels in carbon nitride (C3N4) for enhancing its photocatalytic activity is still a challenging issue. Herein, for the first time, the engineering of C(3)N(4)layers with single-atom Cu bonded with compositional N (Cu-N-x) is demonstrated to address this challenge. The Cu-N(x)is formed by intercalation of chlorophyll sodium copper salt into a melamine-based supramolecular precursor followed by controlled pyrolysis. Two groups of Cu-N(x)are identified: in one group each of Cu atoms is bonded with three in-plane N atoms, while in the other group each of Cu atoms is bonded with four N atoms of two neighboring C(3)N(4)layers, thus forming both in-plane and interlayer charge transfer channels. Importantly, ultrafast spectroscopy has further proved that Cu-N(x)can greatly improve in-plane and interlayer separation/transfer of charge carriers and in turn boost the photocatalytic efficiency. Consequently, the catalyst exhibits a superior visible-light photocatalytic hydrogen production rate (approximate to 212 mu mol h(-1)/0.02 g catalyst), 30 times higher than that of bulk C3N4. Moreover, it leads to an outstanding conversion rate (92.3%) and selectivity (99.9%) for the oxidation of benzene under visible light. |
语种 | 英语 |
内容类型 | 期刊论文 |
源URL | [http://ir.sinap.ac.cn/handle/331007/32687] |
专题 | 上海应用物理研究所_中科院上海应用物理研究所2011-2017年 |
作者单位 | 1.Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China 2.Heilongjiang Univ, Minist Educ Peoples Republ China, Sch Chem & Mat Sci, Key Lab Funct Inorgan Mat Chem, Harbin 150080, Peoples R China 3.Kent State Univ, Dept Chem & Biochem, Kent, OH 44242 USA 4.Univ Sci & Technol China, Synerget Innovat Ctr Quantum Informat & Quantum P, Dept Chem Phys, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Anhui, Peoples R China 5.Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai 201800, Peoples R China 6.JEOL Beijing Co Ltd, 6 Zhongguancun Nansan St, Beijing 100080, Peoples R China 7.Univ Saskatchewan, Canadian Light Source, Saskatoon, SK S7N 2V3, Canada |
推荐引用方式 GB/T 7714 | Xiao, XD,Gao, YT,Zhang, LP,et al. A Promoted Charge Separation/Transfer System from Cu Single Atoms and C(3)N(4)Layers for Efficient Photocatalysis[J]. ADVANCED MATERIALS,2020,32(33):-. |
APA | Xiao, XD.,Gao, YT.,Zhang, LP.,Zhang, JC.,Zhang, Q.,...&Fu, HG.(2020).A Promoted Charge Separation/Transfer System from Cu Single Atoms and C(3)N(4)Layers for Efficient Photocatalysis.ADVANCED MATERIALS,32(33),-. |
MLA | Xiao, XD,et al."A Promoted Charge Separation/Transfer System from Cu Single Atoms and C(3)N(4)Layers for Efficient Photocatalysis".ADVANCED MATERIALS 32.33(2020):-. |
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