Quantum dots in photocatalytic applications: efficiently enhancing visible light photocatalytic activity by integrating CdO quantum dots as sensitizers

Literature Information

Publication Date 2017-08-25
DOI 10.1039/C7CP05312F
Impact Factor 3.676
Authors


View Original

Abstract

The amalgamation of a wide optical band gap photocatalyst with visible-light-active CdO quantum dots (QDs) as sensitizers is one of the most efficient ways to improve photocatalytic performance under visible light irradiation. The photocatalytic performance of cadmium benzoate ((Cd(C7H5O2)2)3(CH3CN)1) is comprehensively investigated. The estimated optical band gap of cadmium benzoate is 2.64 eV and the EPc and EPv are about −0.09 V (vs. NHE) and +2.55 V (vs. NHE), respectively, which implies that cadmium benzoate possesses a high negative reduction potential of excited electrons due to its higher conduction band position, and hence, the locations of the conduction band minimum and the valence band maximum meet the redox capacity. Thus, this composite photocatalyst exhibits superior activity in visible-light-driven photocatalytic H2 evolution. We found that introducing the QDs enhance the photocatalytic performance towards the visible light region. The electronic band structure shows high k-dispersion bands around the Fermi level, which implies low effective masses, and hence, the high mobility carriers favor the enhancement of the charge transfer process. The mobility of the photogenerated carriers significantly influences the photocatalytic efficiency and the higher photogenerated carriers' mobility enhances the photocatalytic performance. Moreover, the result shows a great effective mass difference between electrons (e−) and holes (h+), which can facilitate the e− and h+ migration and separation, and finally improve the photocatalytic performance. The large mobility difference is useful for the separation of e− and h+, the reduction of the e− and h+ recombination rate, and the improvement of the photocatalytic activity. Thus, cadmium benzoate exhibits rapid generation of e−–h+ pairs with photoexcitation and a high negative reduction potential of excited electrons due to its higher CB position. Based on these results one can conclude that cadmium benzoate satisfied all requirements to be an efficient photocatalyst. This will greatly improve the search efficiency and greatly help experimentalists in saving resources in the exploration of new photocatalysts with good photocatalytic performance.

Related Literature

Contents

Front/Back Matter

DOI: 10.1039/C0PY90029J

Inside front cover

Front/Back Matter

DOI: 10.1039/C0PY90019B

Preparation of shell cross-linked nanoparticlesvia miniemulsion RAFT polymerization

Miaojun Ding, Hongyuan Hu

2010-09-14 Paper

DOI: 10.1039/C0PY00170H

E-beam irradiation and UV photocrosslinking of microemulsion-laden poly(N-vinyl-2-pyrrolidone) hydrogels for “in situ” encapsulation of volatile hydrophobic compounds

C. Dispenza, M. Ricca, C. LoPresti, G. Battaglia, M. La Valle, D. Giacomazza, D. Bulone

2010-09-23 Paper

DOI: 10.1039/C0PY00161A

Polymer–protein conjugates: an enzymatic activity perspective

Marc A. Gauthier, Harm-Anton Klok

2010-06-11 Review Article

DOI: 10.1039/C0PY90001J

Thermoresponsive behaviour of poly[(oligo(ethyleneglycol methacrylate)]s and their protein conjugates: importance of concentration and solvent system

Konstantinos Bebis, Mathew W. Jones, David M. Haddleton, Matthew I. Gibson

2011-02-07 Paper

DOI: 10.1039/C0PY00408A

A spoonful of sugar: the application of glycopolymers in therapeutics

Sebastian G. Spain, Neil R. Cameron

2010-07-09 Review Article

DOI: 10.1039/C0PY00149J

Supramolecular complexes of single walled carbon nanotubes with conjugated polymers‡

Patigul Imin, Fuyong Cheng, Alex Adronov

2010-10-29 Paper

DOI: 10.1039/C0PY00286K

Synthesis and characterization of polythiophenes with alkenyl substituents

Nadia Hundt, Kumaranand Palaniappan, Prakash Sista, John W. Murphy, Jing Hao, Hien Nguyen, Eugene Stein, Michael C. Biewer, Bruce E. Gnade, Mihaela C. Stefan

2010-08-31 Paper

DOI: 10.1039/C0PY00176G

Front cover

Cover

DOI: 10.1039/C0PY90027C

You might also like

Compound Q&A

Is 6-(3-Fluorophenyl)picolinic acid (CAS: 887982-40-3) safe?

6-(3-Fluorophenyl)picolinic acid is generally considered safe for laboratory use...

887982-40-36-(3-Fluorophenyl)pi...
Compound Q&A

What industries use (3R)-3-Pyrrolidinol (CAS: 2799-21-5)?

(3R)-3-Pyrrolidinol is used in the pharmaceutical industry as a precursor for dr...

2799-21-5(3R)-3-Pyrrolidinol
Compound Q&A

What precautions should be taken when handling (4R,5R)-4,5-Diethoxycarbonyl-2,2-dimethyldioxolane (CAS: 59779-75-8)?

When handling (4R,5R)-4,5-Diethoxycarbonyl-2,2-dimethyldioxolane (CAS: 59779-75-...

59779-75-8(4R,5R)-4,5-Diethoxy...
Compound Q&A

How is 1-(6-Chloroimidazo[1,2-b]pyridazin-3-yl)ethanone (CAS: 90734-71-7) typically synthesized?

1-(6-Chloroimidazo[1,2-b]pyridazin-3-yl)ethanone is often synthesized via a mult...

90734-71-71-(6-Chloroimidazo[1...
Compound Q&A

What is the market or research trend for N-Ethyl-3,4-dimethylbenzylamine (CAS: 39180-83-1)?

The market for N-Ethyl-3,4-dimethylbenzylamine (CAS: 39180-83-1) remains steady,...

39180-83-1N-Ethyl-3,4-dimethyl...
Compound Q&A

What is Tert-butyl 3-(pyrrolidin-1-yl)azetidine-1-carboxylate (CAS: 1019008-21-9)?

Tert-butyl 3-(pyrrolidin-1-yl)azetidine-1-carboxylate is a chemical compound wit...

1019008-21-9Tert-butyl 3-(pyrrol...
Compound Q&A

What regulatory guidelines apply to 1-Bromo-3-chloro-2,4-dimethoxybenzene (CAS: 1228956-93-1)?

1-Bromo-3-chloro-2,4-dimethoxybenzene (CAS: 1228956-93-1) falls under the classi...

1228956-93-11-Bromo-3-chloro-2,4...
Compound Q&A

Is 8-Bromo-2-methyl-3,4-dihydroisoquinolin-1(2H)-one (CAS: 1368622-07-4) safe?

The safety of 8-Bromo-2-methyl-3,4-dihydroisoquinolin-1(2H)-one (CAS: 1368622-07...

1368622-07-48-Bromo-2-methyl-3,4...
Compound Q&A

Is Benzyl [(3S)-2,6-dioxo-3-piperidinyl]carbamate (CAS: 22785-43-9) safe?

Benzyl [(3S)-2,6-dioxo-3-piperidinyl]carbamate is generally safe when handled wi...

22785-43-9Benzyl [(3S)-2,6-dio...
Compound Q&A

How should 1-{[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]sulfonyl}pyrrolidine (CAS: 928657-21-0) be stored?

1-{[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]sulfonyl}pyrrolidine s...

928657-21-01-{[4-(4,4,5,5-Tetra...

Source Journal

Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
Self-citation Rate: 10.3%
Articles per Year: 3036

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.