Quantum confined colloidal nanorod heterostructures for solar-to-fuel conversion

被引:259
作者
Wu, Kaifeng [1 ]
Lian, Tianquan [1 ]
机构
[1] Emory Univ, Dept Chem, 1515 Pierce Dr, Atlanta, GA 30322 USA
关键词
ULTRAFAST CHARGE SEPARATION; PHOTOCATALYTIC HYDROGEN-PRODUCTION; MULTIPLE EXCITON DISSOCIATION; HOT-ELECTRON TRANSFER; LIQUID-SOLID GROWTH; NOBLE-METAL-FREE; BRIDGED MOLECULAR-SYSTEMS; CARRIER-MULTIPLICATION; SEMICONDUCTOR NANOCRYSTALS; AUGER RECOMBINATION;
D O I
10.1039/c5cs00472a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Solar energy conversion, particularly solar-driven chemical fuel formation, has been intensely studied in the past decades as a potential approach for renewable energy generation. Efficient solar-to-fuel conversion requires artificial photosynthetic systems with strong light absorption, long-lived charge separation and efficient catalysis. Colloidal quantum confined nanoheterostructures have emerged as promising materials for this application because of the ability to tailor their properties through size, shape and composition. In particular, colloidal one-dimensional (1D) semiconductor nanorods (NRs) offer the opportunity to simultaneously maintain quantum confinement in radial dimensions for tunable light absorptions and bulk like carrier transport in the axial direction for long-distance charge separations. In addition, the versatile chemistry of colloidal NRs enables the formation of semiconductor heterojunctions (such as CdSe/CdS dot-in-rod NRs) to separate photogenerated electron-hole pairs and deposition of metallic domains to accept charges and catalyze redox reactions. In this review, we summarize research progress on colloidal NR heterostructures and their applications for solar energy conversion, emphasizing mechanistic insights into the working principle of these systems gained from spectroscopic studies. Following a brief overview of synthesis of various NRs and heterostructures, we introduce their electronic structures and dynamics of exciton and carrier transport and interfacial transfer. We discuss how these exciton and carrier dynamics are controlled by their structures and provide key mechanistic understanding on their photocatalytic performance, including the photo-reduction of a redox mediator (methyl viologen) and light driven H-2 generation. We discuss the solar-driven H2 generation mechanism, key efficiency limiting steps, and potential approaches for rational improvement in semiconductor NR/metal heterostructures (such as Pt tipped CdSe@CdS dot-in-rod NRs). Finally, we conclude by pointing out challenges to be addressed in future research.
引用
收藏
页码:3781 / 3810
页数:30
相关论文
共 287 条
[61]   Photodeposition of Pt on Colloidal CdS and CdSe/CdS Semiconductor Nanostructures [J].
Dukovic, Gordana ;
Merkle, Maxivell G. ;
Nelson, Jaines H. ;
Hughes, Steven M. ;
Alivisatos, A. Paul .
ADVANCED MATERIALS, 2008, 20 (22) :4306-4311
[62]   Band-edge exciton in quantum dots of semiconductors with a degenerate valence band: Dark and bright exciton states [J].
Efros, AL ;
Rosen, M ;
Kuno, M ;
Nirmal, M ;
Norris, DJ ;
Bawendi, M .
PHYSICAL REVIEW B, 1996, 54 (07) :4843-4856
[63]   The electronic structure of semiconductor nanocrystals [J].
Efros, AL ;
Rosen, M .
ANNUAL REVIEW OF MATERIALS SCIENCE, 2000, 30 :475-521
[64]   ABSORPTION AND INTENSITY-DEPENDENT PHOTOLUMINESCENCE MEASUREMENTS ON CDSE QUANTUM DOTS - ASSIGNMENT OF THE 1ST ELECTRONIC-TRANSITIONS [J].
EKIMOV, AI ;
HACHE, F ;
SCHANNEKLEIN, MC ;
RICARD, D ;
FLYTZANIS, C ;
KUDRYAVTSEV, IA ;
YAZEVA, TV ;
RODINA, AV ;
EFROS, AL .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA B-OPTICAL PHYSICS, 1993, 10 (01) :100-107
[65]   Quantum Dot Size Dependent J-V Characteristics in Heterojunction ZnO/PbS Quantum Dot Solar Cells [J].
Gao, Jianbo ;
Luther, Joseph M. ;
Semonin, Octavi E. ;
Ellingson, Randy J. ;
Nozik, Arthur J. ;
Beard, Matthew C. .
NANO LETTERS, 2011, 11 (03) :1002-1008
[66]   Breakdown of Volume Scaling in Auger Recombination in CdSe/CdS Heteronanocrystals: The Role of the Core-Shell Interface [J].
Garcia-Santamaria, Florencio ;
Brovelli, Sergio ;
Viswanatha, Ranjani ;
Hollingsworth, Jennifer A. ;
Htoon, Han ;
Crooker, Scott A. ;
Klimov, Victor I. .
NANO LETTERS, 2011, 11 (02) :687-693
[67]   Suppressed Auger Recombination in "Giant" Nanocrystals Boosts Optical Gain Performance [J].
Garcia-Santamaria, Florencio ;
Chen, Yongfen ;
Vela, Javier ;
Schaller, Richard D. ;
Hollingsworth, Jennifer A. ;
Klimov, Victor I. .
NANO LETTERS, 2009, 9 (10) :3482-3488
[68]   Efficient and Limiting Reactions in Aqueous Light-Induced Hydrogen Evolution Systems using Molecular Catalysts and Quantum Dots [J].
Gimbert-Surinach, Carolina ;
Albero, Josep ;
Stoll, Thibaut ;
Fortage, Jerome ;
Collomb, Marie-Noelle ;
Deronzier, Alain ;
Palomares, Emilio ;
Llobet, Antoni .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2014, 136 (21) :7655-7661
[69]   Solar cell efficiency tables (Version 45) [J].
Green, Martin A. ;
Emery, Keith ;
Hishikawa, Yoshihiro ;
Warta, Wilhelm ;
Dunlop, Ewan D. .
PROGRESS IN PHOTOVOLTAICS, 2015, 23 (01) :1-9
[70]   Direct Evidence of Active-Site Reduction and Photodriven Catalysis in Sensitized Hydrogenase Assemblies [J].
Greene, Brandon L. ;
Joseph, Crisjoe A. ;
Maroney, Michael J. ;
Dyer, R. Brian .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (27) :11108-11111