CdSe Quantum Dot–Fullerene Hybrid Nanocomposite for Solar Energy Conversion: Electron Transfer and Photoelectrochemistry

ACS Nano ◽  
2011 ◽  
Vol 5 (12) ◽  
pp. 9421-9427 ◽  
Author(s):  
Jin Ho Bang ◽  
Prashant V. Kamat
Keyword(s):  
Electron Transfer ◽  
Solar Energy ◽  
Quantum Dot ◽  
Energy Conversion ◽  
Conversion Electron ◽  
Solar Energy Conversion ◽  
Hybrid Nanocomposite ◽  
Cdse Quantum Dot

scholarly journals Nitrogen-Doped and CdSe Quantum-Dot-Sensitized Nanocrystalline TiO2Films for Solar Energy Conversion Applications

2008 ◽  
Vol 112 (4) ◽  
pp. 1282-1292 ◽  
Author(s):  
Tzarara López-Luke ◽  
Abraham Wolcott ◽  
Li-ping Xu ◽  
Shaowei Chen ◽  
Zhenhai Wen ◽  
...  
Keyword(s):  
Solar Energy ◽  
Quantum Dot ◽  
Energy Conversion ◽  
Solar Energy Conversion ◽  
Nitrogen Doped ◽  
Cdse Quantum Dot

scholarly journals A biophotoelectrochemical approach to unravelling the role of cyanobacterial cell structures in exoelectrogenesis

2021 ◽  
Author(s):  
Laura T. Wey ◽  
Joshua M. Lawrence ◽  
Xiaolong Chen ◽  
Robert Clark ◽  
David J. Lea-Smith ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Solar Energy ◽  
Energy Conversion ◽  
Solar Energy Conversion ◽  
Growth Stages ◽  
Whole Cells ◽  
Analytical Technique ◽  
Type Iv ◽  
Cell Structures ◽  
Cell Electrode

AbstractPhotosynthetic microorganisms can export electrons outside their cells, a phenomenon called exoelectrogenesis, which can be harnessed for solar energy conversion. However, the route electrons take from thylakoid membranes to the cell exterior is not understood. Electrochemistry is a powerful analytical technique for studying electron transfer pathways. Here, we show how photoelectrochemistry can be used to compare electron flux from cyanobacterial cells of different growth stages, species and with the outer layers systematically removed. We show that the periplasmic space contributes significantly to the photocurrent profile complexity of whole cells, indicating that it gates electron transfer in exoelectrogenesis. We found that although components of the type IV pili machinery do not have a role in exoelectrogenesis, they contribute significantly to cell-electrode adherence. This study establishes that analytical photoelectrochemistry and molecular microbiology provide a powerful combination to study exoelectrogenesis, enabling future studies to answer biological questions and advance solar energy conversion applications.

Quantum dot nanoscale heterostructures for solar energy conversion

2013 ◽  
Vol 42 (7) ◽  
pp. 2963-2985 ◽  
Author(s):  
Rachel S. Selinsky ◽  
Qi Ding ◽  
Matthew S. Faber ◽  
John C. Wright ◽  
Song Jin
Keyword(s):  
Solar Energy ◽  
Quantum Dot ◽  
Energy Conversion ◽  
Solar Energy Conversion

scholarly journals Watching the dynamics of electrons and atoms at work in solar energy conversion

2015 ◽  
Vol 185 ◽  
pp. 51-68 ◽  
Author(s):  
S. E. Canton ◽  
X. Zhang ◽  
Y. Liu ◽  
J. Zhang ◽  
M. Pápai ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Solar Energy ◽  
Energy Conversion ◽  
Solar Energy Conversion ◽  
Photochemical Reactions ◽  
Atomic Scale ◽  
Intramolecular Electron Transfer ◽  
X Ray ◽  
Ultrafast Optical ◽  
Quantum Chemistry Calculations

The photochemical reactions performed by transition metal complexes have been proposed as viable routes towards solar energy conversion and storage into other forms that can be conveniently used in our everyday applications. In order to develop efficient materials, it is necessary to identify, characterize and optimize the elementary steps of the entire process on the atomic scale. To this end, we have studied the photoinduced electronic and structural dynamics in two heterobimetallic ruthenium–cobalt dyads, which belong to the large family of donor–bridge–acceptor systems. Using a combination of ultrafast optical and X-ray absorption spectroscopies, we can clock the light-driven electron transfer processes with element and spin sensitivity. In addition, the changes in local structure around the two metal centers are monitored. These experiments show that the nature of the connecting bridge is decisive for controlling the forward and the backward electron transfer rates, a result supported by quantum chemistry calculations. More generally, this work illustrates how ultrafast optical and X-ray techniques can disentangle the influence of spin, electronic and nuclear factors on the intramolecular electron transfer process. Finally, some implications for further improving the design of bridged sensitizer-catalysts utilizing the presented methodology are outlined.

scholarly journals Interfacial Electron Transfer in Dye-Sensitized TiO2 Devices for Solar Energy Conversion

2021 ◽  
Author(s):  
Andressa Müller ◽  
Wendel Wierzba ◽  
Mariana Pastorelli ◽  
André Polo
Keyword(s):  
Electron Transfer ◽  
Solar Energy ◽  
Energy Conversion ◽  
Solar Energy Conversion ◽  
Transport Processes ◽  
Transfer Reactions ◽  
Molecular Devices ◽  
Interfacial Electron Transfer ◽  
Electron Transfer Reactions ◽  
Dye Sensitized

The development of cost-effective molecular devices that efficiently capture and convert sunlight into other useful forms of energy is a promising approach to meet the world’s increasing energy demands. These devices are designed through a successful combination of materials and molecules that work synergistically to promote light-driven chemical reactions. Light absorption by a surface-bound chromophore triggers a sequence of interfacial electron transfer processes. The efficiencies of the devices are governed by the dynamic balance between the electron transfer reactions that promote energy conversion and undesirable side reactions. Therefore, it is necessary to understand and control these processes to optimize the design of the components of the devices and to achieve higher energy conversion efficiencies. In this context, this review discusses general aspects of interfacial electron transfer reactions in dye-sensitized TiO2 molecular devices for solar energy conversion. A theoretical background on the Marcus-Gerischer theory for interfacial electron transfer and theoretical models for electron transport within TiO2 films are provided. An overview of dye-sensitized solar cells (DSSCs) and dye-sensitized photoelectrosynthesis cells (DSPECs) is presented, and the electron transfer and transport processes that occur in both classes of devices are emphasized and detailed. Finally, the main spectroscopic, electrochemical and photoelectrochemical experimental techniques that are employed to elucidate the kinetics of the electron transfer reactions discussed in this review are presented.

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