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Journal ArticleDOI

Small molecule semiconductors for high-efficiency organic photovoltaics

Yuze Lin, +2 more
- 15 May 2012 - 
- Vol. 41, Iss: 11, pp 4245-4272
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TLDR
This review summarizes the developments in small molecular donors, acceptors, and donor-acceptor dyad systems for high-performance multilayer, bulk heterojunction, and single-component OPVs and focuses on correlations of molecular chemical structures with properties, such as absorption, energy levels, charge mobilities, and photovoltaic performances.
Abstract
Organic photovoltaic cells (OPVs) are a promising cost-effective alternative to silicon-based solar cells, and possess light-weight, low-cost, and flexibility advantages. Significant progress has been achieved in the development of novel photovoltaic materials and device structures in the last decade. Nowadays small molecular semiconductors for OPVs have attracted considerable attention, due to their advantages over their polymer counterparts, including well-defined molecular structure, definite molecular weight, and high purity without batch to batch variations. The highest power conversion efficiencies of OPVs based on small molecular donor/fullerene acceptors or polymeric donor/fullerene acceptors are up to 6.7% and 8.3%, respectively, and meanwhile nonfullerene acceptors have also exhibited some promising results. In this review we summarize the developments in small molecular donors, acceptors (fullerene derivatives and nonfullerene molecules), and donor–acceptor dyad systems for high-performance multilayer, bulk heterojunction, and single-component OPVs. We focus on correlations of molecular chemical structures with properties, such as absorption, energy levels, charge mobilities, and photovoltaic performances. This structure–property relationship analysis may guide rational structural design and evaluation of photovoltaic materials (253 references).

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Citations
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Journal ArticleDOI

High-Performance Non-Fullerene Acceptor Derived from Diathiafulvalene Wings for Solution-Processed Organic Photovoltaics

TL;DR: A solution-processable small-molecule nonfullerene electron acceptor BAF-2HDT (7,7′-(9,9-didecyl-9H-fluorene-2,7-diyl)bis(4-((4,5-bis(hexylthio)-1,3-dithiol-2 ylidene)methyl)benzo[c][1,2,5]thiadiazole) bearing hexadiathiafulvalene (HDT) wings as end groups has
Journal ArticleDOI

Nanoscale Characterization and Unexpected Photovoltaic Behavior of Low Band Gap Sulfur-Overrich-Thiophene/Benzothiadiazole Decamers and Polymers

TL;DR: In this paper, high-soluble air-stable conjugated decamers and polymers with alternating bis(3,4′-S-alkyl)-2,2′-bithiophenes as the donor units and 2,1,3-benzothiadiazoles as the acceptor units were designed and expediently synthesized with the aid of microwave and ultrasound enabling technologies.
Journal ArticleDOI

Optimized synthesis of π-extended squaraine dyes relevant to organic electronics by direct (hetero)arylation and Sonogashira coupling reactions.

TL;DR: The induced changes and fine structure observed upon post-deposition annealing is unique to these π-extended squaraines with nothing like it reported in the literature for related squaraine based materials.
Journal ArticleDOI

D-A-D-π-D-A-D type diketopyrrolopyrrole based small molecule electron donors for bulk heterojunction organic solar cells.

TL;DR: The enhancement in PCE is mainly due to the improvement in Jsc and FF, related to light absorption in an active layer, a better nanoscale morphology, and an increase in the crystalline nature of the active layer and balanced charge transport, induced by the TSA treatment.
References
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Journal ArticleDOI

C 60 : Buckminsterfullerene

TL;DR: In this article, the authors proposed a truncated icosahedron, a polygon with 60 vertices and 32 faces, 12 of which are pentagonal and 20 hexagonal.
Journal ArticleDOI

Polymer photovoltaic cells : enhanced efficiencies via a network of internal donor-acceptor heterojunctions

TL;DR: In this paper, the carrier collection efficiency and energy conversion efficiency of polymer photovoltaic cells were improved by blending of the semiconducting polymer with C60 or its functionalized derivatives.
Journal ArticleDOI

Conjugated polymer-based organic solar cells

TL;DR: This review gives a general introduction to the materials, production techniques, working principles, critical parameters, and stability of the organic solar cells, and discusses the alternative approaches such as polymer/polymer solar cells and organic/inorganic hybrid solar cells.
Journal ArticleDOI

Two‐layer organic photovoltaic cell

TL;DR: In this paper, a two-layer organic photovoltaic cell was fabricated from copper phthalocyanine and a perylene tetracarboxylic derivative, achieving a power conversion efficiency of about 1% under simulated AM2 illumination.
Journal ArticleDOI

Photoinduced electron transfer from a conducting polymer to buckminsterfullerene.

TL;DR: Because the photoluminescence in the conducting polymer is quenched by interaction with C60, the data imply that charge transfer from the excited state occurs on a picosecond time scale.
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