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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

Indolocarbazoles end-capped with diketopyrrolopyrroles: impact of regioisomerism on the solid-state properties and the performance of solution-processed bulk heterojunction solar cells

TL;DR: In this paper, two regioisomeric indolo [3,2-b] carbazoles end-substituted with diketopyrrolopyrrole dyes (3,9-TDPPIC and 2,8-TPDPIC) were synthesized, and their solid-state properties and performance as donor materials for bulk heterojunction solar cells using [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) as an acceptor material were evaluated.
Journal ArticleDOI

Tuning the Optoelectronic Properties of Naphtho‐Dithiophene‐Based A‐D‐A Type Small Donor Molecules for Bulk Hetero‐Junction Organic Solar Cells

TL;DR: In this paper, four acceptor-donor-acceptor (A-D-A) type small molecules using naphtho-dithiophene as central building block, trithiopehene as -bridges, malononitrile and 2-Thioxo-thiazolidin-4-one as end acceptor are presented.
Journal ArticleDOI

Synthesis and characterization of new [1]benzothieno[3,2-b]benzothiophene derivatives with alkyl-thiophene core for application in organic field-effect transistors

TL;DR: In this paper, new benzo[b]benzo[4,5]thieno[2,3-d]thiophene derivatives were synthesized and characterized as organic semiconductors in top-contact/bottom-gate organic field-effect transistors.
Journal ArticleDOI

Z-Shaped Fused-Chrysene Electron Acceptors for Organic Photovoltaics.

TL;DR: A new fused-chrysene electron-donating core is synthesized, where chrysene is condensed with two thiophenes via two dihydrobenzene rings, and a new Z-shaped fused-ring electron acceptor, FCIC, is designed and synthesized.
Journal ArticleDOI

An A′–A–D–A–A′ type small molecule based on 2,7-carbazole for solution-processed organic solar cells with high open-circuit voltage

TL;DR: In this article, a low-band gap small molecule Cz-TBT-CAC8 with 2,7-carbazole as the center donor and benzothiadiazole as an electron acceptor was designed and synthesized as the donor material for the solution-processed bulk hetero-junction solar cells.
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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