Organic Solar Cells: Materials and Device Physics by Dixon D. S. Fung, Wallace C. H. Choy (auth.), Wallace C.H.

By Dixon D. S. Fung, Wallace C. H. Choy (auth.), Wallace C.H. Choy (eds.)

Organic sunlight cells have emerged as new promising photovoltaic units because of their power purposes in huge zone, printable and versatile sunlight panels. Organic sunlight Cells: fabrics and equipment Physics bargains an up to date evaluate at the subject matters protecting the synthesis, houses and purposes of latest fabrics for varied severe roles in units from electrodes, interface and service shipping fabrics, to the lively layer composed of donors and acceptors.

Addressing the real equipment physics problems with provider and exciton dynamics and interface balance and novel mild trapping buildings, the opportunity of hybrid natural sun cells to supply excessive potency sunlight cells is tested and mentioned intimately. particular chapters covers key components including:

Latest learn and designs for powerful polymer donors/acceptors and interface materials

Synthesis and alertness of hugely obvious and conductive graphene

Exciton and cost dynamics for in-depth knowing of the mechanism underlying natural sunlight cells.

New potentials and rising functionalities of plasmonic results in OSCs

Interface Degradation Mechanisms in natural photovoltaics bettering the complete machine lifetime

Device structure and operation mechanism of natural/ inorganic hybrid sunlight cells for subsequent new release of excessive functionality photovoltaics

This reference might be essentially and theoretically utilized via senior undergraduates, postgraduates, engineers, scientists, researchers, and venture managers with a few basic wisdom in natural and inorganic semiconductor fabrics or devices.

Show description

Read or Download Organic Solar Cells: Materials and Device Physics PDF

Similar organic books

Chemistry of Heterocyclic Compounds: Pyridazines, Volume 28

Content material: bankruptcy I actual homes of Pyridazines (pages 1–22): Anne G. Lenhert and Raymond N. CastleChapter II The Pyridazinones, Alkoxy? and Aryloxy? Pyridazines, and similar Compounds (pages 23–218): James W. Mason and Duane L. AldousChapter III Halopyridazines (pages 219–352): Duane L. Aldous and Raymond N.

Handbook of Heterocyclic Chemistry

This new version is designed to supply a one-volume total photograph of the topic of heterocyclic chemistry

Annual Reports in Organic Synthesis–1975

Annual experiences in natural Synthesis – 1975 is a suite of invaluable information regarding the developments within the box of natural chemistry. acknowledged details is gifted within the kind of photographs and/or natural chemistry equations. The e-book covers subject matters corresponding to carbon-carbon bond forming reactions; oxidations; discounts; synthesis of heterocycles; artificial arrangements; and different miscellaneous reactions.

Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products

Focusing totally on the literature that has seemed on the grounds that 1984, Padwa (chemistry, Emory U. ) and Pearson (chemistry, U. of Michigan) current 12 contributions that survey functions of [3+2]-cycloadditions in natural synthesis. The chapters disguise nitrones, nitronates, azomethine ylides, carbonyl ylides, thiocarbonyl ylides, nitrile oxides, nitrile ylides and nitrile imines, diazoalkanes, azides, mesoionic ring platforms, influence of exterior reagents, and uneven reactions

Extra info for Organic Solar Cells: Materials and Device Physics

Sample text

To extend the conjugation of the backbone, a third thiophene was added as shown in PTDPP. The polymerization was performed via a Suzuki cross-coupling polymerization, using 2,5-thiophenebis(boronic ester) as monomer [48]. 9). DPP was also copolymerized with the other commonly used conjugated components. It is worthy to mention that in comparison with DTBT-based polymers, DPP-based polymers possess much lower band gaps. 57 eV [45, 49], respectively, which are lower than their DTBT-based counterparts (PFDTBT and PCDTBT).

2 Open-circuit voltage distribution of the devices based on BDT polymers; average values are shown as squares imides and diimide-containing conjugated components. These polymers made great success in PSCs. 4. A. A. A. A. A. 2 Electron Acceptors Organic materials with appropriate properties, including conjugated polymers and small molecular compounds, can be used as electron donor materials in OPV. Many organic compounds exhibited potential properties as electron acceptor material, but only a very few electron acceptor materials can be used in highly efficient OPV devices.

The conjugated backbone of PSBTBT would stack tighter than that of PCPDTBT. Therefore, the former exhibits better hole transport property than the latter [24]. The silicon atom of PSBTBT can also be replaced by a nitrogen atom, and the polymer PDTPBT was obtained [30]. 6 eV) than those of PCPDTBT and PSBTBT due to the strong electron donating effect of the amino group. 4 V, which limited its photovoltaic performance tremendously. The polymer PBDTBT exhibited a broader band gap 28 J. Hou and X. 3 eV) compared to PDTPBT.

Download PDF sample

Rated 4.57 of 5 – based on 47 votes