Naphthalenediimide (NDI) polymers for all-polymer photovoltaics

Naphthalenediimide (NDI) polymers are an important class of electron-accepting (acceptor or n-type) semiconductors for organic photovoltaic (OPV) or organic solar cell (OSC) applications. Blending them with compatible electron-donating (donor or p-type) polymers yields an OPV device known as bulk-heterojunction (BHJ) all-polymer solar cells (all-PSCs). Compared to the more extensively studied OPVs using fullerene derivatives as the acceptor material, all-PSCs provide important benefits such as chemical tunability, mechanical flexibility and ambient/stress stability. Through an extensive research on materials design and device optimization in the last five years, all-PSCs employing NDI-based polymers have achieved remarkable improvement in device power conversion efficiency (PCE), now surpassing 10% – a number that approaches the state-of-the-art organic photovoltaic (OPV) cells using fullerenes. In this review, recent development of NDI-based conjugated polymers used in all-PSCs will be highlighted.     

Combined power of perovskites and silicon solar cells

The photovoltaic (PV) or solar cells technology can be categorised into two main groups, the wafer‐based and thin‐film based PVs. The wafer‐based PVs include the commonly known crystalline silicon (c‐Si) and gallium arsenide (GaAs) cells. The GaAs cells exhibit higher efficiency compared to crystalline silicon (c‐Si) cells but it is the later that dominates the commercial market. Thin‐film based (2nd Generation) PVs, including cadmium telluride (CdTe), amorphous silicon (a‐Si:H) and copper‐indium‐gallium‐selenide (CIGS), generally absorb light more efficiently than wafer‐based cells and can allow the use of materials in very thin films form. CdTe PVs have proven to be highly efficient but holds only a few percentage share of the market. There is still a need for more R&D before further commercialisation. An emerging and relatively new class of thin‐film based photovoltaics (3rd Generation) technology that has the potential to overcome the current energy conversion efficiencies and performance by making use of novel materials. This class of PVs include organic photovoltaic (OPV), dye‐synthesised solar cells (DSSC), quantum‐dot (QD) and last but not least, the perovskite PV. Perovskite PVs can offer a low cost energy generation solution with the best device conversion efficiencies have shot from lower than 4% in 2009 to more than 21% in 2016. Perovskite based devices can be fabricated using vacuum thermal evaporation or by solution processing of the active layers. Although most recent perovskite solar cells with record efficiencies (>20%) are prepared via solution processing, the early breakthrough in perovskite solar cells was made with vacuum processed perovskites thin films. Vacuum thermal evaporation offers the ability and flexibility to prepare solar cell devices in various configuration. Recent developments in the field of perovskite demonstrates its compatibility with both, first and second generation PV technologies, and is therefore likely to be embraced by the conventional PV industry and make its way into utility‐scale power generation.     

1 cm2 Organic Photovoltaic Cells for Indoor Application with over 20% Efficiency

Organic photovoltaic (OPV) technologies have the advantages of fabricating larger‐area and light‐weight solar panels on flexible substrates by low‐cost roll‐to‐toll production. Recently, OPV cells have achieved many significant advances with power conversion efficiency (PCE) increasing rapidly. However, large‐scale solar farms using OPV modules still face great challenges, such as device stability. Herein, the applications of OPV cells in indoor light environments are studied. Via optimizing the active layers to have a good match with the indoor light source, 1 cm² OPV cells are fabricated and a top PCE of 22% under 1000 lux light‐emitting diode (2700 K) illumination is demonstrated. In this work, the light intensities are measured carefully. Incorporated with the external quantum efficiency and photon flux spectrum, the integral current densities of the cells are calculated to confirm the reliability of the photovoltaic measurement. In addition, the devices show much better stability under continuous indoor light illumination. The results suggest that designing wide‐bandgap active materials to meet the requirements for the indoor OPV cells has a great potential in achieving higher photovoltaic performance.     

Bacteriorhodopsin-based Langmuir-Schaefer films for solar energy capture

The photovoltaic (PV) solar cell, converting incident solar radiation directly into electrical energy, today represents the most common power source for the Earth-orbiting spacecraft, and the utilization of organic materials in this context is here explored in comparison with the present state of the art placing emphasis in organic nanotechnology. Poly[3-3'(vinylcarbazole)] (PVK) was synthesized by oxidative polymerization with ferric chloride of N-vinylcarbazole. The resulting polymer was then deposited on solid support by using the Langmuir-Schaefer (LS) technique. The pressure-area isotherm of PVK revealed the possibility of compact monolayer formation at the air-water interface. Different layers of PVK were doped with iodine vapors. The cyclic voltammetry investigation of PVK-doped I/sub 2/ showed a distinctive electrochemical behavior. The photoinduced charge transfer across a donor/acceptor (D/A) hybrid interface provided an effective method to study the PV properties of the composite LS films. The results are compared with other approaches within the biological framework, such as bacteriorhodopsin (BR), and organic nanostructured materials.     

Polymer–Fullerene Bulk‐Heterojunction Solar Cells

Solution‐processed bulk heterojunction organic photovoltaic (OPV) devices have gained serious attention during the last few years and are established as one of the leading next generation photovoltaic technologies for low cost power production. This article reviews the OPV development highlights of the last two decades, and summarizes the key milestones that have brought the technology to today’s efficiency performance of over 7%. An outlook is presented on what will be required to drive this young photovoltaic technology towards the next major milestone, a 10% power conversion efficiency, considered by many to represent the efficiency at which OPV can be adopted in wide‐spread applications. With first products already entering the market, sufficient lifetime for the intended application becomes more and more critical, and the status of OPV stability as well as the current understanding of degradation mechanisms will be reviewed in the second part of this article.     

Photovoltaic–Pyroelectric Coupled Effect Induced Electricity for Self‐Powered Photodetector System

Ferroelectric materials have demonstrated novel photovoltaic effect to scavenge solar energy. However, most of the ferroelectric materials with wide bandgaps (2.7–4 eV) suffer from low power conversion efficiency of less than 0.5% due to absorbing only 8–20% of solar spectrum. Instead of harvesting solar energy, these ferroelectric materials can be well suited for photodetector applications, especially for sensing near‐UV irradiations. Here, a ferroelectric BaTiO₃ film‐based photodetector is demonstrated that can be operated without using any external power source and a fast sensing of 405 nm light illumination is enabled. As compared with photovoltaic effect, both the responsivity and the specific detectivity of the photodetector can be dramatically enhanced by larger than 260% due to the light‐induced photovoltaic–pyroelectric coupled effect. A self‐powered photodetector array system can be utilized to achieve spatially resolved light intensity detection by recording the output voltage signals as a mapping figure.     

9,9′-联芴烯衍生物在有机光伏电池中的应用

由于具有独特的14π电子芳香结构和扭曲的非平面构型,9,9′-联芴烯衍生物成为近年来被广泛研究的一类新型有机光伏材料。9,9′-联芴烯衍生物含有两个刚性平面内的联苯单元,因此具有良好的热稳定性和化学稳定性;且其具有优良的光电特性,很容易接受电子,从而提升自身的最低未占分子轨道(LUMO)能级,使得其有机光伏器件的开路电压增大。此外,9,9′-联芴烯有12个不同的取代位,与富勒烯衍生物相比,其结构更具灵活性。但是,该类化合物的电子迁移率较低,使得其光伏电池的光电转化效率过低。如何通过提高该类材料的电子迁移率、拓展其光谱吸收范围和吸收强度来提高光伏器件的光电转换效率,受到越来越多的关注和研究。阐述了近年来联芴烯衍生物在有机光伏电池中的研究进展,并对其结构、性能进行了简要的分析。最后,对联芴烯类材料的发展前景进行了展望。     

Organic Solar Cells: A Review of Materials,Limitations, and Possibilities for Improvement

Significant attention has been given during the last few years to overcome technological and material barriers in order to develop organic photovoltaic devices (OPVs) with comparable cost efficiency similar to the inorganic photovoltaics (PVs) and to make them commercially viable. To take advantage of the low cost for such devices, major improvements are necessary which include: an efficiency of around 10%, high stability from degradation under real-world conditions, novel optically active materials, and development of novel fabrication approaches. In order to meet such stringent requirements, the research and development in OPVs need to improve upon the short diffusion length of excitons, which is one of the factors that are responsible for their low power conversion efficiency. This review discusses some of the most significant technological developments that were presented in the literature and helped improve photovoltaic performance, such as tandem architectures, plasmonics, and use of graphitic nanostructural materials, among others.

Tandem organic solar cells with embedded plasmonics are a promising approach to further increase the power conversion efficiency of organic solar cells, by harvesting complementary spectral regions with high quantum efficiencies. Polymeric nanocomposites incorporating graphitic nanostructures were extensively investigated for the next generation of efficient and low-cost solar cells, since such nanomaterials show excellent electrical and mechanical properties, excellent carrier transport capabilities, and provide an efficient pathway to the dissociated charge carriers.     

Recent Advances in Wide‐Bandgap Photovoltaic Polymers

The past decade has witnessed significant advances in the field of organic solar cells (OSCs). Ongoing improvements in the power conversion efficiency of OSCs have been achieved, which were mainly attributed to the design and synthesis of novel conjugated polymers with different architectures and functional moieties. Among various conjugated polymers, the development of wide‐bandgap (WBG) polymers has received less attention than that of low‐bandgap and medium‐bandgap polymers. Here, we briefly summarize recent advances in WBG polymers and their applications in organic photovoltaic (PV) devices, such as tandem, ternary, and non‐fullerene solar cells. Addtionally, we also dissuss the application of high open‐circuit voltage tandem solar cells in PV‐driven electrochemical water dissociation. We mainly focus on the molecular design strategies, the structure‐property correlations, and the photovoltaic performance of these WBG polymers. Finally, we extract empirical regularities and provide invigorating perspectives on the future development of WBG photovoltaic materials.     

Hybrid solar cells with prescribed nanoscale morphologies based on hyperbranched semiconductor nanocrystals

In recent years, the search to develop large-area solar cells at low cost has led to research on photovoltaic (PV) systems based on nanocomposites containing conjugated polymers. These composite films can be synthesized and processed at lower costs and with greater versatility than the solid state inorganic semiconductors that comprise today's solar cells. However, the best nanocomposite solar cells are based on a complex architecture, consisting of a fine blend of interpenetrating and percolating donor and acceptor materials. Cell performance is strongly dependent on blend morphology, and solution-based fabrication techniques often result in uncontrolled and irreproducible blends, whose composite morphologies are difficult to characterize accurately. Here we incorporate three-dimensional hyperbranched colloidal semiconductor nanocrystals in solution-processed hybrid organic-inorganic solar cells, yielding reproducible and controlled nanoscale morphology.     

Developments of Diketopyrrolopyrrole-Dye-Based Organic Semiconductors for a Wide Range of Applications in Electronics

In recent times, fused aromatic diketopyrrolopyrrole (DPP)-based functional semiconductors have attracted considerable attention in the developing field of organic electronics. Over the past few years, DPP-based semiconductors have demonstrated remarkable improvements in the performance of both organic field-effect transistor (OFET) and organic photovoltaic (OPV) devices due to the favorable features of the DPP unit, such as excellent planarity and better electron-withdrawing ability. Driven by this success, DPP-based materials are now being exploited in various other electronic devices including complementary circuits, memory devices, chemical sensors, photodetectors, perovskite solar cells, organic light-emitting diodes, and more. Recent developments in the use of DPP-based materials for a wide range of electronic devices are summarized, focusing on OFET, OPV, and newly developed devices with a discussion of device performance in terms of molecular engineering. Useful guidance for the design of future DPP-based materials and the exploration of more advanced applications is provided.     

Towards sustainable photovoltaics: the search for new materials

The opportunities for photovoltaic (PV) solar energy conversion are reviewed in the context of projected world energy demands for the twenty-first century. Conventional single-crystal silicon solar cells are facing increasingly strong competition from thin-film solar cells based primarily on polycrystalline absorber materials, such as cadmium telluride (CdTe) and copper indium gallium diselenide (CIGS). However, if PVs are to make a significant contribution to satisfy global energy requirements, issues of sustainability and cost will need to be addressed with increased urgency. There is a clear need to expand the range of materials and processes that is available for thin-film solar cell manufacture, placing particular emphasis on low-energy processing and sustainable non-toxic raw materials. The potential of new materials is exemplified by copper zinc tin sulphide, which is emerging as a viable alternative to the more toxic CdTe and the more expensive CIGS absorber materials.     

25th Anniversary Article: A Decade of Organic/Polymeric Photovoltaic Research

Organic photovoltaic (OPV) technology has been developed and improved from a fancy concept with less than 1% power conversion efficiency (PCE) to over 10% PCE, particularly through the efforts in the last decade. The significant progress is the result of multidisciplinary research ranging from chemistry, material science, physics, and engineering. These efforts include the design and synthesis of novel compounds, understanding and controlling the film morphology, elucidating the device mechanisms, developing new device architectures, and improving large‐scale manufacture. All of these achievements catalyzed the rapid growth of the OPV technology. This review article takes a retrospective look at the research and development of OPV, and focuses on recent advances of solution‐processed materials and devices during the last decade, particular the polymer version of the materials and devices. The work in this field is exciting and OPV technology is a promising candidate for future thin film solar cells.     

Toward clean environment: evaluation of solar electric power technologies using fuzzy logic

The rapid expansion of the use of solar energy power plants worldwide is a subject that is being followed with interest. Fuzzy logic methodology is used for evaluating the solar thermal power technology, it compresses huge amount of data into smaller sets, and it has the ability to decide between different solar technologies on the basis of their benefits and costs. The most often considered solar technologies were parabolic trough, central receiver, dish sterling engine, compact linear Fresnel reflector (CLFR), solar chimney, photovoltaic (PV), and solar pond. The aim of our research is to provide the needed information to make a judgment or a decision of adopting the most preferred solar technology in terms of installation and development using fuzzy set methodology. The criteria of the evaluation were based on different parameters, i.e., power capacity, efficiency, availability, capacity factor, storage capability, cost, maturity, water usage, land usage, and safety. The key barriers and features for each technology on the basis of benefit-to-cost ratios are addressed. The results showed that CLFR was found to be the best choice in terms of research, development, and implementation, followed by parabolic trough technology, then the central receiver technology, dish sterling engine, solar chimney, PV, and solar pond, according to the order of preference.     

基于线路保护反时限特性的含光伏发电系统风险备用优化模型

针对光伏并网后容易引起系统的不安全运行,传统的备用配置方法经济性较差的情况,为保证系统在弃光最小化情况下安全运行的同时提高经济性,引入失负荷及弃光风险指标,建立了光伏并网后不同场景下的备用优化模型。该模型以最小化发电成本和备用成本为目标函数,功率平衡、机组特性及可中断负荷等为约束条件,利用线路保护反时限特性将线路潮流约束转化为对应时间尺度的热稳定极限值,综合求解含光伏发电系统中的各种不确定性场景下,线路保护反时限特性所对应的不同响应速度备用优化调度模型。含光伏系统的IEEE 6机30节点系统算例验证了模型的合理性及方法的有效性。     

Economical study for hydrogen production from seawater using renewable energy in Egypt

This study looks into the possibilities of hydrogen production in the north coast and red-sea Zone, Egypt, to conver renewable energy to hydrogen (power to gas). The main purpose is to estimate the power needed for each kg of hydrogen production from seawater using renewable energy and then the quantity of desalinated seawater needed to cover this cost. We will discuss different scenarios; the main two scenarios are photovoltaic (PV) solar with reverse osmosis (RO) desalination and concentrating solar power (CSP) with multi-effect desalination (MED).     

Efficient small molecule bulk heterojunction solar cells with high fill factors via pyrene-directed molecular self-assembly

Efficient organic photovoltaic (OPV) materials are constructed by attaching completely planar, symmetric end-groups to donor-acceptor electroactive small molecules. Appending C2-pyrene as the small molecule end-group to a diketopyrrolopyrrole core leads to materials with a tight, aligned crystal packing and favorable morphology dictated by π-π interactions, resulting in high power conversion efficiencies and high fill factors. The use of end-groups to direct molecular self-assembly is an effective strategy for designing high-performance small molecule OPV devices.     

Progress and Design Concerns of Nanostructured Solar Energy Harvesting Devices

Integrating devices with nanostructures is considered a promising strategy to improve the performance of solar energy harvesting devices such as photovoltaic (PV) devices and photo‐electrochemical (PEC) solar water splitting devices. Extensive efforts have been exerted to improve the power conversion efficiencies (PCE) of such devices by utilizing novel nanostructures to revolutionize device structural designs. The thicknesses of light absorber and material consumption can be substantially reduced because of light trapping with nanostructures. Meanwhile, the utilization of nanostructures can also result in more effective carrier collection by shortening the photogenerated carrier collection path length. Nevertheless, performance optimization of nanostructured solar energy harvesting devices requires a rational design of various aspects of the nanostructures, such as their shape, aspect ratio, periodicity, etc. Without this, the utilization of nanostructures can lead to compromised device performance as the incorporation of these structures can result in defects and additional carrier recombination. The design guidelines of solar energy harvesting devices are summarized, including thin film non‐uniformity on nanostructures, surface recombination, parasitic absorption, and the importance of uniform distribution of photo‐generated carriers. A systematic view of the design concerns will assist better understanding of device physics and benefit the fabrication of high performance devices in the future.     

Practical roadmap and limits to nanostructured photovoltaics

The significant research interest in the engineering of photovoltaic (PV) structures at the nanoscale is directed toward enabling reductions in PV module fabrication and installation costs as well as improving cell power conversion efficiency (PCE). With the emergence of a multitude of nanostructured photovoltaic (nano-PV) device architectures, the question has arisen of where both the practical and the fundamental limits of performance reside in these new systems. Here, the former is addressed a posteriori. The specific challenges associated with improving the electrical power conversion efficiency of various nano-PV technologies are discussed and several approaches to reduce their thermal losses beyond the single bandgap limit are reviewed. Critical considerations related to the module lifetime and cost that are unique to nano-PV architectures are also addressed. The analysis suggests that a practical single-junction laboratory power conversion efficiency limit of 17% and a two-cell tandem power conversion efficiency limit of 24% are possible for nano-PVs, which, when combined with operating lifetimes of 10 to 15 years, could position them as a transformational technology for solar energy markets.     

Towards Efficient Spectral Converters through Materials Design for Luminescent Solar Devices

Single‐junction photovoltaic devices exhibit a bottleneck in their efficiency due to incomplete or inefficient harvesting of photons in the low‐ or high‐energy regions of the solar spectrum. Spectral converters can be used to convert solar photons into energies that are more effectively captured by the photovoltaic device through a photoluminescence process. Here, recent advances in the fields of luminescent solar concentration, luminescent downshifting, and upconversion are discussed. The focus is specifically on the role that materials science has to play in overcoming barriers in the optical performance in all spectral converters and on their successful integration with both established (e.g., c‐Si, GaAs) and emerging (perovskite, organic, dye‐sensitized) cell types. Current challenges and emerging research directions, which need to be addressed for the development of next‐generation luminescent solar devices, are also discussed.