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Abstract Mangrove forests are critical coastal ecosystems that provide great socio‐ecological services, which are also highly vulnerable to climate change, particularly to sea level rise (SLR). Here we assess changes in mangrove forests in four distinct river/tide/wave‐dominant large deltas along the Indo‐Pacific coast based on 1,336 remote sensing images by machine learning techniques. We find that mangroves are migrating seaward at a rate of 18% ± 12% m/yr, which can offset landward mangroves loss, 67% of which caused by land use conversion. The fact that mangroves are expanding seaward with accretion rates exceeding SLR suggests that climate change has not yet triggered substantial loss in deltaic mangrove forests. Assuming that present environmental conditions do not change and that sediment and organic deposition in the deltaic topsets match SLR rates, we project that 90% of deltaic mangrove forests may start to retreat after 132–194 years. Early inundation of mangroves will occur in wave‐dominated delta. 

Abstract Fluorinated molecule 2,3,5,6‐tetrafluoro‐7,7,8,8‐tetracyanoquinodimethane (F4‐TCNQ) and its derivatives have been used in polymer:fullerene solar cells primarily as a dopant to optimize the electrical properties and device performance. However, the underlying mechanism and generality of how F4‐TCNQ affects device operation and possibly the morphology is poorly understood, particularly for emerging nonfullerene organic solar cells. In this work, the influence of F4‐TCNQ on the blend film morphology and photovoltaic performance of nonfullerene solar cells processed by a single halogen‐free solvent is systematically investigated using a set of morphological and electrical characterizations. In solar cells with a high‐performance polymer:small molecule blend FTAZ:IT‐M, F4‐TCNQ has a negligibly small effect on the molecular packing and surface characteristics, while it clearly affects the electronic properties and mean‐square composition variation of the bulk. In comparison to the control devices with an average power conversion efficiency (PCE) of 11.8%, inclusion of a trace amount of F4‐TCNQ in the active layer has improved device fill factor and current density, which has resulted into a PCE of 12.4%. Further increase in F4‐TCNQ content degrades device performance. This investigation aims at delineating the precise role of F4‐TCNQ in nonfullerene bulk heterojunction films, and thereby establishing a facile approach to fabricate highly optimized nonfullerene solar cells. 

Semitransparent organic photovoltaics (ST‐OPVs) provide a potentially facile route for some applications in building integrated photovoltaics. One of the challenges in developing large‐scale, printable ST‐OPVs is to address the need for high‐performance and fully solution‐processed top electrodes, allowing the replacement of the evaporated thin metallic films (Ag, Au, and Al). Silver nanowire (AgNW) is considered a promising candidate for the substitution due to its excellent transparency, conductivity, and solution processability. Herein, a novel bimodal AgNW (AgNW‐BM) electrode is reported, comprising AgNWs of two different aspect ratios. It is shown that the AgNW‐BM film achieves lower sheet resistance and higher visible transmittance than each monodisperse AgNW film, respectively. Furthermore, ST‐OPVs based on PTB7‐Th:IEICO‐4F with AgNW‐BM top electrodes are fabricated, which can obtain a maximum power conversion efficiency (PCE) of 7.49% with an average visible transmittance (AVT) of 33%. The ST‐devices also demonstrate an enhanced reproducibility and excellent color‐rendering index of 90. In addition, the bimodal top electrode is successfully implemented in the PM6:Y6 system with a higher PCE of 9.79% and with an AVT of 23%, demonstrating the universality for various semiconductor systems. Our work provides a simple strategy to realize fully solution‐processed, highly efficient ST‐OPVs. 

Abstract Casting of a donor:acceptor bulk‐heterojunction structure from a single ink has been the predominant fabrication method of organic photovoltaics (OPVs). Despite the success of such bulk heterojunctions, the task ofcontrolling the microstructure in a single casting process has been arduous and alternative approaches are desired. To achieve OPVs with a desirable microstructure, a facile and eco‐compatible sequential deposition approach is demonstrated for polymer/small‐molecule pairs. Using a nominally amorphous polymer as the model material, the profound influence of casting solvent is shown on the molecular ordering of the film, and thus the device performance and mesoscale morphology of sequentially deposited OPVs can be tuned. Static and in situ X‐ray scattering indicate that applying (R)‐(+)‐limonene is able to greatly promote the molecular order of weakly crystalline polymers and form the largest domain spacing exclusively, which correlates well with the best efficiency of 12.5% in sequentially deposited devices. The sequentially cast device generally outperforms its control device based on traditional single‐ink bulk‐heterojunction structure. More crucially, a simple polymer:solvent interaction parameter χ is positively correlated with domain spacing in these sequentially deposited devices. These findings shed light on innovative approaches to rationally create environmentally friendly and highly efficient electronics. 

Abstract The commercialization of nonfullerene organic solar cells (OSCs) critically relies on the response under typical operating conditions (for instance, temperature and humidity) and the ability of scale‐up. Despite the rapid increase in power conversion efficiency (PCE) of spin‐coated devices fabricated in a protective atmosphere, the efficiencies of printed nonfullerene OSC devices by blade coating are still lower than 6%. This slow progress significantly limits the practical printing of high‐performance nonfullerene OSCs. Here, a new and relatively stable nonfullerene combination is introduced by pairing the nonfluorinated acceptor IT‐M with the polymeric donor FTAZ. Over 12% efficiency can be achieved in spin‐coated FTAZ:IT‐M devices using a single halogen‐free solvent. More importantly, chlorine‐free, blade coating of FTAZ:IT‐M in air is able to yield a PCE of nearly 11% despite a humidity of ≈50%. X‐ray scattering results reveal that large π–π coherence length, high degree of face‐on orientation with respect to the substrate, and small domain spacing of ≈20 nm are closely correlated with such high device performance. The material system and approach yield the highest reported performance for nonfullerene OSC devices by a coating technique approximating scalable fabrication methods and hold great promise for the development of low‐cost, low‐toxicity, and high‐efficiency OSCs by high‐throughput production. 

Abstract Tandem structure provides a practical way to realize high efficiency organic photovoltaic cells, it can be used to extend the wavelength coverage for light harvesting. The interconnecting layer (ICL) between subcells plays a critical role in the reproducibility and performance of tandem solar cells, yet the processability of the ICL has been a challenge. In this work the fabrication of highly reproducible and efficient tandem solar cells by employing a commercially available material, PEDOT:PSS HTL Solar (HSolar), as the hole transporting material used for the ICL is reported. Comparing with the conventional PEDOT:PSS Al 4083 (c‐PEDOT), HSolar offers a better wettability on the underlying nonfullerene photoactive layers, resulting in better charge extraction properties of the ICL. When FTAZ:IT‐M and PTB7‐Th:IEICO‐4F are used as the subcells, a power conversion efficiency (PCE) of 14.7% is achieved in the tandem solar cell. To validate the processability of these tandem solar cells, three other research groups have successfully fabricated tandem devices using the same recipe and the highest PCE obtained is 16.1%. With further development of donor polymers and device optimization, the device simulation results show that a PCE > 22% can be realized in tandem cells in the near future.