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This review article summarizes the current understanding and recent updates to tropical cyclone outer size and structure forecasting and research primarily since 2018 as part of the World Meteorological Organization's 10th International Workshop on Tropical Cyclones. A more complete understanding of tropical cyclone outer wind and precipitation is key to anticipating storm intensification and the scale and magnitude of landfalling hazards. We first discuss the relevance of tropical cyclone outer size and structure, improvements in our understanding of its life cycle and inter-basin variability, and the processes that impact outer size changes. We next focus on current forecasting practices and differences among warning centers, recent advances in operational forecasting, and new observations of the storm outer wind field. We also summarize recent research on projected tropical cyclone outer size and structure changes by the late 21st century. Finally, we discuss recommendations for the future of tropical cyclone outer size forecasting and research. 

1,3-Dimethyl-2,3-dihydrobenzo[d]imidazoles,1H, and 1,1',3,3'-tetramethyl-2,2',3,3'-tetrahydro-2,2'-bibenzo[d]imidazoles,1₂, are of interest as n-dopants for organic electron-transport materials. Salts of 2-(4-(dimethylamino)phenyl)-4,7-dimethoxy-, 2-cyclohexyl-4,7-dimethoxy-, and 2-(5-(dimethylamino)thiophen-2-yl)benzo[d]imidazolium (1g–i⁺, respectively) have been synthesized and reduced with NaBH₄to1gH,1hH, and1iH, and with Na:Hg to1g₂and1h₂. Their electrochemistry and reactivity were compared to those derived from 2-(4-(dimethylamino)phenyl)- (1b⁺) and 2-cyclohexylbenzo[d]imidazolium (1e⁺) salts.E(1⁺/1^•) values for 2-aryl species are less reducing than for 2-alkyl analogues, i.e., the radicals are stabilized more by aryl groups than the cations, while 4,7-dimethoxy substitution leads to more reducingE(1⁺/1^•) values, as well as cathodic shifts inE(1₂^•+/1₂) andE(1H^•+/1H) values. Both the use of 3,4-dimethoxy and 2-aryl substituents accelerates the reaction of the1Hspecies with PC₆₁BM. Because 2-aryl groups stabilize radicals,1b₂and1g₂exhibit weaker bonds than1e₂and1h₂and thus react with 6,13-bis(triisopropylsilylethynyl)pentacene (VII) via a “cleavage-first” pathway, while1e₂and1h₂react only via “electron-transfer-first”.1h₂exhibits the most cathodicE(1₂^•+/1₂) value of the dimers considered here and, therefore, reacts more rapidly than any of the other dimers withVIIvia “electron-transfer-first”. Crystal structures show rather long central C–C bonds for1b₂(1.5899(11) and 1.6194(8) Å) and1h₂(1.6299(13) Å). 

While molecular doping is ubiquitous in all branches of organic electronics, little is known about the spatial distribution of dopants, especially at molecular length scales. Moreover, a homogeneous distribution is often assumed when simulating transport properties of these materials, even though the distribution is expected to be inhomogeneous. In this study, electron tomography is used to determine the position of individual molybdenum dithiolene complexes and their three-dimensional distribution in a semiconducting polymer at the sub-nanometre scale. A heterogeneous distribution is observed, the characteristics of which depend on the dopant concentration. At 5 mol% of the molybdenum dithiolene complex, the majority of the dopant species are present as isolated molecules or small clusters up to five molecules. At 20 mol% dopant concentration and higher, the dopant species form larger nanoclusters with elongated shapes. Even in case of these larger clusters, each individual dopant species is still in contact with the surrounding polymer. The electrical conductivity first strongly increases with dopant concentration and then slightly decreases for the most highly doped samples, even though no large aggregates can be observed. The decreased conductivity is instead attributed to the increased energetic disorder and lower probability of electron transfer that originates from the increased size and size variation in dopant clusters. This study highlights the importance of detailed information concerning the dopant spatial distribution at the sub-nanometre scale in three dimensions within the organic semiconductor host. The information acquired using electron tomography may facilitate more accurate simulations of charge transport in doped organic semiconductors. 

Developing efficient and stable organic photovoltaics (OPVs) is crucial for the technology's commercial success. However, combining these key attributes remains challenging. Herein, we incorporate the small molecule 2-((3,6-dibromo-9 H -carbazol-9-yl)ethyl)phosphonic acid (Br-2PACz) between the bulk-heterojunction (BHJ) and a 7 nm-thin layer of MoO 3 in inverted OPVs, and study its effects on the cell performance. We find that the Br-2PACz/MoO 3 hole-extraction layer (HEL) boosts the cell's power conversion efficiency (PCE) from 17.36% to 18.73% (uncertified), making them the most efficient inverted OPVs to date. The factors responsible for this improvement include enhanced charge transport, reduced carrier recombination, and favourable vertical phase separation of donor and acceptor components in the BHJ. The Br-2PACz/MoO 3 -based OPVs exhibit higher operational stability under continuous illumination and thermal annealing (80 °C). The T 80 lifetime of OPVs featuring Br-2PACz/MoO 3 – taken as the time over which the cell's PCE reduces to 80% of its initial value – increases compared to MoO 3 -only cells from 297 to 615 h upon illumination and from 731 to 1064 h upon continuous heating. Elemental analysis of the BHJs reveals the enhanced stability to originate from the partially suppressed diffusion of Mo ions into the BHJ and the favourable distribution of the donor and acceptor components induced by the Br-2PACz. 

Molecular doping can increase the conductivity of organic semiconductors and plays an increasingly important role in emerging and established plastic electronics applications. 4-(1,3-Dimethyl-2,3-dihydro-1 H -benzimidazol-2-yl)- N , N -dimethylaniline (N-DMBI-H) and tris(pentafluorophenyl)borane (BCF) are established n- and p-dopants, respectively, but neither functions as a simple one-electron redox agent. Molecular hydrogen has been suggested to be a byproduct in several proposed mechanisms for doping using both N-DMBI-H and BCF. In this paper we show for the first time the direct detection of molecular hydrogen in the uncatalysed doping of a variety of polymeric and molecular semiconductors using these dopants. Our results provide insight into the doping mechanism, providing information complementary to that obtained from more commonly applied methods such as optical, electron spin resonance, and electrical measurements.