Facile synthesis and characterization of aza-bridged all-benzenoid quinoidal figure-eight and cage molecules.

Synthesis of conjugated compounds with unusual shape-persistent structures remains a challenge. Herein, utilizing thermodynamically reversible intermolecular Friedel-Crafts alkylation, a dynamic covalent chemistry (DCC) reaction, we facilely synthesized a figure-eight shaped macrocycle FEM and cage molecules CATPA/CACz. X-ray crystallographic analysis confirmed the chemical geometries of tetracation FEM4+(PF6 -)4 and hexacation CACz6+(SbF6 -)6. FEM and CATPA displayed higher photoluminescence quantum yield in solid states compared to that in solution, whereas CACz gave the reverse result. DFT calculations showed that fluorescence-related frontier molecular orbital profiles are mainly localized on their arms consisting of a p-quinodimethane (p-QDM) unit and two benzene rings of triphenylamine or carbazole. Owing to their space-confined structures, variable-temperature 1H NMR measurements showed that FEM, CATPA and FEM4+ have intramolecular restricted motion of phenyl rings on their chromophore arms. Accordingly, FEM and CATPA with flexible triphenylamine subunits displayed aggregation-induced emission behavior (AIE), whereas CACz with a rigid carbazole subunits structure showed no AIE behavior.

Tetrachromatic vision-inspired neuromorphic sensors with ultraweak ultraviolet detection.

Sensing and recognizing invisible ultraviolet (UV) light is vital for exploiting advanced artificial visual perception system. However, due to the uncertainty of the natural environment, the UV signal is very hard to be detected and perceived. Here, inspired by the tetrachromatic visual system, we report a controllable UV-ultrasensitive neuromorphic vision sensor (NeuVS) that uses organic phototransistors (OPTs) as the working unit to integrate sensing, memory and processing functions. Benefiting from asymmetric molecular structure and unique UV absorption of the active layer, the as fabricated UV-ultrasensitive NeuVS can detect 370 nm UV-light with the illumination intensity as low as 31 nW cm-2, exhibiting one of the best optical figures of merit in UV-sensitive neuromorphic vision sensors. Furthermore, the NeuVS array exbibits good image sensing and memorization capability due to its ultrasensitive optical detection and large density of charge trapping states. In addition, the wavelength-selective response and multi-level optical memory properties are utilized to construct an artificial neural network for extract and identify the invisible UV information. The NeuVS array can perform static and dynamic image recognition from the original color image by filtering red, green and blue noise, and significantly improve the recognition accuracy from 46 to 90%.

An n-Type Polythiophene Derivative with Excellent Thermoelectric Performance.

Typical n-type conjugated polymers are based on fused-ring electron-accepting building blocks. Herein, we report a non-fused-ring strategy to design n-type conjugated polymers, i.e. introducing electron-withdrawing imide or cyano groups to each thiophene unit of a non-fused-ring polythiophene backbone. The resulting polymer, n-PT1, shows low LUMO/HOMO energy levels of -3.91 eV/-6.22 eV, high electron mobility of 0.39 cm2  V-1 s-1 and high crystallinity in thin film. After n-doping, n-PT1 exhibits excellent thermoelectric performance with an electrical conductivity of 61.2 S cm-1 and a power factor (PF) of 141.7 µW m-1 K-2 . This PF is the highest value reported so far for n-type conjugated polymers and this is the first time for polythiophene derivatives to be used in n-type organic thermoelectrics. The excellent thermoelectric performance of n-PT1 is due to its superior tolerance to doping. This work indicates that polythiophene derivatives without fused rings are low-cost and high-performance n-type conjugated polymers.

Modulating the Alkylation Position on Terminal Thiophene Ring of Naphtho[2,3-b:6,7-b'] Bithieno[2,3-d] Thiophene (NBTT) for High-Performance Organic Optoelectronic Devices.

Several thiophene terminated thienoacenes with high mobilities in organic thin-film transistors (OTFTs) have been reported; however, the structure-property relationship of thiophene terminated thienoacenes was unclear, especially the impact of α or ß position substitution of terminal thiophene ring on molecular packing and physicochemical properties. Here, we report the synthesis and characterization of a six-ring-fused naphtho[2,3-b:6,7-b'] bithieno[2,3-d] thiophene (NBTT) and its derivatives 2,8-dioctyl-naphtho[2,3-b:6,7-b'] bithieno [2,3-d] thiophene (2,8-C8NBTT) and 3,9-dioctyl-naphtho[2,3-b:6,7-b'] bithieno [2,3-d] thiophene (3,9-C8NBTT). It is found that the alkylation on terminal thiophene ring can effectively tune the molecular stacking from a cofacial herringbone stacking mode (NBTT) to layer-by-layer packing (2,8-C8NBTT and 3,9-C8NBTT). Impressively, a hopping to "band-like" charge transport mechanism evolution of vacuum deposited films is realized by modulating the alkylation position on the terminal thiophene rings. As a result, the OTFTs based on 2,8-C8NBTT characterized by a "band-like" transport presents the highest mobility of 3.58 cm2 V-1 s-1 together with a remarkably high current on/off ratio around 109. Furthermore, organic phototransistors (OPTs) based on 2,8-C8NBTT thin film also exhibits higher photosensitivity (P) of 2.0 × 108, photoresponsivity (R) of 3.3 × 103 A W-1, and detectivity (D*) of 1.3 × 1016 Jones than those based on NBTT and 3,9-C8NBTT.

Polymerized Thermally Activated Delayed-Fluorescence Small Molecules: Long-Axis Polymerization Leads to a Nearly Concentration-Independent Luminescence.

Nowadays numerous thermally activated delayed fluorescence (TADF) polymers have been developed for PLEDs to realize high device performance and tunable emission colors. However, they often possess a strong concentration dependence on their luminescence including aggregation-caused quenching (ACQ) and aggregation-induced emission (AIE). Herein, we first report a nearly concentration-independent TADF polymer based on the strategy of polymerized TADF small molecules. It is found that when a donor-acceptor-donor (D-A-D) type TADF small molecule is polymerized through its long-axis direction, the triplet state is distributed along the polymeric backbone to effectively suppress the unwanted concentration quenching. Unlike the short-axis one with an ACQ effect, the photoluminescent quantum yield (PLQY) of the resultant long-axis polymer remains almost unchanged with the increasing doping concentration. Accordingly, a promising external quantum efficiency (EQE) up to 20 % is successfully achieved in a whole doping control window of 5-100 wt. %.

A high-contrast polymorphic difluoroboron luminogen with efficient RTP and TADF emissions.

A simple N,S-chelated four-coordinated difluoroboron-based emitter is reported with three polymorphs, which emit high contrast green (G), yellow (Y) and red (R) light. Interestingly, the G and R-Crystals show different thermally activated delayed fluorescence (TADF) at 530 nm and 630 nm with a remarkable emission spectral shift of up to 100 nm, while the Y-Crystal exhibits room temperature phosphorescence (RTP) at around 570 nm with a high solid-state quantum yield of 77%. Single crystal analysis and theoretical calculations reveal that different molecular conformations and packing modes lead to distinct triplet exciton conversion channels.

An Amorphous n-Type Conjugated Polymer with an Ultra-Rigid Planar Backbone.

High charge carrier mobility polymer semiconductors are always semi-crystalline. Amorphous conjugated polymers represent another kind of polymer semiconductors with different charge transporting mechanism. Here we report the first near-amorphous n-type conjugated polymer with decent electron mobility, which features a remarkably rigid, straight and planar polymer backbone. The molecular design strategy is to copolymerize two fused-ring building blocks which are both electron-accepting, centrosymmetrical and planar. The polymer is the alternating copolymer of double B←N bridged bipyridine (BNBP) unit and benzobisthiazole (BBTz) unit. It shows a decent electron mobility of 0.34 cm2  V-1 s-1 in organic field-effect transistors. The excellent electron transporting property of the polymer is possibly due to the ultrahigh backbone stiffness, small π-π stacking distance, and high molecular weight.

Correction: Unusual design strategy for a stable and soluble high-molecular-weight copper(I) arylacetylide polymer.

Correction for 'Unusual design strategy for a stable and soluble high-molecular-weight copper(I) arylacetylide polymer' by Li Jiang et al., Chem. Commun., 2021, 57, 12004-12007, DOI: 10.1039/D1CC05080J.

Unusual design strategy for a stable and soluble high-molecular-weight copper(I) arylacetylide polymer.

A long enough side chain, electron-withdrawing ester groups and a chloroform solvent in the polymerization can together relay solubility and/or stability to the copper(I) arylacetylide polymer.

B←N-Incorporated Dibenzo-azaacenes as n-Type Thermoelectric Materials.

Organic thermoelectric materials play a vital role in flexible power generating applications, such as wearable electronics and sensor networks. While there is a wealth of research on p-type organic thermoelectric materials, developments on n-type counterparts as complementary are comparatively limited. Herein, we report a new kind of n-type small-molecule thermoelectric materials based on B←N-incorporated dibenzo-azaacenes 1,2-DBNA-2 and 1,2-DBNA-5. Because of the low-lying lowest unoccupied molecular orbital (LUMO) energy levels, 1,2-DBNA-2 and 1,2-DBNA-5 could be efficiently n-doped, and the rigid and almost planar skeleton could ensure good carrier transfer. When doped with a typical n-dopant (4-(1,3-dimethyl-2,3-dihydro-1H-benzoimidazol-2-yl)phenyl)dimethylamine (N-DMBI), 1,2-DBNA-5 exhibits a moderate conductivity of 0.01 S cm-1 and a power factor of 0.06 µW m-1 K-2 with a Seebeck coefficient of -244.4 µV K-1 in thermoelectric devices. These results not only demonstrate that B←N-incorporated dibenzo-azaacenes are a novel class of n-type thermoelectric materials but also highlight a new strategy to develop n-type organic thermoelectric materials.

Crystallization Control of N,N'-Dioctyl Perylene Diimide by Amphiphilic Block Copolymers Containing poly(3-Hexylthiophene) and Polyethylene Glycol.

The preparation of micron- to nanometer-sized functional materials with well-defined shapes and packing is a key process to their applications. There are many ways to control the crystal growth of organic semiconductors. Adding polymer additives has been proven a robust strategy to optimize semiconductor crystal structure and the corresponding optoelectronic properties. We have found that poly(3-hexylthiophene) (P3HT) can effectively regulate the crystallization behavior of N,N'-dioctyl perylene diimide (C8PDI). In this study, we combined P3HT and polyethylene glycol (PEG) to amphiphilic block copolymers and studied the crystallization modification effect of these block copolymers. It is found that the crystallization modification effect of the block copolymers is retained and gradually enhanced with P3HT content. The length of C8PDI crystals were well controlled from 2 to 0.4 µm, and the width from 210 to 35 nm. On the other hand, due to the water solubility of PEG block, crystalline PEG-b-P3HT/C8PDI micelles in water were successfully prepared, and this water phase colloid could be stable for more than 2 weeks, which provides a new way to prepare pollution-free aqueous organic semiconductor inks for printing electronic devices.

π-Stacked Donor-Acceptor Dendrimers for Highly Efficient White Electroluminescence.

π-Stacked dendrimers consisting of cofacially aligned donors and acceptors are developed by introducing three dendritic teracridan donors with orthogonal configuration and three triazine acceptors in periphery of hexaphenylbenzene skeleton. The dendritic structure and orthogonal configuration of teracridan not only make their outer acridan segments approaching to acceptor in close distance, but also fix donor and acceptor in face-to-face alignment, leading to through-space charge transfer emission with thermally activated delayed fluorescence (TADF) effect. By regulating charge transfer strength via substituent effect of acceptor, emission color of the dendrimers can be tuned from blue to yellow/red region. Solution-processed two-color white organic light-emitting diodes (OLEDs) based on blue and yellow π-stacked donor-acceptor dendrimers exhibit the maximum external quantum efficiency of 20.6 % and maximum power efficiency of 58.9 lm W-1 , representing the state-of-the-art efficiency for all-TADF white OLEDs by solution process.

Applications of UAS in Crop Biomass Monitoring: A Review.

Biomass is an important indicator for evaluating crops. The rapid, accurate and nondestructive monitoring of biomass is the key to smart agriculture and precision agriculture. Traditional detection methods are based on destructive measurements. Although satellite remote sensing, manned airborne equipment, and vehicle-mounted equipment can nondestructively collect measurements, they are limited by low accuracy, poor flexibility, and high cost. As nondestructive remote sensing equipment with high precision, high flexibility, and low-cost, unmanned aerial systems (UAS) have been widely used to monitor crop biomass. In this review, UAS platforms and sensors, biomass indices, and data analysis methods are presented. The improvements of UAS in monitoring crop biomass in recent years are introduced, and multisensor fusion, multi-index fusion, the consideration of features not directly related to monitoring biomass, the adoption of advanced algorithms and the use of low-cost sensors are reviewed to highlight the potential for monitoring crop biomass with UAS. Considering the progress made to solve this type of problem, we also suggest some directions for future research. Furthermore, it is expected that the challenge of UAS promotion will be overcome in the future, which is conducive to the realization of smart agriculture and precision agriculture.

Sterically-Locked Donor-Acceptor Conjugated Polymers Showing Efficient Thermally Activated Delayed Fluorescence.

Donor-acceptor (D-A) conjugated polymers often possess a significant frontier molecular orbital overlap because of the conjugation elongation, leading to no thermally activated delayed fluorescence (TADF) caused by a large singlet-triplet energy splitting (▵EST ). Herein a novel steric locking strategy is proposed by incorporating methyl groups into D-A conjugated polymers. Benefitting from the methyl hindrance, the torsion between the donor and acceptor can be well tuned to form a sterically-locked conformation, so that the unwanted relaxation toward planarity and thus conjugation elongation is prevented to boost hole-electron separation. The resultant D-A conjugated polymer achieves an extremely low ΔEST of 0.09 eV to enable efficient TADF. The corresponding doped and non-doped devices are fabricated via a solution process, revealing a record-high external quantum efficiency (EQE) of 24.0 % (79.4 cd A-1 , 75.0 lm W-1 ) and 15.3 % (50.9 cd A-1 , 47.3 lm W-1 ).

B←N-Incorporated Dibenzo-azaacene with Selective Near-Infrared Absorption and Visible Transparency.

Organic compounds with selective near-infrared absorption and visible transparency are very desirable for fabrication of transparent/semitransparent optoelectronic devices. Herein, we develop a molecule with selective near-infrared absorption property, QBNA-O, in which four B←N units are incorporated to the core and two benzodioxin groups are introduced at the termini of the dibenzo-azaacene skeleton. QBNA-O exhibits a small optical gap of 1.39 eV due to the strong electron-donating benzodioxin groups and the strong electron-withdrawing B←N units. In toluene solution, QBNA-O shows a strong absorption peak at 856 nm with the full width at half maximum (FWHM) of only 41 nm as well as very weak absorption in the visible range from 380 nm to 760 nm. Thin films of QBNA-O exhibit the average visible transparency (AVT) of 78 % at the thickness of 205 nm and 90 % at the thickness of 45 nm. Solution-processed organic field-effect transistors (OFETs) of QBNA-O display ambipolar transporting behavior with the electron mobility of 0.52 cm2 V-1 s-1 and the hole mobility of 0.013 cm2 V-1 s-1 together with excellent air-stability. The selective NIR absorbing property and excellent charge transporting property imply that QBNA-O can be used to fabricate transparent organic optoelectronic devices.

Isomers of B←N-Fused Dibenzo-azaacenes: How B←N Affects Opto-electronic Properties and Device Behaviors?

The B←N unit has a large dipole and it is isoelectronic to C-C moiety with no dipole. Incorporating B←N units into π-conjugated system is a powerful strategy to design organic small molecules and polymers with intriguing opto-electronic properties and excellent opto-electronic device performance. However, it is unclear how the B←N unit affects electronic structures and opto-electronic properties of large π-conjugated molecules. In this work, to address this question, we developed three dibenzo-azaacene molecules in which two B←N units were introduced at different positions. Although the dibenzo-azaacene skeleton is fully π-conjugated, the effect of B←N unit on the electronic structures of the adjacent rings is much stronger than that of the distant rings. As a result, the three molecules with isomerized B←N incorporation patterns possess different electronic structures and exhibit tunable opto-electronic properties. Among the three molecules, the centrosymmetrical molecule exhibits higher LUMO/HOMO energy levels than those of the two axisymmetrical molecules. When used as the active layer in organic field-effect transistors (OFETs), while the two axisymmetrical molecules show unipolar electron transporting property, the centrosymmetrical molecule exhibits ambipolar hole and electron transporting behavior. This work not only deepens our understanding on organoboron π-conjugated molecules, but also indicates a new strategy to tune opto-electronic properties of organic semiconductors for excellent device performance.

Polymerization-induced photothermy: A non-donor-acceptor approach to highly effective near-infrared photothermal conversion nanoparticles.

Photothermal conversion nanoagents based on conjugated polymers (CPs) are attracting increasing attention for in vivo disease theranostics and high-performing ones are in urgent pursuit. Herein, we report a new and non-donor-acceptor approach to photothermal conversion CPs that combine several merits including low bandgaps, strong near-infrared absorption, low intersystem crossing rate and non-emissive nature. Three CPs based on 6,7; 6',7'-fused isoindigos (nIIDs), i.e., P2IIDV, P3IIDV and P4IIDV that have optical bandgaps of 1.30, 1.22 and 1.17 eV, respectively, are synthesized. The nanoparticles (NPs) of the CPs in water are prepared via nanocoprecipitation, which are non-fluorescent due to the rapid intramolecular twisting in the CP backbone within NPs, enabling most of the excitation energy flow to generate heat. The photothermal conversion efficiencies of the NPs as measured under irradiation at 808, 880 and 980 nm are 62.4%, 40.5% and 15.8% for P2IIDV, 65.1%, 41.0% and 38.9% for P3IIDV and 71.5%, 48.9% and 41.7% for P4IIDV, which are significantly higher than indocyanine green and many popularly reported photothermal conversion materials. In vivo studies using xenograft 4T1 tumor-bearing mouse model demonstrate that the P4IIDV NPs can serve as a rather effective photothermal conversion nanoagent for enhanced photoacoustic imaging and photothermal therapy of tumors.

A disk-type polyarene containing four B←N units.

In this manuscript, we report a disk-type polyarene consisting of an all-hexagon π-framework and four B←N units. It exhibits intriguing electronic structures and opto-electronic properties, such as locally modulated (anti)aromaticity, strong red fluorescence and n-type semiconductor characteristics, thus representing a new kind of π-molecule containing B←N units.

Direct Effect of Dielectric Surface Energy on Carrier Transport in Organic Field-Effect Transistors.

The understanding of the characteristics of gate dielectric that leads to optimized carrier transport remains controversial, and the conventional studies applied organic semiconductor thin films, which introduces the effect of dielectric on the growth of the deposited semiconductor thin films and hence only can explore the indirect effects. Here, we introduce pregrown organic single crystals to eliminate the indirect effect (semiconductor growth) in the conventional studies and to undertake an investigation of the direct effect of dielectric on carrier transport. It is shown that the matching of the polar and dispersive components of surface energy between semiconductor and dielectric is favorable for higher mobility. This new empirical finding may show the direct relationship between dielectric and carrier transport for the optimized mobility of organic field-effect transistors and hence show a promising potential for the development of next-generation high-performance organic electronic devices.