Three conjugated pigment molecules with fused hydrogen bonds, 3,7-diphenylpyrrolo[2,3-f]indole-2,6(1H,5H)-dione (BDP), (E)-6,6'-dibromo-[3,3'-biindolinylidene]-2,2'-dione (IIDG), and 3,6-di(thiophen-2-yl)-2,5-dihydropyrrolo-[3,4-c]pyrrole-1,4-dione (TDPP), were studied in this work. The insoluble pigment molecules were functionalized with tert-butoxylcarbonyl (t-Boc) groups to form soluble pigment precursors (BDP-Boc, IIDG-Boc, and TDPP-Boc) with latent hydrogen bonding. The single crystals of soluble pigment precursors were obtained. Upon simple thermal annealing, the t-Boc groups were removed and the soluble pigment precursor molecules with latent hydrogen bonding were converted into the original pigment molecules with fused hydrogen bonding. Structural analysis indicated that the highly crystalline soluble precursors were directly converted into highly crystalline insoluble pigments, which are usually only achievable by gas-phase routes like physical vapor transport. The distinct crystal structure after the thermal annealing treatment suggests that fused hydrogen bonding is pivotal for the rearrangement of molecules to form a new crystal in solid state, which leads to over 2 orders of magnitude enhancement in charge mobility in organic field-effect transistor (OFET) devices. This work demonstrated that crystalline OFET devices with insoluble pigment molecules can be fabricated by their soluble precursors. The results indicated that a variety of commercially available conjugated pigments could be potential active materials for high-performance OFETs.
Novel pigments isoepindolidiones (isoEpi) and di-tert-butyl quinolino [8,7-h]quinoline-1,7-diyl bis(carbonate) (isoEpi-Boc) were synthesized and characterized. The spectroscopic characterizations indicated that the tert-butyloxycarbonyl (t-Boc) units could be removed from soluble isoEpi-Boc by thermal annealing, forming insoluble isoEpi with hydrogen bonding. A solid-state isoEpi-Boc crystal to isoEpi crystal transition was observed during the annealing process and the molecular packing was significantly changed. With the emergence of hydrogen bonds, the isoEpi molecules were arranged into a brick-in-wall structure with π-stacking along the crystal growth axis, leading to a significant enhancement of charge mobility along the crystal growth direction (the hole mobility from 3.4 × 10 −4 to 0.32 cm 2 /(V•s), and the electron mobility from nondetectable to 5.6 × 10 −3 cm 2 /(V•s)). The results indicate that isoEpi is a promising chromophore for organic field-effect transistor (OFET). The crystal-to-crystal transition driven by the formation of hydrogen bonds is a unique method for modulating the charge transport properties in organic semiconductive materials for OFET devices.
This research proposes a seawater desalination system driven by photovoltaic and solar thermal energy for remote regions such as islands and seaside villages where fresh water is not accessible. The performance of this system is demonstrated through experiments, and the main concerns are the output of the photovoltaic power generation system, power quantity, water yield, and the loads under different solar irradiance and temperature. In this system, a PLC is used as the controller to adjust the water pump by the collection and processing of sensor data. A load switching time system is designed to select different operating schemes under different environments in order to save energy. The control method of this system is developed to ensure that the photovoltaic power generation system does not undervoltage while maintaining the normal operation of the desalination system. An improved Perturbation and Observation (P&O) algorithm is also proposed as a new Maximum Point Power Tracking (MPPT) method to solve the problem of misjudgment and oscillation after tracking the maximum power point (MPP) in the traditional P&O algorithm. The simulation test in the MATLAB/Simulink environment shows that when external irradiance changes, the improved P&O algorithm can track the MPP faster than the traditional P&O algorithm, and the amplitude of oscillation on the MPP is smaller. The hardware experiments show that this system can operate stably and flexibly, and it is capable of producing 5.18 kWh of electric energy and 335.81 kg of freshwater per day. The maximum yield of the unit can reach 565.75 kg per day and the maximum daily power generation is 8.12 kWh.
It is necessary to detect cadmium ions in seawater with high sensitivity because the pollution of cadmium ions seriously endangers the health and life of human beings. Nano-Fe3O4/MoS2/Nafion modified glassy carbon electrode was prepared by a drop coating method. The electrocatalytic properties of Nano-Fe3O4/MoS2/Nafion were measured by Cyclic Voltammetry (CV). Differential Pulse Voltammetry (DPV) was used to study the stripping Voltammetry response of the modified electrode to Cd2+. The optimal conditions were determined: In 0.1 mol/L HAc-NaAc solution, the solution pH was 4.2, the deposition potential was − 1.0 V, and the deposition time was 720 s, the membrane thickness was 8 μL. Under the optimum condition, the linear relation of Cd2+ concentration was found in the range of 5–300 μg/L, and the detection limit was 0.053 μg/L. The recovery of Cd2+ in seawater ranged from 99.2 to 102.9%. A composite material with simple operation, rapid response and high sensitivity was constructed for the determination of Cd2+ in seawater. Graphical abstract
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2025 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.