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The organic-based memristive devices are widely studied as a next-generation electronics for eco-friendly wearable applications, thanks to materials` flexibility and biocompatibility. However, poor operational reliability and stability of the devices remain a critical challenge. Here, the study demonstrates a crystalline organohalide, Dabconium ammonium triiodide (DABCO-NH-I, DABCO is 1,4-diazabicyclo[2.2.2] octonium)-based memristive device with exceptionally high reliability and endurance. Owing to the low dielectric constant and anisotropic hexagonal crystal structure consisting of hydrogen bonds with a high bandgap, the DABCO-NH-I-based conductive bridging random access memory device demonstrates millivolt-scale operating voltages with a remarkably high on/off ratio of ≈10, capable of multi-level storage. The relatively higher thermal conductivity of the crystalline organohalide (1.06 W mK), compared to most of organic materials (0.1-0.5 W mK), is found to be beneficial to suppress intense heat accumulation generated by Joule heating effect during device operation. With the facilitated dissipation of the generated heat, the simple planar heterojunction structured device shows remarkably endurable resistive switching over 10 cycles of program-erase at both room temperature and 85 °C with high switching reliability. This study introduced a new class of materials that can overcome the limitations of existing organic materials for high-performance next-generation organic electronic devices.
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http://dx.doi.org/10.1002/adma.202413020 | DOI Listing |
Food Chem
August 2025
School of Light Industry Science and Engineering, Beijing Technology and Business University, Beijing 100048, China.
High-throughput screening of deep eutectic solvents (DESs) was performed using artificial intelligence/quantum mechanical models. Ni-amorphous metal-organic frameworks (aMOFs) was synthesized through amine-DES aqueous solution. The target-specific DES/amorphous MOF nanocomposite was then modified onto screen-printed electrode, serving as sensing platform for dicofol due to high surface properties and excellent electrochemical activity.
View Article and Find Full Text PDFSci Rep
July 2025
Department of Chemistry, Shahid Bahonar University of Kerman, Kerman, 76169-133, Iran.
Organohalide lead perovskites (PVKs) are among the most promising materials for creating high-efficiency and low-cost photovoltaic devices. However, challenges such as high trap densities, low crystallinity, and moisture sensitivity in perovskite films hinder the performance and stability of perovskite solar cells (PSCs). In this work, we address these limitations by incorporating a green, environmentally friendly nanocomposite multi-walled carbon nanotube/zinc oxalate (MWCNT/Zn(COO)₂) into the electron transport layer (ETL) to enhance the performance, stability, and cost-effectiveness of PSCs.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Department of Materials Science and Engineering, City University of Hong Kong, Hong Kong SAR, 999007, China.
Organohalides are commonly found pollutants with long-term persistence in industrial wastewater and drinkable water. Although these pollutants only constitute a small portion of the total organic carbon (TOC), they contribute major toxicity, posing a threat to ecosystem, biodiversity, and public health. Selective removal of organohalides from wastewater/drinkable water is costly due to the orders of magnitude lower concentration of organohalides as compared to interferences.
View Article and Find Full Text PDFAdv Mater
July 2025
Department of Nano Science and Technology and Department of Nanoengineering, SKKU Advanced Institute of Nanotechnology (SAINT), Sungkyunkwan University, Suwon, 16419, Republic of Korea.
Chempluschem
April 2023
Institut für Chemie und Biochemie, Freie Universität Berlin, Fabeckstr. 34/36, 14195, Berlin, Germany.
A co-crystalline adduct consisting of a phosphinine selenide and an organohalide was obtained by slow evaporation of the solvent from a mixture of 2,6-bis(trimethylsilyl)phosphinine selenide and 1,4-diiodotetrafluorobenzene (1,4-TFDIB). The crystallographic characterization of the product shows π-π stacking, F⋅⋅⋅H hydrogen bonding between 1,4-TFDIB and the phosphinine selenide, as well as F⋅⋅⋅F interactions between 1,4-TFDIB molecules. Moreover, the phosphorus heterocycle could be crystallized with diiodine to form a 1 : 1 adduct.
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