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Recently, utilizing the air breakdown effect in the charge excitation strategy proves as an efficient charge injection technique to increase the surface charge density of dielectric polymers for triboelectric nanogenerators (TENGs). However, quantitative characterization of the ability of dielectric polymers to trap reverse charges and the effect on the startup time of secondary self-charge excitation (SSCE) are essential for extensive applications. Here, an ultra-fast charge self-injection technique based on a self-charge excitation strategy is proposed, and a standard method to quantify the charge trapping and de-trapping abilities of 23 traditional tribo-materials is introduced. Further, the relationship among the distribution of dielectric intrinsic deep, shallow trap states, and transportation of trapped charges is systematically analyzed in this article. It shows that the de-trapping rate of charges directly determines the reactivation and failure of SSCE. Last, independent of TENG contact efficiency, an ultra-high charge density of 2.67 mC m and an ultra-fast startup time of SSCE are obtained using a 15 µm poly(vinylidene fluoride-trifluoroethylene) film, breaking the historical record for material modification. As a standard for material selection, this work quantifies the charge trapping and de-trapping ability of the triboelectric dielectric series and provides insights for understanding the charge transport in dielectrics.
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http://dx.doi.org/10.1002/adma.202312148 | DOI Listing |
Chem Sci
August 2025
Department of Chemistry and Biochemistry, Auburn University Auburn Alabama 36849 USA
Organic mixed ionic-electronic conducting polymers remain at the forefront of materials development for bioelectronic device applications. During electrochemical operation, structural dynamics and variations in electrostatic interactions in the polymer occur, which affect dual transport of the ions and electronic charge carriers. Such effects remain unclear due to a lack of spectroscopic methods capable of capturing these dynamics, which hinders the rational design of higher-performance polymers.
View Article and Find Full Text PDFInt J Mass Spectrom
December 2025
Department of Chemistry, Purdue University, 560 Oval Drive, West Lafayette, IN 47907-2084, USA.
An electrostatic linear ion trap (ELIT) is used to trap ions between two ion mirrors with image current detection by central detection electrode. Transformation of the time-domain signal to the frequency-domain via Fourier transform (FT) yields an ion frequency spectrum that can be converted to a mass-to-charge scale. Injection of ions into an ELIT from an external ion source leads to a time-of-flight ion separation that ultimately determines the range of over which ions can be collected from a given ion injection step.
View Article and Find Full Text PDFSmall Sci
September 2025
Infrared photodetectors are crucial for autonomous driving, providing reliable object detection under challenging lighting conditions. However, conventional silicon-based devices are limited in their responsivity beyond 1100 nm. Here, a scallop-structured silicon photodetector integrated with tin-substituted perovskite quantum dots (PQDs) that effectively extends infrared detection is demonstrated.
View Article and Find Full Text PDFNanoscale
September 2025
Department of Chemistry, Utkal University, Vani Vihar, Bhubaneswar, 751004, India.
Designing heterostructure-based nanocomposites has gained considerable interest in solving energy scarcity and environmental contamination issues. Herein, a heterojunction assembly of ternary SnS/MoS/g-CN nanocomposites with varying Sn and Mo weight ratios was synthesized through a single-step hydrothermal method. At an optimized ratio of tin to molybdenum (1 : 2), denoted as SM-3, promising electrochemical and photocatalytic performances were observed compared to bare SnS/g-CN and MoS/g-CN.
View Article and Find Full Text PDFACS Nano
September 2025
School of Microelectronics, Hefei University of Technology, Hefei 230009, China.
Near-infrared (NIR) narrowband photodetectors, featuring high sensitivity, excellent wavelength selectivity, and narrow full width at half-maximum (fwhm), enable efficient detection of specific NIR wavelengths and are widely used in optical communication, environmental monitoring, spectroscopy, and scientific research. In this study, we present a self-powered NIR photodetector based on a silicon nanowire (SiNW) array, exhibiting an ultranarrowband response centered at 1120 nm. The device employs a simple Schottky junction architecture.
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