Publications by authors named "Chong'an Di"

Molecular doping plays a crucial role in modulating the performance of polymeric semiconductor (PSC) materials and devices. Despite the development of numerous molecular dopants and doping methods over the past few decades, achieving highly efficient doping of PSCs remains challenging, primarily because of the inadequate matching of frontier energy levels between the host polymers and the dopants, which is critical for facilitating charge transfer. In this work, we introduce a novel doping method termed photoexcitation-assisted molecular doping (PE-MD), capable of transcending limitations imposed by energy level disparities through the mediation of efficient photoinduced electron transfer between polymers and dopants.

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Article Synopsis
  • * The unique porous structure minimizes thermal conductivity by over 50%, improving charge transport and significantly boosting the materials' figure of merit (ZT) to 0.52 at 363 K.
  • * This innovative approach highlights the versatility of microstructural engineering in developing advanced plastic thermoelectric materials across various polymer systems.
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Reusable point-of-care biosensors offer a cost-effective solution for serial biomarker monitoring, addressing the critical demand for tumour treatments and recurrence diagnosis. However, their realization has been limited by the contradictory requirements of robust reusability and high sensing capability to multiple interactions among transducer surface, sensing probes and target analytes. Here we propose a drug-mediated organic electrochemical transistor as a robust, reusable epidermal growth factor receptor sensor with striking sensitivity and selectivity.

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Conjugated polymers promise inherently flexible and low-cost thermoelectrics for powering the Internet of Things from waste heat. Their valuable applications, however, have been hitherto hindered by the low dimensionless figure of merit (ZT). Here we report high-ZT thermoelectric plastics, which were achieved by creating a polymeric multi-heterojunction with periodic dual-heterojunction features, where each period is composed of two polymers with a sub-ten-nanometre layered heterojunction structure and an interpenetrating bulk-heterojunction interface.

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Nanoresolved doping of polymeric semiconductors can overcome scaling limitations to create highly integrated flexible electronics, but remains a fundamental challenge due to isotropic diffusion of the dopants. Here we report a general methodology for achieving nanoscale ion-implantation-like electrochemical doping of polymeric semiconductors. This approach involves confining counterion electromigration within a glassy electrolyte composed of room-temperature ionic liquids and high-glass-transition-temperature insulating polymers.

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  • The musculoskeletal system is the largest physiological system in humans, crucial for support, movement, and protection of organs.
  • The emerging field of "musculoskeletal electronics" focuses on advanced materials and technologies for motion capture, health monitoring, and rehabilitation.
  • The review highlights key advancements, strategies for developing materials and devices, and outlines future directions for research in this innovative area.
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The ability of n-type polymer thermoelectric materials to tolerate high doping loading limits further development of n-type polymer conductivity. Herein, two alcohol-soluble n-type polythiophene derivatives that are n-PT3 and n-PT4 are reported. Due to the ability of two polymers to tolerate doping loading more significantly than 100 mol%, both achieve electrical conductivity >100 S cm .

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The thermoelectric (TE) performance of organic materials is limited by the coupling of Seebeck coefficient and electrical conductivity. Herein a new strategy is reported to boost the Seebeck coefficient of conjugated polymer without significantly reducing the electrical conductivity by incorporation of an ionic additive DPPNMe Br. The doped polymer PDPP-EDOT thin film exhibits high electrical conductivity up to 1377 ± 109 S cm but low Seebeck coefficient below 30 µV K and a maximum power factor of 59 ± 10 µW m K .

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Humans rely increasingly on sensors to address grand challenges and to improve quality of life in the era of digitalization and big data. For ubiquitous sensing, flexible sensors are developed to overcome the limitations of conventional rigid counterparts. Despite rapid advancement in bench-side research over the last decade, the market adoption of flexible sensors remains limited.

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The development of high-performance organic thin-film transistor (OTFT) materials is vital for flexible electronics. Numerous OTFTs are so far reported but obtaining high-performance and reliable OTFTs simultaneously for flexible electronics is still challenging. Herein, it is reported that self-doping in conjugated polymer enables high unipolar n-type charge mobility in flexible OTFTs, as well as good operational/ambient stability and bending resistance.

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The deep sea remains the largest uncharted territory on Earth because it's eternally dark under high pressure and the saltwater is corrosive and conductive. The harsh environment poses great difficulties for the durability of the sensing method and the device. Sea creatures like sharks adopt an elegant way to detect objects by the tiny temperature differences in the seawater medium using their extremely thermo-sensitive thermoelectric sensory organ on the nose.

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In the development of high-performance organic thermoelectric devices, n-type materials, especially with small molecule semiconductors, lags far behind p-type materials. In this paper, three small molecules are synthesized based on electron-deficient naphthalene bis-isatin building blocks bearing different alkyl chains with the terminal functionalized with 3-ethylrhodanine unit and studied their aggregation and doping mechanism in detail. It is found that crystallinity plays an essential role in tuning the doping behavior of small molecules.

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Breaking the thermoelectric (TE) trade-off relationship is an important task for maximizing the TE performance of polymeric semiconductors. Existing efforts have focused on designing high-mobility semiconductors and achieving ordered molecular doping, ignoring the critical role of the molecular orientation during TE conversion. Herein, the achievement of ZT to 0.

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Article Synopsis
  • Adaptive devices adjust their electrical functions automatically in response to changes in their environment, making them promising for future artificial perception systems.
  • The review covers advancements in materials and devices that replicate biological sensory adaptation, particularly in tactile and visual systems.
  • It also outlines five strategies for developing adaptive devices and discusses current challenges and future directions for research in this area.
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Organic transistor with DNA-damage evaluation ability can open up novel opportunities for bioelectronic devices. Even though trace amounts of drugs can cause cumulative gene damage in vivo, the extremely low occurrence proportion makes them hardly transduced into detectable electric signals. Here, an ultrasensitive DNA-damage sensor based on an oligonucleotide-distortion-responsive organic transistor (DROT) is reported by creating controllable conformation change of double-stranded DNA on the surface of organic semiconductors.

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Solution-processable highly conductive polymers are of great interest in emerging electronic applications. For p-doped polymers, conductivities as high a nearly 10 S cm have been reported. In the case of n-doped polymers, they often fall well short of the high values noted above, which might be achievable, if much higher charge-carrier mobilities determined could be realized in combination with high charge-carrier densities.

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Doping is essential to manipulate the electrical performance of both thermoelectric (TE) materials and organic semiconductors (OSCs). Although organic thermoelectric (OTE) materials have experienced a rapid development over the past decade, the chemical doping of OSCs for TE applications lags behind, which has limited further breakthroughs in this cutting-edge field. Recently, increasing efforts have been devoted to the development of energetically matched host and dopant molecules, exploring novel doping methods and revealing the doping mechanisms.

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N-doping plays an irreplaceable role in controlling the electron concentration of organic semiconductors thus to improve performance of organic semiconductor devices. However, compared with many mature p-doping methods, n-doping of organic semiconductor is still of challenges. In particular, dopant stability/processability, counterion-semiconductor immiscibility and doping induced microstructure non-uniformity have restricted the application of n-doping in high-performance devices.

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Article Synopsis
  • * The authors demonstrate that using an electric field can significantly improve the photo-thermoelectric effect in n-type organic semiconductors, yielding over ten times the usual photoinduced carrier concentration.
  • * This improvement leads to a unique trade-off in the Seebeck coefficient and electrical conductivity, resulting in a 500% increase in power factor, paving the way for advanced organic materials in energy harvesting applications.
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Experimental discovery of organic topological insulators (OTI) is a dream for both topological matters and organic materials. Despite great challenges, we anticipate that the dream will become a reality by engineered studies on materials chemistry, characterization techniques and device physics of conjugated molecules.

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Optically tunable field-effect transistors (FETs) with near infra-red (NIR) light show promising applications in various areas. Now, arylazopyrazole groups are incorporated in the side chains of a semiconducting donor-acceptor (D-A) polymer. The cis-trans interconversion of the arylazopyrazole can be controlled by 980 nm and 808 nm NIR light irradiation, by utilizing NaYF :Yb,Tm upconversion nanoparticles and the photothermal effect of conjugated D-A polymers, respectively.

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2D conductive metal-organic frameworks (2D c-MOFs) feature promising applications as chemiresistive sensors, electrode materials, electrocatalysts, and electronic devices. However, exploration of the spin-polarized transport in this emerging materials and development of the relevant spintronics have not yet been implemented. In this work, layer-by-layer assembly was applied to fabricate highly crystalline and oriented thin films of a 2D c-MOF, Cu (HHTP) , (HHTP: 2,3,6,7,10,11-hexahydroxytriphenylene), with tunable thicknesses on the La Sr MnO (LSMO) ferromagnetic electrode.

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Development of high-performance organic thermoelectric (TE) materials is of vital importance for flexible power generation and solid-cooling applications. Demonstrated here is the significant enhancement in TE performance of selenium-substituted diketopyrrolopyrrole (DPP) derivatives. Along with strong intermolecular interactions and high Hall mobilities of 1.

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Mimicking sensory adaptation with transistors is essential for developing next-generation smart circuits. A key challenge is how to obtain controllable and reversible short-term signal decay while simultaneously maintaining long-term electrical stability. By introducing a buried dynamic-trapping interface within the dielectric layer, an organic adaptive transistor (OAT) with sensory adaptation functionality is developed.

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  • The charge-transport characteristics of charge-transfer complexes (CTCs) are crucial for advancing optoelectronic devices.
  • Systematic first-principles calculations on perylene-FTCNQ CTCs reveal that a 1:1 ratio (1P1F) has better charge-carrier mobility compared to a 3:2 ratio (3P2F), attributed to strong interlayer interactions in the latter.
  • Introducing fluorine atoms in the perylene-FTCNQ framework enhances charge-carrier mobility, and experimental results from field-effect transistors support these theoretical findings, suggesting that optimizing donor-acceptor ratios can lead to better organic electronic materials.
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