Publications by authors named "Fengxing Jiang"

Conducting polymers (CPs), a significant class of electrochemical capacitor electrode materials, exhibit exceptional capacitive energy storage performance in aqueous electrolytes. Current research primarily concentrates on enhancing the electrical conductivity and capacitive performance of CPs via molecular design and structural control. However, the absence of a comprehensive understanding of the impact of molecular chain spatial order on ion/electron transport and capacitive performance impedes the development and optimization of advanced electrode materials.

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Infrared light accounts for the vast majority of natural light energy, however, the challenge of converting infrared light directly into electricity is too difficult. The photothermoelectric (PTE) effect (connecting the photothermal (PT) and thermoelectric (TE) effects) provides a feasible solution for the indirect conversion of infrared light into electrical energy. Therefore, it is of great significance to actively seek and explore materials with good PT and TE performance to fully harvest infrared light energy.

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Low-dimensional noble-metal materials (LDNMs) with different structural advantages have been considered as the high-performance catalysts for C2 alcohol electrooxidation. However, it is still a great challenging to precisely construct nanomaterials with low-dimensional composite structure thus to take advantages of various dimension, especial without the surfactant participation. Most studies focus on the modulation of the single dimensional nanocatalysts, the correlation between electrocatalytic performances and low-dimension composite have been rarely reported.

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Liver fibrosis is a common pathological feature of end-stage liver disease and has no effective treatment. MicroRNAs (miRNAs) have been found to modulate gene expression in liver disease. But the potential role of miRNA in hepatic fibrosis is still unclear.

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Attracted by the capability of light to heat and electricity conversion, the photothermoelectric (PTE) effect has drawn great attention in the field of energy conversion and self-powered electronics. However, it still requires effective strategies to convert electricity from light based on the corresponding photothermoelectric generator. Herein, considering the broad photoresponse and large Seebeck effect of tellurium nanowires (Te NWs) as well as the high electrical conductivity of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS), PEDOT:PSS/Te NW hybrid thin films were fabricated to enhance the conversion efficiency by the photothermoelectric effect with respect to single thermoelectric performance.

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The development of poly(3,4-ethylenedioxythiophene) (PEDOT) with high specific capacitance is the key to pursuing high-performance supercapacitors, and the electrochemical properties of PEDOT are closely related to the oxidation degree and conjugated chain length of its molecular chain. In this work, the influences of various oxidants (FeCl, Fe(Tos) and MoCl) on the molecular chain structure and capacitive properties of PEDOT via vapor phase polymerization were systematically investigated. Fe(Tos) can significantly improve the degree of oxidation and the length of the conjugated chain of PEDOT compared to FeCl and MoCl, enhancing the conductivity and providing more active sites for Faraday reaction.

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Rational design of fiber-shaped gas sensors with both excellent mechanical properties and sensing performance is of great significance for boosting future portable and wearable sensing electronics, however, it is still a challenge. Herein, we develop a novel fiber-shaped hydrogen (H) sensor by directly electrochemically growing palladium (Pd) sensing layer on conductive poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) fiber electrode. This approach produces free-standing functional fiber (PEDOT:PSS@Pd) with promising mechanical features of flexibility, light weight, knittability and high mechanical strength, and good H sensing performance at room temperature.

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Indole molecules with fused heteroaromatic structures can be adsorbed on the N-doped graphene surface through the π-π interaction. Therefore, the indole-functionalized N-doped graphene (InFGN) with mesopores is successfully fabricated by a simple hydrothermal method and subsequent vacuum freeze-drying process. The microstructure, thickness, element composition, pore structure, and electrochemical performance of InFGN are analyzed via SEM, TEM, AFM, BET, UV-vis, FT-IR, XPS, Raman, XRD, and electrochemical technologies.

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In this paper, a two dimensional/two dimensional (2D/2D) heterostructure of TiC/g-CN (T/CN) was constructed and used to activate peroxymonosulfate (PMS) for the degradation of diclofenac (DCF) in water in the presence of light illumination. Compared with single photocatalytic process by T/CN (0.040/min) and with pure g-CN nanosheets in PMS system (0.

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Rational and smart design of hydrogen (H) sensors especially those featured with flexibility and light weight is highly desirable, to meet the requirements for future development of portable H sensors. In this work, we demonstrate a novel paper film H sensor employing TiCT MXene nanosheets with Pd colloidal nanoclusters (Pd CNC) as the activator. The MXene@ Pd CNC paper film was facilely prepared via an all-colloidal solution-based vacuum-filtration process, which is flexible, light-weight and endowed with a compact, glossy surface.

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Two electrochromic polymers based on thiophene-benzene derivatives were prepared using an electrochemical method and exhibited multiple separate redox couples due to the introduction of side chains. The energy storage states of electrochromic supercapacitors based on the resulting polymers could be monitored by their appearance colour.

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Electrochromic devices with low-cost, energy-saving advantages, and controllable color switching have gained widely attention. Yet, electrochromic materials are limited for smart window due to challenges such as difficulty freestanding, monotonous color change, slow switching capability, and low optical contrast. In this work, a freestanding copolymers based on Poly(N-vinylcarbazole) (PVK) and 3, 4-ethoxylenedioxythiophene (EDOT) are designed.

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In this paper, a comparision of Pt Pd /C catalysts for ethanol-oxidation in acidic and alkaline media has been investigated. We prepared Pt Pd /C catalysts with different ratios of Pt/Pd ( at% = 0, 27, 53, 77 and 100) by the formic acid reduction method. The obtained Pt Pd /C catalysts were characterized by X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDX), induced coupled plasma-atomic emission spectroscopy (ICP-AES), X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM).

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The low specific capacitance and energy density of carbon electrode has extremely limited the wide application of supercapacitors. For developing a high-performance carbon electrode using a simple and effective method, a fishnet-like, N-doped porous carbon (FNPC) film is prepared by calcining the KOH-activated polyindole precoated on carbon cloths. The FNPC film is tightly anchored on carbon cloths without any binder.

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Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is a readily available copolymer that comes as an aqueous dispersion with good processability. A flexible voltammetric sensor for the widely used food stabilizer tert.-butylhydroquinone (TBHQ) was constructed by using a film of PEDOT:PSS.

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Background: Hypoxia is an important factor in malignant tumors, and glycolysis is a major metabolic contributor in their development. Glycolytic enzymes have gained increasing attention as potential therapeutic targets because they are associated with cancer-specific metabolism. Fructose-bisphosphate aldolase A (ALDOA), a key glycolytic enzyme, reportedly is associated with hepatocellular carcinoma (HCC).

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The regulation of oxidation levels is of great importance as an efficient way to optimize the thermoelectric (TE) performance of conducting polymers. Many efforts have been devoted to the acquisition of a high TE performance for poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) by oxidation/reduction post treatment to achieve an effective compromise. However, a strong oxidant/reductant is usually employed to tune the TE performance of PEDOT:PSS with high electrical conductivity (σ) and Seebeck coefficient ( S), and it also presents a number of operational challenges depending on a fast reaction rate.

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Conducting polymer-based composite aerogel film is desired to be used as thermoelectric (TE) materials due to its good flexibility and ultralow thermal conductivity. Here, we proposed the simple freeze drying method to fabricate free-standing poly(3,4-ethylenedioxythiophene)/poly(styrenesulfonate) (PEDOT:PSS)-based aerogel films without any crosslinker addition. The evolutions of morphology and TE performance were systemically investigated with various organic solvent addition.

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The requirement of a portable electron is functioning as a driving force for a wearable energy instrument. Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS), as one of the most promising organic electron materials, has been widely studied in energy conversion devices. However, the efforts for PEDOT:PSS fibers are insufficient to boost the development of wearable thermoelectric energy harvesting.

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Aims: We aimed to determine whether cancer-associated fibroblasts (CAFs) are associated with microvessel density (MVD) and lymphatic vessel density (LVD) in lung squamous cell carcinoma, as well as their clinical significance in predicting survival.

Methods: 122 patients were enrolled in the study. Samples were obtained on resection at the Department of Thoracic Surgery of the Qingdao Municipal Hospital between January 2011 and December 2014.

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Conductive thiophene-based polymers have garnered great attention for use in organic electron materials such as electrochromic and thermoelectric materials. However, they suffer from poor electron transport properties and long-term stability, leading to limited development eventually. Here, we proposed a strategy of functionalized thiophene-based polymers with oligo(ethylene glycol) or alkyl side chains and synthesized a series of poly(3,4-ethylenedioxy bithiophene)s (PEDTs) to tune their electrochromic and thermoelectric properties.

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Graphene-based two-dimensional (2D) heterostructures have ignited intensive interest in recent years because of their excellent physical performance. However, the most common method to prepare them uses chemical vapor deposition, which has the drawback of a complex process unsuitable for large-scale production. In this respect, reduced graphene oxide and transitional metal dichalcogenides (rGO-TMDs) composite thin-films were fabricated by a simple solution-processing method and their thermoelectric performance was investigated systematically.

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The wet-chemical approach is of great significance for the synthesis of two-dimensional (2D) bismuth telluride nanoplatelets as a potential thermoelectric (TE) material. Herein, we proposed a simple and effective solution method with the assistance of aniline for the fabrication of bismuth telluride nanoplatelets at a low temperature of 100 °C. The choice of aniline with its dual function avoided the simultaneous use of a capping regent and a toxic reductant.

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Organic semiconductors have great potential as flexible thermoelectric materials. A fluorene-based covalent organic framework (FL-COF-1) was designed with the aim of creating an enhanced π-π interaction among the crystalline backbones. By the introduction of fluorene units into the frameworks, the FL-COF-1 had high thermal stability with a BET surface area over 1300 m g.

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MoS2 has been predicted to be an excellent thermoelectric material due to its large intrinsic band gap and high carrier mobility. In this work, we exfoliated bulk MoS2 by the assistance of lithium intercalation and fabricated the restacked MoS2 thin-film using a simple filtration technique. These MoS2 thin-films with different thickness showed different thermoelectric performance.

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