APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING
·
2025
·Vol. 131
·期 10
·1-14
·
IF 2.8
Ning Qiyun,Li Bingwei,Zhou Wang,Xu Xiaoting,Li Jun
In this study, Bi₂O₂Se nanosheets were synthesized via a hydrothermal method, and a Bi₂O₂Se/WSe₂ heterostructure was subsequently constructed using a mechanical compounding approach to develop a photoelectrochemical photodetector. By optimizing the mass ratio and KOH electrolyte concentration, the Bi₂O₂Se/WSe₂ heterostructure exhibited optimal performance at a 7:1 ratio in 0.1 M KOH. Benefiting from the interfacial heterojunction between the two materials, the Bi₂O₂Se/WSe₂ heterostructure achieved a photocurrent density of -2.74 µA/cm² under zero external bias, representing an order-of-magnitude enhancement compared to pristine Bi₂O₂Se nanosheets. Concurrently, the rise time was significantly reduced from 0.86 s to 0.28 s, And the decay time decreased from 4.85 s to 0.32 s, demonstrating superior self-powered characteristics. Furthermore, the Bi₂O₂Se/WSe₂ heterostructure exhibited a maximum photoresponsivity of 61 µA/W. The optimized Bi₂O₂Se/WSe₂ photodetector showed no notable performance degradation during a 10,000 s cyclic on/off illumination test. This work highlights the immense potential of the Bi₂O₂Se/WSe₂ heterostructure-based self-powered photodetector in delivering exceptional self-driven functionality, outstanding optoelectronic properties, and robust stability for practical applications.
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Science Bulletin
·
2025
·
IF 21.1
Hailin Lu,Mengjie Wang,Zhiwei Chen,Gengchen Yu,Yanan Ma,Li Wen,Yang Yue,Siliang Wang
Human-machine intelligent interaction (HMII) technology, which is an advanced iteration of human-machine interaction technology, has garnered widespread attention owing to its significant achievements in healthcare and virtual reality research. Nonetheless, these fields often depend on elaborate multi-sensor integrations and face challenges in achieving precise control over robotic manipulation. Herein, a novel transistor-like iontronics pressure sensor based on an MXene/Bi 2D heterojunction is proposed. This transistor-like, flexible, all-solid-state, self-powered iontronics device exhibited a fast response time (66.59 ms), long lifetime (up to 50,000 cycles), and static/dynamic response with linear sensitivity. A deep-learning-assisted single-device HMII system was further constructed. Crucially, the system is adept at monitoring subtle skin deformations triggered by the median and ulnar nerves, efficient real-time decoding of sophisticated hand gestures (recognition accuracy of 95.83%), and precise control of robotic hands using tactile perception feedback. This approach addresses the inherent redundancy in multi-sensor devices used to decode motion across multiple finger joints, marking a significant step forward for iontronics in enhancing the perceptual interaction between humans and machines.
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PubMed
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Light-Science & Applications
·
2024
·Vol. 13
·期 1
·1-12
·
IF 20.6
Liu Bo-Mei,Lin Yue,Liu Yingchun,Lou Bibo,Ma Chong-Geng,Zhang Hui,Wang Jing
Materials capable of dynamic persistent luminescence (PersL) within the visible spectrum are highly sought after for applications in display, biosensing, and information security. However, PersL materials with eye-detectable and excitation-wavelength-dependent characteristics are rarely achieved. Herein, a nonstoichiometric compound CaGa x O 4 :Bi ( x < 2) is present, which demonstrates ultra-long, color-tunable PersL. The persistent emission wavelength can be tuned by varying the excitation wavelength, enabling dynamic color modulation from the green to the orange region within the visible spectrum. Theoretical calculations, in conjunction with experimental observations, are utilized to elucidate the thermodynamic charge transitions of various defect states, thereby providing insights into the relationship between Bi 3+ emitters, traps, and multicolored PersL. Furthermore, the utility of color-tunable PersL materials and flexible devices is showcased for use in visual sensing of invisible ultraviolet light, multicolor display, information encryption, and anti-counterfeiting. These discoveries create new opportunities to develop smart photoelectric materials with dynamically controlled PersL for various applications.
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Journal of Water Process Engineering
·
2024
·
IF 6.3
Jian Dong,Yi Wang,Liangliang Dong,Tatsuo Kaneko,Weifu Dong,Dongjian Shi,Mingqing Chen
To address the membrane challenges such as the trade-off effect between water permeance and separation selectivity, development of a desirable nanofiltration membrane structure is crucial. And, it is important to design a positively charged surface to enhance charge repulsion force between membrane surface and ions due to lithium (Li) extraction problem as the close hydration diameter of magnesium (Mg) and lithium ions. Herein, a strategy that involves regulating membrane structure to create a loose and dense double-layer structure via bi-directional interfacial polymerization has been proposed to form selectivity-enhanced nanofiltration membranes for Li + /Mg 2+ separation. The incorporation of dopamine (DA) and trimesoyl chloride (TMC) in first loose layer could improve the membrane stability, while the amine groups from polyethyleneimine (PEI) or polyvinylamine (PVAm) in the second dense layer surface, provided by rich amine polymers, could improve the rejection of divalent magnesium ion. The as-fabricated membrane DA-TMC-PEI shows enhanced permeance (around 15.4 L m −2 h −1 bar −1 ) and the membrane DA-TMC-PVAm demonstrates outstanding ion selectivity with Li + /Mg 2+ separation factor of 30. Moreover, the DA-TMC-PEI and DA-TMC-PVAm membranes could efficiently purify the ratio of Mg 2+ /Li + solution from 50 to 0.43. We believe the strategy could provide a promising potential in lithium extraction.
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ADVANCED FUNCTIONAL MATERIALS
·
2023
·Vol. 33
·期 20
·2214771
·
IF 19
Jun Pei,Jian-Lei Shi,Hezhang Li,Yilin Jiang,Jinfeng Dong,Hua-Lu Zhuang,Bowen Cai,Bin Su,Jincheng Yu,Wei Zhou,Bo-Ping Zhang,Jing-Feng Li
GeTe and (Bi,Sb) 2 Te 3 are two representative thermoelectric (TE) materials showing maximum performance at middle and low temperature, respectively. In order to achieve higher performance over the whole temperature range, their segmented one-leg TE modules are designed and fabricated by one-step spark plasma sintering (SPS). To search for contact and connect layers, the diffusion behavior of Fe, Ni, Cu, and Ti metal layers in GeTe is studied systematically. The results show that Ti with a similar linear expansivity (10.80 × 10 −6 K −1 ) to GeTe, has low contact resistance (3 µΩ cm 2 ) and thin diffusion layer (0.4 µm), and thus is an effective metallization layer for GeTe. The geometric structure of the GeTe/(Bi,Sb) 2 Te 3 segmented one-leg TE module and the ratio of GeTe to (Bi,Sb) 2 Te 3 are determined by finite element simulation method. When the GeTe height ratio is 0.66, its theoretical maximum conversion efficiency (η max ) can reach 15.9% without considering the thermal radiation and thermal/electrical contact resistance. The fabricated GeTe/(Bi,Sb) 2 Te 3 segmented one-leg TE module showed a η max up to 9.5% with a power density ≈ 7.45 mW mm −2 , which are relatively high but lower than theoretical predictions, indicating that developing segmented TE modules is an effective approach to enhance TE conversion efficiency.
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POLYMERS FOR ADVANCED TECHNOLOGIES
·
2021
·Vol. 32
·期 8
·2843-2855
·
IF 3.665
Pengfei Ji,Yihua Cui,Dongyue Liu,Tianlong Zhang,Jipeng Lv
A novel functionalized graphene oxide (F-GO) decorated with a double-phosphaphenanthrene structure was fabricated using a covalent modification method. The F-GO with Bi-DOPO groups then was introduced into the epoxy matrix as a highly effective flame retardant. The Flame retardant epoxy resins (FREP) containing F-GO exhibited superior fire-resistant performance with extremely low loading. When the content of F-GO was 1 wt%, the limiting oxygen index value of the FREP was increased from 19.9% to 30.8%, and the total heat release and the peak heat release rate was decreased by 44.0% and 55.5%, respectively. Meanwhile, the tensile and impact tests results indicated that the mechanical properties of the epoxy resins were improved with the addition of F-GO. Furthermore, the thermogravimetric analysis showed that F-GO greatly increased the char-yield of the cured FREP. Based on the char analyses of SEM images, F-GO was conducive to form a more protective char barrier for FREP during combustion. F-GO developed a synergistic flame-retardant effect of the Bi-DOPO derivative and graphene layer structures on epoxy resins.
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JOURNAL OF POWER SOURCES
·
2022
·
IF 9.794
Junying Yin,Xin Xu,Sen Jiang,Yue Lei,Yunfang Gao
Solid-state lithium metal batteries (SSLMBs) with high safety and high energy densities draw widespread attention in recent years. Nevertheless, the intrinsic defects of the solid-state electrolyte (SSE) such as the poor compatibility with electrodes and low ionic conductivity hamper the application of SSMLBs. Herein, we introduce rigid two-dimensional hexagonal boron nitride (BN) nanosheets and flexible One-dimensional aramid nanofibers (ANFs) as bi-nanofillers into the polyethylene oxide (PEO)-based SSEs to fabricate a composite solid-state electrolyte (CSE) ANF-PEO-BN with network structure boosting the comprehensive performance of SSMLBs. ANF and BN with special properties and structures are prone to be dispersed homogeneously in the PEO matrix to build the ANF-PEO-BN electrolyte, whose rigid and flexible network structure ensures the formation of Li dendrites inhibited. Furthermore, the dissociation of lithium bis(trifluoromethanesulphonyl)imide (LiTFSI) is promoted and more ion transport channels are provided due to the strong affinity between Lewis acid centers of ANF/BN and Li + /TFSI − . As a result, the LiFePO 4 /Li batteries deliver high-capacity retention of 86% after 500 cycles and Li/Li cells stably cycle beyond 3300 h with small overpotential of 10 mV at 0.1 mA cm −2 /0.2 mAh cm −2 .
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2020
·Vol. 31
·期 12
·9595-9604
·
IF 2.22
Zhou Junyi,Zhang Huimin,Chang Aimin,Zhao Yifeng
La x Bi 1− x FeO 3 (LBFO) materials were synthesized by sol–gel method with x = 0.0, 0.1, 0.2, and 0.3. LBFO ceramics were obtained by rapid liquid phase sintering and conventional sintering, respectively. X-ray diffraction (XRD) and Raman spectroscopy indicated that the phase transition from twisted diamond R3C to orthogonal Pbnm occurs in the course of the increase of La element doping. Scanning electron microscopy demonstrated that the grain size of LBFO ceramics decreased from 10 to 1 μm, with the increase of La ion doping, and the volatilization of Bi decreases from 6.48 to 1.43%. It was found that LBFO ceramics have the characteristic of negative temperature coefficient (NTC), the resistivity (100 °C) is from 4.32 × 10 6 to 2.71 × 10 8 Ω cm, the material constant ( B 100/700 value) is about 6000–9000 K, the activation energy of LBFO is around 0.56 to 0.82 eV, and the temperature range of LBFO is from 100 to 700 °C. The resistivity change of LBFO is less than 1% after 500 h of ageing at 300 °C.
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JOURNAL OF COORDINATION CHEMISTRY
·
2017
·
IF 1.795
Yong-Qiang Chen,Yuan Tian,Dao-Li An
A new coordination framework, [Co2(L)2(bpy)2(H2O)]n (1) (H2L = (4-phenyl)-2,6-bis(4-carboxyphenyl)pyridine and bpy = 2,2′-bipyridine), has been prepared and structurally characterized. Complex 1 shows an interesting bi-chain substructure bridged by coordinated water molecules, which is further extended into a three-dimensional (3-D) supramolecular structure by π–π stacking interactions. Moreover, the magnetic properties and photocatalytic activity for degradation of methyl orange have been investigated.
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INORGANIC CHEMISTRY
·
2021
·
IF 5.165
Yuanyuan Li,Puxian Xiong,Gaochao Liu,Mingying Peng,Zhijun Ma
Bismuth (Bi)-activated luminescence materials have attracted much attention for their tunable broad emissions ranging from a visible to near-infrared (NIR) region. However, it remains a challenge to regulate the Bi valence state and achieve NIR emission via a facile way. Here, we report the design and preparation of Ba3Sc4O9:Bi phosphors, which emit visible and NIR emissions simultaneously even prepared in the air condition. The self-reduction mechanism of Bi3+ species in Ba3Sc4O9 with a rigid crystal structure is illustrated based on the charge compensation model, and the coexistence of different Bi-active centers, Bi3+ for visible emission, while Bi+ and Bi0 for NIR emission, is confirmed by the spectroscopic data and X-ray photoelectron spectroscopy (XPS) analysis. The enhanced NIR emission was further achieved through controlled reducing treatment and the related mechanism has also been clarified. This work paves a new way to control bismuth valence and tune the emission of Bi-based luminescence materials for emerging photonics applications.
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高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2019
·
IF 7.65
Li Song,Yuefeng Feng,Changqing Zhu,Fuqiang Liu,Aimin Li
Cr(VI) and Cd(II) are typical heavy metal ions and their co-removal is significant. Nitrogen-doped, bi-functional, and biomass-based composites (CP-BA) were successfully applied for efficient and synergistic removal of Cr(VI) and Cd(II). The mutual promotion ratios of adsorption capacity by Cr(VI) and Cd(II) were 161.32 % and 14.13 %, respectively. In addition, all coexisting inorganic anions could extremely promote the removal of Cd(II) with the best promotion ratio upon phosphate ions as high as 80.00 %. The following co-removal mechanisms were deeply revealed: (1) Cr(VI) combined with protonated imine groups could weaken the electrostatic repulsion between CP-BA and Cd(II) by electrostatic shielding, and further promoted the coordination of Cd(II) with hydroxyl, carboxyl and neutral imine groups. (2) Cd(II) which were coordinated to neutral imine groups could form cation bridges, and thus promoted the interaction with Cr(VI) because of the electrostatic attraction. Moreover, the removal capacity for Cr(VI) and Cd(II) did not display obvious reduction even after four cycles. Therefore, CP-BA showed a great potential in the co-removal of inorganic anion-cation complexes from wastewater.
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Journal of Energy Chemistry
·
2021
·
IF 9.676
Qihao Sun,Bao Xiao,Leilei Ji,Dou Zhao,Jinjin Liu,Wei Zhang,Menghua Zhu,Wanqi Jie,Bin-Bin Zhang,Yadong Xu
All-inorganic Cs 3 Bi 2 I 9 (CBI) halide perovskites are sought to be candidate for photoelectrical materials because of their low toxicity and satisfactory stability. Unfortunately, the discrete molecular [Bi 2 I 9 ] 3− clusters limit the charge-transport behaviors. Herein, the defect halide perovskite based on trivalent Bi 3+ is expanded to Cs 3 Bi 2 I 6 Br 3 (CBIB). Centimeter-size CBIB single crystal ( Φ 15 × 70 mm 3 ) was grown by the vertical Bridgeman method. The powder X-ray diffraction analysis shows that CBIB has P 3 ¯ m 1 structure with lattice parameters of a = b = 8.223 Å, c = 10.024 Å, α = β = 90° and γ = 120°. The density functional theory (DFT) calculations demonstrate that the charge density distribution was enhanced after the dimensional expansion. The enhancement of carrier transport ability of (00 l ) in-plane is characterized before and after dimensional improvement. The obtained CBIB (001) exhibited an electron mobility up to 40.03 cm 2 V −1 s −1 by time-of-flight (TOF) technique, higher than 26.46 cm 2 V −1 s −1 of CBI (001) . Furthermore, the X-ray sensitivity increases from 707.81 μC Gy −1 cm −2 for CBI (001) to 3194.59 μC Gy −1 cm −2 for CBIB (001) . This research will deepen our understanding of Bi-based perovskite materials and afford more promising strategies for lead-free perovskite optoelectronic devices modification.
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