APPLIED SURFACE SCIENCE
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2022
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IF 7.392
Shuo Li,Nan Yao,Lulu Fan,Zhengjia Li,Linyan Yang,Jie Cen,Xiaonian Li
How to break the activity-selectivity dependence in halonitrobenzene hydrogenation remains a challenge. In this work, Ni@C N/SiO 2 were synthesized and examined in the hydrogenation of p -chloronitrobenzene. It showed that the electron transferred from nitrogen doped carbon shell to Ni 0 core (core–shell synergistic effect) dominated the intrinsic activities of Ni@C N/SiO 2 with dual-reaction surfaces (H 2 dissociated on Ni 0 core, while p -chloronitrobenzene was hydrogenated on carbon shell) in the thiophene-free hydrogenation, leading to their higher turnover frequencies than Raney Ni catalyst. During the thiophene-involved hydrogenation, the adsorption of thiophene on Ni 0 changed its electron density and blocked the active sites. These enhanced the selectivity, but significantly reduced the activity for Raney Ni catalyst. Comparatively, the carbon shell protected Ni 0 core from thiophene adsorption so that the hydrogen dissociated on Ni 0 as usual. However, the adsorption of thiophene on the carbon shell reduced the available sites for p -chloronitrobenzene adsorption. Although Ni@C N/SiO 2 had lower activities in the thiophene-involved reactions than those of thiophene-free reactions, they achieved ∼100 % p-chloroaniline selectivities and 8-fold higher turnover frequencies than Raney Ni, breaking the activity-selectivity dependence. This reveals that the available sites on the carbon shell and the core–shell synergistic effect determine the thiophene-involved hydrogenation activities of Ni@C N/SiO 2 catalysts.
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CHINESE JOURNAL OF POLYMER SCIENCE
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2022
·Vol. 40
·期 11
·1441-1450
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IF 3.815
Tong Li-Fen,He Liang,Zhan Chen-Hao,Xia Yun-Qing,Liu Xiao-Bo
High-quality film capacitors are widely used in many fields such as new energy vehicles, electronic communications, etc., due to their advantages in wide frequency response and low dielectric loss. The dielectric film is a crucial part of the film capacitor, and its properties have an important impact on the performance and use conditions of the film capacitor. In this work, a novel high-temperature-resistant dielectric film was prepared. Firstly, the Bi 2 S 3 /rGO-CN fillers were prepared by hydrothermal method combined with cyanation treatment, and then added to the poly(arylene ether nitrile) (PEN) matrix to prepare the dielectric film materials (PEN/Bi 2 S 3 /rGO-CN). After high temperature treatment, the fillers Bi 2 S 3 /rGO-CN reacted with the PEN matrix, and the composites materials transformed into a thermosetting hybrid film (PEN-Bi 2 S 3 /rGO) with gel content of 97.88%. The prepared hybrid dielectric films did not decompose significantly before 400 °C, and showed a glass transition temperature ( T g ) of up to 252.4 °C, which could increase the effective use temperature of the materials. Compared with the composite films without heat treatment, they exhibit better mechanical properties, with further improvement in tensile strength and elastic modulus, and a decrease in elongation at break. The dielectric constant of the hybrid films can be up to 6.8 while the dielectric loss is only about 0.02 at 1 kHz. Moreover, the hybrid films showed excellent dielectric stability during temperature changes, and remain relatively stable before 250 °C, which is suitable as a high-temperature-resistant high-dielectric material and is more advantageous for practical applications.
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JOURNAL OF POWER SOURCES
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2014
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IF 5.211
Guofu Ma,Jiajia Li,Kanjun Sun,Hui Peng,Jingjing Mu,Ziqiang Lei
A gel polymer PVA–KOH–K 3 [Fe(CN) 6 ] is prepared by potassium hydroxide and potassium ferricyanide doped polyvinyl alcohol, and a solid-state supercapacitor is assembled using the gel polymer as electrolyte and separator, activated carbons as electrode. The gel polymer exhibits flexible, high ionic conductivity and wide potential properties. The electrochemical properties of the supercapacitor are investigated using cyclic voltammetry , galvanostatic charge/discharge, and impedance spectroscopy techniques. The electrode specific capacitance of the supercapacitor can be as high as 430.95 F g −1 , and after 1000 cycles at a current density of 1 A g −1 it still remains higher than 380 F g −1 . The energy density and power density of the supercapacitor reach 57.94 Wh kg −1 and 59.84 kW kg −1 , respectively. These novel flexible gel polymers are desirable for applications in supercapacitor devices.
研究领域:
材料科学
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电化学
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COLLOIDS AND SURFACES B-BIOINTERFACES
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2023
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IF 5.8
Xi Lan,Junchen Zhuo,Linpin Luo,Hao Sun,Yanmin Liang,Jianxing Feng,Rui Shu,Yuechun Li,Tianyu Wang,WenTao Zhang,Jianlong Wang
A tannate-iron network-derived peroxidase-like catalyst loaded with Fe ions on carbon nitride (C 3 N 4 ) was reported for detection of total antioxidant capacity (TAC) in food in this study. Metal-phenolic networks (MPNs) was employed to form a low coordination compound on C 3 N 4 , and calcined catalyst formed hollow structure with abundant and uniform Fe sites and surface folds. CN-FeC exhibited significant peroxidase-like activity and high substrate affinity. The homogeneous distribution of amorphous Fe elements on the C 3 N 4 substrate provides more active sites, resulting in provided excellent catalytic activity to activate H 2 O 2 to 1 O 2 and O 2 ·– . The established CN-FeC/TMB/H 2 O 2 colorimetric system can detect AA in the concentration range of 5-40 μM, with the detection limits of 1.40 μM, respectively. It has good accuracy for the detection of vitamin C tablets, beverages. Taken together, this work shows that metal-phenolic networks can be an effective way to achieve efficient utilization of metal atoms and provides a promising idea for metal-phenolic networks in nanoparticle enzyme performance enhancement.
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
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2020
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IF 3.232
Xiaoye Wen,Li Yan,Zhefeng Fan
New strategies still need to be proposed that can be used to sense and remove toxic environmental pollutants in a sensing system. In this research, a novel NIR fluorescence sensor 1 was designed and prepared with aggregation induced emission (AIE) property. The fluorescence intensity of the sensor 1 in DMSO/H 2 O mixed solvent was changed along with the proportion of water. The sensor 1 can be successfully used for real-time detection and removal of Hg 2+ in 20% DMSO aqueous solution with high selectivity, quick response and so on. Furthermore it can be efficiently reused and recycled without any loss through Na 2 S. In addition, the sensor 1 displayed high sensitivity and selectivity to cyanide ions in 1% DMSO aqueous solution with the presence of other interference anions. The sensing mechanism for Hg 2+ and cyanide ion was evaluated by 1 H NMR spectra, Mass spectrometry. The sensor 1 exhibited low cytotoxicity for biological applications, which was used as an outstanding fluorescent transducer for detection of cyanide ion in living cells. Based on the visible fluorescence change for the sensor 1 to cyanide ion, the measurement was performed for food materials containing cyanide, such as potato, cassava powder and almond. This research provides perspective potential in solving the problem of other pollution and stimulating new thinking for designing of the novel fluorescence materials.
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APPLIED CATALYSIS B-ENVIRONMENTAL
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2019
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IF 14.229
Yanyan Zhao,Yongbo Wang,Xuhua Liang,Huanxian Shi,Cunjin Wang,Jun Fan,Xiaoyun Hu,Enzhou Liu
A visible-light-induced antibiotics degradation system based on a nano-Ag, CsPbBr 3 quantum dot (QDs) and bulk g-C 3 N 4 (CN) ternary assembly (Ag-CsPbBr 3 /CN) has been firstly constructed under an organic phase environment, oleylamine (OLA) and oleic acid (OA) were used as surfactants to stabilize the CsPbBr 3 , l -cysteine was used to facilitate the interaction between nano-Ag, CsPbBr 3 and CN. The new ternary assembly of Ag-CsPbBr 3 /CN composite was used to degrade 7-aminocephalosporanic acid (7-ACA) under visible light irradiation, and the 7%-Ag-CsPbBr 3 /CN composite displayed the superior photocatalytic activity, approximately 92.79% of 7-ACA has been degraded to CO 2 , H 2 O and other small molecules at 140 min, which was approximately 1.49-folds, 1.56-folds, 3.01-folds and 11.43-folds higher than 9%-CsPbBr 3 /CN, 7%-Ag/CN, pure CN and pure CsPbBr 3 , respectively. A possible mechanism for 7-ACA degradation over Ag-CsPbBr 3 /CN composite were proposed according to detailed measurements of adsorption test, Brunauer-Emmett-Teller (BET) measurement, UV–vis diffuse reflectance spectra (DRS), photoluminescence spectra (PL), transient photocurrent response and electrochemical impedance spectroscopy (EIS) measurement, and the enhanced photocatalytic activity of Ag-CsPbBr 3 /CN composite could be attributed to the excellent adsorbability, the enhanced light-harvesting and reduced charge recombination, as well as the synergistic effects of nano-Ag and CsPbBr 3 co-loaded with CN. In addition, Holes (h + ) and hydroxyl radicals ( OH) played major roles, electronic (e − ) and superoxide radical ( O 2 -) played minor roles based on the reactive-species-trapping experiments, the NBT transformation and the 7-hydroxycoumarin fluorescent experiments. Furthermore, a possible 7-ACA degradation pathway was investigated based on the Liquid Chromatography-Mass spectroscopy (LC-MS) experiment to better understand the degradation process. The present opens up a new insight for using CsPbBr 3 as photocatalyst to degrade antibiotics.
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ACS Applied Materials & Interfaces
·
2018
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IF 8.097
Jingying Duan,Guohui Qin,Luofu Min,Yuchen Yang,Chengyang Wang
The photochemistry and sodium storage process have been generally considered as two separated approaches without strong connection. Here, ultraviolet (UV) irradiation was applied to sodium-ion batteries to improve the electrochemical performance of MoS2-based composites. C@MoS2@CN nanospheres consist of double protective structures, including inner hollow carbon spheres with a thin wall (C) and outer N-doping carbon nanosheets (CNs) derived from polydopamine. The special nanostructure possesses the virtues such as wide-interlayer spacing, flexible feature with great structure integrity, and rich active sites, which endow the fast electron transfer and shorten the ion diffusion pathways. Under the excitation of UV-light, intense electrons and holes are accumulated within MoS2-based composites. The excited electrons can promote the preinsertion of Na+. More importantly, dense electrons promote the electrolyte to decompose and hence form a stable solid electrolyte interphase in advance. After UV-light irradiation treatment in the electrolyte, the initial Coulombic efficiency of C@MoS2@CN electrodes increased from 48.2 to 79.6%, and benefiting from the fine nanostructure, the C@MoS2@CN electrode with UV irradiation treatment delivered a great rate performance 116 mAh g–1 in 20 s and super cycling stability that 87.6% capacity was retained after 500 cycles at 500 mA g–1. When employed as anode for sodium-ion hybrid capacitors, it delivered a maximum power density of 6.84 kW kg–1 (with 114.07 Wh kg−1 energy density) and a maximum energy density of 244.15 Wh g–1 (with 152.59 W kg–1 power density). This work sheds new viewpoints into the applications of photochemistry in the development of energy storage devices.
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INORGANIC CHEMISTRY
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2018
·
IF 4.7
Qian Peng,J. Timothy Sage,Yulong Liu,Zijian Wang,Michael Y. Hu,Jiyong Zhao,E. Ercan Alp,W. Robert Scheidt,Jianfeng Li
Compared to well studied diatomic ligands (NO, CN–, CO), the axial bonds of carbene hemes is much less known although its significance in biological chemistry. The unusually large quadrupole splitting (ΔEQ = +2.2 mm·s–1) and asymmetric parameter (η = 0.9) of the five-coordinate heme carbene [Fe(TTP)(CCl2)], which is the largest among all known low spin ferrohemes, has driven investigations by means of Mössbauer effect Nuclear Resonance Vibrational Spectroscopy (NRVS). Three distinct measurements on one single crystal (two in-plane and one out-of-plane) have demonstrated comprehensive vibrational structures including stretch (429) and bending modes (472 cm–1) of the axial Fe–CCl2, and revealed iron vibrational anisotropy in three orthogonal directions for the first time. Frontier orbital analysis especially comparisons with diatomic analogues (NO, CN–, CO) suggest that CCl2, similar to NO, has led to strong but anisotropic π bonding in a ligand-based “4C”-coordinate which induced the vibrational anisotropies and very large Mössbauer parameters. This is contrasted to CN– and CO complexes which possess a porphyrin-based “4N”-coordinate electronic and vibrational structures due to inherent on-axis linear ligation.
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ACS Applied Materials & Interfaces
·
2024
·
IF 8.3
Ming-Xuan Liu,Yu-Ting Cai,Ruo-Jia Wang,Peng-Fei Zhu,Yan-Chao Liu,Hao Sun,Yong Ling,Wei-Zhong Zhu,Jing Chen,Xiao-Ling Zhang
Hypoxia can lead to liver fibrosis and severely limits the efficacy of photodynamic therapy (PDT). Herein, carbon nitride (CN)-based hybrid nanoparticles (NPs) VPSGCNs@TSI for light-driven water splitting were utilized to solve this problem. CNs were doped with selenide glucose (Se-glu) to enhance their red/NIR region absorption. Then, vitamin A-poly(ethylene glycol) (VA-PEG) fragments and aggregation-induced emission (AIE) photosensitizers TSI were introduced into Se-glu-doped CN NPs (VPSGCNs) to construct VPSGCNs@TSI NPs. The introduction of VA-PEG fragments enhanced the targeting of the NPs to activated hepatic stellate cells (HSCs) and reduced their toxicity to ordinary liver cells. VPSGCN units could trigger water splitting to generate O2 under 660 nm laser irradiation, improve the hypoxic environment of the fibrosis site, downregulate HIF-1α expression, and activate HSC ferroptosis via the HIF-1α/SLC7A11 pathway. In addition, generated O2 could also increase the reactive oxygen species (ROS) production of TSI units in a hypoxic environment, thereby completely reversing hypoxia-triggered PDT resistance to enhance the PDT effect. The combination of water-splitting materials and photodynamic materials showed a 1 + 1 > 2 effect in increasing oxygen levels in liver fibrosis, promoting ferroptosis of activated HSCs and reversing PDT resistance caused by hypoxia.
研究领域:
材料科学
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生物医学工程
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治疗学
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纳米技术
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分子生物学
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JOURNAL OF ALLOYS AND COMPOUNDS
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2026
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IF 6.7
Yi Li,Yong Tang,Yujing Wang,Junyin Chen,Chun Huang,Jianwei Zhao,Lirong Qin
Aqueous zinc‑ion batteries (AZIBs) are promising for safe and low‑cost energy storage, yet their practical application is hindered by limited cathode cyclability and poor low‑temperature performance. Herein, a ternary composite of V 3 O 4 /Fe 3 O 4 /V 1.5 Fe(CN) 6 nanorods is directly grown on carbon cloth via a simple hydrothermal method. The electrode exhibits a unique activation behavior: its specific capacity gradually increases by more than 300% during the initial galvanostatic charge‑discharge cycles, reaching 530.1 mAh/g at 1 A/g. Ex situ XRD and XPS reveal that activation induces lattice expansion and an increase in V 4 + and Fe 3+ contents without phase transformation. The VF‑20 electrode delivers exceptional long‑term stability (89% retention after 4200 cycles at 4 A/g) and remarkable low‑temperature performance (69 mAh/g at −40 °C and 0.1 A/g). This work provides a new paradigm of activation‑driven performance enhancement for multiphase cathodes in AZIBs.
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JOURNAL OF ALLOYS AND COMPOUNDS
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2026
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IF 6.7
Hongxia Zhang,Junxin Huang,Ming Zhong,Bitao Su,Ziqiang Lei
Carbon nitride-based heterojunction catalysts show broad application prospects for the degradation of wastewater pollutants (e.g. antibiotics and dyes), yet their performance remains challenges in narrow light absorption range and high carrier recombination rate. The introduction of components with matched band structures and surface plasmon resonance can mitigate these limitations. Herein, a Schottky heterojunction composed of plasma Bi and MoO 2 -incorporated carbon nitride (Bi/MoO 2 @CN) is designed and synthesized via solvothermal-calcination method. Multiple preparation parameters are optimized to achieve the reduction of Bi 2 MoO 6 (BMO) to plasma Bi metal and MoO 2 . The synergistic structural and compositional effects endow the optimal material with exceptional adsorption-photocatalytic activity, achieving 96.19% tetracycline (TC) degradation within 90 min under visible light. The first-order kinetic constant is seven times higher than CN. The catalyst also demonstrates versatility in removing diverse organic dyes. Active species trapping experiments identify holes (h + ) and superoxide radicals ( ⸱O 2 − ) as primary reactive species. Furthermore, enhanced photocatalytic mechanism is elucidated through band structure analysis, Schottky heterojunction characterization, and TC degradation pathway study.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2025
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IF 6.3
Zhiru Yang,Zi Yang,Wentao Hou,Hai Zhou,Hao He,Chao Jin
Three-dimensional S-CN/NC/CNTs network composites were synthesized via a combined hydrothermal and high-temperature treatment strategy. And their electrochemical behavior as supercapacitor electrodes was investigated. Compared with conventional synthesis routes, this method provides distinct advantages. Cobalt and nickel nanoparticles catalyze the directional growth of carbon nanotubes (CNTs) from melamine, forming a uniform coating structure that significantly enhances the electrical conductivity of the electrode. Concurrently, the sulfidation of cobalt and nickel nanoparticles dispersed within the nitrogen-doped carbon (NC) matrix and CNT network generates abundant redox-active sites, thereby improving the specific capacitance. Within this composite, Co-Ni-S functions as the electrochemically active phase, NC serves as the structural scaffold, and CNTs form an interconnected three-dimensional conductive framework that facilitates efficient electron transport. The synergistic interaction among these components endows the material with superior electrochemical performance. The optimized composite exhibits a high specific capacitance of 2104 F g⁻¹ at 0.5 A g⁻¹ in 6 M KOH electrolyte. Furthermore, a flexible quasi-solid-state supercapacitor assembled using this material as the positive electrode, activated carbon as the negative electrode, and a gel polymer electrolyte achieves an energy density of 40.3 Wh kg⁻¹ at a power density of 750 W kg⁻¹ , maintaining 87.6 % capacitance retention after 5000 cycles at 10 A g⁻¹ with excellent mechanical flexibility. This study presents an effective route for enhancing the electrochemical performance of three-dimensional composite electrodes through hierarchical conductive network design and controlled active-site dispersion, offering valuable insights for the development of high-performance energy storage materials.
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