CHEMICAL ENGINEERING JOURNAL
·
2021
·
IF 13.273
Yingqiao Jiang,Gang Cheng,Yuehua Li,Zhangxing He,Jing Zhu,Wei Meng,Lei Dai,Ling Wang
The application of metal oxide is limited due to low conductivity, weak combination, poor dispersion, and hard nanocrystallization in vanadium redox flow battery. Herein, metal–organic framework (MOF) was firstly employed to prepare metal oxide and porous carbon nanocomposite, which was used to ultra-uniformly decorate graphite felt by in-situ growth. Graphite felt was modified with UiO-66 (Zr-MOF) nanoparticle using hydrothermal synthesis followed by conversion into porous nanocomposite (ZrO 2 @C) via high-temperature carbonization. ZrO 2 @C owns large surface area, regular arrangement of ZrO 2 , and high conductivity, which provides large reaction place, high active site density, and rapid electron transfer for redox reaction. Therefore, ZrO 2 @C can boost the electrochemical performance of graphite felt for VO 2+ /VO 2 + and V 3+ /V 2+ reactions by promoting diffusion, charge transfer, and electron transport, systematically. The modified flow cell using ZrO 2 @C/GF has better stability and higher utilization of electrolyte than pristine cell during 500-cycle test. ZrO 2 @C/GF decreases electrochemical polarization of cell at different current densities. At 200 mA cm −2 , voltage efficiency (77.5%) and energy efficiency (75.2%) of modified cell increase by 14.6% and 13.9% respectively compared with pristine cell. The modified cell can operate at a high current density up to 300 mA cm −2 and shows a 62.4% of energy efficiency. The cell performance in this study is superior to that reported in previous metal oxide-related works. This work presents a design allowing MOF-derived catalyst with nano size, high conductivity, good adhesion, and uniform dispersion, simultaneously.
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Materials Today Chemistry
·
2021
·
IF 8.301
Y. Ji,W. Luo,Y. Liu,Z. He,N. Cheng,Z. Zhang,X. Qi,J. Zhong,L. Ren
The bottleneck of alkaline hydrogen evolution reaction lies in the kinetically sluggish brought from multistep reaction processes involving water adsorption and dissociation, as well as hydrogen adsorption. In this work, we successfully synthesized o-CoSe 2 /c-CoSe 2 heterostructures anchored on MoSe 2 nanosheets to powerfully promote reaction processes. As an electrocatalyst , it exhibits a low overpotential of 112 mV at 10 mA/cm 2 and a Tafel slope of 96.9 mV/dec for an alkaline hydrogen evolution reaction . Moreover, the as-prepared catalyst can behave as both cathode and anode for overall water splitting , which only requires 1.61 V cell voltage at 10 mA/cm 2 . Significantly, the cell voltage can be further reduced to 1.53 V at 10 mA/cm 2 for water electrolysis under the simulated solar irradiation owing to such a semiconductor-based heterostructure that facilitates the separation of photogenerated charges. Here, the improving overall performance of this ternary electrocatalyst is attributed to the multifunctionality and synergistic interaction of different components in this heterogeneous material . The work provides a novel strategy to design active catalysts simultaneously using electric energy and solar energy for effective water splitting.
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NANOTECHNOLOGY
·
2023
·Vol. 35
·期 6
·065704
·
IF 3.5
Xiaomei Yu,Wei Shi,Jiajiao Wei,Tiantian Liu,Yuanyuan Li,Mengyuan He,Zhengyu Wei,Dehai Ping,Panfei Sun,Jin You Zheng,Songjie Li
Developing non-noble-metal electrocatalysts for hydrogen evolution reactions with high activity and stability is the key issue in green hydrogen generation based on electrolytic water splitting. It has been recognized that the stacking of large CoP particles limits the intrinsic activity of as-synthesized CoP catalyst for hydrogen evolution reaction. In the present study, N-MoxC/CoP-0.5 with excellent electrocatalytic activity for hydrogen evolution reaction was prepared using N-MoxC as decoration. A reasonable overpotential of 106 mV (at 10 mA cm−2) and a Tafel slope of 59 mV dec−1 in 1.0 M KOH solution was achieved with N-MoxC/CoP-0.5 electrocatalyst, which exhibits superior activity even after working for 37 h. Uniformly distributed ultrafine nanoclusters of the N-MoxC/CoP-0.5 hybrids could provide sufficient interfaces for enhanced charge transfer. The effective capacity of the hydrogen evolution reaction could be preserved in the complex, and the enlarged electrocatalytic surface area could be expected to offer more active sites for the reaction.
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CRYSTENGCOMM
·
2015
·Vol. 17
·期 45
·8697-8702
·
IF 4.034
Xiaolin Wu,Jiang-Long Wang,Hongrui Zhang,Shufang Wang,Shengjun Zhai,Yaguang Li,Dogheche Elhadj,Guangsheng Fu
c-axis oriented Bi1−xPbxCuSeO (0 ≤ x ≤ 0.8) single crystalline thin films have been successfully epitaxially grown on SrTiO3 (001) substrates via the pulsed laser deposition technique. Detailed X-ray diffraction and transmission electron microscopy measurements reveal the excellent c-axis and ab-plane texture of the films. As the Pb doping concentration increases, both the resistivity and the Seebeck coefficient decrease due to the increase in hole carrier concentration. The highest power factor of about 1.2 mW m−1 K−2 has been achieved in Bi0.96Pb0.06CuSeO single crystalline thin films at 673 K, which is much higher than those of polycrystalline ceramics with random orientation, suggesting that c-axis oriented BiCuSeO-based single crystalline thin films might have great potential for application in thermoelectric thin film devices.
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JOURNAL OF THE AMERICAN CERAMIC SOCIETY
·
2024
·Vol. 108
·期 1
·e20151
·
IF 3.5
Zhitong Xu,Jian Zhao,Malin Liu,Zebing Liu,Xinyu Cheng,Jiaxing Chang,Xu Yang,Bowen Li,Bing Liu,Rongzheng Liu
Developing high strength and tough silicon carbide (SiC) composite ceramics remains a significant challenge. Here, we report the process of synthesizing fully densified SiC/C composite ceramics using SiC@graphene (SiC@G) core–shell nanoparticles as raw materials through spark plasma sintering (SPS) at 1700°C and 45 MPa. The SiC@G nanoparticles were synthesized by the fluidized bed chemical vapor deposition (FB-CVD) method. During the sintering process, graphene coated, the surface of nanosized SiC particles exhibited high electrical and thermal conductivity, facilitating the uniform distribution of pulse current and heat and promoting the densification of SiC/C composite ceramics. For the prepared SiC/C composite ceramic, the carbon content reaches as high as 14.3 wt%, with carbon uniformly dispersed in a particulate form within the SiC matrix and stable interface bonding. Consequently, the introduction of excessive carbon does not compromise the hardness (28.8 GPa) and flexural strength (517.34 MPa) of the SiC/C composite ceramics. Furthermore, the carbon particles effectively enhance the toughness of the SiC/C composite material through mechanisms such as crack branching, bridging, and deflection, resulting in a fracture toughness of 7.38 MPa m 1/2 . The preparation strategy in this study provides a novel route for sintering SiC composites with high-carbon content through nanoscale powder structure design, resulting in the attainment of high-performance lightweight composite materials.
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APPLIED SURFACE SCIENCE
·
2021
·
IF 6.707
Chuanxu Hou,Junye Cheng,Huibin Zhang,Ziheng Lu,Xiuying Yang,Guangping Zheng,Deqing Zhang,Maosheng Cao
With the continuous advances in detection and early-warning technologies, stealth technologies have widely integrated in modern combat systems and armament research. The development of high-performance electromagnetic wave absorbing materials is important for electromagnetic stealth and shielding applications. Herein, biomass-derived carbon (BDC) from glucose is coated on the surface of folded and stacked WS 2 nanosheets, forming WS 2 @BDC via a simple hydrothermal method and subsequent annealing carbonization. The amount of the BDC coating on the WS 2 nanosheets is effectively controlled by the glucose solution concentration, and the electromagnetic wave (EMW) absorption performance in the low-frequency bands can be adjusted by the regulation of annealing temperature. The effective absorption band of WS 2 @BDC is shifted to a lower frequency region and the absorption performance is substantially enhanced, compared to those of pure WS 2 nanosheets. The minimum reflection loss of WS 2 @BDC corresponding to 14 mL of glucose and a carbonization temperature of 800 °C can reach up to −51.40 dB at 5.52 GHz. The study provides a novel and facile method for improving the EMW absorption performance of WS 2 in the low-frequency bands.
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APPLIED ORGANOMETALLIC CHEMISTRY
·
2014
·Vol. 28
·期 9
·673-677
·
IF 2.017
Limin Ren,Wenyi Chu,Dinghui Guan,Yanjun Hou,Man Wang,Xiaobin Yuan,Zhizhong Sun
A simple and efficient route for the preparation of terphenyl derivatives via palladium-catalyzed sequential directed C―H arylation/Suzuki–Miyaura cross-coupling in ‘one-pot’ has been developed. 4,4′-(Cyclohexane-1,1-diyl)diphenol is an essential ligand. This reaction can tolerate a series of functional groups and provides the terphenyl derivatives in moderate to good yield. Copyright © 2014 John Wiley & Sons, Ltd.
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IONICS
·
2023
·Vol. 30
·期 2
·697-708
·
IF 2.8
Wang Guanzheng,Lei Huazhi,Wang Zheng,Yuan Zhentao,Zhan Zhaolin,Li Lu,Wang Xiao
Amorphous GeO 2 @C anode materials were successfully prepared from commercial GeO 2 and C 6 H 12 O 6 .H 2 O by a hydrothermal method combined with sintering under nitrogen atmosphere protection. The anode materials showed an ideal spherical shape of about 3 μm and their surface was uniformly covered with C. GeO 2 @C composite anodes exhibited better storage performance for Li-ion batteries. The discharge-specific capacities of GeO 2 @C-3 sample were 1143, 1049, 776, 551, and 308 mAh g -1 at current densities of 0.2, 0.5, 1, 2, and 5 A g -1 , and restored to 1136 mAh g -1 when the current density returned to 0.2 A g -1 . The reversible specific capacity was 756 mAhg -1 after 1000 cycles at a current density of 1 A g -1 . The GeO 2 @C anode was stable in the process of charge and discharge, and no obvious pulverization occurred. GeO 2 @C composites stabilized the electrochemical properties through carbon and amorphous structure to improve the overall electrical conductivity in Li + embedding/de-embedding processes.
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CRYSTENGCOMM
·
2019
·Vol. 21
·期 40
·6010-6017
·
IF 3.382
Shuai Fang,Hongan Ma,Zhanke Wang,Zhiqiang Yang,Zheng-hao Cai,Luyao Ding,Xinyuan Miao,Liangchao Chen,XiaoPeng Jia
FeS is the main sulfur-containing compound in natural diamond inclusions. The research on FeS-doped diamond crystals plays an extremely important role in exploring the growth environment of natural diamond and the chemical composition of the earth. In our work, the characteristics of FeS doped diamond crystals were studied by using a China-type large volume cubic high-pressure apparatus with an iron–nickel alloy as a catalyst at 6.0 GPa and 1300–1350 °C. The crystals were characterized by OM, SEM, XPS, FTIR and Raman. Scanning electron microscopy of the crystal shows that the {100} plane of the crystal is rougher than {111}, which is related to the number of dangling bonds on different crystal faces of the crystal. The residue on the surface of the crystal was detected by mapping, and the test result showed that it was a sulfur iron and a sulfur nickel compound. FeS will decompose in the synthesis system, and the decomposition products are Fe and S2.The XPS spectrum of the crystal shows that S was successfully incorporated into the diamond lattice by forming C–S–O and C–S–SO2–C bonds, and the peak intensity was strong. The infrared spectrum shows that the N content in the crystal gradually increases as the doping ratio increases. Raman spectroscopy analysis shows that the S-doped Ib-type diamond single crystal has a high-quality sp3 structure, and the full width at half maximum (FWHM) of the crystal gradually broadens as the doping ratio increases.
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Current Research in Food Science
·
2025
·
IF 7
Le Cheng,Haoyue Bai,Mingfang Zhang,Fengping Yang,Difeng Ren,Yunpeng Du
The emerging technology of inhibiting polyphenol oxidase (PPO) is crucial for preventing enzymatic browning in food. This study aimed to investigate the effects of 4.5 kJ/m 2 ultraviolet (UV)-C radiation and 0.02 mg/mL L-cysteine (L-cys) treatment on the enzyme activity, physico-chemical properties, thermal properties, structure, and molecular microstructure of PPO. UV-C/L-cys decreased PPO activity and had the highest aggregation index and turbidity of PPO. UV-C/L-cys further reduced the denaturation temperature point and increased the denaturation enthalpy of PPO. UV-C/L-cys turned the α-helix to random coil of PPO and destroyed the tertiary structure. This combined treatment aggregated the microstructure of PPO, which led to covering the active center of the enzyme, leading to its inactivation. Molecular docking simulation confirmed that L-cys bound to PPO through hydrogen bonding and ionic contact. This study established a foundation for the application of UV-C radiation and L-cys treatment to control food browning.
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产品关联
DOI
PubMed
高影响因子
JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
·
2025
·
IF 14.3
Martin C. Koo,Yu Zhang,Bo Cai,Chen-Ming Liang,Shao-Hang Shi,Hua-Long Peng,Shu-Hao Yang,Xiao-Bo Sun,Guang-Sheng Wang
Microwave-absorbing materials (MAMs) play an important role in reducing electromagnetic pollution. However, achieving a balance between low filler loading, low minimum reflection loss (RL min ) and wide effective absorption bandwidth (EAB) for efficient absorption of microwaves remains challenging. In this work, an innovative method of using CO 2 atmosphere annealed Ti 3 C 2 T x MXene (C/TiO 2 ) combined with nickel nanowires (NiNW) via ultrasonic treatment was performed to yield C/TiO 2 /NiNW (CTN) composites with abundant NiNW/TiO 2 contacts. The electromagnetic (EM) parameters of the as-synthesized composites were closely studied through a series of experiments and computed theoretical calculations. Through the establishment of built-in electric fields (BIEFs) at the NiNW/TiO 2 interface, the derived CTN composite demonstrated improved dielectric properties and impedance matching characteristics that are clearly reflected on the microwave absorption performance of our as-synthesized MAMs, with RL min improving by 127.9% from −31.93 dB to −72.77 dB, and widest EAB increasing by 25.9% from 4.25 GHz to 5.35 GHz, at a low filler loading of 10 wt.%. This work investigates the mechanisms by which BIEFs influence EM parameters, providing critical insights into improving microwave absorption performance via BIEF structural design.
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Turkish Journal of Gastroenterology
·
2025
·Vol. 36
·期 9
·573
·
IF 1.6
Hailiang Liu,Xile Wei,Ye Nie,Jianshan Liu,Ming Fan
Background/Aims: The function and mechanism of ubiquitin-specific protease 34 (USP34) in hepatocellular carcinoma (HCC) were explored to provide new molecular targets for treating HCC. Materials and Methods: In the present study, bioinformatics techniques, quantitative real-time polymerase chain reaction, and western blot were used to detect the level of USP34 in HCC tissues and cell lines. Small interfering RNA of USP34 was transfected into HCC cells, and then Cell Counting Kit-8 (CCK-8) assay, wound healing assay, and transwell assay were performed to verify the proliferation, migration and invasion of HCC cells. Enzyme-linked immunosorbent assay was utilized to assess the glycolysis level in HCC cells. Co-immunoprecipitation was used to evaluate the ubiquitination level of cellular Myc (c-Myc). Results: The expression of USP34 was upregulated in HCC patients and strongly associated with worse outcomes. Meanwhile, interference with USP34 suppressed the proliferation, migration, and invasion of HCC cells. In addition, silencing of USP34 reduced the glucose uptake, lactate production and ATP content in HCC cells, as well as downregulated the expression levels of glycolysis-related proteins (hexokinase 2, glucose transporter 1, pyruvate kinase M2, and lactate dehydrogenase A). Furthermore, the knockdown of USP34 enhanced the ubiquitination level of c-Myc and increased the degradation of c-Myc. Overexpression of c-Myc reverted the inhibitory effects of si-USP34 on the malignant biological behavior in HCC cells. Conclusion: TheUSP34 regulates aerobic glycolysis and inhibits the progression of HCC by accelerating c-Myc ubiquitinated degradation.
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PubMed
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