JOURNAL OF ALLOYS AND COMPOUNDS
·
2018
·
IF 3.779
Xuebin Hou,Sarah Louise Stanley,Min Zhao,Jin Zhang,Huimin Zhou,Yibing Cai,Fenglin Huang,Qufu Wei
As the most widely used metal oxide catalysts in photocatalytic degradation, the fast recombination of charge carriers limits the photocatalytic performance of multiform TiO 2 , resulting from its direct-band-gap property. In the present work, we designed C-doped coupled TiO 2 /ZnO nanofibrous membrane based on the derivation of ZnO from the metal organic framework (MOF). The morphology and catalytic properties of the composite membrane could be manipulated by the growth of ZIF-8 crystals. Compared to pristine TiO 2 nanofibers (11.4341 m 2 g −1 ), the composite membrane with an optimized ZnO cubes exhibited larger specific surface area (30.2475 m 2 g −1 ) after introducing ZnO cubes. Furthermore, the crossed-network connection between TiO 2 and ZnO cubes is propitious to increase the synergy of the heterojunction , subsequently effectively inhibiting the recombination of photogenetrated holes and electrons. Benefitting from the trinomial synergistic effect of carbon doping, ZnO and TiO 2 , the as-designed composite membrane exhibited excellent photocatalytic performance to Rhodamine compared to pure TiO 2 nanofibers. This study not only presents the strategy of preparing a C-doped coupled TiO 2 /ZnO composites with crossed network connection for effective photocatalysis , but also exploit the application of MOFs.
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高影响因子
CARBON
·
2019
·
IF 7.466
Yudi Mo,Junchen Liu,Chao Meng,Min Xiao,Shan Ren,Luyi Sun,Shuanjin Wang,Yuezhong Meng
The low electronic conductivity and poor Li + diffusion coefficient of conventional LiFePO 4 (LFP) materials severely impede its high-rate applications for lithium-ion batteries (LIBs). To break these limits, one novel poly(1,3-diethynylbenzene) (PAB) acetylenic carbon-rich polymer with extremely high-carbon content (96.75 wt%) and good solubility has been prepared by an oxidative coupling reaction. One definite advantage is that this carbon-rich PAB polymer will release, upon pyrolysis , very low amounts of gas, forming therefore uniform and dense highly conductive carbon network. Besides, the specific resistivity of continuous PAB-C layer can be as low as ∼0.01 Ω cm, which can effectively improve electrical conductivity and maintain mechanical integrity of LFP cathode. As a result, the prepared LFP@PAB-C nanocomposites with approximately 3.8 wt% carbon content and 2.5 nm carbon layer exhibit an excellent high-rate capability, e.g. even at a considerable discharge rate of 50 C, while the capacity can still be remained at 129.6 mA h g −1 . Moreover, the LFP@PAB-C nanocomposites also reveal a remarkable cycling stability with as high as 100.6% capacity retention at 20 C over 1000 cycles. This kind of LFP@PAB-C composite was demonstrated to be an ideal cathode material for high-power LIBs.
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高影响因子
SENSORS AND ACTUATORS B-CHEMICAL
·
2016
·
IF 4.758
Yehui Guan,Fangmeng Liu,Bin Wang,Xue Yang,Xishuang Liang,Hui Suo,Peng Sun,Yanfeng Sun,Jian Ma,Jie Zheng,Yue Wang,Geyu Lu
In this paper, a novel amperometric CO sensor using Nafion and Pt/C composite electrodes was fabricated. Three kinds of carbon materials (carbon fibers, multiwall carbon nanotubes and carbon blacks) were utilized as the supports of the sensing and reference electrodes for the CO sensors. The results revealed that the effective Pt loadings on the electrodes increased in the following order: carbon fibers (CFs) > multiwall carbon nanotubes (MWCNTs) > carbon blacks (CBs), leading to the increasing of the sensitivities toward CO in same order. In other words, the sensor using Pt/CFs as the sensing electrode (SE) showed the highest sensitivity with the value of 0.077 μA/ppm and shortest response time in the range of CO concentration from 1 to 200 ppm at room temperature . Further, a reproducible and stable response against 50 ppm CO was obtained for the sensor with Pt/CFs SE materials . Moreover, a low detection limit of 0.1 ppm for CO was also examined, suggesting that the sensor can be convenient for detecting very low traces of CO.
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高影响因子
CARBON
·
2022
·
IF 11.307
Wenjun Huyan,Junru Yao,Jiaqi Tao,Feng Yang,Xuewei Tao,Zhengjun Yao,Jintang Zhou,Zibao Jiao
0D-2D Polydopamine (PDA)-derived carbon nanoparticles @ MXene composites (PCM) with high microwave absorption properties were prepared by in-situ self-polymerization combined with vacuum pyrolysis . As the “nano clothing” of MXene , the moderate accumulation of PDA-derived carbon nanoparticles makes enough interface contact with MXene nanosheets , which not only improves the impedance matching of MXene reasonably but also optimizes the dielectric loss . Based on the multi-dimension structure and multi-component synergistic effect , when the filling amount of the composite is only 7.5 wt% and the thickness is 2.8 mm, the best reflection loss at 10 GHz is −46.92 dB and the maximum effective absorption bandwidth is 7.01 GHz. This work provides a synthesis strategy of crystal/amorphous heterointerface and offers a new way for the preparation of lightweight, broadband, and efficient microwave absorption materials , showing great application potential.
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高影响因子
JOURNAL OF THE ELECTROCHEMICAL SOCIETY
·
2022
·Vol. 169
·期 6
·062501
·
IF 4.386
Chanez Maouche,Yazhou Zhou,Bing Li,Chao Cheng,Zirui Wu,Xue Han,Shaosheng Rao,Yi Li,Nasir Rahman,Juan Yang
Iron-nitrogen-carbon graphitic (Fe-N-C), a noble metal-free catalyst holds a lot of promise to substitute platinum (Pt) as an efficient catalyst in the oxygen reduction reaction (ORR). However, the synthesis process and the stabilization of single atoms that tend to aggregate, without jeopardizing the catalytic activity remain challenging. Here we demonstrate a stabilized assisted method for the preparation of Fe-N-C electrocatalyst by using graphitic carbon nitride (g-C3N4) nanosheet as a template. Fe ions are absorbed on the surface of g-C3N4 and imprisoned after the addition of pyrrole, preventing Fe migration that may result in nanoparticles. During the pyrolysis, Fe atoms coordinated with N provided by g-C3N4 and pyrrole on graphitic carbon to form Fe-N-C with a metal loading of 5.4 wt%. Moreover, FeNx species were introduced in the graphitic carbon, where the coexistence of micro and mesopores were favorable to offer a larger density of active sites compared to Fe/NP without pyrrole. Fe-N-C demonstrated a good electrocatalytic performance with a half-wave potential (E1/2) of 0.82 V (vs reversible hydrogen electrode (RHE)) higher than Fe/NP (0.76 V) and close to Pt/C, with a superior long stability of 85% in alkaline media after 40000 s.
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高影响因子
JOURNAL OF THE ELECTROCHEMICAL SOCIETY
·
2021
·Vol. 168
·期 12
·123509
·
IF 4.316
Xianglin Liu,Yongsong Ma,Peng Li,Huayi Yin,Dihua Wang
MoB2 is synthesized by the electrochemical reduction of solid MoS2/B mixture in molten NaCl-KCl at 700 °C. Unlike the traditional methods, the electrolysis method employs the low-cost MoS2 feedstock and the boronization reaction happens at a low temperature of 700 °C. The electrochemically induced boronization involves two steps: the electrochemical desulfurization to generate Mo and the reaction of Mo with B to form MoB2. The S2− released from the reduction of MoS2 transfers to the carbon anode and is oxidized to sulfur gas, realizing a green synthetic process. In addition, the influences of molar ratio of MoS2 and amorphous boron and electrolysis cell voltage on the phase composition and morphology of electrolytic products were studied. The obtained MoB2 particles possess a uniform nodular morphology. Overall, this paper provides a straightforward and green process to prepare MoB2 nanoparticles using economically affordable raw materials at low temperature, and this method can be extended to prepare other borides.
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高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2020
·
IF 16.683
Pijun Duan,Yuanfeng Qi,Shanshan Feng,Xiaoming Peng,Wei Wang,Yue Yue,Yanan Shang,Yanwei Li,Baoyu Gao,Xing Xu
FeMn bimetallic nanoparticles coated with nitrogen-doped graphene shells (FeMn@N-C) were prepared to decompose clothianidin (CTD) through activation of peroxymonosulfate (PMS). The redox cycles of encapsulated FeMn bimetallic nanoparticles with multiple valence states could accelerate the radical generation and ensure the stability of FeMn@N-C with continuous PMS activation. Coexisting NaH 2 PO 4 could unusually accelerate CTD degradation through facilitating reactive oxygen species (ROS) generation and decreasing bonding dissociation energies of CTD molecule. DFT calculation indicated that the C-Cl bond in CTD molecule was weakened after being surrounded by NaH 2 PO 4 . Two main degradation pathways were proposed in the absence of phosphate and a new dechlorination pathway was first reported after CTD molecule bonding with phosphate, which was confirmed by DFT. This work provides a feasible strategy of PMS activation by graphene coated bimetallic nanoparticles and give a new insight into accelerated degradation of recalcitrant pollutants with phosphate surrounding.
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高影响因子
ACS Sustainable Chemistry & Engineering
·
2017
·
IF 5.951
Yueling Cao,Minghui Tang,Mingming Li,Jiang Deng,Fan Xu,Lei Xie,Yong Wang
A novel N-doped carbon supported Rh catalyst was developed via one-pot pyrolysis of chitin and (NH4)3RhCl6. The catalyst exhibited excellent catalytic activity and recyclability for the hydrogenation of benzoic acid to cyclohexane carboxylic acid. Characterization indicated that the high catalytic performance of Rh/N–C-700 is mainly attributed to the proportion of Rh0 to Rh3+ and Rh particle size. More importantly, this novel synthesis strategy significantly increased the interaction between Rh nanoparticles and N-doped carbon in contrast with the conventional impregnation and NaBH4 reduction methods, thus preventing the Rh nanoparticles from migration, aggregation, and leaching from the support surface and therefore improving the reusability of the catalyst. This synthetic method may pave a new way for producing N-doped carbon supported metal catalysts from chitin on a large scale, which is attractive for industrial applications.
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高影响因子
COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING
·
2024
·Vol. 27
·期 13
·1919-1929
·
IF 1.6
Zhang Fei,Chu Mingliang,Liu Jiemin,Zhao Qi,Zhu Yanqiu,Wu Xuefang
Aim: The study aimed to study the potential roles and mechanisms of shikonin in gastric cancer by network pharmacology and biological experiments. Methods: The key genes and targets of shikonin in gastric cancer were predicted by network pharmacology and molecular docking study.
The effect of shikonin on the proliferation, migration, and invasion of gastric cancer cells was detected by the CCK8 method, and wound healing and transwell assays. The expression levels of c-Myc and Yap-1 were detected via western blotting in gastric cancer cells after shikonin intervention.
Results: The results of network pharmacology revealed the key target genes of shikonin on gastric cancer cells to be c-Myc, Yap-1, AKT1, etc. GO and KEGG analysis showed regulation of cell migration, proliferation, adhesion, and other biological processes, including the PI3K-Akt signaling
pathway, HIF-1 signaling pathway, necroptosis, and other cancer pathways. Molecular docking showed shikonin to be most closely combined with protooncogenes c-Myc and Yap-1. In vitro experiments showed that the proliferation rate, migration, and invasion ability of the gastric cancer cell group
decreased significantly after shikonin intervention for 24h. The expression levels of c-Myc and Yap-1 in gastric cancer cells were found to be significantly decreased after shikonin intervention. Conclusion: This study showed protooncogenes c-Myc and Yap-1 to be the core target genes
of shikonin on gastric cancer cells. Shikonin may suppress gastric cancer cells by inhibiting the protooncogenes c-Myc and Yap-1. This suggests that shikonin may be a good candidate for the treatment of gastric cancer.
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PubMed
高影响因子
APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY
·
2022
·Vol. 194
·期 11
·5167-5184
·
IF 3.094
An Peide,Zhu Fenfen,Liu Shiji,Zhou Xiaolin,Wang Chunfang,Liu Yufeng,Meng Hao,Zhang Xia
Recently, metal–organic frameworks (MOFs) are considered to be the moderate hosts for the bio-enzymes owing to their unique 3D pores and controllable surface affinity to the target molecules. In this work, the benzoic acid (BA)–modulated UiO-66-NO 2 was introduced, and cytochrome c (Cyt C) was chosen as the target enzyme to evaluate the immobilization efficiency of the resulting UiO-66-NO 2 -BA. The immobilization conditions including pH, adsorption time, and temperature and the initial concentrations of BA were optimized. The adsorption kinetics and thermodynamics were analyzed to further explore the enhanced adsorption mechanism. It is worth noted that all the UiO-66-NO 2 -BA exhibited evidently enhanced adsorption capacities in comparison with the unmodified UiO-66-NO 2 due to the formation of the chemical bonds between the UiO-66-NO 2 -BA and cytochrome C, indicating the positive roles of BA modification. Finally, the activities of the immobilized cytochrome C were assessed by using the catalytic oxidation of ABTS in the presence of H 2 O 2 , which reactions were also conducted over the free cytochrome C for comparison. The evidently improved stability under definite pH range, prolonged durability against the organic solvents, and the good reusability of the immobilized cytochrome C highlight the prospect applications of functional MOF immobilized enzymes in the practical catalytic reactions. Graphical abstract
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高影响因子
CERAMICS INTERNATIONAL
·
2021
·
IF 4.527
Nali Li,Yong Yu,Yanwei Tong,Tiantian Liu,Xuefeng Zhang
An enhanced sol-gel combustion method was used to synthesize different porous Sc 3+ -doped Li 3 V 2-x Sc x (PO 4 ) 3 /C (x = 0.00, 0.05, 0.10 and 0.15) compounds. The substitution of Sc 3+ into the V 3+ sites of Li 3 V 2-x Sc x (PO 4 ) 3 /C expands the lattice volume along with the enlargement of Li + diffusion channel, which is beneficial for Li + transportation and ionic conductivity improvement. Besides, the Sc 3+ doping content exhibits a great impact on the morphology of Li 3 V 2-x Sc x (PO 4 ) 3 /C composite. The pristine Li 3 V 2 (PO 4 ) 3 /C are constituted of porous particles and nanorods , and the ratio of nanorods to particles can be controlled by adjusting the amount of Sc 3+ doping since the ratio of nanorods to particles decreases with increasing Sc 3+ doping content. When Sc 3+ doping content increases to a certain level (x = 0.15, Li 3 V 1.85 Sc 0.15 (PO 4 ) 3 /C), the nanorods are hardly seen. Li 3 V 1.90 Sc 0.10 (PO 4 ) 3 /C with higher tapped density, better reversibility, smaller resistance and larger Li + diffusion coefficient demonstrates outstanding rate performance and cyclic stability, together with high specific discharge capacities of 130.2 and 92.9 mAh g −1 at 0.5 and 20 C, respectively. Furthermore, a superior specific discharge capacity of 85.8 mAh g −1 was retained at 20 C following 1000 cycles. Overall, a novel approach for the preparation of high-performance Li 3 V 2-x Sc x (PO 4 ) 3 /C cathodes with different morphologies for lithium-ion batteries is provided.
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高影响因子
JOURNAL OF THE ELECTROCHEMICAL SOCIETY
·
2019
·Vol. 166
·期 4
·B193
·
IF 3.12
Sheying Dong,Hao Cui,Dandan Zhang,Mengmeng Tong
Several reports reveal that high level of C-reactive protein (CRP) in serum enhances venture of diabetes. In this article, we presented a platform which blended Zr(IV)-organic framework with 2,5-thiophenedicarboxylate ligand (Zr-tdc) and ionic liquid (IL) to form a steady composite membrane on the carbon paste electrode (CPE). The platform was applied to CRP and glucose biosensors which were connected with diabetes and displayed well performances. Firstly, a sensitive immunosensor for label-free and direct detection of CRP was developed at Zr-tdc/IL modified electrode. Under optimal conditions, differential pulse voltammetry (DPV) response showed the low detection limit of CRP was 0.2 ng/mL. Secondly, the glucose biosensor immobilized glucose oxidase (GOX) was constructed and studied by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and amperometric response. The Michaelis–Menten constant (KM) of immobilized GOX was 0.16 mM, and the detection limit was 2.7 μM for glucose. Two novel biosensors displayed well selectivity, stability and lower detection limit. This work improved the performance of electrochemical sensing and expand the utilization of the material by carrying on the effective immobilization of enzyme and antibody.
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高影响因子