ACS Applied Materials & Interfaces
·
2025
·
IF 8.2
Xiaoqing Li,Min Zuo,Ziwei Lan,Fengling Jiang,Dickon H. L. Ng,Jia Li
C/OVs-Ni-Cu-LDHs@MnO2 tubular micromotors with enzyme-like activity and abundant oxygen vacancies (OVs) were synthesized hydrothermally using kapok as a biotemplate. MnO2 acted as the micromotor’s “driving engine”, catalyzing the generation of H2O2 bubbles to provide driving force for the motor, enabling efficient motion (144.45 ± 3.97 μm/s in 5% H2O2). The micromotors also exhibited enzyme-like activity, oxidizing 3,3′,5,5′-tetramethylbenzidine (TMB) via reactive radicals. A sensor for the colorimetric detection of GLY (lowest detection limit 0.63 μM) was developed by utilizing the enzyme inhibition induced by Cu2+-glyphosate (N-(phosphonomethyl)glycine, GLY) chelation. Meanwhile, the micromotor catalyzes H2O2 and activates peroxymonosulfate (PMS), efficiently generating hydroxyl radicals (•OH), superoxide radicals (O2•–), and single-linear oxygen (1O2). Under the synergistic effect of self-driven propulsion and efficient catalysis, achieving 93.71% GLY degradation in 40 min. This study provides an intelligent strategy for developing dynamic sensors with dual functions of simultaneous detection and degradation of GLY.
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产品关联
DOI
PubMed
高影响因子
APPLIED SURFACE SCIENCE
·
2017
·
IF 3.387
Xuedong Wei,Na Li,Xianming Zhang
It remains a huge challenge to develop non precious electrocatalysts with high activity to substitute commercial Pt catalysts for hydrogen evolution reactions (HER). Here, the C-Cu-DI and C-Cu materials with the copper based nanoporous carbon structures were synthesized by carbonizing MOF199 and DI-MOF199. The composite structure and HER electrocatalytic properties of the C-Cu-DI and C-Cu materials are studied. The results show that C-Cu-DI and C-Cu samples exhibit good catalytic activity. And C-Cu-DI sample through the addition of Dimethyl imidazole(DI) in the DI-MOF199 precursor has higher electrocatalytic activity than the C-Cu sample. The superior catalytic activity is attributed to the special composite structure of nanoscale deposition particles on the framework with plenty of nano pores and nano copper and few copper oxidation particles distributed or wrapped into the amorphous porous carbon phase. The nano copper and few copper oxidation particles in the C-Cu and C-Cu-DI catalysts maybe provide the more effective catalytic activity sites. The C-Cu-DI composite with large size spherical hollow deposition particles has higher conductivity, better BET surface area and reasonable micro-meso-macro porous distribution, so the overpotentials at the current density of 1 mA cm −2 and 10 mA cm −2 are respectively 270 mV and 390 mV vs. RHE. Although the HER activity has a big gap with commercial platinum catalyst, this study can provide an important experimental exploration for the design of copper based non noble metal/nano porous carbon composite HER electrocatalyst.
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DOI
高影响因子
Nanoscale
·
2019
·Vol. 11
·期 31
·14844-14856
·
IF 6.97
Haoru Shan,Xiangyang Dong,Xiaota Cheng,Yang Si,Jianyong Yu,Bin Ding
The development of inorganic membranous catalysts with both large mesopores and superb flexibility is extremely favorable for the enhancement of their catalytic oxidation activity for the degradation of antibiotic pollutants in wastewater via sulfate radical-based advanced oxidation processes; however, there still exists a huge challenge for inorganic materials to simultaneously realize these two properties. Herein, metallic copper-doped carbon/silica nanofibrous membranes (Cu@C/SiO2 NFMs) with large mesopores, superb flexibility, and robust mechanical strength were fabricated through a sol–gel electrospinning and subsequent in situ carbonization reduction method. The synthesized Cu nanoparticles were homogeneously distributed throughout the mesoporous C/SiO2 nanofiber matrix, which enabled the resultant Cu@C/SiO2 NFMs to be applied as heterogeneous catalysts, and their catalytic performance was systematically assessed through activating persulfate for the elimination of tetracycline hydrochloride (TCH) in water. The fabricated Cu@C/SiO2 NFMs provided outstanding catalytic performance towards TCH with a high removal efficiency of 95% in 40 min and a rapid removal speed of 0.054 min−1. Moreover, the membranes could be facilely recycled through being directly separated from water without any post-processing. Such a facile strategy for preparing mesoporous and flexible metal-doped inorganic nanofibrous membranes may offer novel insights for designing new types of heterogeneous catalysts for antibiotic-containing wastewater treatment or other potential applications.
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DOI
高影响因子
COMPOSITES PART B-ENGINEERING
·
2022
·
IF 11.322
Zhiyuan Wang,Haohui Zhang,Xinyu Zhang,Xiaomei Wang,Xu Zhang
High-capacity SiO x anodes are fatally limited by poor electrical conductivity and huge volume fluctuations. Nano-engineering can effectively extend battery life, but achieving the transformation of nanostructures from laboratory synthesis to industrial mass production still remains a great challenge. Conventional synthetic routes are plagued by harsh conditions, complex processes, and especially low yields; even if they are adopted by industrial production, the large amounts of solvents in traditional wet chemical methods will pose a potential risk of pollution and energy waste. Herein, a solvent-free and mass-producible strategy is presented to prepare SiO x /C@C nanocomposite via solvent-free sol-gel, ball milling , and carbon coating process . The production exhibits favorable powder properties for conventional LIB fabrication technology, such as narrow particle size distribution , suitable specific surface area, as well as a high yield (40.5%). The prepared SiO x /C@C anode displays a high initial coulombic efficiency (71.4%) and reversible capacity (1279 mAh g −1 at 0.1 A g −1 ), and a great durability (80.08% capacity retention after 1000 cycles at 1.0 A g −1 ). Furthermore, the superior matching performance of SiO x /C@C//LiCoO 2 full-cell is also clearly demonstrated, especially the high energy density (347 Wh kg −1 ). This ingenious and scalable strategy will remarkably promote the commercialization of nanostructures.
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DOI
高影响因子
INORGANIC CHEMISTRY
·
2018
·
IF 4.7
Ming Zhong,Wei-Wei He,Wei Shuang,Ying-Ying Liu,Tong-Liang Hu,Xian-He Bu
Metal–organic frameworks (MOFs) with diverse structures, adjustable pore sizes, and high surface areas have exhibited awesome potential in many fields. Here we report a simple carbonization strategy to obtain a series of core–shell structured Co/Co3O4 nanoparticles encapsulated into nitrogen-doped carbon shells from cobalt-based metal–organic framework precursors at different carbonization temperatures. When it is applied as an anodes for lithium ion batteries, the Co/Co3O4@N-C-700 electrode delivers a maximum initial discharge capacity of 1535 mAh g–1, the highest reversible capacity (903 mAh g–1 at a current density of 100 mA g–1 after 100 cycles), and the best rate performance (i.e., 774 mAh g–1 at a current density of 1.0 A g–1 after 100 cycles) in comparison with those of Co/Co3O4@N-C-600 and Co/Co3O4@N-C-800 electrodes. The excellent electrochemical performance could be mainly attributed to the unique core–shell structure, abundant graphited carbon, and the well-dispersed Co/Co3O4 nanoparticles which can promote the specific capacity through conversion reactions.
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DOI
高影响因子
ACS Applied Materials & Interfaces
·
2020
·
IF 8.758
Yansong Bai,Xiaoyan Zhang,Hongbo Shu,Zhigao Luo,Hai Hu,Qinglan Zhao,Ying Wang,Xianyou Wang
The poor electronic conductivity of Na2FeSiO4 always limits its electrochemical reactivities and no effective solution has been found to date. Herein, the novel Ni-substituted Na2Fe1–xNixSiO4@C nanospheres (50–100 nm) encapsulated with a 3D hierarchical porous skeleton (named as alveolation-like configuration) constructed using in situ carbon are first synthesized via a facile sol–gel method, and the effects of Ni substitution combined with the design of a unique carbon network on Na-storage properties are assessed systematically, focusing on alleviating the inherent defects of the Na2FeSiO4 cathode material. A series of characterization technologies such as X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy and so forth, coupled with the electrochemical measurements and first-principles calculations, are used to explore the structure, morphology and electrochemical behaviors of the as-prepared materials. The results show that the synergism between Ni substitution and the special alveolation-like configuration enables fast Na ions mobility (from 10–14 to 10–12 cm2 s–1), reduces band gap energy (from 2.82 to 1.79 eV) and lowers Na-ion diffusion barriers, finally reciprocating the vigorous electrochemical kinetics of the electrode. Especially, the elaborately designed material—Na2Fe0.97Ni0.03SiO4@C—displays superior Na-storage properties of around 197.51 mA h g–1 (corresponding to 1.43 Na+ intercalation) at 0.1 C within 1.5–4.5 V along with desirable capacity retention (84.44% after 100 cycles), and the rate capability is also markedly enhanced (a capacity of 133.62 mA h g–1 at 2 C). Such the effective methodology employed in this work opens a potential pathway to synthesize the silicate cathode material with excellent electrochemical properties.
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DOI
高影响因子
ACS Nano
·
2019
·
IF 13.903
Fei Wang,Bo Wang,Tingting Ruan,Tiantian Gao,Rensheng Song,Fan Jin,Yu Zhou,Dianlong Wang,Huakun Liu,Shixue Dou
Silicon (Si), a promising candidate for next-generation lithium-ion battery anodes, is still hindered by its volume change issue for (de)lithiation, thus resulting in tremendous capacity fading. Designing carbon-modified Si materials with a void-preserving structure (Si@void@C) can effectively solve this issue. The preparation of Si@void@C, however, usually depended on template-based routes or chemical vapor deposition, which involve toxic reagents, tedious operation processes, and harsh conditions. Here, a facile templateless approach for preparing Si@void@C materials is reported through controlling the growth kinetics of resin, without the use of toxic hydrofluoric acid or harsh conditions. This approach allows great flexibility in tuning the crucial parameters of Si@void@C, such as the carbon shell thickness, the reserved void size, and the number of Si cores coated by a carbon shell. The optimized Si@void@C delivers a large specific capacity (1993.2 mAh g–1 at 0.1 A g–1), excellent rate performance (799.4 mAh g–1 at 10.0 A g–1), and long cycle life (73.5% capacity retention after 1000 cycles at 2.0 A g–1). In addition, a full cell fabricated with a Si@void@C anode and commercial LiFePO4 cathode also displays an impressive cycling performance.
✓ 已验证
DOI
高影响因子
ADVANCED POWDER TECHNOLOGY
·
2024
·
IF 4.2
Jiuxiang Zhang,Xiaoping Zhang,Shengxing Lu,Yian Wang,Yulei Sui,Keyi Sun,Mengting Deng,Wenbin Fei,Ling Wu
Na 4 MnCr(PO 4 ) 3 is a promising cathode material with high redox potential and high energy density, but the intrinsic poor electronic conductivity and substandard structural stability restrict its practical application. Herein, porous Na 4 MnCr(PO 4 ) 3 /C with conductive networks and improved electrochemical properties is synthesized by a facile modified solid-state process using citric acid as a multifunctional additive. The results reveal that citric acid can be used as a grinding aid to make the raw materials mix more evenly and speed up the efficiency of ball milling. Besides, 3D conductive network and porous structure originated from polycondensation and carbonization of citric acid can promote the electrochemical properties of Na 4 MnCr(PO 4 ) 3 /C by enhancing the electronic/ionic conductivity and (de)intercalation reaction kinetics. As expected, the optimal Na 4 MnCr(PO 4 ) 3 /C delivers a high reversible capacity of 130.5 mAh g −1 at 0.1C rate, and exhibits a capacity retention of 82.62% at 10C rate after 500 cycles. In addition, the reversible biphasic reaction of the cathode is confirmed by the constant galvanostatic intermittent titration technique and ex-situ XRD, which shows great potential of the synthesized Na 4 MnCr(PO 4 ) 3 /C for practical applications.
✓ 已验证
DOI
高影响因子
Water Supply
·
2013
·Vol. 14
·期 3
·493-503
·
IF 0
Ou Hua-Se,Wei Chao-Hai,Deng Yang,Gao Nai-Yun
Polyaluminum chloride (PAC) coagulation, short wavelength ultraviolet (UV-C at 254 nm) treatment and UV-C/PAC treatment of algae-laden water from Meiliang Gulf (Lake Taihu) were conducted. The intrinsic characteristics and correlations of chromophoric dissolved organic matter (CDOM), algae biomass and other contaminants were investigated. Parallel factor analysis determined four CDOM components, and principal component analysis (PCA) identified three integrated principal factors. PCA Factor 1 had correlations with dissolved organic carbon (DOC) ( r = 0.798), UV 254 (0.645), humic-like CDOM component C3 (0.892) and C4 (0.876), and Factor 2 correlated with in vivo chlorophyll-a (0.768), microcystin-LR (0.713), protein-like C1 (0.782) and C2 (0.759). Factor 3 had correlations with NH 3 -N (0.851) and total phosphorus (T-P) (0.716). The variation in PCA factor scores revealed that single PAC coagulation preferentially removed algal cells (Factor 2) but had little effect on NH 3 -N and T-P (Factor 3). Single UV-C treatment induced degradation of protein-like CDOM and decrease of algal biomass (Factor 2), followed by humic-like CDOM increase from ruptured cells (Factors 1 and 3). Compared with single PAC coagulation (20 mg L −1 ), the combined UV-C/PAC treatment (700 mJ cm −2 + 20 mg L −1 ) enhanced the removal of PCA Factors 1, 2 and 3 (15%, 32% and 10%).
✓ 已验证
DOI
CHEMISTRY-A EUROPEAN JOURNAL
·
2017
·Vol. 23
·期 19
·4644-4650
·
IF 5.317
Lianshan Sun,Chunli Wang,Qujiang Sun,Yong Cheng,Limin Wang
With the aim of finding efficient non-noble metal catalysts for water splitting, hierarchical Ni-Mo-polydopamine microflowers (Ni-Mo 2 C/C MF) were synthesized through a facile aqueous-phase reaction at room temperature. NiMoO 4 nanowires were utilized as both Ni and Mo source; they can complex with dopamine to form a hierarchical structure and affect the scale of the final product. The energy dispersive spectroscopy (EDS) measurement of Ni-Mo 2 C/C microflowers (MF) shows a high content of Mo 2 C and Ni (>90 wt %). For the hydrogen evolution reaction (HER), the Ni-Mo 2 C/C MF displays a low overpotential of 99 mV at a current density of −10 mA cm −2 and a small Tafel slope of 73 mV dec −1 in 1.0 m KOH. By comparison with Mo 2 C/C microspheres (MS), the nanosized Ni-doped particles offer more active sites and enhance the kinetic performance. This facile synthesis strategy is also suitable for preparing other metal-Mo 2 C/C composites that can be used in the fields of catalysis and energy conversion. Graphical In flower : A flowerlike Ni-Mo-dopamine complex is first synthesized by a facile method under room temperature. Ni doping in situ is realized by utilizing NiMoO 4 nanowire as both template and precursor. An enlarged surface area and nanosized Ni doping greatly enhance the electrocatalytic properties of Ni-Mo 2 C/C due to more active sites.
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DOI
高影响因子
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
·
2015
·Vol. 2016
·期 2
·325-330
·
IF 3.065
Wannian Zhao,Lei Xu,Yingcai Ding,Ben Niu,Ping Xie,Zhaogang Bian,Denghong Zhang,Aihua Zhou
Coumarin derivatives are highly valuable compounds in drug discovery. Herein, we have developed two new coupling reactions that involve coumarins and either aldehydes or di- tert -butyl peroxide (DTBP) in the presence of inexpensive copper or iron catalysts. Both of these reactions proceed through a C(sp 2 )–H functionalization process to regioselectivity generate keto- or methyl-substituted coumarin derivatives in moderate to good yields These coupling reactions will enrich current coumarin chemistry. Graphical Two coupling reactions that regioselectively yield either keto- or methyl-substituted coumarin derivatives by proceeding through a C(sp 2 )–H functionalization process were successfully developed. The coupling of coumarins with either aldehydes or di- tert -butyl peroxide (DTBP) generated the corresponding products in moderate to good yields.
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DOI
高影响因子
CEMENT & CONCRETE COMPOSITES
·
2022
·
IF 9.93
Xing Ming,Qing Liu,Miaomiao Wang,Yongqing Cai,Binmeng Chen,Zongjin Li
Chloride-induced corrosion in reinforced concrete is a primary durability issue that causes large economic loss every year. To improve the intrinsic chloride binding capacity and realize a favorable corrosion protection of cement-based materials are thus crucial to prolong the service life of concrete structures. Here, alumina nano particles (ANPs) were incorporated to improve the chloride binding capacity of cement pastes in chloride solutions and the anti-corrosion performance of mortars under accelerated corrosion process. The ANPs facilitated the formation of alumino-ferrite-mono (AFm)-type phases, thereby improved the content of chemically bound chlorides. Solution calcium (Ca) ions benefited the chloride captured by calcium-(alumino-)silicate-hydrates (C-(A-)S-H) in the assistance of ANPs, especially at high initial chloride concentrations , and further evoked a pH-related chloride binding response. Moreover, the enhanced corrosion resistance was finally realized by incorporating appropriate amount of ANPs because of the filling and chemical effects induced low permeability of mortars. In general, the ANPs possess dual functions in the aspects of chloride binding and corrosion inhibition . These findings are expected to advance the design of high-durable cement-based materials serviced in the marine environment.
研究领域:
建筑材料
·
土木工程材料
·
腐蚀科学
·
纳米材料应用
·
混凝土耐久性
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DOI
高影响因子
危险品化学品经营许可证（带存储）