APPLIED SURFACE SCIENCE
·
2022
·
IF 7.392
Chitengfei Zhang,Liuyi Cai,Rong Tu,Yingqiu Zheng,Bao-Wen Li,Song Zhang
Due to its nontoxicity, suitable bandgap, high defect tolerance and high electron mobility, layered BiI 3 has been gaining attention in photoelectric device and nonlinear optics field. However, the growth of large-size single crystal 2D BiI 3 has not been achieved. Herein, the synthesis of single crystal 2D BiI 3 on mica substrate via a cooling-induced growth method is reported, with the thickness of 8 ∼ 1000 nm and a lateral dimension of 110 ∼ 1000 μm. X-ray diffraction and selected area electron diffraction demonstrate the single crystal nature of 2D BiI 3 flakes. The high temperature during heat preservation step prevents the deposition of BiI 3 vapor, and then, when proceeding to cooling-induced growth step, single crystal 2D BiI 3 flakes start to nucleate on colder mica substrate and grow up to ∼ 1000 μm (lateral dimension) rapidly. The stability test indicates the 2D BiI 3 flake decomposes with the present of both O 2 and water. Finally, the cooling rate, height of crucible, holding temperature and type of substrate have also been investigated to show the structural evolution of 2D BiI 3 flakes.
研究领域:
材料科学
·
凝聚态物理
·
纳米材料
·
晶体生长
·
光电器件
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DOI
高影响因子
MICROPOROUS AND MESOPOROUS MATERIALS
·
2012
·
IF 3.285
Yi Liu,Hai-Xiao He
Mesoporous alumina with a narrow pore size distribution is synthesized by direct thermolysis of Al-based coordination polymer. By applying the appropriate thermolysis temperature, both high surface area and large pore volume are obtained with the collapses and elimination of the 1,4-benzenedicarboxylate linkers of Al-based coordination polymer. This new class of mesoporous alumina display better adsorption properties and higher thermal stability, which retain mesoporous properties and high surface area after calcination in 900 °C. This thermolysis method provides a new approach to synthesize mesoporous alumina with high thermal stability by using coordination polymers.
研究领域:
材料科学
·
无机化学
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纳米材料
·
多孔材料
·
热分析
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DOI
高影响因子
Sustainable Energy & Fuels
·
2017
·Vol. 2
·期 2
·444-454
·
IF 0
Xiaohong Xia,Chunming Wang,Lang Liu,Yonglin Du,Weichun Ye
Transition metal dichalcogenides for electrocatalytic water splitting are important in renewable energy research, with studies showing that the edge structure and specific surface area are crucial to their electrocatalytic activity. Herein, the design and construction of yolk–shell nanospheres based on molybdenum diselenide-encapsulated molybdenum oxide are reported. Their structures were characterized using various techniques, which showed that the void space between the interior core and outer shell increased the number of active sites. This yolk–shell structure exhibited enhanced and stable electrocatalytic activity in the hydrogen evolution reaction (HER). The HER current density at −0.5 V vs. the reversible hydrogen electrode was increased by 95% (to −256 mA cm−2) compared to that of traditional flower-like molybdenum diselenide. The overpotential of this yolk–shell structure, which was required to drive a current density of −10 mA cm−2, was 65 mV lower than that of flower-like molybdenum diselenide (286 mV). Furthermore, long-term potential cycling and potentiostatic measurement of this catalyst showed favorable stability and durability of electrocatalytic activity. This yolk–shell structure plays a key role in energy conversion processes central to several renewable energy technologies.
研究领域:
材料科学
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纳米科技
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电化学
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能源化学
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催化化学
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DOI
Journal of Materials Chemistry A
·
2018
·Vol. 6
·期 24
·11370-11376
·
IF 9.931
Qinglong Fu,Pan Yang,Jingchuan Wang,Hefang Wang,Lijun Yang,Xiaochong Zhao
Simple, safe and economic methods to prepare Ni nanofibers are required for their practical application. Herein, an in situ vacuum thermal reduction strategy is proposed to synthesize Ni nanofibers on a large scale, which involves electrospinning of a nickel acetate/polyvinylpolypyrrolidone/ethyl cellulose (NiAc/PVP/EC) precursor solution, followed by vacuum thermal treatment. Characterization of the morphology and microstructure reveals that the as-prepared Ni nanofibers are composed of nano-size Ni grains and possess a large surface area. Moreover, it has been demonstrated that the content of EC is closely related to the size of Ni grains and thus the surface area of Ni nanofibers. On account of their high specific surface area, the as-prepared Ni nanofibers exhibit efficient catalytic properties for H2 generation from hydrous hydrazine in an alkaline solution.
研究领域:
材料科学
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纳米技术
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催化化学
·
能源材料
·
物理化学
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DOI
高影响因子
Progress in Natural Science-Materials International
·
2019
·Vol. 29
·期 4
·379-383
·
IF 3.31
Yongsheng Fu,Jun Li,Jianguo Li
The effect of CdS content on the photo-induced improvement of hydrogen evolution reaction activity of the Pt/CdS electrocatalyst was investigated. Although the electrons transferred from CdS to Pt in the Pt/CdS electrocatalyst increased with the CdS content under illumination, the electrochemical active surface area of the Pt/CdS electrocatalyst decreased with the CdS content, resulting that the photo-induced improvement of hydrogen evolution reaction activity of the Pt/CdS electrocatalyst decreased with the CdS content.
研究领域:
材料科学
·
催化化学
·
物理化学
·
纳米材料
·
能源化学
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DOI
高影响因子
RSC Advances
·
2014
·Vol. 4
·期 98
·55256-55262
·
IF 3.708
Zhijian Wu,Ya Xiong,Guoqiang Guan,Lingjun Kong,Shuanghong Tian
A new pyrolytic process was successfully used to prepare hollow-like spherical sludge chars (HSC). In the process, pre-formed cotton spheres with a low density were firstly coated by a layer of sludge paste containing ZnCl2 to form cotton fiber@sludge spheres and then pyrolyzed at 500 °C for 2 h. The resulting HSC possessed a diameter of about 3 mm, a low density of 0.1008 g cm−3 and a high surface area of 1008 m2 g−1. The column adsorption behavior showed that the adsorption capacity and rate constant of HSC for methylene blue reached 186.4 mg g−1 and 0.232 mL min−1 mg−1. The adsorption capacity is about 8.4 and 12 fold of the adsorption capacities of GAC (22.28 mg g−1) and SC (15.26 mg g−1), respectively, and the adsorption rate constant is about 1.3 fold of that of GAC and SC. The great adsorption capacity and rate constant can be considerably dependent on the special hollow-like spherical structure of HSC.
研究领域:
环境科学
·
材料科学
·
化学工程
·
污染控制
·
吸附技术
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DOI
高影响因子
ENVIRONMENTAL POLLUTION
·
2021
·
IF 8.071
Yanping Bao,Jinhao Lai,Yishun Wang,Zheng Fang,Yongshi Su,Daniel S. Alessi,Nanthi S. Bolan,Xiaolian Wu,Yan Zhang,Xueding Jiang,Zhihong Tu,Hailong Wang
Iron (III) co-precipitation with dissolved organic matter (DOM) is pervasive in many natural environments. However, the effects of DOM on the formation of Fe(III) hydroxysulfate (FHS) and its environmental implications are poorly understood. In this study, fulvic acid (FA) was used as a model DOM compound, and experiments were devised to investigate the effects of FA on the formation of FHS. In addition, the Pb(II) adsorption capabilities of FHSs biosynthesized under various FA dosages, including kinetics and sorption isotherm experiments, were conducted. These experiments showed that co-precipitation of FA promoted the formation of Fe-FA composites, FA-doped schwertmannite , and small particles of jarosite . Co-precipitates are more enriched in carboxyl (–COOH) functional groups due to their preferential binding with FHS. The adsorption kinetics , isotherms and mechanisms of Pb onto the biosynthesized FHSs were then comprehensively characterized and modeled. Though the specific surface area decreased with increasing FA loading, the introduction of FA into FHSs increased Pb(II) adsorption, with the highest concentration of FA addition improving the removal capacity of Pb(II) to 91.54%. Kinetics studies and intra-particle diffusion models indicated that the adsorption of Pb(II) onto the FHSs was correlated with the number of active sites, and two adsorption steps: surface adsorption and the diffusion of Pb(II) in channels inside the biosynthesized FHSs, are suggested. The adsorption mechanism was attributed to cation exchange between Pb(II) and –OH and –COOH functional groups, and the co-precipitated FA provided additional sites for Pb(II) adsorption by FHS.
研究领域:
环境地球化学
·
水处理技术
·
胶体与界面化学
·
污染控制化学
·
功能材料
·
吸附科学
✓ 已验证
DOI
高影响因子
JOURNAL OF MOLECULAR LIQUIDS
·
2020
·
IF 5.065
Jianwei Bai,Xiaofei Ma,Cen Gong,Yiming Chen,Huijun Yan,Kewei Wang,Jun Wang
Traditional adsorption resin prepared by a low efficiency method has a low porosity and surface area , which limits the adsorption performance of the resin. Therefore, a novel porous resin was developed by structural design of the resins through post- modification with HPA and a post-crosslinked method. The novel porous post-modification resin was successfully prepared by the multistep method. Meanwhile, the high surface area and abundant micropores in HCR-AO can improve the adsorption rate by accelerating the diffusion of uranium in the external diffusion stage. The removal capacity of HCR-AO increased 366% for HCR and 120% for PSD-AO at the same initial concentration. HCR-AO takes less time to reach equilibrium than PSD-AO and HCR. Excitingly, the adsorption amount of the material dropped only slightly even after 8 cycles. The short equilibrium time and outstanding removal efficiency makes it a novel candidate for further extraction of U (VI) from seawater .
研究领域:
环境化学
·
核化学
·
材料科学
·
吸附分离
·
海洋资源提取
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DOI
高影响因子
ENVIRONMENTAL RESEARCH
·
2021
·
IF 6.498
Xiulei Fan,Zixuan Ma,Yefeng Zou,Jiaqiang Liu,Jun Hou
In recent years, tire wear particles (TWP), as the significant proportion of microplastics (MPs), has adsorbed much attention due to its widespread presence in aquatic ecosystem . Compared with typical MPs, TWP exists significant differences in composition, additives, characteristics and so on. With TWP and polypropylene (PP) as target MPs, Cd 2+ and Pb 2+ as target pollutants, the adsorption-desorption characteristics of heavy metal ions on original and aged MPs were studied. Compare with the PP, the S BET of TWP increased more significantly after the UV ageing process. Meanwhile, the zeta potential of TWP increased from −8.01 to −14.6 mV and PP from −5.36 to −9.52 mV, and the surface of the TWP were more negatively-charged. In addition, the hydrophilicity of MPs enhanced due to the increased oxygen-containing functional groups after ageing process. Compared with PP, the physicochemical properties of TWP changed more obviously during UV ageing processes. The adsorption results showed that the pseudo-second-order model could better describe the adsorption processes of Cd 2+ and Pb 2+ on MPs. Meanwhile, the orders of adsorption capacity of MPs for Cd 2+ and Pb 2+ were aged TWP > aged PP > original TWP > original PP. The phenomenon of adsorption confirmed that TWP had better vector effects for heavy metal ions than PP, and the ageing processes could enhance the adsorption capacity of MPs. Moreover, the desorption results demonstrated that, compared with PP, the TWP (with higher adsorption capacity) also had the better desorption capacity for heavy metal ions in simulated gastric fluid. Compared with PP, the TWP might cause a more serious hazard to aquatic environment and organisms. These investigations would contribute to assessing the potential environmental and biological risk of TWP, especially considering the effect of the ageing process.
研究领域:
环境科学
·
生态毒理学
·
微塑料污染
·
水生生态系统
·
环境化学
✓ 已验证
DOI
高影响因子
Journal of Nanomaterials
·
2019
·Vol. 2019
·期 1
·5290496
·
IF 2.233
Zhenzhu Yu,Fei Nan,Lu Su,Shaofei Zhang,Yan He
Intercalation and exfoliation are key steps in the preparation of graphene by thermal exfoliation, and they determine the quality of the final product. Therefore, it is important to explore the influence of intercalation agents on the intercalation and exfoliation of graphite. In this article, ammonium bicarbonate is intercalated into graphite with different degrees of oxidation to form a graphite intercalation compound (GIC) by means of ultrasound and stirring. Then, they are exfoliated by being heated at high temperatures. After ammonium bicarbonate intercalation and heating treatment, XRD, TG, and BET show that the intercalation and exfoliation effect of graphite oxide (GO) is better than that of graphite (G) and expanded graphite (EG). The intercalation mechanism is that the ammonia molecule in ammonium bicarbonate solution contains a wedge-shaped structure and active point, which provides empty orbits for graphite electrons and forms edge intercalation through physical interaction at the same time.
研究领域:
材料科学
·
纳米材料
·
物理化学
·
碳材料
·
功能材料
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DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2018
·
IF 6.735
Wei Teng,Nan Bai,Zehan Chen,Junming Shi,Jianwei Fan,Wei-xian Zhang
Porous carbon is the most important and most common adsorbent for the separation and treatment of organic pollutants. Characteristics such as accessible and large surface area, physical and chemical stability, and low-cost manufacturing method are desired for any adsorbent. Herein, a hierarchically porous carbon (HPC) was prepared by pyrolysis and graphitization of crystalline metal–organic frameworks (MOF-5) for enhanced adsorption of aromatic contaminants. The material treated at high temperature (950 °C) possesses large surface area (1512 m 2 /g), high porosity (0.94 cm 3 /g), and hierarchically porous structures. The generated mesopores around 4 nm improve the interconnectivity of micro- and macropores to make the porous material ideal for sorption of organic pollutants such as aromatic hydrocarbons. Effects of adsorbent dose, pH, ionic strength, contact time, and initial concentration on the adsorption of p -nitrophenol (PNP, as a model) were investigated. Adsorption isotherms and kinetics suggest that the adsorption is a spontaneous and endothermic physisorption process with monolayer surface coverage. The surface sites are electron-rich due to the graphitic layer, which has high affinity toward π electrons of the aromatic ring. The adsorption capacity of the hierarchically porous carbon (HPC) is nearly over 100% higher that of conventional activated carbon.
研究领域:
环境科学
·
材料科学
·
物理化学
·
吸附分离
·
污染治理
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DOI
高影响因子
Asia-Pacific Journal of Chemical Engineering
·
2022
·Vol. 17
·期 4
·e2769
·
IF 1.777
Hao Qiu,Shanshan Jiang,Yingjie Niu,Qi Zhang,Yingping Pang,Chao Su
The electrochemical performance of solid oxide fuel cells (SOFCs) is highly reliant upon the properties of cathodes, including crystal structure, electrical conductivity, electrode thickness, and so on. Here, Ba 0.5 Sr 0.5 Co 0.8 Fe 0.2 O 3-δ (BSCF) is synthesized and served as the electrode for enabling high-performance SOFCs. The effect of electrode thickness on the electrocatalytic activity is systematically investigated. The electrode thickness is adjusted in two ways. One is spray-coating and then calcining once, and the other is performing the above process twice. On the basis of symmetrical cells configuration, the oxygen reduction reaction (ORR) activity of BSCF electrode with different thickness is evaluated and analyzed by the electrochemical impedance spectroscopy (EIS) technique and distribution of relaxation time (DRT). The obtained area-specific resistances (ASRs) of electrodes on the oxygen ion conducting electrolyte Sm 0.2 Ce 0.9 O 1.90 (SDC) demonstrate the thickness-dependent electrochemical activity in ORR of BSCF electrode. With an electrode thickness of 24 μm that controlled by conducting “spray-coating and calcining” twice, the BSCF electrode displays the optimal electrochemical performance with an ASR of 0.072 Ω cm 2 in ambient air at 600°C. This strategy has allowed us to produce an electrode layer with optimal thickness, paving a new path for the design of high-performance SOFCs.
研究领域:
材料科学
·
电化学
·
能源材料
·
固体离子学
·
燃料电池技术
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DOI
高影响因子