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RSC Advances · 2015 ·Vol. 5 ·期 27 ·20741-20746 · IF 3.84

Cost-effective preparation and sensing application of conducting polymer PEDOT/ionic liquid nanocomposite with excellent electrochemical properties

Ge Sheng,Guiyun Xu,Shenghao Xu,Shiying Wang,Xiliang Luo

A conducting polymer based composite material of poly(3,4-ethylenedioxythiophene) (PEDOT) doped with pure insoluble ionic liquid (IL), 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, was prepared through a cost-effective electrodeposition method. A very tiny amount of insoluble IL (less than 15 μL), containing 0.1 M conducting polymer monomer, was drop-coated on an electrode surface and then used for electropolymerization using a homemade electrochemical cell filled with aqueous supporting electrolyte. With this design, the consumption of expensive IL for the preparation of the PEDOT/IL composite was greatly reduced, and thus effectively reduced the cost. The prepared PEDOT/IL composite was found to be highly conductive and stable, and it exhibited a highly nanoporous microstructure and excellent electrocatalytic activity toward the oxidation of dopamine (DA). Based on the excellent stability and electrocatalytic activity of the PEDOT/IL nanocomposite, a highly stable, sensitive and selective DA sensor with a detection limit of about 51 nM was developed.

研究领域: 分析化学 · 生物传感器 · 纳米材料 · 电化学 · 神经化学 · 转化医学
✓ 已验证 DOI 高影响因子
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Journal of Materials Chemistry A · 2018 ·Vol. 7 ·期 11 ·5991-6000 · IF 9.931

A bimetallic thermally regenerative ammonia-based battery for high power density and efficiently harvesting low-grade thermal energy

Weiguang Wang,Hua Tian,Gequn Shu,Dongxing Huo,Fang Zhang,Xiuping Zhu

A bimetallic thermally regenerative ammonia-based battery (B-TRAB) using inexpensive materials efficiently converts low-grade thermal energy into electricity with high power density. Through thermal regeneration of the anolyte, the B-TRAB system realized high-voltage discharge (1.38 V) with redox couples [Cu(II)/Cu and Zn(NH3)42+/Zn] and low-voltage charge (0.72 V) with Zn(II)/Zn and Cu(NH3)42+/Cu. Adding 2 M NH3 to the anolyte of a Cu/Zn-TRAB produced a peak discharge power density of 525 W m−2-electrode (120 W m−2-membrane), and the voltage (or current) and peak power could be doubled by connecting two cells in series (or parallel). In successive regeneration cycles, a maximum power density of 115 W m−2-electrode (26 W m−2-membrane) and a net energy density of 714 W h m−3 were produced at a constant current density of 100 A m−2. The power density was enhanced to 515 W m−2-electrode (118 W m−2-membrane) and maintained in successive cycles by adding acid to the regenerated catholytes, with a net energy density of 299 W h m−3 (discharged at a constant load of 12 Ω and charged at a constant current density of 100 A m−2). A thermal-electricity conversion efficiency of 0.95% (10.7% relative to the Carnot efficiency) was achieved.

研究领域: 能源材料 · 电化学工程 · 热电转换技术 · 可持续能源 · 功能材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2012 ·Vol. 378 ·期 1 ·30-35 · IF 3.07

Preparation of bamboo-like PPy nanotubes and their application for removal of Cr(VI) ions in aqueous solution

Shangkun Li,Xiaofeng Lu,Xiang Li,Yanpeng Xue,Chengcheng Zhang,Junyu Lei,Ce Wang

A reactive-template vapor phase polymerization method for the preparation of bamboo-like polypyrrole (PPy) nanotubes has been successfully demonstrated in this paper. Herein, electrospun V 2 O 5 nanofibers were chosen as templates to deposit PPy, which served as the oxidants as well. This method can provide the fabrication of PPy nanostructures more easily than conventional routes due to its independence of removing template, which is usually a complex and tedious experimental process. The application of bamboo-like PPy nanotubes for Cr(VI) ions removal in aqueous solution has been explored. The resulting bamboo-like PPy nanotubes exhibited much higher adsorption performance than traditional PPy nanoparticles.

研究领域: 环境科学 · 纳米材料 · 高分子化学 · 环境污染治理 · 吸附技术
✓ 已验证 DOI 高影响因子
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CERAMICS INTERNATIONAL · 2021 ·Vol. 47 ·期 14 ·20310-20316 · IF 4.527

Hollow Co3O4 nanoparticles immobilized rGO/Carbon monolith as an electrode material for high-performance supercapacitors

Yang Yan,Linlin Zang,Tianwei Dou,Haicheng Li,Liguo Sun,Yanhong Zhang

In this work, we prepared a hollow Co 3 O 4 nanoparticles (NPs) immobilized reduced graphene oxide (rGO)/carbon monolith (HCGCM) via a one-step carbonization method. The doping of nanomaterial and transition metal oxide can improve the poor conductivity and low capacitance of pure carbonaceous materials. The optimal addition concentration of polystyrene microspheres as a template provided the HCGCM composite with a hierarchical pore structure and a large specific surface area (1600 cm 2 /g), which is conducive to generating sufficient electroactive sites. At the same time, three dimensional (3D) interconnected pores shorten ion transport paths and reduced diffusion resistance of ions. Due to the existence of pseudocapacitive behavior, the HCGCM composite, as an electrode material working in a three-electrode system, achieved a high capacitance value of 1106 F/g at a current density of 1 A/g. In two-electrode system, the asymmetric supercapacitor had excellent stability performance and remained about 86.7% capacitance after 5000 cycles test. Moreover, it also exhibited a maximum energy density of 66.7 Wh/kg at power density of 750 W/kg. Thus, the strategy of manufacturing 3D porous electrodes is beneficial to improve the overall electrochemical performance of supercapacitors .

研究领域: 材料科学 · 电化学 · 纳米科技 · 能源存储 · 功能材料
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2018 · IF 6.735

Sedimentary phosphorus immobilization with the addition of amended calcium peroxide material

Jing Zhou,Dapeng Li,Shutong Chen,Yao Xu,Xue Geng,Chaoran Guo,Yong Huang

The immobilization of sedimentary phosphorus (P) by capping sediments with amended calcium peroxide material (ACPM) and CaO 2 was investigated, the sediments and overlying water from a black-odor river. Under the capping with ACPM and CaO 2 , the pH and dissolved oxygen (DO) in the overlying water were higher than in the control. This contributed to the more loss of external P under the ACPM (the phosphate sorption was fitted well by the Langmuir equation, the maximum P sorption capacity up to 29.28 mg P g −1 ). Additionally, ACPM improves the decrease of the reduction materials (e.g., NH 4 + -N, Fe 2+ ) in the pore water compared to that associated with CaO 2 , resulting in a less obvious dissolved inorganic P (DIP) in the pore water, but the accumulation of DIP in the pore water with CaO 2 suggested an explosive release once the micro-environment conditions encounters adverse conditions. The sharp reduction of Fe/Al-P and Res-P contributes to the increase of DIP in the pore water, with a release of up to 390.60 mg P kg −1 DW (dry weight), whereas the value is only 62.55 mg P kg −1 DW when capped with ACPM. Correspondingly, the percentage of the bioavailable P to Tot-P decreases rapidly from 17.27% (control, 0–2 cm) to 7.21% (ACPM, 0–2 cm) and 10.57% (CaO 2 , 0–2 cm), indicating the obvious P immobilization. The implication is that the application of CaO 2 is not suitable for direct use, while the combination with other materials (e.g., WPS) is a better choice.

研究领域: 环境科学 · 水体修复 · 环境化学 · 污染控制 · 沉积物管理
✓ 已验证 DOI 高影响因子
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Journal of Energy Chemistry · 2023 · IF 13.1

Reducing voltage hysteresis of metal oxide anodes to achieve high energy efficiency for Li-ion batteries

Xuexia Lan,Xingyu Xiong,Jie Cui,Renzong Hu

In the past two decades, a lot of high-capacity conversion-type metal oxides have been intensively studied as alternative anode materials for Li-ion batteries with higher energy density. Unfortunately, their large voltage hysteresis (0.8–1.2 V) within reversed conversion reactions results in huge round-trip inefficiencies and thus lower energy efficiency (50%–75%) in full cells than those with graphite anodes. This remains a long-term open question and has been the most serious drawback toward application of metal oxide anodes. Here we clarify the origins of voltage hysteresis in the typical SnO 2 anode and propose a universal strategy to minimize it. With the established in situ phosphating to generate metal phosphates during reversed conversion reactions in synergy with boosted reaction kinetics by the added P and Mo, the huge voltage hysteresis of 0.9 V in SnO 2 , SnO 2 -Mo, and 0.6 V in SnO 2 -P anodes is minimized to 0.3 V in a ternary SnO 2 -Mo-P (SOMP) composite, along with stable high capacity of 936 mA h g −1 after 800 cycles. The small voltage hysteresis can remain stable even the SOMP anode operated at high current rate of 10 A g −1 and wide-range temperatures from 60 to −30 °C, resulting in a high energy efficiency of 88.5% in full cells. This effective strategy to minimize voltage hysteresis has also been demonstrated in Fe 2 O 3 , Co 3 O 4 -basded conversion-type anodes. This work provides important guidance to advance the high-capacity metal oxide anodes from laboratory to industrialization.

研究领域: 电化学 · 材料科学 · 能源存储 · 纳米材料 · 固态化学 · 电池技术
✓ 已验证 DOI 高影响因子
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PHYSICAL CHEMISTRY CHEMICAL PHYSICS · 2020 ·Vol. 22 ·期 17 ·9362-9367 · IF 3.43

Unveiling the atomic defects and electronic structure of Cu2.2Zn0.8SnSe4−xTex (x = 0 to 0.04) by X-ray absorption fine structure spectroscopy

Weifeng Huang,Yingcai Zhu,Yong Liu,Lijuan Liu,Changchun Yang,Wei Xu

The quaternary chalcogenides consisting of earth-abundant elements such as Cu2ZnSnSe4 (CZTSe) have promising electrical and optical properties prompting enormous technological interest. Understanding different types of defects including Cu/Zn ordering is believed to be the key point to tackle technological challenges such as a large open circuit voltage deficit in CZTSe. The Te doped Cu2.2Zn0.8SnSe4−xTex (x = 0.01–0.04) were investigated using X-ray absorption fine structure spectroscopy at the Cu, Zn, and Se K-edges as well as at the Te L3-edge. Cu at the zinc site with anti-site defects and oxygen interstitials are identified. The detailed electronic structure upon Te doping is studied, providing insights into the rich defect chemistry present in this compound.

研究领域: 材料科学 · 凝聚态物理 · 无机化学 · 半导体材料 · 光电功能材料
✓ 已验证 DOI 高影响因子
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PROGRESS IN ORGANIC COATINGS · 2020 · IF 4.469

Phosphorylated polymer/anionic surfactant doped polypyrrole in waterborne epoxy matrix toward enhanced mechanical and chemical resistance

Haihua Wang,Wenjing Zhang,Yongning Ma,Guiqiang Fei,Huan Wen,Liyu Sun,Yanming Shao,Yong-Mook Kang

The compatibility between polypyrrole (PPy) and waterborne epoxy coating (EP) remains the main challenge. Here, phosphorylated poly (vinyl alcohol) (PPVA) and p-toluene sulfonic acid sodium (p-TSA) were simultaneously utilized as dopants to modify PPy and prepare water dispersible PPVA/p-TSA/PPy (PPVAT/PPy) solution. Additionally, poly (vinyl alcohol) (PVA) and TSA were also adopted to prepare PVA/p-TSA/PPy (PVAT/PPy) for comparison. Denser film with granular morphology was observed for PPVAT/PPy nanocomposite film. Compared with PVAT/PPy-40 %, the tensile strength of PPVAT-8.0 %/PPy-40 % increased from 248.8–283.9 MPa. PPVAT/PPy displayed higher compatibility and interactions with EP compared to PPy-TSA and PVAT/PPy. Compared with EP, the impedance modulus of PVAT/PPy+EP and PPVAT/PPy+EP increased from 3.17×10 5 to 1.07×10 8 and 1.62×10 9 Ω·cm 2 ; corrosion current density I corr decreased from 1.49×10 −6 to 7.72×10 -8 and 4.01×10 -9 A·cm -2 ; corrosion potential E corr displayed a positive shift of 230 mV and 269 mV, respectively. The corrosion inhibition efficiency of PPVAT/PPy+EP reached 99.83 %, which is much higher than that of PVAT/PPy+EP (93.97 %). PPVAT/PPy+EP nanocomposite coating has been proved to have preferable long-term corrosion resistance based on electrochemical impedance spectra (EIS), polarization curves and salt water spray test. The simultaneous incorporation of phosphate anions, sulfate ions and PPy into EP was beneficial to fabricate high-performance anticorrosion coating.

研究领域: 材料科学 · 高分子化学 · 腐蚀防护 · 纳米复合材料 · 表面工程
✓ 已验证 DOI 高影响因子
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MATERIALS LETTERS · 2017 · IF 2.572

Synthesis of bioactive polyvinyl alcohol/silica hybrid fibers for bone regeneration

Shu-Hui Xia,Shu-Hua Teng,Peng Wang

Polyvinyl alcohol/silica (PVA/SiO 2 ) hybrid fibers were prepared via a sol–gel combined electrospinning technique, and their potential application in bone tissue engineering was evaluated in terms of in vitro bioactivity. When the PVA concentration was 8%, the obtained PVA/SiO 2 hybrid fibers exhibited a uniform and continuous morphology, with an average fiber diameter of about 542.9 nm. The SiO 2 xerogel phase was uniformly distributed within the PVA matrix, and its actual content was very close to the theoretical value. After 3 days of immersion in simulated body fluid (SBF), the PVA/SiO 2 hybrid fibers displayed a vigorous precipitation of lamellar apatite crystals, reflecting their excellent in vitro bioactivity.

研究领域: 生物材料学 · 组织工程 · 纳米医学 · 生物医学工程 · 无机非金属材料 · 再生医学
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

A multifunctional nano filler for solid polymer electrolyte toward stable cycling for lithium-metal anodes in lithium–sulfur batteries

XinLong Zhang,HaiYan Zhang,Yuan Geng,ZhangQin Shi,Sheng Zhu,QunJie Xu,YuLin Min

Lithium–sulfur (Li–S) batteries are considered as very promising energy storage systems due to their higher theoretical performance and lower active material cost. However, the notorious shuttle effect and lithium dendrite growth have severely restricted the industrial production of Li–S batteries. In this study, we used polyethylene oxide (PEO) as the matrix and added multifunctional nanofillers (nano In 2 O 3 ) to effectively inhibit the shuttle effect caused by the dissolution of lithium polysulphides (LiPSs) in Li–S batteries. As a multifunctional filler, nano-In 2 O 3 not only improves the ionic conductivity of the PEO electrolyte, but also forms a Li–In alloy layer in situ at the polymer/anode interface, which can cause the rapid diffusion of lithium ions and prevent the side reactions between lithium metal anode and the electrolyte. Achieving the effect of stabilizing the lithium metal anode and suppressing the shuttle effect. Multiple problems in the system are solved by introducing a single component with multiple functions. The symmetrical lithium battery based on the PEO/LiTFSI/In 2 O 3 solid polymer electrolyte (PEO/LiTFSI/In 2 O 3 SPE) has higher cycle stability (over 1200 h) because it is more stable to the lithium metal anode. The Li–S full battery also exhibits excellent electrochemical performance. After 500 cycles at 1C, its capacity can be maintained at 570 mAh g −1 , the capacity decay rate is 0.038%. The coulombic efficiency (CE) during the cycle is also close 100%.

研究领域: 电化学 · 能源材料 · 固态离子学 · 电池技术 · 纳米复合材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF CATALYSIS · 2018 · IF 6.759

Catalytic oxidation of ethyl acetate over Ru–Cu bimetallic catalysts: Further insights into reaction mechanism via in situ FTIR and DFT studies

Xiaolong Liu,Qingzhen Han,Wenbo Shi,Cheng Zhang,Erwei Li,Tingyu Zhu

In this work, ruthenium-based bimetallic catalysts of 1Ru-5 M/TiO 2 (M = Co, Ce, Fe, Mn, Cu, Ni) were prepared and evaluated in ethyl acetate oxidation. It was found that 1Ru-5Cu/TiO 2 gave the highest catalytic activity. The influence of CuO content and the preparation method on the catalytic activity was also studied. 1Ru-5Cu/TiO 2 showed great catalytic stability in the on-stream reaction test. The influence of H 2 O on the catalytic activity is presented. The bimetallic catalyst 1Ru-5Cu/TiO 2 showed better catalytic performance than the monometallic catalysts 1Ru/TiO 2 and 5Cu/TiO 2 . XRD, TEM, HAADF-STEM, H 2 -TPR, and XPS characterizations were conducted, and the synergistic effect between Ru and Cu was well presented. In situ FTIR studies were also conducted, and the reaction intermediates were revealed on the catalyst surface. The theoretical calculations suggested that ethyl acetate is more easily adsorbed on the CuO surface, while it reacts more easily on the RuO 2 surface . Accordingly, a reaction mechanism for the catalytic oxidation of ethyl acetate over a Ru-Cu bimetallic catalyst is proposed.

研究领域: 催化化学 · 环境化学 · 表面科学 · 材料化学 · 物理化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF HAZARDOUS MATERIALS · 2021 · IF 10.588

Three porous shapeable three-component hydrogen-bonded covalent-organic aerogels as backfill materials in a simulated permeable reactive barrier (PRB) for trapping levofloxacin

Fangyuan Zhang,Mei Hong,Jing Bai,Zhi Liu,Aiyuan Jia,Zhisheng Liu,Can Shi,Yangxue Li

Levofloxacin (LEV) infiltrated in groundwater has threatened the safety of drinking water . For in-situ remediation of LEV-contaminated groundwater, there exists a main challenge of exploiting proper high efficient backfill medium in utilizing charming permeable reactive barriers (PRBs). Herein, three porous shapeable three-component hydrogen-bonded covalent organic aerogels (H C OA-1, H C OA-2 and H C OA-3) were fabricated based on a multiple-linking-site strategy to evaluate for adsorptive removal of LEV. The three H C OAs exhibited satisfactory performance in LEV adsorption that could integrate high adsorption capacity, good antiion interference, excellent recyclability and wide pH tolerance. The different regularity of kinetics and isotherms of three H C OAs signified that electrostatic effect, pore preservation, hydrogen bonding probably govern the adsorption process in combination, coupling with π-π electron-donor-acceptor (EDA), dipole-dipole and hydrophobic-hydrophobic interaction besides. In addition, the response surface methodology (RSM) was employed for studying the single and synergetic effects of selected variables and optimizing operation conditions. Furthermore, a laboratory PRB column packed with processable H C OA-2 was set up to investigate the LEV removal, and the breakthrough data was explained by Adams-Bohart, Thomas, BDST and Yoon-Nelson models. We believe could hopefully bring H C OAs into the real in-situ remediation of such challenging and persistent LEV-polluted groundwater with further massive-scale efficiently.

研究领域: 环境科学 · 材料科学 · 水污染控制 · 环境功能材料 · 污染物吸附 · 可持续修复技术
✓ 已验证 DOI 高影响因子
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