The composites of carbon nanotube (CNT) supported by Sn-doped MnO2 with enhanced capacitance have been fabricated with varying dopant concentrations. The composites have been subjected to physiochemical, configurational, and morphological analyses by FTIR, UV–Vis spectroscopy, X-ray diffraction and field emission scanning electron microscopy, high resolution transmission electron microscopy and selected area electron diffraction studies. The electrochemical performance of the composite has been evaluated by cyclic voltammetry and charge/discharge techniques. Highest specific capacitances of 940 F g−1 at a current density of 0.35 A g−1 and 927 F g−1 at 5 mV s−1 in 1 M Na2SO4 electrolyte solution was achieved in the case of 5% Sn doped composite. Moreover, the electrode demonstrated good cycling performance and retaining 79.7% of the initial capacitance over 3000 cycles. The superior electrochemical performance is accredited mainly to the porous sheath hierarchical architecture, which consist of inter connected MnO2 nanoneedles uniformly coated over the CNT surface. This peculiar architecture is responsible for fast ion/electron transfer and easy access of the active material.
Effects of multi-walled carbon nanotube (MWCNT) type and flow type (shear and elongational flow) on the electrical conductivity of polycarbonate (PC)/MWCNT nanocomposites were investigated. Two different MWCNTs produced a huge difference in electrical conductivity in an injection molded PC/MWCNT nanocomposite. It was observed that MWCNTs having a higher aspect ratio provide much lower electrical conductivity in injection molded PC/MWCNT nanocomposites while the conductivities of compression molded samples from two different MWCNTs were the same. We found that this is due to a difference in the deformability of the two MWCNTs. Nanocomposite samples prepared at a higher extensional rate and shear rate showed lower electrical conductivity. This is attributed to flow induced orientation of the MWCNTs. The experimental results were discussed in relation to variation in the tube–tube contact due to the change of the MWCNT orientation.
탄소나노튜브(CNT) 기반의 멤브레인은 높은 물 전달률과 직경에 따른 이온 배제율로 해수담수, 물질 정화 등을 위한 분리막으로써의 가능성을 보여 주었다. 이온 선택성은 CNT 기반 멤브레인의 응용 분야를 확대하기 위한 중요한 요소이며, 기능기를 이용하여 이온 선택성의 조절이 가능함이 보고되었다. 다양한 원자가/크기의 이온이 혼합될 경우, 이온-기능기간 작용력 뿐만 아니라 이온-이온간의 작용력, 이온의 크기에 의한 반발력 등이 복합적으로 작용한다. 이에 본 연구에서는 분자동역학 전산모사를 통하여, 상이한 원자가/크기를 가진 이온의 혼합이 기능화된 CNT의 이온 선택성에 미치는 영향을 연구 하였다. Potential of Mean Force 계산을 통하여 이온 투과에 대한 자유 에너지 장벽을 계산하였으며, CNT 크기 변화, 전하량 변화를 통하여 이온 선택성과 배제에 영향을 미치는 요소를 분석하였다. 본 연구는 CNT 멤브레인을 이용한 분리막 설계, 생체 이온 전달 채널 모사 등에 유용할 것으로 기대한다.
본 연구에서는 탄소나노튜브/화이버/폴리머 복합소재 구조에 대한 재료 물성 및 강성 추정을 다룬다. 수정된 Halpin-Tsai 모델을 적용한 멀티 스케일 해석은 탄소나노튜브의 함유량 비율, CNT 두께-길이 비율, 화이버 부피 함유량, 그리고 화이버 보강각도 변화에 따라서 수행되었다. 본 연구에서 제시한 멀티-스케일 접근방법은 기존 모델을 적용하여 얻은 결과와 비교하여 검증하였다. 매개변수 해석을 통하여 CNT의 적절한 함유량은 적층된 CNTFPC 구조의 구조성능의 향상시킬 수 있는 중요한 특성을 규명하였다.
A conductive additive is prepared by dispersing multi-walled carbon nanotubes (MWCNTs) on Cu powder by mechanical milling and is distributed in epoxy to enhance its electrical conductivity. During milling, the MWCNTs are dispersed and partially embedded on the surface of the Cu powder to provide electrically conductive pathways within the epoxy-based composite. The degree of dispersion of the MWCNTs is controlled by varying the milling medium and the milling time. The MWCNTs are found to be more homogeneously dispersed when solvents (particularly, non-polar solvent, i.e., NMP) are used. MWCNTs gradually disperse on the surface of Cu powder because of the plastic deformation of the ductile Cu powder. However, long-time milling is found to destroy the molecular structure of MWCNTs, instead of effectively dispersing the MWCNTs more uniformly. Thus, the epoxy composite film fabricated in this study exhibits a higher electrical conductivity than 1.1 S/cm.
Nickel oxide(NiO) thin films, nanorods, and carbon nanotube(CNT)/NiO core-shell nanorod structures are fabricated by sputtering Nickel at different deposition time on alumina substrates or single wall carbon nanotube templates followed by oxidation treatments at different temperatures, 400 and 700 oC. Structural analyses are carried out by scanning electron microscopy and x-ray diffraction. NiO thinfilm, nanorod and CNT/NiO core-shell nanorod structurals of the gas sensor structures are tested for detection of H2S gas. The NiO structures exhibit the highest response at 200 oC and high selectivity to H2S among other gases of NO, NH3, H2, CO, etc. The nanorod structures have a higher sensing performance than the thin films and carbon nanotube/NiO core-shell structures. The gold catalyst deposited on NiO nanorods further improve the sensing performance, particularly the recovery kinetics.
Free-standing electrodes of CuO nanorods in carbon nanotubes (CNTs) are developed by synthesizing porous CuO nanorods throughout CNT webs. The electrochemical performance of the free-standing electrodes is evaluated for their use in flexible lithium ion batteries (LIBs). The electrodes comprising CuO@CNT nanocomposites (NCs) were characterized by charge-discharge testing, cyclic voltammetry, and impedance measurement. These structures are capable of accommodating a high number of lithium ions as well as increasing stability; thus, an increase of capacity in long-term cycling and a good rate capability is achieved. We demonstrate a simple process of fabricating free-standing electrodes of CuO@ CNT NCs that can be utilized in flexible LIBs with high performance in terms of capacity and cycling stability.
We fabricated a Li-S battery with post-treated carbon nanotube (CNT) films which offered better support for sulfur, and investigated the effect of the surface properties and pore structure of the post-treated CNT films on Li-S battery performance. Post-treatments, i.e., acid treatment, unzip process and cetyltrimethylammonium bromide (CTAB) treatment, effectively modified the surface properties and pore structure of the CNT film. The modified pore structure impacted the ability of the CNT films to accommodate the catholyte, resulting in an increase in initial discharge capacity.
This paper presents a method to deice concrete pavement with carbon nanotube (CNT) so as to avoid the adverse effects of conventional deicing method such as salt on the structure, function and environment. To meet the research objective, laboratory tests were incorporated with finite element method. Laboratory tests conducted with CNT embedded inside the slab to investigate how far the heat transfers on the surface temperature of above 0oC when CNT generates the target temperature of 60oC in the freezer temperature of -10oC. Also, the cases of three different spacing of 15, 20 and 30 cm between CNTs were conducted to determine the maximum allowable spacing of CNT. Along with these experimental tests, heat transferring analysis conducted to validate the test results.
본 연구에서는 해수를 유도용액으로 사용하고 하수처리수를 공급수로 사용하는 정삼투막 공정의 유기/바이오 오염물에 의한 막오염을 저감하기 위해 폴리도파민/탄소 나노 튜브 복합 분리막을 제작하였다. 분리막은 기존 계면중합반응에 탄소 나노 튜브를 첨가하여 초박형 복합 분리막을 제조한 후, 폴리도파민으로 코팅시켜 제조하였다. 제작 된 분리막은 알긴산나트륨(Sodium alginate)용액과 미생물(Pseudomonas aeruginosa PA01) 부착 실험을 통하여 수투과도와 막오염도를 평가하였다. 그 결과, 폴리도파민/탄소 나노 튜브 복합 분리막은 복합되지 않은 분리막에 비하여 높은 수투과도와 낮은 막오염 성능을 보였다.
The microstructure, flexural properties, electrical conductivity, thermal conductivity and electromagnetic interference (EMI) shielding effectiveness (SE) of epoxy composites filled with multi-walled carbon nanotubes (CNTs), exfoliated graphite nanoplatelets (xGnPs) and CNT-xGnP hybrid filler were investigated. The EMI SE of the CNT-xGnP hybrid composite was higher than 25 dB at 100 MHz while that of the xGnP based composite was almost zero. The flexural modulus of the CNT-xGnP based epoxy composite continuously increased to 3.32 GPa with combined filler content up to 10 wt% while that of the CNT based epoxy composites slightly decreased to 1.96 GPa at 4 wt% CNT, and dropped to 1.57 GPa at 5 wt% loading, which is lower than that of epoxy. The CNT and CNT-xGnP samples had the same EMI SE at the same surface resistivity, because samples with the same surface conductivity have the same amount of the charge carriers.
The formation mechanism and photocatalytic properties of a multiwalled carbon nanotube (MWCNT)/TiO2- based nanotube (TNTs) composite are investigated. The CNT/TNT composite is synthesized via a solution chemical route. It is confirmed that this 1-D nanotube composite has a core-shell nanotubular structure, where the TNT surrounds the CNT core. The photocatalytic activity investigated based on the methylene blue degradation test is superior to that of with pure TNT. The CNTs play two important roles in enhancing the photocatalytic activity. One is to act as a template to form the core-shell structure while titanate nanosheets are converted into nanotubes. The other is to act as an electron reservoir that facilitates charge separation and electron transfer from the TNT, thus decreasing the electronhole recombination efficiency.
The thermoelectric Seebeck and Peltier effects of a single walled carbon nanotube (SWCNT) quantum dot nanodevice are investigated, taking into consideration a certain value of applied tensile strain and induced ac-field with frequency in the terahertz (THz) range. This device is modeled as a SWCNT quantum dot connected to metallic leads. These two metallic leads operate as a source and a drain. In this three-terminal device, the conducting substance is the gate electrode. Another metallic gate is used to govern the electrostatics and the switching of the carbon nanotube channel. The substances at the carbon nanotube quantum dot/ metal contact are controlled by the back gate. Results show that both the Seebeck and Peltier coefficients have random oscillation as a function of gate voltage in the Coulomb blockade regime for all types of SWCNT quantum dots. Also, the values of both the Seebeck and Peltier coefficients are enhanced, mainly due to the induced tensile strain. Results show that the three types of SWCNT quantum dot are good thermoelectric nanodevices for energy harvesting (Seebeck effect) and good coolers for nanoelectronic devices (Peltier effect).
In this study, we report a general method for preparation of a one-dimensional (1D) arrangement of Au nanoparticles on single-walled carbon nanotubes (SWNTs) using biologically programmed peptides as structure-guiding 1D templates. The peptides were designed by the combination of glutamic acid (E), glycine (G), and phenylalanine (F) amino acids; peptides efficiently debundled and exfoliated the SWNTs for stability of the dispersion and guided the growth of the array of Au nanoparticles in a controllable manner. Moreover, we demonstrated the superior ability of 1D nanohybrids as flexible, transparent, and conducting materials. The highly stable dispersion of 1D nanohybrids in aqueous solution enabled the fabrication of flexible, transparent, and conductive nanohybrid films using vacuum filtration, resulting in good optical and electrical properties.
A TiO2/CNT nanohybrid photocatalyst is synthesized via sol-gel route, with titanium (IV) isopropoxide and multi-walled carbon nanotubes (MWCNTs) as the starting materials. The microstructures and phase constitution of the nanohybrid TiO2/CNT (0.005wt%) samples after calcination at 450oC, 550oC and 650oC in air are compared with those of pure TiO2 using field-emission scanning electron microscopy and X-ray diffraction, respectively. In addition, the photocatalytic activity of the nanohybrid is compared with that of pure TiO2 with regard to the degradation of methyl orange under visible light irradiation. The TiO2/CNT composite exhibits a fast grain growth and phase transformation during calcination. The nanocomposite shows enhanced photocatalytic activity under visible light irradiation in comparison to pure TiO2 owing to not only better adsorption capability of CNT but also effective electron transfer between TiO2 and CNTs. However, the high calcination temperature of 650oC, regardless of addition of CNT, causes a decrease in photocatalytic activity because of grain growth and phase transformation to rutile. These results such as fast phase transformation to rutile and effective electron transfer are related to carbon doping into TiO2.
탄소나노튜브(MWCNT)는 그 구조적 특징에 따라 열적, 기계적 안정성이 우수하며 고분자 매트릭스 내에 소량만 첨가하여도 향상된 물성을 얻을 수 있다. 그러나 탄소나노튜브를 고분자 복합체에 응용 시 분산이 필수적으로 요구되기 때문에 전처리 기술이 필요하다. 본 연구에서는 PEO 막의 CO2 투과도 향상을 위해 PEO/EVA 혼합물에 산처리를 통해 표면에 친수성기가 도입된 다중벽 탄소나노튜브(MWCNT-COOH)를 첨가하여 PEO/EVA/MWCNT 혼성막을 제조하였다. 제조된 혼성막의 특성을 FT-IR, TGA, SEM 분석으로 확인하였다.
Heavy metals are typical contaminant in water and need to be removed because they are non-biodegradable and can accumulate in human body. To remove metal and other contaminants from water, chemical absorbents are widely used due to their low cost. Herein, hybrid materials comprised of amylose and single wall carbon-nanotube (swCNT) was developed as the absorbent for water purification. A high adsorption properties of carbon-nanotubes have been utilized in designing effective absorbent but its poor dispersity in water is a limiting factor for practical use. Single wall carbon-nanotube was hybridized with amylose chain produced by enzyme reaction of amylosucrase and their tendency to self-assemble in aqueous environment. The amylose-swCNT microparticles were characterized by FE-SEM and turned out to be spherical structure with CNTs embedded throughout the amylose matrix. The ability of amylose-CNT microparticles to remove copper was examined. Concentration of copper was decreased after reaction with amylose-swCNT microparticles. Although amount of decreasing copper was less than swCNT on same total mass, Adsorption efficiency of amylose-swCNT microparticles was good because their swCNT content was only 10% of total mass.