그래핀 기반 소재는 높은 가공성과 초박성으로 인하여 분리막 소재로서 각광받고 있다. 본 연구에서는, 스핀 코팅 법을 이용하여 제조된 산화그래핀 분리막의 기체 투과 거동을 평가하였다. 산화그래핀 분리막의 구조는 산화그래핀의 크기와 산화그래핀 용액의 pH 조절을 통하여 조절될 수 있다. 산화그래핀의 크기가 작을수록 굴곡률이 작아짐에 따라 분리막의 기 체 투과도 및 선택도가 증가하는 경향을 보인다. 또한 산화그래핀에서의 기체 투과 거동은 적층된 산화그래핀 사이의 채널 크기에 따라 영향을 받는다. 특히 산화그래핀 분리막의 좁은 기공과 이산화탄소 선택적인 산화그래핀 자체의 특성으로 인하 여 산화그래핀 분리막은 이산화탄소에 대한 높은 투과도 및 선택성을 가지며, 이는 이산화탄소 포집에 적합한 특성을 가진다. 이러한 산화그래핀 분리막의 특이한 기체 투과 거동은 흡착-촉진 확산 거동(표면 확산 기작)으로 설명될 수 있다. 본 연구를 통하여 이산화탄소 선택성 분리막 소재 설계와 슬릿 형태의 기공과 적층 구조를 가진 분리막을 통한 기체 투과 거동 연구가 활발히 이루어질 것으로 기대한다.

식품 포장, 전자 기기 등에 활용되고 있는 고분자 기반 기체 차단성 필름은 경량성, 낮은 제조 원가, 높은 가공성 으로 인하여 많은 주목을 받고 있다. 특히 전자기기에 활용되기 위하여, 기체 차단 필름은 매우 높은 수준의 기체 차단성을 요구받고 있다. 하지만 현재 수준의 고분자 기반 기체 차단 필름은 다른 소재와 비교하여 상대적으로 높은 수준의 기체 투과 유량을 보이고 있다. 따라서 기존의 고분자 필름이 가지고 있는 장점을 유지하면서 더 높은 수준의 기체 차단성을 부여하기 위한 요구가 증대되고 있다. 최근 그래핀 소재는 기체 차단을 위한 2차원 소재로서 각광받고 있다. 그러나 그래핀 소재의 낮 은 가공성과 어려운 대면적화 문제 때문에 산화그래핀이 그 대안으로서 떠오르고 있다. 산화그래핀은 높은 종횡비를 가지는 2차원 층상구조의 그래핀에 산소관능기를 함유한 형태로서, 수용성 혹은 극성 용매에 잘 분산되는 성질을 가지며, 따라서 대 량 생산에 용이한 특성을 가지고 있다. 본 연구에서는, 산화그래핀이 함유된 폴리이미드 나노복합막을 제조하였다. 폴리이미 드는 현재 널리 이용되고 있는 기체 차단성 고분자 중의 하나로서 높은 기계적 강도, 열적 안정성 및 내화학성을 가지고 있 다. 본 연구를 통하여 산화그래핀이 함유된 폴리이미드 나노복합막이 기체 차단성을 가지고 있음을 확인하였다. 더 나아가, Triton X-100이나 sodium deoxycholate (SDC) 등의 계면활성제를 나노복합막에 도입함으로써 산화그래핀의 고분자 매트릭스 내에서의 분산성을 향상시켜 기체 차단성을 높이고자 하였다. 그 결과로서, Triton X-100이 도입된 나노복합막이 예상치와 유 사한, 향상된 기체 차단성을 보임을 확인하였다. 본 연구를 기반으로 고분자 기반 나노복합막의 기체 차단성 분야로의 활용성 이 증대될 것으로 기대한다.

A highly facile and eco-friendly green synthesis of Annona squamosa (custard apple) leaf extract reduced graphene oxide (CRG) nanosheets was achieved by the reduction of graphene oxide (GO). The as-prepared CRG was characterized with X-ray diffraction (XRD), transmission electron microscope (TEM), Fourier-transform infrared spectroscopy (FT-IR), ultraviolet-visible (UV-Vis), X-ray photoelectron spectroscopy (XPS) and Raman spectroscopic techniques. Removal of oxygen containing moieties from the GO was confirmed by UV-Vis, FT-IR and XPS spectroscopic data. The XRD and Raman data further confirmed the formation of the CRG. TEM images showed the sheet structure of the synthesized CRG. These results show that the phytochemicals present in custard apple leaf extract act as excellent reducing agents. The CRG showed good dispersion in water.

연구에서는 고분자전해질 연료전지(PEMFC)의 전해질막의 성능향상을 위하여 sulfonated graphene oxide (sGO)와 Nafion을 이용하여 복합막을 개발하였다. sGO/Nafion 복합막 안의 sGO의 균일한 분산을 위해 각기 다른 용매를 사 용한 sGO 분산액과 Nafion 현탁액을 혼합하여 복합막들을 제조하였다. 제조된 복합막들의 물성 및 전기화학적 특성을 평가 하기 위해 SEM, FT-IR, 이온 전도도, 이온 교환 용량, 함수율, 열안정성 등을 수행하였다. 연구 결과 ODB와 DMAc 혼합 용 매로 sGO를 분산하여 고분자 용액 내에서의 분산도를 향상시켰으며, 이 결과 11 wt%의 낮은 함수율에도 불구하고, 0.06 S cm-1의 기존 연구와 유사한 이온 전도도를 나타내었다.

PTMSP[poly(1-trimethylsilyl-1-propyne)]는 구조적으로 trimethylsilyl의 크기와 큰 자유부피를 인하여 기체의 투과도가 매우 우수한 장점을 가지고 있으나, 선택도가 낮은 단점이 있다. GO(Graphene oxide)는 흑연으로부터 제조하여 재료의 습득이 용이하고, 단일막 제조시, 기체투과에 선택적 배리어로서 작용한다. 본 연구에서는 PTMSP-GO 복합막을 제조하여 물리화학적 특성을 분석하고, 기체투과도를 측정하여 상대적 선택도를 도출하는 연구를 실행하였다.

Graphene oxide (GO) has received a lot of attention in membrane science for its CO2-philic nature, which can facilitate CO2 separation performance. In addition, GO has attractive properties for gas separation membrane material due to thin-film membrane formation and tunable transport channel. GO membrane can be generally prepared by coating GO nanosheets on microporous polymer supports for mechanical stability. However, the substrates for in thin GO layer should be carefully chosen for good adhesion between GO layer and support surface with maintaining good separation performance. In this study, we tried to modify the surface properties of high permeable support membranes by using gutter layer as an intermediate layer, and measured the gas transport properties of these GO thin-film composite membranes.

Recently, graphene oxide (GO) has been extensively investigated for gas and liquid separation because thin-film GO membranes show quite interesting separation performance. However, even GO membranes exhibit relatively low gas permeability due to high tortuosity caused by high aspect ratio of GO. Normally, the size of GO is in the range from a few hundred nanometers to a few micrometers, so inherent gas permeability would be very varied. For practical applications of GO membranes, the gas permeability should be improved. As such, in this study, we have modified the pristine GO sheets to reduce the gas permeation pathway, with maintaining GO’s excellent gas separation properties. This study will provide a further insight on how such two-dimensional nanosheets can be used for membrane applications, competing with existing membrane materials.

Graphene oxide (GO) is an intriguing two-dimensional nanosheet, a highly oxidized graphene sheet. Due to its various oxygen-containing polar functional groups, graphene oxide shows high CO2 sorption properties, and also thin-film GO membranes exhibit good CO2 separation properties, particularly in the presence of water molecules. Recently, GO nanosheets have been incorporated into polymer membranes, in the form of mixed-matrix membranes, to expect the synergistic effect of GO and polymer matrix. Here, we prepared novel GO/polymer membranes via crosslinking reactions between polar groups on basal plane of GO and bi-functional crosslinking agents, and then conducted the gas permeation measurements to see the possible enhancement for permeability/selectivity performance.

Graphene oxide (GO) can be used as a membrane material itself or a nanofiller to enhance gas separation performance of polymer membranes. Since GO has high CO2 affinity due to some polar groups, particularly GO membranes or GO/polymer membranes have been extensively studied for CO2 separation. Although ultrathin GO membranes show outstanding CO2 separation properties, the gas permeance through GO membranes is still low owing to high tortuosity caused by high aspect ratio of GO sheets. In this study, mixed-matrix membranes consisting of modified GO (as a dispersed phase) and high permeable polymer were prepared by combining each advantage of GO and high permeable polymer for improving gas separation performance. Both single-gas and mixed-gas permeation experiments were conducted with or without humidified feeds for post-combustion CO2 capture.

Carbon nanomaterials such as graphene and its derivatives can be used for membrane applications due to its scalable area and one-atom-thickness, if pores or channels can be well-engineered. Particularly, graphene oxide (GO), a highly oxidized graphene sheet, shows promising membrane building block for gas separation as well as liquid separation. Due to its various polar groups, GO-based membranes also show good candidate for CO2 separation. In this regard, we tried to prepare large-scale GO-based, thin-film composite membrane for post-combustion CO2 capture, and also fabricated membrane modules (e.g., spiral wound membrane or plate-and-frame modules) to apply for real flue gas separation. In this study, the separation performance of two kinds of membrane modules will be compared in terms of gas permeance, selectivity, and pressure drop.

본 연구에서는 유연성을 갖는 전극 제조를 위해 환원된 그래핀 옥사이드/단일벽 탄소나노튜 브 복합체를 금이 코팅된 PET 기판 위에 스프레이 코팅하였다. 제조된 플렉시블한 전극의 전기 용량 값 은 1 M의 황산 전해질과 100 mV s-1 의 주사속도에서 82 F g-1 으로 측정 되었으며, 이 용량 값은 500 번의 굽힘 시험 후에 38 F g-1 로 감소되는 현상을 확인 하였다. 또한, 이러한 결과는 정전류 충 방전과 전기화학 임피던스법을 포함한 전기화학적 분석 결과와도 부합하는 결과를 나타내었다. 유연성을 갖는 환원된 그래핀 옥사이드/단일벽 탄소나노튜브 복합체 전극은 500회의 반복적인 굽힘 시험 후에도 대략 50%의 초기 전기 용량 값을 유지 할 수 있었으며, 이러한 여러 가지 전기화학적 특성을 고려하여 볼 때 미래 개발 가능한 플렉시블한 에너지 저장 매체로써의 적용이 가능 하다는 점을 확인 할 수 있었 다.

Graphene oxide (GO) powder processed by Hummer's method is mixed with p-type Bi2Te3 based thermoelectric materials by a high-energy ball milling process. The synthesized GO-dispersed p-type Bi2Te3 composite powder has a composition of Bi0.5Sb1.5Te3 (BSbT), and the powder is consolidated into composites with different contents of GO powder by using the spark plasma sintering (SPS) process. It is found that the addition of GO powder significantly decreases the thermal conductivity of the pure BSbT material through active phonon scattering at the newly formed interfaces. In addition, the electrical properties of the GO/BSbT composites are degraded by the addition of GO powder except in the case of the 0.1 wt% GO/BSbT composite. It is found that defects on the surface of GO powder hinder the electrical transport properties. As a result, the maximum thermoelectric performance (ZT value of 0.91) is achieved from the 0.1% GO/BSbT composite at 398 K. These results indicate that introducing GO powder into thermoelectric materials is a promising method to achieve enhanced thermoelectric performance due to the reduction in thermal conductivity.

Sulphonated polysulphone (SPS) has been synthesized and subsequently applied as binder for graphene oxide (GO)-based electrodes for development of electrochemical supercapacitors. Electrochemical performance of the electrode was investigated using cyclic voltammetry in 1M Na2SO4 and 1M KOH solution. The fabricated supercapacitors gave a specific capacitance of 161.6 and 216.8 F/g with 215.4 W/kg and 450 W/kg of power density, in 1M Na2SO4 and 1M KOH solutions, respectively. This suggests that KOH is a better electrolyte than Na2SO4 for studying the electrochemical behavior of electroactive material, and also suggests SPS is a good binder for fabrication of a GO based electrode.

In this work, recent progress on graphene/metal oxide composites as advanced materials for HgCl2 and CO2 capture was investigated. Density Functional Theory calculations were used to understand the effects of temperature on the adsorption ability of HgCl2 and water vapor on CO2 adsorption on CaO (001) with reinforced carbon-based nanostructures using B3LYP functional. Understanding the mechanism by which mercury and CO2 adsorb on graphene/CaO (g-CaO) is crucial to the design and fabrication of effective capture technologies. The results obtained from the optimized geometries and frequencies of the proposed cluster site structures predicted that with respect to molecular binding the system possesses unusually large HgCl2 (0.1- 0.4 HgCl2 g/g sorbent) and CO2 (0.2-0.6 CO2 g/g sorbent) uptake capacities. The HgCl2 and CO2 were found to be stable on the surface as a result of the topology and a strong interaction with the g-CaO system; these results strongly suggest the potential of CaO-doped carbon materials for HgCl2 and CO2 capture applications, the functional gives reliable answers compared to available experimental data.

Usually olefin/paraffin separations (e.g., ethane/ethylene and propane/ propylene) by distillation process are energy-intensive because such molecules have very similar molecular size and boiling point. Membrane process has been considered as an alternative method to achieve energy- efficient olefin/paraffin separation. However, based on solution-diffusion mechanism, it is hard to design good membrane materials to separate them efficiently. Here we report fundamental separation properties of olefin/paraffin through graphene oxide (GO) membranes having slit-like channels. Analogue to carbon molecular sieve membranes, GO membranes showed ability to separate these molecules. To improve the separation properties, GO membranes have been modified by various methods.

Graphene oxide (GO), a highly oxidized graphene sheet, is a distinguished 2-D nanosheet. GO membranes exhibit good CO2 separation properties due to its various polar functional groups with oxygen resulting in high CO2 sorption properties. Recently, GO nanosheets have been incorporated into polymer membranes expecting the synergistic effect. There is, however, little research on GO as a crosslinker even though it has high potential due to available functional groups for further reaction. Here, we prepared GO/polymer membranes by crosslinking reactions between polar groups of GO and bi-functional polymer matrix at different temperatures. Optimum crosslinking condition was found by analyzing gas transport, chemical properties of samples. Degree of crosslinking in GO/polymer nanocomposites affected gas transport behavior.

Graphene oxide (GO) has been extensively studied for membrane material for gas and liquid separation due to its outstanding features such as selective CO2 or water vapor transport properties. Although GO membranes can be easily fabricated in the form of thin-film composite membranes by using high-flux polymeric support membranes, it shows relatively low gas permeability due to high tortuosity. Here we report the way to improve gas permeation rate through porous graphene oxide by reducing the gas permeation pathway, with maintaining GO’s two-dimensional structure. We also used polymer, which has high CO2/N2 selectivity, and prepared GO/polymer composite membranes as a function of GO concentration. This study will provide a further insight on how such two-dimensional nanosheets can be harmonized with polymer and improved membrane properties.