• 제목/요약/키워드: Double Mesoporous

검색결과 19건 처리시간 0.031초

Fabrication of nitrogen doped ordered mesoporous carbon derived from glucosamine with hybrid capacitive behaviors

  • Zhang, Deyi;Han, Mei;Li, Yubing;Wang, Bing;Wang, Yi;Wang, Kunjie;Feng, Huixia
    • Carbon letters
    • /
    • 제23권
    • /
    • pp.9-16
    • /
    • 2017
  • This paper introduces a nitrogen-doped ordered mesoporous carbon (NOMC) derived from glucosamine with hybrid capacitive behaviors, achieved by successfully combining electrical double-layer capacitance with pseudo-capacitance behaviors. The nitrogen doping content of the fabricated NOMC reached 7.4 at% while its specific surface area ($S_{BET}$) and total pore volume reached $778m^2g^{-1}$ and $1.17cm^3g^{-1}$, respectively. A dual mesoporous structure with small mesopores centered at 3.6 nm and large mesopores centered at 9.9 nm was observed. The specific capacitance of the reported materials reached up to $328Fg^{-1}$, which was 2.1 times higher than that of pristine CMK-3. The capacitance retention rate was found to be higher than 87.9% after 1000 charge/discharge cycles. The supplementary pseudocapacitance as well as the enhanced wettability and conductivity due to the incorporation of nitrogen heteroatoms within the carbon matrixes were found to be responsible for the excellent capacitive performance of the reported NOMC materials.

층상이중 수산화물을 이용한 5가 비소 흡착 특성 (Adsorption of Arsenate on the Synthesized Layered Double Hydroxide Materials)

  • 최영무;최원호;김정환;박주양
    • 대한토목학회논문집
    • /
    • 제29권1B호
    • /
    • pp.91-96
    • /
    • 2009
  • LDH(Layered double hydroxide) 물질을 제조하고 이를 이용하여 비소를 흡착시키는 실험을 수행하였다. TEM을 이용하여 제조한 LDH 물질의 형상을 살펴본 결과 열처리를 거친 시료는 나노크기의 결정화된 구조를 가지고 있고 열처리를 거치지 않은 시료는 아직 결정화가 완전히 이루어지지 않았으며 크기도 마이크로 범위에서 나타났다. X선 회절분석 결과를 보면 이 같은 결과가 뚜렷이 나타났으며, 열처리를 거친 경우는 뚜렷한 결정화를 보이고 있었다. $N_2$ 흡착 및 탈착 결과를 통해 LDH가 mesoporous한 공극 형태를 가지고 있다는 것을 알 수 있었다. 비표면적은 열처리를 거친 시료가 열처리를 거치지 않은 시료보다 2배 이상 크게 나타났다. 흡착 등온 실험 결과에서도 두 시료는 비슷한 흡착량을 보이며 기존 철산화 물에 못지않은 흡착능을 나타내고 있다. 금번에 합성한 Mg Fe-LDH 물질을 이용하여 토양 및 지하수의 비소 제거 공정에 적용할 수 있음을 확인하였다.

EDLC의 전기화학적 성능에 대한 메조기공 구조의 효과 (Effect of pore structure on electrochemical performance of EDLC)

  • 이명숙;신윤성;이종대
    • 한국응용과학기술학회지
    • /
    • 제27권3호
    • /
    • pp.310-317
    • /
    • 2010
  • The electrochemical properties of electric double layer capacitor(EDLC) was studied by controlling pore size distribution and specific surface area of the activated carbon fiber(ACF). The mesoporous ACF, which was prepared by the iron exchange method, showed the tendency of increasing average pore size and decreasing total surface area. The mesoporous ACF (surface area = 2225 $m^2$/g, pore size=1.93 nm) showed increased mesopore(pore size=1~3nm) volume from 0.055 cc/g to 0.408 cc/g compared to its raw ACF. The charging capacity of the EDLC which uses the prepared mesoporous ACF also increased from 0.39 F/$cm^2$ to 0.55 F/$cm^2$. From these results, it can be known that the electrochemical properties of EDLC are mainly dependent on the specific surface area, but above the surface area 2200 $m^2$/g, it is the mesopore volume that affects the performance of the capacitor considerably. Because the increased mesopore volume results in a decreased ion mobility resistance, the charge capacitance is enhanced.

EDLC 전극용 메조기공 활성탄소 섬유의 전기화학적 특성 (The Electrochemical Characteristics of Mesopore Active Carbon Fiber for EDLC Electrode)

  • 강채연;신윤성;이종대
    • Korean Chemical Engineering Research
    • /
    • 제49권1호
    • /
    • pp.10-14
    • /
    • 2011
  • 철 이온 교환방법에 의해 메조기공을 갖는 활성탄소 섬유(ACF)를 제조하고, 이를 사용하여 전기 이중층 커패시터(EDLC)의 전극소재 성능을 조사하였다. 질산처리에 의해 제조된 메조기공 ACF는 비표면적이 1,249, 664 $m^2/g$이고, 메조 기공 분율이 70.6-81.3%이고, 평균 기공크기는 약 2.78~4.14 nm이다. 질산처리시간이 짧을수록 비표면적이 크고 메조 기공이 적게 발달됨을 알 수 있었다. 전기이중층 커패시터의 성능을 조사하기 위해서, 메조기공 ACF, 도전제, 바인더를 사용하여 단위 셀을 제조하였으며, 유기 전해질을 사용하였다. 2시간 질산으로 처리된 ACF의 비 축전양은 0.47 $F/cm^2$이고, 20회 충.방전 테스트에서 안정된 실험결과를 얻을 수 있었다. EDLC의 전기화학적 성능은 ACF 전극의 비표면적에 크게 영향을 받으며 메조기공은 전하의 확산저항을 감소시키는 것을 알 수 있었다.

Methanol-involved heterogeneous transformation of ginsenoside Rb1 to rare ginsenosides using heteropolyacids embedded in mesoporous silica with HPLC-MS investigation

  • Mengya Zhao;Yusheng Xiao;Yanyan Chang;Lu Tian;Yujiang Zhou;Shuying Liu;Huanxi Zhao;Yang Xiu
    • Journal of Ginseng Research
    • /
    • 제48권4호
    • /
    • pp.366-372
    • /
    • 2024
  • Background: The biological activity and pharmacological effects of rare ginsenosides have been proven to be superior to those of the major ginsenosides, but they are rarely found in ginseng. Methods: Ginsenoside Rb1 was chemically transformed with the involvement of methanol molecules by a synthesized heterogeneous catalyst 12-HPW@MeSi, which was obtained by the immobilization of 12-phosphotungstic acid on a mesoporous silica framework. High-performance liquid chromatography coupled with mass spectrometry was used to identify the transformation products. Results: A total of 18 transformation products were obtained and identified. Methanol was found to be involved in the formation of 8 products formed by the addition of methanol molecules to the C-24 (25), C-20 (21) or C-20 (22) double bonds of the aglycone. The transformation pathways of ginsenoside Rb1 involved deglycosylation, addition, elimination, cycloaddition, and epimerization reactions. These pathways could be elucidated in terms of the stability of the generated carbenium ion. In addition, 12-HPW@MeSi was able to maintain a 60.5% conversion rate of Rb1 after 5 cycles. Conclusion: Tandem and high-resolution mass spectrometry analysis allowed rapid and accurate identification of the transformation products through the characteristic fragment ions and neutral loss. Rare ginsenosides with methoxyl groups grafted at the C-25 and C-20 positions were obtained for the first time by chemical transformation using the composite catalyst 12-HPW@MeSi, which also enabled cyclic heterogeneous transformation and facile centrifugal separation of ginsenosides. This work provides an efficient and recyclable strategy for the preparation of rare ginsenosides with the involvement of organic molecules.

Synthesis of Core-Shell Silica Nanoparticles with Hierarchically Bimodal Pore Structures

  • 윤석본;박대근;윤완수
    • 한국진공학회:학술대회논문집
    • /
    • 한국진공학회 2011년도 제40회 동계학술대회 초록집
    • /
    • pp.467-467
    • /
    • 2011
  • Reflecting the growing importance of nanomaterials in science and technology, controlling the porosity combined with well-defined structural properties has been an ever-demanding pursuit in the related fields of frontier researches. A number of reports have focused on the synthesis of various nanoporous materials so far and, recently, the nanomaterials with multimodal porosity are getting an emerging importance due to their improved material properties compared with the mono porous materials. However, most of those materials are obtained in bulk phases while the spherical nanoparticles are one of the most practical platforms in a great number of applications. Here, we report on the synthesis of the core-shell silica nanoparticles with double mesoporous shells (DMSs). The DMS nsnoparticles are spherical and monodispersive and have two different mesoporous shells, i.e., the bimodal porosity. It is the first example of the core-shell silica nanoparticles with the different mesopores coexisting in the individual nanoparticles. Furthermore, the carbon and silica hollow capsules were also fabricated via a serial replication process.

  • PDF

Optimal Porous Structure of MnO2/C Composites for Supercapacitors

  • Iwamura, Shinichiroh;Umezu, Ryotaro;Onishi, Kenta;Mukai, Shin R.
    • 한국재료학회지
    • /
    • 제31권3호
    • /
    • pp.115-121
    • /
    • 2021
  • MnO2 can be potentially utilized as an electrode material for redox capacitors. The deposition of MnO2 with poor electrical conductivity onto porous carbons supplies them with additional conductive paths; as a result, the capacitance of the electrical double layer formed on the porous carbon surface can be utilized together with the redox capacitance of MnO2. However, the obtained composites are not generally suitable for industrial production because they require the use of expensive porous carbons and/or inefficient fabrication methods. Thus, to develop an effective preparation procedure of the composite, a suitable structure of porous carbons must be determined. In this study, MnO2/C composites have been prepared from activated carbon gels with various pore sizes, and their electrical properties are investigated via cyclic voltammetry. In particular, mesoporous carbons with a pore size of around 20 nm form a composite with a relatively low capacitance (98 F/g-composite) and poor rate performance despite the moderate redox capacitance obtained for MnO2 (313 F/g-MnO2). On the other hand, using macro-porous carbons with a pore size of around 60 nm increases the MnO2 redox capacitance (399 F/g-MnO2) as well as the capacitance and rate performance of the entire material (203 F/g-composite). The obtained results can be used in the industrial manufacturing of MnO2/C composites for supercapacitor electrodes from the commercially available porous carbons.

다공성 탄소전극의 전위에 따른 복소캐패시턴스 분석 (Potential-dependent Complex Capacitance Analysis for Porous Carbon Electrodes)

  • 장종현;윤성훈;가복현;오승모
    • 전기화학회지
    • /
    • 제6권4호
    • /
    • pp.255-260
    • /
    • 2003
  • 다공성 탄소전극의 전위에 짜른 EDLC(e)ectric double-layer capacitor)특성을 조사하기 위해 복소캐패시턴스분석(complex capacitance analysis)을 수행하였다. 하나의 원통형 기공에 대해 복소캐패시턴스를 이론적으로 유도하였고, 기공의 분포를 고려하여 다공성 전극에 대하여서도 계산하였다. 복소캐패시턴스의 허수부를 주파수에 대해 도시하면 피크 형태의 곡선이 얻어지는데, 이때 피크의 면적은 캐패시턴스 값의 크기와, 피크의 위치는 다공성전극의 전기화학 파라매터와 기공구조에 의해 결정되는 $\alpha_0$와 상관관계가 있음을 알 수 있었다. 이를 이용하면, 동일한 기공구조를 갖는 전극에 대해, 전위에 따른 캐패시턴스와 기공 내 이온전도도의 변화를 측정할 수 있다. 메조포러스 탄소전극에 대하여 전위를 변화시키며 electrochemical impedance spectroscopy를 측정하고 이를 복소캐패시턴스법에 의해 분석하였다. 피크 면적으로부터 구한 전위에 따른 캐패시턴스는 0.3V부근에서 최대값을 가졌는데, 이는 cyclic voltammetry 실험결과와도 일치하였다. 한편, 피크 위치로부터 구한 기공 내 이온전도도는 0.2V에서 최대 값을 가지고 전위가 증가할 수록 서서히 감소하였다. 이를 탄소 표면전하의 증가로 인해 이온/표면의 전기적 작용력이 커졌기 때문으로 해석하였다.