• 제목/요약/키워드: 나노촉매

검색결과 529건 처리시간 0.026초

다중벽 탄소 나노 튜브에 담지한 PtxM(1-x)(M = Co, Cu, Ni) 합금촉매의 제조 및 고분자 전해질 연료전지에서 산소환원 특성 (Synthesis and Oxygen Reduction Reaction Characteristics of Multi-Walled Carbon Nanotubes Supported PtxM(1-x) (M = Co, Cu, Ni) Alloy Catalysts for Polymer Electrolyte Membrane Fuel Cell)

  • 정동원;박순;안치영;최성호;김준범
    • 한국재료학회지
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    • 제19권12호
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    • pp.667-673
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    • 2009
  • The electrocatalytic characteristics of oxygen reduction reaction of the $PtxM_{(1-x)}$ (M = Co, Cu, Ni) supported on multi-walled carbon nanotubes (MWNTs) have been evaluated in a Polymer Electrolyte Membrane Fuel Cell (PEMFC). The $Pt_xM_{(1-x)}$/MWNTs catalysts with a Pt : M atomic ratio of about 3 : 1 were synthesized and applied to the cathode of PEMFC. The crystalline structure and morphology images of the $Pt_xM_{(1-x)}$ particles were characterized by X-ray diffraction and transmission electron microscopy, respectively. The results showed that the crystalline structure of the Pt alloy particles in Pt/MWNTs and $Pt_xM_{(1-x)}$/MWNTs catalysts are seen as FCC, and synthesized $Pt_xM_{(1-x)}$ crystals have lattice parameters smaller than the pure Pt crystal. According to the electrochemical surface area (ESA) calculated with cyclic voltammetry analysis, $Pt_{0.77}Co_{0.23}$/MWNTs catalyst has higher ESA than the other catalysts. The evaluation of a unit cell test using Pt/MWNTs or $Pt_xM_{(1-x)}$/MWNTs as the cathode catalysts demonstrated higher cell performance than did a commercial Pt/C catalyst. Among the MWNTs-supported Pt and $Pt_xM_{(1-x)}$ (M = Co, Cu, Ni) catalysts, the $Pt_{0.77}Co_{0.23}$/MWNTs shows the highest performance with the cathode catalyst of PEMFC because they had the largest ESA.

ICP-CVD 방법에 의해 성장된 탄소나노튜브의 Ni 및 Co 촉매 두께에 따른 구조적 물성 및 전계 방출 특성 분석 (Characterization of structural and field emissive properties of CNTs grown by ICP-CVD method as a function of Ni and Co catalysts thickness)

  • 김종필;김영도;박창균;엄현석;박진석
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 2003년도 하계학술대회 논문집 C
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    • pp.1574-1576
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    • 2003
  • Carbon nanotubes (CNTs) were grown on the TiN-coated silicon substrate with different thickness of Ni and Co catalysts layer at $600^{\circ}C$ using inductively coupled plasma-chemical vapor deposition (ICP-CVD). The Ni and Co catalysts were formed using the RF magnetron sputtering system with various deposition times. It was found that the growth of CNTs was strongly influenced by the surface morphology of Ni and Co catalysts. With increasing deposition time, the thickness of catalysts increased and the grain boundary size of catalysts increased. The surface morphology of catalysts and CNTs were elucidated by SEM. The Raman spectrum further confirmed the graphitic structure of the CNTs. The turn-on field of CNTs grown on Ni and Co catalysts was about 2.7V/pm and 1.9V/pm respectively. Field emission current density of CNTs grown on Ni and Co catalysts was measured as $11.67mA/cm^2$ at $5.5V/{\mu}m$ and $1.5mA/cm^2$ at $5.5V/{\mu}m$ respectively.

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수소발생반응을 위한 Ni4Cr 나노 섬유 전기화학 촉매 합성 및 특성 분석 (Synthesis and Characterization of Ni4Cr Nanofiber Electrocatalyst for Hydrogen Evolution Reaction)

  • 이정훈;장명제;박유세;최승목;김양도;이규환
    • 한국표면공학회지
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    • 제50권5호
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    • pp.322-331
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    • 2017
  • Hydrogen evolution reaction(HER) was studied over $Ni_4Cr$ nanofibers(NFs) prepared by electrospinning method and oxidation/reduction heat treatment for alkaline water electrolysis. The physicochemical and electrochemical properties such as average diameter, lattice parameter, HER activity of synthesized $Ni_4Cr$ NFs could be modified by proper electrospinning process condition and reduction temperature. It was shown that $Ni_4Cr$ NFs had average diameter from 151 to 273 nm. Also, it exhibited the overpotential between 0.419 V and 0.526 V at $1mA/cm^2$ and Tafel slope of -334.75 mV to -444.55 mV per decade in 1 M KOH solution. These results indicate that $Ni_4Cr$ NFs with reduction heat treatment at $600^{\circ}C$ show thinnest diameter and highest HER activity among the other catalysts.

광전자촉매시스템(PECS) 적용을 위한 고효율 광촉매의 제조와 특성 (Preparation and Characterization of High-performance Photocatalyst for Photoelectrocatalytic System (PECS))

  • 박성애;유동식;이지호;도영웅;하진욱
    • 한국산학기술학회논문지
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    • 제7권6호
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    • pp.1302-1307
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    • 2006
  • 본 연구는 고효율의 광촉매 제조와 그것의 환경적 응용에 관한 것이다. 가시광 영역에서도 $TiO_2$와 유사한 빛 흡수와 광분해속도를 갖는 나노 광촉매를 제조하였고, 낮은 온도에서도 활성 높은 rutile상이 형성하는 $TiO_2$ 광촉매를 제조하여 $SiO_2$위에 분산시켰다 또한, 광촉매에 적용 가능한 바인더와 안정한 $TiO_2$ 광촉매 졸을 제조하였다. 이와같은 물질들은 자외선/가시광선 분광광도계, X선 회절분석기, SEM, 광촉매활성 측정과 $TiO_2$ 코팅 표면의 물성으로 평가하였다. 이 결과들은 공기정화를 위하여 POF나 금속판을 이용하는 효율적인 광촉매 시스템에 적용 할 수 있다.

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폴리스티렌 구형입자를 주형으로 이용한 할로우 메조포러스 질화탄소 구형입자의 합성 (Synthesis of Hollow Mesoporous Carbon Nitride Spheres Using Polystyrene Spheres as Template)

  • 박성수;하창식
    • 접착 및 계면
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    • 제15권2호
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    • pp.63-68
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    • 2014
  • 주형으로 구형의 폴리스티렌을 사용하고 질소와 탄소원으로 시안아미드를 사용하여 열처리 과정을 거친 후 구형의 할로우 메조포러스 질화탄소 물질을 합성하였다. 이때 할로우 메조포러스 질화탄소 물질을 합성하는 과정에서 실리카와 같은 무기물 주형을 사용하지 않기 때문에 이차적인 실리카 제거 공정이 필요 없고 용매를 전혀 사용하지 않는다. 구형의 폴리스티렌 입자는 약 170 nm 크기였고 그리고 할로우 메조포러스 질화탄소 구형입자의 할로우 직경은 약 82 nm, 벽 두께는 약 13 nm이었다. 또한 할로우 메조포러스 질화탄소 물질의 표면적, 나노세공 크기, 세공부피는 각각 $188m^2g^{-1}$, 3.8 nm, $0.35cm^3g^{-1}$이었다. 한편, 할로우 벽은 흑연구조와 유사한 박막층의 쌓임 구조를 가졌으며 이러한 할로우 메조포러스 질화탄소 물질은 연료전지, 촉매, 광촉매, 전자방출 소자 등과 같은 분야에 매우 높은 응용 가능성을 가질 것으로 기대된다.

탄소층으로 캡슐화된 Ni나노입자 촉매의 CO2 메탄화 반응 (Carbon-Encapsulated Ni Catalysts for CO2 Methanation)

  • 김혜정;김승보;김동현;윤재랑;김민재;전상구;이경자;이규복
    • 한국재료학회지
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    • 제31권9호
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    • pp.525-531
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    • 2021
  • Carbon-encapsulated Ni catalysts are synthesized by an electrical explosion of wires (EEW) method and applied for CO2 methanation. We find that the presence of carbon shell on Ni nanoparticles as catalyst can positively affect CO2 methanation reaction. Ni@5C that is produced under 5 % CH4 partial pressure in Ar gas has highest conversions of 68 % at 350 ℃ and 70 % at 400 ℃, which are 73 and 75 % of the thermodynamic equilibrium conversion, respectively. The catalyst of Ni@10C with thicker carbon layer shows much reduced activity. The EEW-produced Ni catalysts with low specific surface area outperform Ni catalysts with high surface area synthesized by solution-based precipitation methods. Our finding in this study shows the possibility of utilizing carbon-encapsulated metal catalysts for heterogeneous catalysis reaction including CO2 methanation. Furthermore, EEW, which is a highly promising method for massive production of metal nanoparticles, can be applied for various catalysis system, requiring scaled-up synthesis of catalysts.

유기 리간드 제어를 통한 고분산 팔라듐 나노 촉매의 합성 및 음이온교환막 연료전지를 위한 산소 환원 반응 특성 분석 (Synthesis of Highly Dispersed Pd Nanocatalysts Through Control of Organic Ligands and Their Electrochemical Properties for Oxygen Reduction Reaction in Anion Exchange Membrane Fuel Cells)

  • 성후광;;장정희;정남기
    • 한국재료학회지
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    • 제28권11호
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    • pp.633-639
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    • 2018
  • In anion exchange membrane fuel cells, Pd nanoparticles are extensively studied as promising non-Pt catalysts due to their electronic structure similar to Pt. In this study, to fabricate Pd nanoparticles well dispersed on carbon support materials, we propose a synthetic strategy using mixed organic ligands with different chemical structures and functions. Simultaneously to control the Pd particle size and dispersion, a ligand mixture composed of oleylamine(OA) and trioctylphosphine(TOP) is utilized during thermal decomposition of Pd precursors. In the ligand mixture, OA serves mainly as a reducing agent rather than a stabilizer since TOP, which has a bulky structure, more strongly interacts with the Pd metal surface as a stabilizer compared to OA. The specific roles of OA and TOP in the Pd nanoparticle synthesis are studied according to the mixture composition, and the oxygen reduction reaction(ORR) activity and durability of highly-dispersed Pd nanocatalysts with different particles sizes are investigated. The results of this study confirm that the Pd nanocatalyst with large particles has high durability compared to the nanocatalyst with small Pd nanoparticles during the accelerated degradation tests although they initially indicated similar ORR performance.

다공성 탄소층이 코팅된 하이브리드 표면 구조를 갖는 산소 환원 반응용 PtCo 합금 나노 촉매 (Hybrid PtCo Alloy Nanocatalysts Encapsulated by Porous Carbon Layers for Oxygen Reduction Reactions)

  • 장정희;모니카 샤르마;성후광;김순표;정남기
    • 한국재료학회지
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    • 제28권11호
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    • pp.646-652
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    • 2018
  • During a long-term operation of polymer electrolyte membrane fuel cells(PEMFCs), the fuel cell performance may degrade due to severe agglomeration and dissolution of metal nanoparticles in the cathode. To enhance the electrochemical durability of metal catalysts and to prevent the particle agglomeration in PEMFC operation, this paper proposes a hybrid catalyst structure composed of PtCo alloy nanoparticles encapsulated by porous carbon layers. In the hybrid catalyst structure, the dissolution and migration of PtCo nanoparticles can be effectively prevented by protective carbon shells. In addition, $O_2$ can properly penetrate the porous carbon layers and react on the active Pt surface, which ensures high catalytic activity for the oxygen reduction reaction. Although the hybrid catalyst has a much smaller active surface area due to the carbon encapsulation compared to a commercial Pt catalyst without a carbon layer, it has a much higher specific activity and significantly improved durability than the Pt catalyst. Therefore, it is expected that the designed hybrid catalyst concept will provide an interesting strategy for development of high-performance fuel cell catalysts.

젖산 연료전지용 효소전극 제작 및 특성 분석 (Fabrication and Characterization of Enzyme Electrode for Lactate Fuel Cell)

  • 장연청;김창준
    • Korean Chemical Engineering Research
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    • 제59권3호
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    • pp.373-378
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    • 2021
  • 본 연구는 땀에 존재하는 젖산을 연료로 사용하여 전기를 생산하는 웨어러블 연료전지용 고전력 젖산 산화효소 전극을 개발하는 데 그 목적이 있다. 유연성 있는 탄소종이 기반의 고정화효소 전극을 제작하고 평가하였다. 전해질 내 젖산농도 증가에 따라 젖산 산화효소(lactate oxidase, LOx)의 촉매작용으로 전류생성량이 증가하였다. 금 나노입자가 부착된 탄소종이에 고정화된 LOx가 탄소종이에 부착된 LOx보다 1.5배 많은 전류를 생성하였다. 빌리루빈 산화효소(bilirubin oxidase, BOD)가 고정화된 cathode는 질소로 퍼지(purge)된 전해질보다 산소로 포화된 전해질에서 높은 환원전류를 발생시켰다. 두 전극으로 구성된 연료전지를 제작하여 방전전류 변화에 따른 셀전압을 측정하였다. 방전 전류밀도 값이 66.7 ㎂/cm2에서 셀 전압은 0.5±0.0 V였고, 셀 전력량은 최대치인 33.8±2.5 ㎼/cm2를 나타내었다.

화학적 공침법을 이용한 침상형 페라이트 합성 (Preparation and Characterization of Nanocrystalline Spinel Ferrites by Chemical Co-precipitation)

  • ;임윤희;조영민
    • 공업화학
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    • 제22권2호
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    • pp.185-189
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    • 2011
  • 본 연구에서는 화학적 공침법을 적용하여 가스상 이산화탄소 분해를 위한 나노크기의 M-페라이트(M=Co, Ni, Cu, Zn)를 제조하였다. 열중량 분석 결과, 시험제조한 모든 시료의 최고 무게 감소율은 $350^{\circ}C$ 미만에서 발생하였다. 소성온도가 증가할수록 결정형은 우수하여 표면촉매활성화를 기대할 수 있지만, 입자결정의 크기가 크고, 비표면적이 낮은 페라이트가 합성됨을 알 수 있었다. FT-IR 분석으로부터 $375{\sim}406cm^{-1}$의 범위에서 octahedral site에 착화물이 존재함을 확인 할 수 있었으며, 이는 페라이트 내 스피넬 구조가 형성되어 있음을 보여주는 것이라고 믿는다. 본 연구로부터 얻은 이산화탄소 분해반응을 위한 금속페라이트의 최적 열처리 온도는 $500^{\circ}C$인 것으로 나타났다.