• 제목/요약/키워드: $CO_2$ Evolution

검색결과 421건 처리시간 0.028초

MOF-Derived FeCo-Based Layered Double Hydroxides for Oxygen Evolution Reaction

  • Fang Zheng;Mayur A. Gaikwad;Jin Hyeok Kim
    • 한국재료학회지
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    • 제33권10호
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    • pp.377-384
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    • 2023
  • Exploring earth-abundant, highly effective and stable electrocatalysts for electrochemical water splitting is urgent and essential to the development of hydrogen (H2) energy technology. Iron-cobalt layered double hydroxide (FeCo-LDH) has been widely used as an electrocatalystfor OER due to its facile synthesis, tunable components, and low cost. However, LDH synthesized by the traditional hydrothermal method tends to easily agglomerate, resulting in an unstable structure that can change or dissolve in an alkaline solution. Therefore, studying the real active phase is highly significant in the design of electrochemical electrode materials. Here, metal-organic frameworks (MOFs) are used as template precursors to derive FeCo-LDH from different iron sources. Iron salts with different anions have a significant impact on the morphology and charge transfer properties of the resulting materials. FeCo-LDH synthesized from iron sulfate solution (FeCo-LDH-SO4) exhibits a hybrid structure of nanosheets and nanowires, quite different from other electrocatalysts that were synthesized from iron chloride and iron nitrate solutions. The final FeCo-LDH-SO4 had an overpotential of 247 mV with a low Tafel-slope of 60.6 mV dec-1 at a current density of 10 mA cm-2 and delivered a long-term stability of 40 h for the OER. This work provides an innovative and feasible strategy to construct efficient electrocatalysts.

고전압 구동 Li2MnO3-LiMO2(M=Ni, Co, Mn)/graphite 시스템에서의 전지 수명 및 고온 방치 특성 향상에 효과적인 플루오로 화합물계 전해액에 대한 연구 (Improved Cycle Life and Storage Performance in High-Voltage Operated Li2MnO3-LiMO2(M=Ni, Co, Mn)/Graphite Cell System by Fluorine Compounds as Main Electrolyte Solvent)

  • 유정이;신우철;이병곤
    • 전기화학회지
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    • 제16권3호
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    • pp.162-168
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    • 2013
  • $Li_2MnO_3-LiMO_2$(M=Ni, Co, Mn) 나노 복합체는 높은 이론 용량을 가지고 있어 전기 자동차용 2차 전지 활물질 재료로 많은 연구가 진행되고 있다. 하지만 $Li_2MnO_3-LiMO_2$(M=Ni, Co, Mn)로부터 250 mAh/g 이상의 용량을 구현하기 위해서는 4.4 V 이상의 구동전압이 필요하며, 이러한 높은 구동 전압은 전지의 수명 및 고온 방치 특성의 저해 요소로 작용하고 있다. 본 연구에서는 이러한 문제점을 개선하기 위해서 FEC (Fluoroethylene carbonate), 플루오로알킬 에테르, $LiPF_6$가 주성분인 신규 전해액(F-based EL)을 설계하였다. F-based EL은 1.3 M $LiPF_6$ EC/EMC/DMC (3/4/3, v/v/v) (STD) 대비 안정한 SEI를 형성하며, 산화 안정성이 뛰어나 $Li_2MnO_3-LiMO_2$(M=Ni, Co, Mn)/graphite 셀의 수명 및 방치 중 가스 저감에 효과가 있음을 확인할 수 있었다.

5ZrSiO4-xCaCO3 혼합계에서 CaCO3첨가량이 CaZrO3와 m-ZrO2의 합성 및 미세구조변화에 미치는 영향 (Influence of Addition Amount of CaCO3on the Synthesizing behavior and Microstructural Evolution of CaZrO3 and m-ZrO2 in 5ZrSiO4-xCaCO3 Mixture System)

  • 김재원;이재언;조창용;이재현;정연길
    • 한국재료학회지
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    • 제13권9호
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    • pp.572-580
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    • 2003
  • Synthesizing behavior and microstructural evolution of $CaZrO_3$and $m-ZrO_2$in a thermal reaction process of $ZrSiO_4$-$xCaCO_3$mixtures, where x is 7 and 19, were investigated to determine the addition amount of CaO in CaO:$ZrO_2$:$SiO_2$ternary composition. CaZrO$_3$-Ca$_2$SiO$_4$precursor prepared by the mixture of $ZrSiO_4$and CaCO$_3$in aqueous suspending media was controlled to the acidic (pH=4.0) condition with HCI solution to enhance the thermal reaction. The addition amount of dispersant into the $ZrSiO_4$-$xCaCO_3$slip increased with increasing mole ratio of $CaCO_3$, which was associated with the viscosity of slip. Decarbonation reaction was activated with an increase of the addition amount of $CaCO_3$, showing different final temperatures in $ZrSiO_4$-$7CaCO_3$and $ZrSiO_4$-$19CaCO_3$mixtures as about 980 and 116$0^{\circ}C$, respectively, for finishing decarbonation reaction. The grain morphology was changed to spherical shape for all samples with an increase of sintering temperature. The grain size and phase composition of the synthesized composites depended on the mixture ratio of Zrsi04 and CacO3 powders, indicating that the main crystals were m-ZrO2 ($\leq$3 $\mu\textrm{m}$) and $CaZrO_3$ ($\leq$ 7 $\mu\textrm{m}$) in $ZrSiO_4$$>-7CaCO_3$and $ZrSiO_4$-$19CaCO_3$mixtures, respectively.

EVOLUTION OF THE SPIN OF LATE-TYPE GALAXIES CAUSED BY GALAXY-GALAXY INTERACTIONS

  • Hwang, Jeong-Sun;Park, Changbom;Nam, Soo-hyeon;Chung, Haeun
    • 천문학회지
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    • 제54권2호
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    • pp.71-88
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    • 2021
  • We use N-body/hydrodynamic simulations to study the evolution of the spin of a Milky Way-like galaxy through interactions. We perform a controlled experiment of co-planar galaxy-galaxy encounters and study the evolution of disk spins of interacting galaxies. Specifically, we consider cases where the late-type target galaxy encounters an equally massive companion galaxy, which has either a late or an early-type morphology, with a closest approach distance of about 50 kpc, in prograde or retrograde sense. By examining the time change of the circular velocity of the disk material of the target galaxy from each case, we find that the target galaxy tends to lose the spin through prograde collisions but hardly through retrograde collisions, regardless of the companion galaxy type. The decrease of the spin results mainly from the deflection of the orbit of the disk material by tidal disruption. Although there is some disk material which gains the circular velocity through hydrodynamic as well as gravitational interactions or by transferring material from the companion galaxy, it turns out that the amount of the material is generally insufficient to increase the overall galactic spin under the conditions we set. We find that the spin angular momentum of the target galaxy disk decreases by 15-20% after a prograde collision. We conclude that the accumulated effects of galaxy-galaxy interactions will play an important role in determining the total angular momentum of late-type galaxies.

Fe-doped β-Ni(OH)2의 산소발생반응 증가를 위한 Mo의 동시도핑효과 (Effects of Mo co-doping into Fe doped β-Ni(OH)2 microcrystals for oxygen evolution reactions)

  • 박제홍;유시범;안태광;김병준;유정호
    • 한국결정성장학회지
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    • 제34권1호
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    • pp.30-35
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    • 2024
  • 수소에너지 생산을 위한 물분해 시스템의 효율을 향상시키기 위해서는, 수소발생반응(HER)과 산소발생반응(OER) 각각에서 촉매로 인한 전기화학적 반응에서의 높은 과전압의 감소가 수반되어야 한다. 그 중에서도 전이금속 기반의 화합물들은 현재 상용되고 있는 백금 등의 귀금속을 대체할 촉매 재료로써 주목받고 있다. 본 연구에서는, 저렴한 금속 다공성 소재인 니켈폼(Ni foam)을 지지체로 사용하고, 수열합성 공정을 통해 Fe-doped β-Ni(OH)2 마이크로결정을 합성하였다. 또한 OER 특성을 향상시키기 위하여 Mo을 동시도핑하여 합성된 Fe-Mo co-doped β-Ni(OH)2 마이크로결정의 형상, 결정구조 및 수전해 특성의 변화를 관찰하였으며, 상용 수전해 시스템의 촉매로서의 적용가능성을 검토하였다.

코발트살리사이드를 위한 습식세정 공정 (Wet Cleaning Process for Cobalt Salicide)

  • 정성희;송오성
    • 한국표면공학회지
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    • 제35권6호
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    • pp.377-382
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    • 2002
  • We investigated the appropriate wet cleaning process for Co-Ti-Si compounds formed on top of cobalt disilicide made from Co/Ti deposition and two rapid thermal annealing (RTA). We employed three wet cleaning processes, WP1 ($H_2$SO$_4$ etchant), WP2 ($NH_4$OH etchant), and WP3 which execute sequentially WP1 and WP2 after the first RTA. All samples were cleaned with BOE etchant after the second RTA. We characterized the sheet resistance with process steps by a four-point probe, the microstructure evolution by a cross detail sectional transmission electron microscope, a Auger depth profiler, and a X-ray diffractometer (XRD). We confirmed WP3 wet cleaning process were the most suitable to remove CoTiSi layer selectively.

중공 ZIF를 이용한 RuO2/h-Co3O4 촉매의 합성 및 산소 발생 반응으로의 활용 (Synthesis of RuO2/h-Co3O4 Electrocatalysts Derived from Hollow ZIF and Their Applications for Oxygen Evolution Reaction)

  • 구윤모;이영빈;임경민;김진수
    • 공업화학
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    • 제34권2호
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    • pp.180-185
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    • 2023
  • 물의 전기 분해 효율을 향상시키기 위해 산소발생반응(OER)의 반응 속도를 가속화하며 고성능과 장기 안정성을 가진 OER 전기촉매 개발이 필수적이다. 본 연구에서는 고효율의 OER 전기촉매를 합성하기 위해 중공 금속-유기골격체 (MOF)로부터 유도된 루테늄-코발트 산화물 촉매를 개발하였다. 합성된 촉매는 루테늄의 표면 노출을 증대시킴으로 낮은 Tafel 기울기와 10 mA/cm2의 전류밀도에서 386 mV의 낮은 과전위가 관찰되었다. 또한 상용 RuO2 촉매 대비 높은 질량 활성과 안정성을 보여, 귀금속 촉매를 대체할 수 있을 것으로 기대된다.

진공 소결공정에 의한 고밀도 바인더리스 및 극저바인더 초경합금의 제조 (Consolidation of Binderless and Low-Binder WC hardmetal by Vacuum Sintering)

  • 민병준;박용호;이길근;하국현
    • 한국분말재료학회지
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    • 제14권5호
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    • pp.315-319
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    • 2007
  • Pure WC or WC with low Co concentration less than 0.5 wt.% is studied to fabricate high density WC/Co cemented carbide using vacuum sintering and post HIP process. Considering the high melting point of WC, it is difficult to consolidate it without the use of Co as binder. In this study, the effect of lower Co addition on the microstructure and mechanical properties evolution of WC/CO was investigated. By HIP process after vacuum sintering, hardness and density was sharply increased. The hardness values was $2,800kgf/mm^2$ using binderless WC.

WC 첨가 방법에 따른 Ti(CN)-Co/Ni 계 서멧트의 미세조직 및 특성변화 (Microstructural Evolution and Properties in Ti(CN)-Co/Ni Cermet Depending on the Starting Material for Incorporation of WC)

  • 정태주;안선용;안승수;신명수;김학규;김경배;오경식;이혁재
    • 한국분말재료학회지
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    • 제14권2호
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    • pp.132-139
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    • 2007
  • In the Ti(CN)-Co/Ni cermet, WC is an effective additive for increasing sinterability and mechanical properties such as toughness and hardness. In this work, WC, (WTi)C and (WTi)(CN) were used as the source of WC and their effects were investigated in the respect of microstructural evolution and mechanical properties. Regardless of the kinds of WC sources, the hard phase with dark core and bright rim structure was observed in the Ti(CN)-Co/Ni cermet under the incorporation of relatively small amount of WC. However, hard phases with bright core began to appear and their frequency increased with the increase of all kinds of WC source addition. The ratio of bright core to dark one in the (TiW)(CN)-Co/Ni cermet was greatest under the incorporation of (WTi)C compared at the same equivalent amount of WC. The mechanical properties were improved with the addition of WC irrespective of the kinds of sources, but the addition of (WTi)(CN) was less effective for the increase of fracture toughness.

원자층증착법을 이용한 수소 생성용 광전기화학 전극 소재 개발 동향 (Recent Developments in H2 Production Photoelectrochemical Electrode Materials by Atomic Layer Deposition)

  • 한정환
    • 한국분말재료학회지
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    • 제25권1호
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    • pp.60-68
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    • 2018
  • The design and fabrication of photoelectrochemical (PEC) electrodes for efficient water splitting is important for developing a sustainable hydrogen evolution system. Among various development approaches for PEC electrodes, the chemical vapor deposition method of atomic layer deposition (ALD), based on self-limiting surface reactions, has attracted attention because it allows precise thickness and composition control as well as conformal coating on various substrates. In this study, recent research progress in improving PEC performance using ALD coating methods is discussed, including 3D and heterojunction-structured PEC electrodes, ALD coatings of noble metals, and the use of sulfide materials as co-catalysts. The enhanced long-term stability of PEC cells by ALD-deposited protecting layers is also reviewed. ALD provides multiple routes to develop improved hydrogen evolution PEC cells.