• Bulletin of the Korean Chemical Society
• /
• 제34권11호
• /
• pp.3253-3256
• /
• 2013

Lithium is a highly attractive material for high-energy-concentration batteries, since it has low weight and high potential. Rechargeable lithium-ion batteries (LIBs), which have the extremely high gravimetric and volumetric energy densities, are currently the most preferable power sources for future electric vehicles and various portable electronic devices. In order to improve the efficiency and lifetime, new electrode compounds for lithium intercalation or insertion have been investigated for rechargeable batteries. Solid-state nuclear magnetic resonance (NMR) is a very useful tool to investigate the structural changes in electrode materials in actual working lithium-ion batteries. To detect the in-situ microstructural changes of electrode and electrolyte materials, $^7Li-^{19}F$ double-resonance solid-state NMR probe with a static solenoidal coil for a 600-MHz narrow-bore magnet was designed, constructed, and tested successfully.

• 반도체디스플레이기술학회지
• /
• 제22권1호
• /
• pp.28-32
• /
• 2023

Recently, the use of stable lithium nanostructures as substrates and electrodes for secondary batteries can be a fundamental alternative to the development of next-generation system semiconductor devices. However, lithium structures pose safety concerns by severely limiting battery life due to the growth of Li dendrites during rapid charge/discharge cycles. Also, enabling long cyclability of high-voltage oxide cathodes is a persistent challenge for all-solid-state batteries, largely because of their poor interfacial stabilities against oxide solid electrolytes. For the development of next-generation system semiconductor devices, solid electrolyte nanostructures, which are used in high-density micro-energy storage devices and avoid the instability of liquid electrolytes, can be promising alternatives for next-generation batteries. Nevertheless, poor lithium ion conductivity and structural defects at room temperature have been pointed out as limitations. In this study, a low-dimensional Graphene Oxide (GO) structure was applied to demonstrate stable operation characteristics based on Li+ ion conductivity and excellent electrochemical performance. The low-dimensional structure of GO-based solid electrolytes can provide an important strategy for stable scalable solid-state power system semiconductor applications at room temperature. The device using uncoated bare NCA delivers a low capacity of 89 mA h g-1, while the cell using GO-coated NCA delivers a high capacity of 158 mA h g−1 and a low polarization. A full Li GO-based device was fabricated to demonstrate the practicality of the modified Li structure using the Li-GO heterointerface. This study promises that the lowdimensional structure of Li-GO can be an effective approach for the stabilization of solid-state power system semiconductor architectures.

• Composites Research
• /
• 제30권1호
• /
• pp.46-51
• /
• 2017

질량 및 부피 증가없이 전지와 구조물기능을 복합재에 결합시키는 구조전지 연구가 광범위하게 진행되고 있다. 탄소섬유 및 유리섬유를 하중지지 및 음극, 분리막 용도로 사용하고, 하중전달이 가능한 고체전해질을 모재로 쓰는 것이 현재 아이디어 이지만, 고체전해질이 두 성능을 충분히 만족시키지 못하는 수준이라 구조전지를 구현하지 못하고 있는 실정이다. 그래서, 본 연구는 유리섬유 분리막 및 액체전해질을 사용하여 하중지지 및 전지의 기능을 동시에 수행하는 실험을 구성하여 액체전해액을 사용한 구조전지의 가능성 및 전기적 물성 변화를 관찰하였다. 인장된 분리막은 안정성을 떨어트리는 영향을 미치는데, 이는 양극의 미세입자들이 늘어난 유리섬유의 틈새로 침투하는 것을 분리막이 막지 못하기 때문이라 예상하였고, 상용 분리막을 추가로 사용 하여 그 예상되는 원인을 확인해 보았다. 그리고, 이러한 구조전지 시스템을 구현하기 위해서는 유리섬유 특성의 연구와 전극과 분리막의 계면에 대한 연구가 필요하다.

• 전기화학회지
• /
• 제8권4호
• /
• pp.181-185
• /
• 2005

알루미나 기판을 사용하여 백금 박막 전류 집전체상에 $2.9{\mu}m$ 두께 및 $4cm^2$의 전극면적을 갖는 $LiCoO_2$ 박막을 R.F. 마그네트론 스퍼터링법에 의해 증착하였으며, 아르곤 공정 압력 및 인가된 R.F. 전력량에 따른 Li/Co 몰 비 의존성에 대해 고찰하였다. 비정질계 고체전해질인 Lipon 및 Li 음극이 순차적으로 증착된 박막전지를 제조하여 정전류충, 방전 시험하였으며, 고율방전 특성 및 충, 방전 횟수에 따른 전지 용량 변화를 측정하였다. 교류임피던스를 통해 전지내부의 저항성분을 측정하였으며, 이에 대한 등가회로를 구성하여 시뮬레이션한 결과와 비교하였다.

• 한국자기공명학회:학술대회논문집
• /
• 한국자기공명학회 1999년도 하계총회 및 제15회 자기공명 학술발표회
• /
• pp.15-15
• /
• 1999

• 한국재료학회:학술대회논문집
• /
• 한국재료학회 2001년도 추계 학술발표강연 및 논문개요집
• /
• pp.83-83
• /
• 2001

• 한국자기공명학회논문지
• /
• 제18권2호
• /
• pp.63-68
• /
• 2014

$^7Li$ nuclear magnetic resonance (NMR) spectra have been observed for $LiMPO_4$ (M = Fe, Mn) samples, as a promising cathode material of lithium ion battery. Observed $^7Li$ shifts of $LiFe_{1-x}Mn_xPO_4$ (x = 0, 0.6, 0.8, and 1) synthesized with solid-state reaction are compared with calculated $^7Li$ shift ranges based on the supertranferred hyperfine interaction of Li-O-M. Ex situ $^7Li$ NMR study of $LiFe_{0.4}Mn_{0.6}PO_4$ in different cut-off voltage for the first charge process is also performed to understand the relationship between $^7Li$ chemical shift and oxidation state of metals affected by delithiation process. The increment of oxidation state for metals makes to downfield shift of $^7Li$ by influencing the supertranferred hyperfine interaction.

• 한국세라믹학회지
• /
• 제56권2호
• /
• pp.111-129
• /
• 2019

Recently, all-solid-state batteries (ASSBs) have attracted increasing interest owing to their higher energy density and safety. As the core material of ASSBs, the characteristics of the solid electrolyte largely determine the performance of the battery. Thus far, a variety of inorganic solid electrolytes have been studied, including the NASICON-type, LISICON-type, perovskite-type, garnet-type, glassy solid electrolyte, and so on. The garnet Li₇La₃Zr₂O₁₂ (LLZO) solid electrolyte is one of the most promising candidates because of its excellent comprehensively electrochemical performance. Both, experiments and theoretical calculations, show that cubic LLZO has high room-temperature ionic conductivity and good chemical stability while contacting with the lithium anode and most of the cathode materials. In this paper, the crystal structure, Li-ion transport mechanism, preparation method, and element doping of LLZO are introduced in detail based on the research progress in recent years. Then, the development prospects and challenges of LLZO as applied to ASSBs are discussed.

• 한국전기전자재료학회논문지
• /
• 제11권9호
• /
• pp.733-738
• /
• 1998

본 논문에서는 고체 리듐 전지를 개발하기 위하여 poly(ethylene oxide) [PEO] 에 $LiClO_4$, poly (vinylidene fluoride) [PVDF] 및 가소제로 propylene carbonate [PC] 와 ethylene carbonate[EC] 등을 혼합여 고분자 저해질을 제조하였다. 또한 고체 리듐 전지용 정극으로써 우수한 특성이 기대되는 $Li_xV_3O_8$을 졸-겔법에 의해 합성하여 $Li_xV_3O_8$SPE/Li cell 의 전기화학적 특성을 측정하였다. 고분자 matrix는 PEO와 PVDE를 혼합 사용한 결과 $PEO_4 PVDF_4LiCIO_4PC_5EC_5$ 고분자 전해질이 상온에서 $5.2 {\times} 10{-3}$ S/cm 의 높은 이온 전도도를 나타냈으며 리듐 이온 transference number는 0.3이었다. 졸-겔법에 의해 제조된 $Li_xV_3O_8$을 사용한 $Li_xV_3O_8$SPE/Li cell의 방전시 cell 저항이 방전 초기에는 비소한 증가를 하다가 방전 말기 전압인 2.0V에서 크게 증가하였다. $Li_xV_3O_8$ composite 정극의 첫 번째 방전 용량은 295㎃h/g이었으며 8번째 충방전 싸이클부터 방전 용량이 안정화 되었고 15번째 방전 용량도 212㎃h/g으로 고체 전지용 정극으로써 우수한 특성을 보였다.

• 한국세라믹학회지
• /
• 제48권5호
• /
• pp.379-383
• /
• 2011

This paper presents the synthesis of one-dimensional spinel $LiMn_2O_4$ nanostructures using a facile and scalable two-step process. $LiMn_2O_4$ nanorods with average diameter of 100 nm and length of 1.5 ${\mu}m$ have been prepared by solid-state lithiation of hydrothermally synthesized ${\beta}$-$MnO_2$ nanorods. $LiMn_2O_4$ nanowires with diameter of 10 nm and length of several micrometers have been fabricated via solid-state lithiation of ${\beta}$-$MnO_2$ nanowires. The precursors have been lithiated with LiOH and reaction temperature and pressure have been controlled. The complete structural transformation to cubic phase and the maintenance of 1-D nanostructure morphology have been evaluated by XRD, SEM, and TEM analysis. The size distribution of the spinel $LiMn_2O_4$ nanorods/wires has been similar to the $MnO_2$ precursors. By control of reaction pressure, cubic 1-D spinel $LiMn_2O_4$ nanostructures have been fabricated from tetragonal $MnO_2$ precursors even below $500^{\circ}C$.