Small-film-type ion sensors are garnering considerable interest in the fields of wearable healthcare and home-based monitoring systems. The performance of these sensors primarily relies on electrode capacitance, often employing nanocomposite materials composed of nano- and sub-micrometer particles. Traditional techniques for enhancing capacitance involve the creation of nanoparticles on film electrodes, which require cost-intensive and complex chemical synthesis processes, followed by additional coating optimization. In this study, we introduce a simple one-step electrochemical method for fabricating gold nanoparticles on a carbon nanotube (Au NP–CNT) electrode surface through cyclic voltammetry deposition. Furthermore, we assess the improvement in capacitance by distinguishing between the electrical double-layer capacitance and diffusion-controlled capacitance, thereby clarifying the principles underpinning the material design. The Au NP–CNT electrode maintains its stability and sensitivity for up to 50 d, signifying its potential for advanced ion sensing. Additionally, integration with a mobile wireless data system highlights the versatility of the sensor for health applications.

The pitch-based activated carbons were prepared with KOH/KMnO4 as a multiple function activation agent to increase the specific capacitance of a supercapacitor electrode active material. And the porous structure and electrochemical properties of activated carbon were analyzed on varying amounts of KMnO4. KMnO4 was decomposed into K2O, MnO, and O2 at the activation temperature of KOH, and MnO was introduced to activated carbon. K2O/ O2 reacts with a surrounding pitch to generate micropores and forms a pathway that exposes MnO to the outside. It also affects to the specific surface area of activated carbon like KOH chemical activation. The enhanced specific surface area and introduced MnO in activated carbon led to a 28.9% increase in specific capacitance.

본 실험은 토마토(Solanum lycopersicum L. ‘Hoyong’ ‘Super Doterang’) 암면재배에서 배지 전체의 정전용량을 측정할 수 있는 장치(Substrate capacitance measurement device, SCMD)를 기반으로 한 적정 급액 방법을 구명하기 위하여 누적일사량 제어구(Integrated solar radiation automated irrigation, ISR)와 물관수액흐름 제어구(sap flow automated irrigation, SF)를 대조구로 비교하면서 봄부터 여름철과 겨울철에 재배를 실시하였다. SCMD 제어구는 급액 개시 후 배지 한 개당 설정된 배액 목표량이 처음 발생하는 시점까지 10분간격으로 급액하였고 첫 배액이 배출되면 그 때의 배지의 정전용량(Capacitance)을 100%로 간주하고 그 기준치의 급액제어 점(Capacitance threshold, CT)에 도달하면 급액 되었고 그 뒤 목표 배액량이 발생하면 급액이 멈추는 방식으로 제어되었다. 봄부터 여름재배에서 실험 처리를 위해 SCMD제어구의 일회 급액량 (Irrigation volume per event)을 50, 75, 또는 100mL로 설정하였고 겨울철 재배에서는 CT가 0.65, 0.75, 또는 0.90가 되면 급액 되도록 설정하였다. 봄부터 여름철 재배에서 일회 급액량을 50, 75, 100mL로 설정하였을 때 급액 횟수는 각각 39, 29, 19회 였고 배액율은 각각 3.04, 9.25, 20.18%였다. 겨울철 재 배에서 CT를 0.65, 0.75, 0.90로 설정하였을 때 급액횟수는 각각 5.67, 6.50, 14.67회였고 배액율은 9.91, 10.78, 35.3%였다. 봄부터 여름철 재배에서 일회 급액량 처리에 따른 물관수액흐름속도(SF) 변화는 1회 급액량과 배액량을 각각 50과 75mL로 제한한 경우 100mL로 제 한한 경우와 비교하여SF 신호가 외부 광량 신호 (SI) 보다 늦어지는 경향(time lag)을 보였고 겨울철 재배에서 CT를 0.65로 설정한 경우는 물관수액흐름 속도나 함수율이 매우 낮아졌고 CT를 0.90로 설정한 경우는 함수율과 물관수액흐름 속도는 매우 높았으나 많은 배액이 배출되었다. 따라서 토마토 봄부터 여름철 재배에서 SCMD를 활용하여 CT를 0.9로, 배지 한 개당 배액 목 표량을 100mL로 설정하였을 때 일회 급액량은 75~100mL 범위가 적합하고 겨울철 재배에서는 1회 급 액량을 75mL로, 배액 목표량을 70mL로 설정하였을 때 CT는 0.75이상 0.9이하 범위가 적합할 것으로 판단되었다. 앞으로 정전용량 값과 배지 용적수분함량의 관계성을 구명하고 보정계수를 구하는 연구가 필요할 것으로 판단된다.

Electrochemical properties and performance of composites performed by incorporating metal oxide or metal hydroxide on carbon materials based on graphene and carbon nanotube (CNT) were analyzed. From the surface analysis by field emission scanning electron microscopy and field emission transmission electron microscopy, it was confirmed that graphene, CNT and metal materials are well dispersed in the ternary composites. In addition, structural and elemental analyses of the composite were conducted. The electrochemical characteristics of the ternary composites were analyzed by cyclic voltammetry, galvanostatic charge-discharge tests, and electrochemical impedance spectroscopy in 6 M KOH, or 1 M Na2SO4 electrolyte solution. The highest specific capacitance was 1622 F g–1 obtained for NiCo-containing graphene with NiCo ratio of 2 to 1 (GNiCo 2:1) and the GNS/single-walled carbon nanotubes/Ni(OH)2 (20 wt%) composite had the maximum specific capacitance of 1149 F g–1. The specific capacitance and rate-capability of the CNT/MnO2/reduced graphene oxide (RGO) composites were improved as compared to the MnO2/RGO composites without CNTs. The MnO2/RGO composite containing 20 wt% CNT with reference to RGO exhibited the best specific capacitance of 208.9 F g–1 at a current density of 0.5 A g–1 and 77.2% capacitance retention at a current density of 10 A g–1.

Resistance switching memory cells were fabricated using atomically dispersed Pt-SiO2 thin film prepared via RF co-sputtering. The memory cell can switch between a low-resistance-state and a high-resistance-state reversibly and reproducibly through applying alternate voltage polarities. Percolated conducting paths are the origin of the low-resistance-state, while trapping electrons in the negative U-center in the Pt-SiO2 interface cause the high-resistance-state. Intermediate resistance-states are obtained through controlling the compliance current, which can be applied to multi-level operation for high memory density. It is found that the resistance value is related to the capacitance of the memory cell: a 265-fold increase in resistance induces a 2.68-fold increase in capacitance. The exponential growth model of the conducting paths can explain the quantitative relationship of resistance-capacitance. The model states that the conducting path generated in the early stage requires a larger area than that generated in the last stage, which results in a larger decrease in the capacitance.

In this study, polyaniline (PANI)/graphene nanosheet (GNS) composites were synthesized through chemical oxidation polymerization by changing the weight ratio of aniline mono-mers. To examine the morphological structure of the composites, scanning electron micros-copy and transmission electron microscopy (TEM) were conducted. TEM results revealed that fibril-likePANI with a diameter of 50 nm was homogeneously coated on the surface of the GNS. The electrochemical properties of the composites were studied by cyclic voltam-metry in 1 M H2SO4 electrolyte. Among the prepared samples, the PANI/GNS (having 40 wt% aniline content) showed the highest specificcapacitance, 528 Fg-1, at 10 mVs-1. The im-proved performance was attributed to the GNS, which provides a large number of active sites and good electrical conductivity. The resulting composites are promising electrode materials for high capacitative supercapacitors.

In this study, cobalt oxide (Co3O4)/graphene composites were synthesized through a simple chemical method at various calcination temperatures. We controlled the crystallinity, particle size and morphology of cobalt oxide on graphene materials by changing the annealing temperatures (200, 300, 400℃). The nanostructured Co3O4/graphene hybrid materials were studied to measure the electrochemical performance through cyclic voltammetry. The Co3O4/graphene sample obtained at 200℃ showed the highest capacitance of 396 Fg-1 at 5 mVs-1. The morphological structures of composites were also examined by scanning electron microscopy and transmission electron microscopy (TEM). Annealing Co3O4/graphene samples in air at different temperatures significantly changed the morphology of the composites. The flower-like cobalt oxides with higher crystallinity and larger particle size were generated on graphene according to the increase of calcination temperature. A TEM analysis of the composites at 200℃ revealed that nanoscale Co3O4 (~7 nm) particles were deposited on the surface of the graphene. The improved electrochemical performance was attributed to a combination effect of graphene and pseudocapacitive effect of Co3O4.

We estimated on the stability of W/O type emulsified fuel using by capacitance sensor, so it concluded the following conclusions. For the first 24 hours, prepared emulsified fuel reveals phase separation ratio of 5%, maintains stable status which verifies the stability of emulsified fuel. Adding more water increases the phase separation ratio rapidly, and adding more surfactant displays stable emulsification. Adding water causes larger size of water droplet diameter, and adding surfactant mixture causes smaller size of water droplet diameter. In conclusion, the size of W/O type emulsified fuel water droplet diameter is directly related to the volume of surfactant, and density of water droplet diameter changes thedistribution according to water contents.

We designed capacitance sensor in order to examine characteristics of W/O type emulsified fuel, so it concluded the following conclusions. The capacitance value of emulsified fuel, using with capacitance sensor, increases as water content increases due to the coalescence. When surfactant increases, the capacitance value decreases, the condition of W/O type emulsified fuel was maintained stably. There was revealed the capacitance value difference of W/O type emulsified fuel in in according to water content. We checked the phase separation of emulsified fuel with the capacitance value difference. The surfactant(HLB=5.4) had better stable condition than surfactant(HLB=4.3). Also, we confirmed that two mixture surfactants were better than one surfactant.

Mesoporous activated carbon fiber (ACF) was prepared from phenolic resin containing a small amount (0.1 wt %) of organic nickel complex through carbonization and steam activation. Microporous ACF as reference sample was also prepared from phenolic resin without agent. In both cases of the mesoporous ACFs and the microporous ACFs, the electric double layer capacitance of the nonaqueous electrolyte (0.5 M TEABF4/PC or 1.0 M LiClO4/PC) was not proportional to the BET specific surface area. This is owing to the low permeability of nonaqueous electrolyte or the low mobility of ion in narrow micropores. However, the mesoporous ACF showed higher double layer capacitance than the microporous (normal) ACF. This result suggests that the presence of many mesopores promotes the formation of effective double layer or the transfer of ion in the micropore.

전해콘텐서용 알루미늄박의 직류에칭에서 1M 염산욕에 부식억제제로 1M 황산을 첨가했을 때의 영향을 조사하기 위하여 에치 피트의 밀도, 에치 터널의 길이와 직경, 정전 용량 등의 변화를 분석하였다. 황산이온은 부식억제제로서 염소이온보다 시료의 표면에서 에치 피트의 밀도를 증가시키며 에치 터널의 직경은 감소하나 길이를 증가시킴으로써 전체적으로 표면적이 커지고 또한 정전 용량 값이 증가하였다. 황산이온을 첨가하였을 경우 전류 밀도가 0.9A/cm2 보다 낮은 경우에는 정전 용량 값이 작지만 그 이상에서는 정전용량이 현저하게 증가하였다.

플라즈마 화학 증착법으로 (100)p-type Si wafer위에 Y2O3-Stabilzed ZrO2박막을 증착하였다. 반응 기체로는 zirconium triflouracethylacetonate[Zr(tfacac) [Zr(tfacac)4], tri(2.2.6.6 tetramethy1-3, 5-heptanate) yttrium [Y(DPM)3]과 oxygen gas를 사용하였다. X-ray diffraction(XRD)과 fourier Particle induced x-ray emission(PIXE)을 통하여 Y(DPM)3 bubbling temperature가 160˚C, 165˚C, 170˚C일때 Y2O3함량이 12.1mo1%, 20.4mol%, 31.6mol%임을 알 수 있었다. C-V측정에서 Y(DPM)3 bubbling temperature가 증가함에 따라 flat band voltage가 더욱더 음의 방향으로 이동하였다.