Photoanode optimization is a fascinating technique for enlightening the power conversion efficiency (PCE) of dye-sensitized solar cells (DSSCs). In this present study, V2O5/ ZnO and reduced graphene oxide (rGO)-V2O5/ZnO nanocomposites (NCs) were prepared by the solid-state technique and used as photoanodes for DSSCs. A wet chemical technique was implemented to generate individual V2O5 and ZnO nanoparticles (NPs). The structural characteristics of the as-synthesized NCs were investigated and confirmed using powder X-ray diffraction (XRD), X-ray photoelectron spectra (XPS), and Scanning electron microscope (SEM) with energy dispersive X-ray (EDX) analysis. The average crystallite size (D) of the as-synthesized V2O5/ ZnO and rGO-V2O5/ZnO NCs was determined by Debye-Scherer’s formula. The bandgap (eV) energy was calculated from Tauc’s plots, and the bonding nature and detection of the excitation of electrons were investigated using the Ultra violet (UV) visible spectra, Fourier Transform infrared (FTIR) and photoluminescence (PL) spectral analysis. Electrical studies like Hall effect analysis and the Nyquist plots are also described. The V2O5/ ZnO and rGO-V2O5/ZnO NCs based DSSCs exhibited 0.64% and 1.27% of PCE and the short circuit current densities and open circuit voltages improved from 7.10 to 11.28 mA/cm2 and from 0.57 to 0.68 V, respectively.

For the selective catalytic reduction of NOx with ammonia (NH3-SCR), a V2O5WO3/TiO2 (VW/nTi) catalyst was prepared using V2O5 and WO3 on a nanodispersed TiO2 (nTi) support by simple impregnation process. The nTi support was dispersed for 0~3 hrs under controlled bead-milling in ethanol. The average particle size (D50) of nTi was reduced from 582 nm to 93 nm depending on the milling time. The NOx activity of these catalysts with maximum temperature shift was influenced by the dispersion of the TiO2. For the V0.5W2/nTi-0h catalyst, prepared with 582 nm nTi-0h before milling, the decomposition temperature with over 94 % NOx conversion had a narrow temperature window, within the range of 365-391 °C. Similarly, the V0.5W2/nTi-2h catalyst, prepared with 107 nm nTi-2h bead-milled for 2hrs, showed a broad temperature window in the range of 358~450 °C. However, the V0.5W2/Ti catalyst (D50 = 2.4 μm, aqueous, without milling) was observed at 325-385 °C. Our results could pave the way for the production of effective NOx decomposition catalysts with a higher temperature range. This approach is also better at facilitating the dispersion on the support material. NH3-TPD, H2-TPR, FT-IR, and XPS were used to investigate the role of nTi in the DeNOx catalyst.

This study describes the doping effect of Yb2O3 on microstructure, electrical and dielectric properties of ZnO-V2O5- MnO2-Nb2O5 (ZVMN) ceramic semiconductors sintered at a temperature as low as 900°C. As the doping content of Yb2O3 increases, the ceramic density slightly increases from 5.50 to 5.54 g/cm3; also, the average ZnO grain size is in the range of 5.3-5.6 μm. The switching voltage increases from 4,874 to 5,494 V/cm when the doping content of Yb2O3 is less than 0.1 mol%, whereas further doping decreases this value. The ZVMN ceramic semiconductors doped with 0.1 mol% Yb2O3 reveal an excellent nonohmic coefficient as high as 70. The donor density of ZnO gain increases in the range of 2.46-7.41×1017 cm−3 with increasing doping content of Yb2O3 and the potential barrier height and surface state density at the grain boundaries exhibits a maximum value (1.25 eV) at 0.1 mol%. The dielectric constant (at 1 kHz) decreases from 592.7 to 501.4 until the doping content of Yb2O3 reaches 0.1 mol%, whereas further doping increases it. The value of tanδ increases from 0.209 to 0.268 with the doping content of Yb2O3.

We have investigated a glass-forming region of V2O5- P2O5-ZnO glass and the effects of the addition of modifier oxides (B2O3) to the glass systems as a sealing material to improve the adhesion between the glass frits and a soda lime substrate. Thermal properties and coefficient of thermal expansion were measured using a differential scanning calorimetry, a dilatometer and a hot stage microscopy. Structural changes and interfacial reactions between the glass substrate and the glass frit after sintering (at 400 oC for 1 h) were measured by Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy and scanning electron microscope. The results showed that the adhesion strength increases as the content of B2O3 at 5 mol% increases because of changes in the structural properties. It seems that the glass structures change with B2O3, and the Si4+ ions from the substrate are diffused to the sealing glass. From these results, we could understand the mechanism of strengthening of the adhesion of soda lime silica substrate by ion-diffusion from the substrate to the glass.

For the aim of low-temperature co-fired ceramic microwave components, sintering behavior and microwave properties (dielectric constant , quality factor Q, and temperature coefficient of resonant frequency ) are investigated in [BCZN] ceramics with addition of . The specimens are prepared by conventional ceramic processing technique. As the main result, it is demonstrated that the additives () show the effect of lowering of sintering temperature and improvement of microwave properties at the optimum additive content. The addition of 0.25 wt% lowers the sintering temperature to utilizing liquidphase sintering and show the microwave dielectric properties (dielectric constant = 75, quality factor = 572 GHz, temperature coefficient of resonance frequency ). The estimated microwave dielectric properties with addition (increase of , decrease of , shift of to negative values) can be explained by the observed microstrucure (sintered density, abnormal grain structure) and possibly high-permittivity (BZN) phase determined by X-ray diffraction.

We designed new compositions for lead free and low temperature sealing glass frit of ZnO-V2O5-P2O5 system, which can be used for PDP (Plasma Display Panel) or other electronic devices. The ZnO-V2O5-P2O5 system can be used as a sealing material at temperatures even lower than 430˚C. This system, however, showed lower bonding strength with glass substrate compared to commercialized Pb based sealing materials. So, we added TiO2 as a promoter for bonding strength. We examined the effect of TiO2 addition on sealing behaviors of ZnO-V2O5-P2O5 glasses with the data for flow button, wetting angle, temporary & permanent residual stress of glass substrate, EPMA analysis of interface between sealing materials and glass substrate, and bonding strength. As a result, sealing characteristics of ZnO-V2O5-P2O5 system glasses were improved with TiO2 addition, but showed a maximum value at 5 mol% TiO2 addition. The reason for improved bonding characteristics was considered to be the chemical interaction between glass substrate and sealing glass, and structural densification of sealing glass itself.

진공증착법으로 제작한 V2O5 박막의 두께 및 결정성에 따른 전기변색 특성을 체계적으로 조사하였다. 증착된 박막은 노란색을 띄고 있었으며 140˚C 보다 높은 기판온도에서 증착된 V2O5 박막은 결정질로 낮은 기판온도에서 증착된 박막들은 비정질로 밝혀졌다. 리튬 이온 주입에 따른 V2O5 박막의 광 변조 특성 결과 V2O5 박막의 두께와 결정성에 관계없이 300~500nm 파장영역에서는 산화발색이 500~1100nm 파장영역에서는 환원 발색이 나타났다. 비정질과 결정질 Lix V2O5 박막의 optical band gap 에너지는 리튬 이온 주입양이 증가함에 따라 (x=0.0~0.6) 각각 0.75 [eV], 0.17 [eV]씩 높은 에너지쪽으로 이동하였다. 비정질 Lix V2O5 박막의 coloration efficiency는 근적외선 영역에서는 리튬 이온 주입과 박막두께에 따라 거의 변화가 없었으나 blue와 near-UV 영역에서는 absorption edge가 500nm 파장근처에서 높은 에너지 부근으로 이동됨으로 인하여, 박막두께가 증가하고 리튬 이온주입양이 감소할수록 coloration efficiency가 상당히 증가하는 것으로 나타났다. 그러나 결정질 Lix V2O5 박막의 경우 coloration efficiency는 전파장영역에서 리튬 이온 주입양과 박막두께에 거의 영향을 받지 않는 것으로 밝혀졌다.

V2O5-TiO2 catalysts were prepared by various methods. V2O5-TiO2 were prepared by sol-gel method with different drying conditions (aerogel and xerogel), and V2O5 supported on TiO2 obtained by sol-gel method with precipitation-deposition method and impregnation method. The performance of the V2O5-TiO2 catalysts was investigated for the selective oxidation of hydrogen sulfide in the stream containing both ammonia and excess water. All the catalysts showed good dispersion of vanadium and they had high H2S conversion with no or little production of sulfur dioxide. The V2O5-TiO2 aerogel catalyst prepared by sol-gel method with drying under super critical condition had the highest surface area which led to better catalytic activity compared to those by other synthesis methods.

질소산화물 등의 배출규제 강화로 인한 사용처의 확대로 SCR(선택적 촉매 환원) 촉매 수요가 증가하고 있으며, 이에 따라 폐촉매 발생량도 증가할 것으로 예상된다. 폐촉매는 지정폐기물로 분류되어 처리시에 비용이 발생하여, 물리적으로 재생하여 재사용 하거나 유가금속을 회수하는 방법으로 재활용하고 있다. 그러나 재생의 횟수가 제한적이고, 유가금속 회수는 비용이 고가이며 촉매의 85~90%를 차지하는 TiO2가 폐기된다는 문제점이 있다. 따라서, 본 연구에서는 SCR 촉매를 경제적이며 지속적으로 사용하기 위해 피독된 SCR 촉매 내 피독물질만 화학적으로 수세 및 정제하고 유가금속/TiO2의 함량을 높이는 최적의 세정 용매를 도출하는 촉매 재활성을 위한 기초연구를 수행하였다. 비교대상 촉매인 Poisoned 촉매를 5가지 세정용매로 화학적 처리결과, acetic acid 용매가 V2O5 1.19 wt%의 높은 함량과 57.6%의 높은 피독물질 제거효율을 나타내며 다른 산 처리 용매에 비해 촉매 재생성이 높은 것으로 분석되었다. 세정 용매의 농도와 세정 시간에 따른 V2O5 함량과 피독물질 제거효율에 미치는 영향을 알아보기 위해 각각 변수를 두어 실험을 진행하였다. 본 연구를 통해 0.1 N acetic acid로 처리한 촉매가 가장 높은 NOX전환율을 나타냈으며, 유가금속/TiO2 함량 또한 높게 나타나 본 연구 목표에 가장 적합한 세정용매로 판단되었다.

This study examined the catalytic destruction of 1,2-dichlorobenzene on V2O5/TiO2 nanoparticles. The V2O5/TiO2 nanoparticles were synthesized by the thermal decomposition of vanadium oxytripropoxide and titanium. The effects of the synthesis conditions, such as the synthesis temperature and precursor heating temperature, were investigated. The specific surface areas of V2O5/TiO2 nanoparticles increased with increasing synthesis temperature and decreasing precursor heating temperature. In addition, the removal efficiency of 1,2-dichlorobenzene was promoted by a decrease in heating temperature. However, the removal efficiency of 1, 2-dichlorobenzene was decreased by an anatase to rutile phase transformation at temperatures 1,300℃.

V2O5/TiO2 catalyst impregnated ceramic candle filters are in principle, capable of performing shallow-bed dust filtration plus a catalytic reaction, promoted by a catalytic deposited in their inner structure. Pilot-scale V2O5/TiO2 catalyst impregnated ceramic candle filters were prepared, characterized and tested for their activity towards the SCR reaction. The effect on NO conversion of operating temperature, gas hourly space velocity, amount of deposited catalyst, pressure drops and long-term experiment (life of catalytic filter) was determined. The following effects of V2O5/TiO2 catalyst impregnated ceramic candle filters in SCR reaction are observed: (1) It increases the activity and widens the temperature window for SCR. (2) When the content of V2O5 catalyst increases further from 3 to 9wt.%, activity of NO increases. (3) NO conversion at first increases with temperature and then decreases at high temperatures (above 400℃ over), possibly due to the occurrence of the ammonia oxidation reaction.

A (5 wt.%)Mn-(1 wt.%)V2O5/TiO2 catalyst were prepared by co-precipitation method and used for low-temperature selective catalytic reduction (SCR) of NOx with ammonia in the presence of oxygen. The properties of the catalysts were studied by X-ray diffraction (XRD), temperature programmed reduction (TPR) and scanning electron microscope-energy dispersive X-ray spectroscopy (SEM-EDS). The experimental results showed that (5 wt.%)Mn-(1 wt.%)V2O5/TiO2 catalyst yielded 81% NO conversion at temperature as low as 150℃ and a space velocity of 2,400 h-1. Crystalline phase of Mn2O3 was present at ≥15% Mn on V2O5/TiO2. XRD confirmed the presence of manganese oxide (Mn2O3) at 2θ=32.978°(222). The XRD patterns presented of (5 wt.%)Mn-(1 wt.%)V2O5/TiO2 did not show intense or sharp peaks for manganese oxides and vanadia oxides. The TPR profiles of (5 wt.%)Mn-(1 wt.%)V2O5/TiO2 catalyst showed main reduction peak of a maximum at 595℃.

V2O5/TiO2 catalysts promoted with Mn were prepared and tested for selective catalytic reduction of NOx in NH3. The effects of promoter content, degree of catalyst loading were investigated for NOx activity while changing temperatures, mole ratio, space velocity and O2 concentration. Among the various V2O5 catalysts having different metal loadings, V2O5(1 wt.%) catalyst showed the highest activity(98%) under wide temperature range of 200-250℃. When the V2O5 catalyst was further modified with 5 wt.% Mn as a promoter, the highest activity(90-47%) was obtained over the low temperature windows of 100-200℃. From Mn-V2O5/TiO2, it was found that by addition of 5 wt.% Mn on V2O5/TiO2 catalyst, reduction activity of catalyst was improved, which resulted in the increase of catalytic activity and NOx reduction. According to the results, NOx removal decreased for 10%, but the reaction temperature down to 100℃.