• 한국수소및신에너지학회논문집
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• 제18권3호
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• pp.244-249
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• 2007

The present work considers the concept of enzymatic photoelectrochemical generation of hydrogen through water splitting using a Xe lamp as a source of light. A solar cell was applied to the system in order to shift the level of electrochemical energy of the system, resulting in the rate of hydrogen production at $43\;{\mu}mol/(cm^2{\times}hr)$ in cathodic compartment with an anodized tubular $TiO_2$ electrode(ATTE, $5^{\circ}C$/1hr in 0.5 wt% HF-$650^{\circ}C$/5hr). The trend of the rate of hydrogen production, for the ATTEs with different annealing temperature from $350^{\circ}C$ to $850^{\circ}C$, fairly well coincided with the photoelectrical properties measured by potentiostat. The actual chemical bias through imposition of two electrolytes of different pHs between anode(13.68) and cathode(7.5) was 0.24eV.

• Food Science and Biotechnology
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• 제14권6호
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• pp.828-831
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• 2005

The content of vitamin $D_2$, including its precursor ergosterol, was determined in some cultivated mushrooms to manufacture fortified Doenjang (Korean traditional soybean paste) with vitamin D by supplementation with mushroom. Ergosterol was the most abundant sterol in the mushrooms (50 to 140 mg/100 g dry weight) but the ergocalciferol portion made up only 0.065% (Pleurotus eryngii) to 2.5% (stipe part of Lentinus edodes, shiitake) of the total vitamin $D_2$ of each mushroom. Changes in these compounds in L. edodes caused by UV or solar irradiation were also evaluated. Ergocalciferol content in the pileus part of L. edodes went up to $424\;{\mu}g/100\;g$ dry weight and ergosterol levels reached 139.3 mg per 100 g dry weight at maximum levels. Ergocalciferol content increased about 50% when exposed to solar radiation and increased 377% with UV irradiation. These compounds level in Doenjang was enriched as much as supplied UV irradiated L. edodes powder to before fermentation, and the supplemented mushroom did not influence the palatability of Doenjang.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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• pp.75-75
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• 2011

Recently, dye-sensitized solar cell (DSSC) attracts great attention as a promising alternative to conventional silicon solar cells. One of the key components for the DSSC would be the nanocrystalline TiO2 electrode, and the control of interface between TiO2 and TCO is a highly important issue in improving the photovoltaic conversion efficiency. In this work, we applied various interfacial layers, and analyzed their effect in enhancing photovoltaic properties. In overall, introduction of interfacial layers increased both the Voc and Jsc, since the back-reaction of electrons from TCO to electrolyte could be blocked. First, several metal oxides with different band gaps and positions were employed as interfacial layer. SnO2, TiO2, and ZrO2 nanoparticles in the size of 3-5 nm have been synthesized. Among them, the interfacial layer of SnO2, which has lower flat-band potential than that of TiO2, exhibited the best performance in increasing the photovoltaic efficiency of DSSC. Second, long-range ordered cubic mesoporous TiO2 films, prepared by using triblock copolymer-templated sol-gel method via evaporation-induced self-assembly (EISA) process, were utilized as an interfacial layer. Mesoporous TiO2 films seem to be one of the best interfacial layers, due to their additional effect, improving the adhesion to TCO and showing an anti-reflective effect. Third, we handled the issues related to the optimum thickness of interfacial layers. It was also found that in fabricating DSSC at low temperature, the role of interfacial layer turned out to be a lot more important. The self-assembled interfacial layer fabricated at room temperature leads to the efficient transport of photo-injected electrons from TiO2 to TCO, as well as blocking the back-reaction from TCO to I3-. As a result, fill factor (FF) was remarkably increased, as well as increase in Voc and Jsc.

• 한국분말재료학회지
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• 제17권3호
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• pp.216-222
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• 2010

Self-standing $TiO_2$ nanotube arrays were fabricated by potentiostatic anodic oxidation method using pure Ti foil as a working electrode and ethylene glycol solution as electrolytes with small addition of $NH_4F$ and $H_2O$. The influences of anodization temperature and time on the morphology and formation of $TiO_2$ nanotube arrays were investigated. The fabricated $TiO_2$ nanotube arrays were applied as a photoelectrode to dye-sensitized solar cells. Regardless of anodizing temperature and time, the average diameter and wall thickness of $TiO_2$ nanotube show a similar value, whereas the thickness show a different trend with reaction temperature. The thickness of $TiO_2$ nanotube arrays anodized at $20^{\circ}C$ and $30^{\circ}C$ was time-dependent, but on the other hand its at $10^{\circ}C$ are independent of anodization time. The conversion efficiency is low, which is due to a morphology breaking of the $TiO_2$ nanotube arrays in manufacturing process of photoelectrode.

• 공업화학
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• 제24권4호
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• pp.396-401
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• 2013

Benzo[1,2,5]thiadiazole, carbazole 및 phenanthrene을 기본 골격으로 한 교대공중합체인 poly[9-(2-octyl-dodecyl)-9H-carbazole-alt-4,7-di-thiophen-2-yl-benzo[1,2,5]thiadiazole] (PCD20TBT)와 poly[9,10-bis-(2-octyl-dodecyloxy)-phenanthrene-alt-4,7-di-thiophen-2-yl-benzo[1,2,5]thiadiazole] (PN40TBT)을 Suzuki coupling reaction을 이용하여 중합하였다. 합성한 고분자들은 chloroform, chlorobenzene, 1,2-dichlorobenzene, tetrahydrofuran, toluene과 같은 유기용매에 대한 용해도가 우수하였다. PCD20TBT의 최대흡수 파장과 밴드갭은 각각 535 nm와 1.75 eV이고, PN40TBT의 최대흡수 파장과 밴드갭은 각각 560 nm과 1.97 eV이었다. PCD20TBT의 HOMO 및 LUMO 에너지준위는 각각 - 5.11 eV와 - 3.36 eV이고, PN40TBT의 HOMO 및 LUMO 에너지준위는 각각 -5.31 eV와 -3.34 eV이었다. 합성한 고분자와 (6)-1-(3-(methoxycarbonyl)-{5}-1-phenyl[5,6]-fullerene(PCBM)을 1:2의 중량비로 블랜딩하여 제작한 이종접합형태(bulk heterojunction) 태양전지를 제작하였다. PCD20TBT의 광전변환효율은 0.52%, PN40TBT의 광전변환효율은 0.60%이었다. 그리고 소자의 단락 전류밀도, 충진 인자와 개방전압은 PCD20TBT가 각각 $-1.97mA/cm^2$, 38.2%, 0.69 V이며, PN40TBT의 경우 각각 $-1.77mA/cm^2$, 42.9%, 0.79 V이었다.

• 한국재료학회:학술대회논문집
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• 한국재료학회 2010년도 춘계학술발표대회
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• pp.3.1-3.1
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• 2010

Water splitting reaction using photocatalysts is of great interest in the utilization of solar energy [1]. In the present work, visible light-responsive $TiO_2$ thin films (Vis-$TiO_2$) were prepared by a radio frequency magnetron sputtering (RF-MS) deposition method and applied for the separate evolution of $H_2$ and $O_2$ from water as well as the photofuel cell. Special attentions will be focused on the effect of HF treatment of Vis-$TiO_2$ thin films on their photocatalytic activities. Vis-$TiO_2$ thin films were prepared by an RF-MS method using a calcined $TiO_2$ plate and Ar as the sputtering gas. The Vis-$TiO_2$ thin films were then deposited on the Ti foil substrate with the substrate temperature at 873 K (Vis-$TiO_2$/Ti). Vis-$TiO_2$/Ti thin films were immersed in a 0.045 vol% HF solution at room temperature. The effect of HF treatments on the activity of Vis-$TiO_2$/Ti thin films for the photocatalytic water splitting reaction have been investigated. Vis-$TiO_2$/Ti thin films treated with HF solution (HF-Vis-$TiO_2$/Ti) exhibited remarkable enhancement in the photocatalytic activity for $H_2$ evolution from a methanol aqueous solution as well as in the photoelectrochemical performance under visible light irradiation as compared with the untreated Vis-$TiO_2$/Ti thin films. Moreover, Pt-loaded HF-Vis-$TiO_2$/Ti thin films act as efficient and stable photocatalysts for the separate evolution of $H_2$ and $O_2$ from water under visible light irradiation in the presence of chemical bias. Thus, HF treatment was found to be an effective way to improve the photocatalytic activity of Vis-$TiO_2$/Ti thin films. Furthermore, unique separate type photofuel cell was fabricated using a Vis-$TiO_2$ thin film as an electrode, which can generate electrical power under solar light irradiation by using various kinds of biomass derivatives as fuel. It was found that the introduction of an iodine ($I^-/{I_3}^-$) redox solution at the cathode side enables the development of a highly efficient photofuel cell which can utilize a cost-efficient carbon electrode as an alternative to the Pt cathode.

• 공업화학
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• 제23권4호
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• pp.377-382
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• 2012

CIGS 화합물 반도체 태양전지에서 광흡수층과 상부투명전극 간의 격자부정합을 낮추기 위해 buffer layer로써 CdS 박막이 적용된다. 높은 광투과도와 낮은 비저항을 갖는 CdS 박막을 제조하기 위하여 화학적 용액 증착법에 의해 반응용액 내의 S 용액의 농도를 고정하고 Cd 용액의 농도를 변화시켜 CdS 박막을 제조하여 특성을 조사하였다. $[S^{2-}]/[Cd^{2+}]$ 농도비에 따른 박막의 구조적, 광학적 및 전기적 특성을 조사하였다. Cd의 농도가 S의 농도보다 높을 경우에는 균일반응이 촉진되어 CdS 결정들이 클러스터 형태로 기판에 흡착되어 결정 크기가 증가하고 광투과율이 감소하였다. 반면, Cd의 농도가 S의 농도보다 낮을 경우에는 용액 내에서 보다 기판위에서 CdS 결정입자가 생성되는 불균일반응에 의해 결정이 생성 및 성장되었고 수백 옹스트롱의 작고 균일한 구형 입자가 생성되었다. Cd 농도가 증가할수록 과잉 Cd가 증가하여 S 공극 생성으로 $[S^{2-}]/[Cd^{2+}]$ 조성비는 감소하였고 CdS 박막의 전하 농도가 증가되어 비저항이 감소되었다.

• 공업화학
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• 제25권1호
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• pp.84-89
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• 2014

본 연구에서는 초음파환원법을 이용하여 이산화티탄($TiO_2$) 미립자 표면에 은나노메탈이 도핑된 Ag-$TiO_2$ 나노복합체를 제조하였다. $TiO_2$ 표면에 생성되는 은나노금속은 약 1~3 nm의 사이즈분포를 나타내었고, 환원반응시 첨가되는 $AgNO_3$의 양이 증가할수록 $TiO_2$ 표면에 형성되는 은나노금속의 개수가 증가하였다. 이렇게 얻어진 일정량의 Ag-$TiO_2$ 나노복합체를 대장균(E-coli)과 함께 고체멸균배지에 도말하여 태양광모사 제논램프로부터 30 min간 $600{\sim}1800{\mu}w/cm^2$의 빛을 조사한 후 $37^{\circ}C$에서 24 h 배양한 후 생존한 콜로니의 개수를 측정하였다. 실험 결과 대조군대비 순수한 $TiO_2$를 첨가했을 때보다 Ag-$TiO_2$를 첨가 시 항균활성도가 더 높게 나타났다. 또한 Ag-$TiO_2$ 주입양이 증가할수록 콜로니의 개수가 감소하였고, 초기 30 min간 조사한 빛의 세기가 증가할수록 Ag-$TiO_2$의 항균효과가 증가하였다. 또한 은나노금속의 도핑양이 증가할수록 광촉매 효율은 감소하였지만 항균효과는 지속적으로 증가하는 경향을 나타내었다.

• Bulletin of the Korean Chemical Society
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• 제24권4호
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• pp.446-452
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• 2003

Some new nanohybrid materials have been synthesized by intercalating the oxotitanium(IV) meso-tetrakis(4- sulfonatophenyl) porphyrin$(O=Ti^{(IV)} TSPP)$ into the Zn/Al layered double hydroxides (LDHs), and their structures and photophysical properties have been investigated by various laser spectroscopic techniques. According to the XRD pattern of the synthesized nanohybrid materials, the macrocycle plane of $O=Ti^{(IV)}$ TSPP are grafted perpendicular to the LDH layers. The $O=Ti^{(IV)}$ TSPP-intercalated LDH exhibits band broadening of the absorption spectrum and a blue shift of Q-band as compared to that observed in solution. Resonance Raman spectral measurements demonstrate that the positively charged LDHs give rise to a slight decrease of the electronic density of the porphyrin ring accompanying a small change of the electronic distribution of the $O=Ti^{(IV)}$ TSPP. Consequently the LDH environment affects the energies of the two highest occupied molecular orbitals (HOMOs) of the $O=Ti^{(IV)}$) TSPP, $a_{1u}$ and $a_{2u}$, producing a mixed orbital character. Being consistent with these electronic structural changes of $O=Ti^{(IV)}$ TSPP in LDH, both the fluorescence spectral change and the fsdiffuse reflectance transient measurements imply that the photoexcitation of the $O=Ti^{(IV)}$ TSPP intercalated into LDH undergoes fast relaxation to the O=Ti(IV) $TSPP^+-LDH^- $charge transfer (CT) state within a few picoseconds, followed by a photoinduced electron transfer between the O=Ti(IV) TSPP and LDHs with a rate constant greater than %1×10^{10}S^{-1}$. No evidence is found for back electron transfer. In conclusion, the $O=Ti^{(IV)}$ TSPP intercalated LDH seems to be a possible candidate for an artificial reaction center for an efficient solar energy conversion system.

• 공업화학
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• 제27권1호
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• pp.16-20
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• 2016

본 연구에서는 $TiO_2$/마이카 혼성 복합 재료의 합성과 적외선 반사 특성에 관한 연구를 수행하였다. 마이카 입자의 존재 하에 아세트산 수용액에서 titanium isopropoxide의 가수 분해 반응과 축합 반응에 의해 $TiO_2$/마이카 복합 재료를 합성하였다. $TiO_2$/마이카 복합 재료의 열처리($600{\sim}1000^{\circ}C$, 1~3 h)에 의해 마이카 표면에 형성된 비결정성 상의 $TiO_2$은 anatase 상을 거쳐 결정성 rutile 상으로 전환되었으며 열처리 조건에 의해 결정의 크기가 제어되었다. FE-SEM 분석, ED-XRF 분석, XRPD 분석을 통하여 마이카와 $TiO_2$/마이카 복합 재료의 물리화학적 특성을 규명하였다. 확산 반사-근적외선 분광 분석을 통하여 측정한 $TiO_2$/마이카 혼성 복합 재료의 근적외선 범위(780~2,500 nm)에서의 일사 반사율은 88.6%로, 순수한 소성 마이카의 86.6%보다 다소 높았다. 따라서 $TiO_2$/마이카 혼성 복합 재료는 높은 광반사율을 나타내는 차열 도료의 안료로 사용할 수 있을 것이다.