• 공업화학
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• 제18권4호
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• pp.356-360
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• 2007

나노 다공질 $TiO_2$ 전극막, 광 감응형 염료, 전해질 그리고 상대전극으로 구성된 염료감응형 태양전지(Dye-Sensitized Solar Cells, DSSCs)는 최근에 많은 관심을 받아오고 있다. 염료감응형 태양전지에서 $TiO_2$ 전극막은 태양광의 흡수량을 증가시키기 위해 가능한 많은 양의 Ru 착물을 표면에 흡착시켜야 하는데 이를 위해 높은 비표면적과 나노 다공성 입자로 구성된 광전극이 요구된다. 또한 에너지 전환 효율을 증가시키기 위한 방법으로 $TiO_2$ 페이스트의 제작시 산을 첨가 후 열처리하는 방법이 보고되고 있다. 이 논문에서는 산이 첨가된 페이스트로 제조한 $TiO_2$ 광전극이 염료감응형 태양전지의 에너지 변환 효율에 미치는 영향을 체계적으로 이해하기 위해 FE-SEM, XPS, EXAFS 그리고 AFM 등을 이용하여 제조된 광전극의 물리적 화학적 특성을 조사하였다. 또한 광전류-전압 곡선으로부터 산처리된 페이스트를 이용하여 제조한 염료감응형 태양전지의 에너지 전환효율을 평가하였다. 산처리된 페이스는 염료감응형 태양전지의 에너지 전환효율에 크게 영향을 미침을 알 수 있었다.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2010년도 춘계학술대회 초록집
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• pp.75.1-75.1
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• 2010

Dye sensitized solar cells(DSSCs) have been extensively studied due to their various advantages such as low production cost, colorful design, and eco-friendly process. Long optical path length is one of the most effective method to improve light harvest efficiency for DSSCs. Multi-layered $TiO_2$ nano-structured film with scattering layer has been studied to generate scattering effect by many researchers. It was expected that the difference of refractive index between $TiO_2$ particles and glass frit would generate the light scattering effect and provide the long optical path length. Therefore, to enhance the scattering effect, the frits of $Bi_2O_3-B_2O_3$-ZnO glass system that has the different refractive index were added to $TiO_2$ pastes in this study. First of all, the absorbance and haze factor of $TiO_2$ electrode with dyes and the refractive index of glass frit and $TiO_2$ were measured, respectively. To study the effect of frits, the efficiencies of DSSCs added glass frit and without glass frit were compared. Our results showed slightly higher efficiency with the different absorbance and haze factor of $TiO_2$ and glass frit. It was considered that the light scattering effect would be improved with adding frits to $TiO_2$ paste. Our preliminary studies will be useful for increasing efficiency of DSSCs.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2010년도 춘계학술대회 초록집
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• pp.90.1-90.1
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• 2010

Due to the rapidly diminishing energy sources and higher energy production cost, the interest in dye-sensitized solar cells (DSSCs) has been increasing dramatically in recent years. A typical DSSC is constructed of wide band gap semiconductor electrode such as $TiO_2$ or ZnO that are anchored by light-harvesting sensitizer dyes and surrounded by a liquid electrolyte with a iodide ion/triiodide ion redox couple. DSSCs based on one-dimensional nano-structures, such as ZnO nanorods, have been recently attracting increasing attention due to their excellent electrical conductivity, high optical transmittance, diverse and abundant configurations, direct band gap, absence of toxicity, large exiton binding energy, etc. However, solar-to-electrical conversion performances of DSSCs composed of ZnO n-type photo electrode compared with that of $TiO_2$ are not satisfactory. An important reason for the low photovoltaic performance is the dissolution of $Zn^{2+}$ by the adsorption of acidic dye followed by the formation of agglomerates with dye molecules which could block the I-diffusion pathway into the dye molecule on the ZnO surface. In this paper, we prepared the DSSC with the ZnO electrode using the chemical bath deposition (CBD) method under low temperature condition (< $100^{\circ}C$). It was demonstrated that the ZnO seed layers played an important role on the formation of the ZnO nanostructures using CBD. To achieve truly low-temperature growth of the ZnO nanostructures on the substrates, a two-step method was developed and optimized in the present work. Firstly, ZnO seed layer was prepared on the FTO substrate through the spin-coating method. Secondly, the deposited ZnO seed substrate was immersed into an aqueous solution of 0.25M zinc nitrate hexahydrate and 0.25M hexamethylenetetramine at $90^{\circ}C$ for hydrothermal reaction several times.

• Bulletin of the Korean Chemical Society
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• 제31권1호
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• pp.116-119
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• 2010

Adsorption structures of the self-assembled thin films of $\alpha$-cyano-4-hydroxycinnamic acid (CHCA) anchoring on $TiO_2$ surfaces have been studied by using temperature-dependent diffuse reflectance infrared Fourier-transform (DRIFT) spectroscopy. From the presence of the strong $\nu(COO^-)$ band at ~1390 $cm^{-1}$ along with the disappearance of the OH bands in the carboxylic acid group in the DRIFT spectra at room temperature, CHCA appeared to adsorb onto $TiO_2$ surfaces as a carboxylate form. The absence of the out-of-plane benzene ring modes of CHCA in the DRIFT spectra suggests a rather vertical orientation of CHCA on $TiO_2$. Above ~220$ ^{\circ}C$, CHCA seemed to start to thermally degrade on $TiO_2$ surfaces referring from the disappearance of most vibrational modes in the DRIFT spectra, whereas the $\nu$(C ≡ N) bands were found to remain relatively conspicuous as the temperature increased even up to ~460$^{\circ}C$.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제45회 하계 정기학술대회 초록집
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• pp.69-69
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• 2013

In the area of artificial photosynthesis, particularly for the generation of hydrogen form water, much attention has been paid on organic-inorganic hybrid system. Most of all, a dye/TiO2-combined system has been suggested and its potential utility was well manifested. However, due to its complicated nature of charge interactions in between dye and TiO2 -interface there remains a great challenge to establish the charge-activity relationship, per se light driven charge generation and recombination kinetics with respect to the amount of hydrogen produced. Further complexity of that hybrid system has been witnessed when sacrificial donor and aqueous media are considered. To unveil the operating mechanism on such a dye/TiO2-combined system, we have prepared organic dyes suitable to account for the effect of sacrificial donor as well as water interactions, and prepared the typical dye-grafted TiO2 films to investigate charge-activity relationship. Femtosecond flash photolysis clearly defined the dye effects anchored on to the TiO2 platform. In addition, photodynamic data contemplated well to the dye orientation proposed by the DFT calculations. Recent findings provide fundamental understanding on the dye-grafted TiO2 system and establish a firm background how future dye-sensitized organic-inorganic hybrid system can be designed for the light driven hydrogen generation from water.

• Bulletin of the Korean Chemical Society
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• 제32권spc8호
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• pp.3081-3089
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• 2011

A series of new bis-thienylanthracene derivatives D1~D5 containing 9,10-antharcene moiety in the center and 2-methylenemalonotitrile or 2-cyanoacrylic acid functional group on the terminal thiophenes were synthesized and characterized by $^1H$-NMR and high-resolution mass spectroscopy. Their optical, electrochemical, and thermal properties were measured. They have absorption ${\lambda}_{max}$ in the range of 437~480 nm and max of $7.4{\times}10^3{\sim}2.0{\times}10^4M^{-1}cm^{-1}$. The substitution of 2-cyanoacrylic acid group allows greater value of ${\varepsilon}_{max}$ than that of 2-methylenemalonotitrile. TGA curves showed that D4 and D5 which have 2-cyanoacrylic acid functional group on the terminal thiophene(s) exhibit good thermal stability and D4 was thermally stable up to $400^{\circ}C$. Their optical properties and LUMO energy levels measured suggest that they can serve as potential candidates for electron donor materials of organic photovoltaic cells (OPVs) or D4 and D5 which contain 2-cyanoacrylic acid group can be used as organic dyes of dye-sensitized solar cells (DSSCs).