Optimization of interface structures in crystalline silicon heterojunction solar cells

In heterojunction solar cells consisting of hydrogenated amorphous silicon (a-Si:H) and crystalline silicon (c-Si), suppression of epitaxial growth at the heterointerface is found to be crucial to achieve high solar cell efficiencies. In order to avoid the epitaxial growth, wide-gap hydrogenated amorphous silicon oxide (a-SiO:H) has been applied to the heterojunction solar cells. We have fabricated a-SiO:H/c-Si solar cells using n-type and p-type c-Si substrates and demonstrated that incorporation of the a-SiO:H i layer prevents the harmful epitaxial growth at the heterointerface completely.     

Luminescent properties of doped freestanding silicon nanocrystals embedded in MEH-PPV

We demonstrate that the electrochemical etching and pulverization of porous silicon films allow the fabrication of boron- and phosphorous-doped freestanding silicon nanocrystals (Si-ncs). The presence of boron in freestanding Si-ncs was confirmed from low-temperature photoluminescence (PL) analysis. The temperature dependence of PL for both types of doped Si-ncs reveals two PL bands due to the quantum confinement effect and surface state defects. Blending of Si-ncs into poly[methoxy-ethylexyloxy-phenylenevinilene] polymer leads to suppression of the PL band originated from surface states. More importantly, those blends showed a photoconductivity response under illumination AM1.5 at room temperature.     

Back surface reflectors with periodic textures fabricated by self-ordering process for light trapping in thin-film microcrystalline silicon solar cells

Back surface reflectors (BSRs) with grating structures have been developed to enhance light trapping in thin-film hydrogenated microcrystalline Si (μc-Si:H) solar cells. As a grating structure, a periodic honeycomb-like dimple pattern with a period of ～450 nm has been fabricated on Al substrates by a self-ordering process using anodic oxidation of Al. The clear diffraction effect has been confirmed on the patterned Al from the angle-dependent reflection. From quantum efficiency measurements, we found that the periodically patterned BSR can confine the incident light more effectively than the random textured BSR, especially at longer wavelengths.     

Preparation of carbon-coated W18O49 and its photoactivity under visible light

Carbon-coated W₁₈O₄₉ powders were prepared from the mixture of para-ammonium tungstate with poly(vinyl alcohol) by heat treatment in inert atmosphere at a temperature between 750 and 900 °C for 1 h. The synthesized W₁₈O₄₉ crystals had prismatic morphology in small size, less than 0.5 μm in diameter and about 1 μm in length. Carbon-coated W₁₈O₄₉ was shown to have photoactivity under visible light irradiation by comparing the concentration changes of methylene blue, phenol and dimethylsulfoxide with time under the irradiation of visible light to that in the dark. Photoactivity of W₁₈O₄₉ was supposed to be due to the formation of OH radicals on the basis of the degradation of dimethylsulfoxide, its quantitative transformation to methanesulfonic acid. Carbon coating seemed to have various roles: to reduce WO₃ to W₁₈O₄₉, to inhibit the sintering and crystal growth of W₁₈O₄₉ to keep them small size, and also to concentrate pollutants around W₁₈O₄₉ crystal by adsorption.     

A concentrator module of spherical Si solar cell

Spherical Si solar cell, which is made up of Si spheres with a diameter of approximately 1.0 mm, is expected to be a promising candidate for low consumption of Si feedstock and simple process technology. This paper describes the formation process and the structure of a concentrator module in detail. The concentrator lens was formed by casting with ultraviolet light hardening resin. The concentration ratio was 4.4 times and the pitch between the spheres was 2.0 mm. By this module design, it was possible to realize a consumption of the Si feedstock of about 3.0 g/W. Conversion efficiencies of 11.3% from single-sphere cell, 8.5% from a 23-spheres module and 5.2% from a 105-spheres module under AM1.5, 100 mW/cm² illumination were achieved.     

Intermolecular Interaction of [60]Fullerene with Tröger's Base Analogues

Tröger's base (TB, 1) and its analogues were synthesized and were subject to the titration experiments to evaluate their ability of supramolecular complexation with C₆₀. Results demonstrate clearly that the fluorene-based TB analogue (2) and the bioctylfluorene-based TB analogue (3) show 1:1 binding with C₆₀ to form the corresponding complexes while TB 1 does not. Titration experiments exhibited that the association constant (K_ass) of 3/C₆₀ (48.1 ± 7.9 M ^?1) was larger than that of 2/C₆₀ (13.7 ± 1.4 M ^?1)_. The formation of the 1:1 binding complexes 2/C₆₀ and 3/C₆₀ was also confirmed by MALDI-TOF mass spectrometry. Theoretical calculations suggest that 2 and 3 have appropriate cavities to embrace C₆₀. These findings indicate that not only the π/π interaction between the fluorene moieties and the C₆₀ surface but also the CH/π interaction between the octyl groups and the C₆₀ surface serve efficiently in the supramolecular complexation with C₆₀.     

Photocarrier generation in organic thin-film solar cells with an organic heterojunction

Photocurrent–voltage characteristics for organic solar cells with a heterojunction formed between copper phthalocyanine and a perylene derivative (or C₆₀) were studied. The photocurrent was observed under both reverse and forward biases. From the analysis of the photocurrent action spectra, the origin of the reverse photocurrent was attributed to the excitons formed in both the organic layers, whereas that of the forward photocurrent was attributed to the excitons formed in the perylene derivative (or C₆₀) layer. The photocurrent density under reverse bias increased at higher temperatures, suggesting that the charge recombination possibility was lowered at higher temperatures. On the basis of the time responses of the photocurrents observed after pulsed photoirradiation, the charge separation and transport processes are discussed.     

Application of nuclear energy for environmentally friendly hydrogen generation

It is universally admitted that hydrogen is one of the best energy media and its demand will increase greatly in the near future. However, little hydrogen exists naturally, so that how to generate hydrogen without bringing forth much CO₂${}_2$ will be very important research subject. Hydrogen generation from water using nuclear energy is one of the solutions for this problem. Especially, the high temperature gas cooled reactor (HTGR) has a possibility to generate hydrogen economically compared with other types of nuclear reactors. As for long-lived radioactive waste to be generated by nuclear reactors, it is expected to significantly reduce its burden to the human environment by applying transmutation technologies. This report describes the feature of the hydrogen generation with HTGR and the development of the accelerator-driven subcritical system to reduce radioactive waste ongoing at JAEA.     

Occurrence and formation potential of N-nitrosodimethylamine in ground water and river water in Tokyo

N-nitrosodimethylamine (NDMA), a disinfection byproduct of water and wastewater treatment processes, is a potent carcinogen. We investigated its occurrence and the potential for its formation by chlorination (NDMA-FP_2Cl) and by chloramination (NDMA-FP_2NHCl) in ground water and river water in Tokyo. To characterize NDMA precursors, we revealed their molecular weight distributions in ground water and river water. We collected 23 ground water and 18 river water samples and analyzed NDMA by liquid chromatography-tandem mass spectrometry. NDMA-FP_2Cl was evaluated by chlorinating water samples with free chlorine for 24 h at pH 7.0 while residual free chlorine was kept at 1.0-2.0 mgCl₂/L. NDMA-FP_2NHCl was evaluated by dosing water samples with monochloramine at 140 mgCl₂/L for 10 days at pH 6.8. NDMA precursors and dissolved organic carbon (DOC) were fractionated by filtration through 30-, 3-, and 0.5 kDa membranes. NDMA concentrations were <0.5-5.2 ng/L (median: 0.9 ng/L) in ground water and <0.5-3.4 ng/L (2.2 ng/L) in river water. NDMA concentrations in ground water were slightly lower than or comparable to those in river water. Concentrations of NDMA-FP_2Cl were not much higher than concentrations of NDMA except in samples containing high concentrations of NH₃ and NDMA precursors. The increased NDMA was possibly caused by reactions between NDMA precursors and monochloramine unintentionally formed by the reaction between free chlorine and NH₃ in the samples. NDMA precursors ranged from 4 to 84 ng-NDMA eq./L in ground water and from 11 to 185 ng-NDMA eq./L in river water. Those in ground water were significantly lower than those in river water, suggesting that NDMA precursors were biodegraded, adsorbed, or volatilized during infiltration. The molecular weight of NDMA precursors in river water was dominant in the <0.5 kDa fraction, followed by 0.5-3 kDa. However, their distribution was inconsistent in ground water: one was dominant in the <0.5 kDa fraction, and the other in 0.5-3 kDa. Molecular weight distributions of NDMA precursors were very different from those of DOC. This is the first study to reveal the widespread occurrence and characterization of NDMA precursors in ground water.