Solar energy conversion from water photolysis by biological and chemical systems

The production of chemicals and fuels, or energy-rich compounds, from water by sunlight is described as a particularly attractive means for the conversion of solar energy to a valuable renewable resource. The redox properties of photoexcited molecules and the operating mechanism of light-driven systems are first considered. The mechanism of water oxidation carried out by higher plants and green algae-which is actually one of the most important biochemical reactions—as well as that of artificial photosystems, up-to-now designed trying to simulate the natural process with higher efficiency and simplicity, are likewise discussed. A number of biological and chemical light-driven systems are presented as practical ways to solar energy conversion.     

用磁控溅射和退火方法制备AlSb多晶薄膜

采用磁控溅射法在玻璃衬底上制备Al/Sb预制多层薄膜,然后将Al/Sb预制多层薄膜在退火炉中退火得到AlSb多晶薄膜.用X射线衍射(XRD)法测薄膜结构;用扫描电镜(SEM)测薄膜Al/Sb成分比,结果表明AlSb多晶薄膜具有单一的晶相、均匀的结构,以及粒径大约20nm的晶粒.根据电导率(lnσ)与温度(T)的关系得到电导激活能为0.21和0.321eV,为制备出适用于太阳电池的AlSb多晶薄膜奠定了一定的技术基础.     

Oligothiophene-based small molecules with 3,3′-difluoro-2,2′-bithiophene central unit for solution-processed organic solar cells

Two new oligothiophene-based small molecules, namely DRCN6T-F and DRCN8T-F, with 3,3′-difluoro-2,2′-bithiophene as the central building block and 2-(1,1-dicyanomethylene)-rhodanine as end groups, were designed and synthesized. Compared to their non-fluorinated counterparts DRCN6T and DRCN8T, DRCN6T-F and DRCN8T-F exhibit enhanced intermolecular interactions and lower HOMO energy levels. However, PCEs of 2.26% and 5.07% were obtained for DRCN6T-F and DRCN8T-F based optimized devices, respectively, lower than those of non-fluorinated molecules DRCN6T and DRCN8T. The relatively poor performance for the DRCN6T-F and DRCN8T-F were mainly caused by their low short-circuit current densities, due to their unfavorable morphologies and low charge carrier mobilities.     

Photovoltaic polymers based on difluoroqinoxaline units with deep HOMO levels

We report the synthesis of low bandgap polymers with a difluoroquinoxaline unit by Stille polymerization for use in polymer solar cells (PSCs). A new series of copolymers with 2,3‐didodecyl‐6,7‐difluoro quinoxaline as the electron‐deficient unit and alkyloxybenzo[1,2‐b:4,5‐b′]dithiophene and thiophene as the electron‐rich unit were synthesized. The photovoltaic properties of the devices based on the synthesized polymers revealed that the fluorine atoms at the quinoxaline units aid in decreasing the highest occupied molecular orbital (HOMO) energy levels; this in turn increased the open circuit voltage of the devices. The polymers with long alkyl chains exhibited good solubility that increased their molecular weight, but the power conversion efficiency was low. Efficient polymer solar cells were fabricated by blending the synthesized copolymers with PC₇₁BM, and the PCE increased up to 5.11% under 100 mW cm⁻² AM 1.5 illumination. These results demonstrate that the importance of having a control polymer to be synthesized and characterized side by side with the fluorine analogues. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018 , 56, 1489–1497     

Color Bricks: Building Highly Organized and Strongly Absorbing Multicomponent Arrays of Terpyridyl Perylenes on Metal Oxide Surfaces

Terpyridine‐substituted perylenes containing cyclic anhydrides in the peri position were synthesized. The anhydride group served as an anchor for assembly of the terpyridyl‐crowned chromophores as monomolecular layers on metal oxide surfaces. Further coordination with Zn²⁺ ions allowed for layer‐by‐layer formation of supramolecular assemblies of perylene imides on the solid substrates. With properly selected anchor and linker molecules it was possible to build high quality structures of greater than ten successive layers by a simple and straightforward procedure. The prepared films were stable and had a broad spectral coverage and high absorbance. To demonstrate their potential use, the synthesized dyes were employed in solid‐state dye‐sensitized solar cells, and electron injection from the perylene antennas to titanium dioxide was observed.     

Rational design of perylenediimide-based polymer acceptor for efficient all-polymer solar cells

Perylenediimide (PDI)-based small molecules have significantly contributed to the development of non-fullerene acceptors, whereas the development of PDI-based polymer acceptors is relatively lagging behind. In this study, we designed and synthesized two PDI-based n-type polymers named as PF-PDI and PBDT-PDI, in which PDI was used as electron-deficient unit and fluorene (F) or benzodithiophene (BDT) were used as electronrich components. The density functional theory (DFT) calculations and grazing incidence wide-angle X-ray scattering (GIWAXS) results indicate that the PF-PDI shows larger steric hindrance and relatively weaker lamellar packing than that of PBDT-PDI. Comparing with PBDT-PDI, PF-PDI shows red-shift absorption and lower-lying HOMO level, which agrees well with the DFT results. A well-known wide bandgap polymer donor, PDBT-T1 was employed to fabricate polymer solar cells (PSCs) with the two acceptors. The all polymer solar cells (all-PSCs) based on PDBT-T1:PF-PDI showed a high power conversion efficiency (PCE) of 4.47%, which is approximately 2-fold larger than that of devices with PDBT-T1:PBDT-PDI (PCE = 2.70%).     

Preparation of dye sensitized titanium oxide nanoparticles for solar cell applications

A new method for synthesis of titanium dioxide (TiO₂)-dye nanoparticles is reported. TiO₂ nanocrystals were obtained at 150 and 200 °C by using chemically bonded TiO₂-sensitizer dye as a precursor. Titanium tetraisopropoxide was first modified with a dye molecule and then precipitated by dropping into acidic water. A strongly colored precipitate was obtained. Hydrothermal growth of a colloidal solution was carried out in a Teflon-lined stainless steel autoclave. Dye sensitized solar cell efficiencies obtained were comparable and fill factor values were close to the analogous cells prepared by the use of conventional TiO₂ paste techniques. This method allows the use of different substrates together with nanocrystalline TiO₂ for many technological applications.     

A new direction in design and manufacture of co-sensitized dye solar cells: Toward concurrent optimization of power conversion efficiency and durability

A novel methodology was implemented in the present study to concurrently control power conversion efficiency (η) and durability (D) of co-sensitized dye solar cells. Applying response surface methodology (RSM) and Desirability Function (DF), the main influential assembling (dye volume ratio and anti-aggregation agent concentration) and operational (performance temperature) parameters were systematically changed to probe their main and interactive effects on the η and D responses. Individual optimization based on RSM elucidated that D can be solely controlled by changing the ratio of vat-based organic photosensitizers, whereas η takes both effects of dye volume ratio and anti-aggregation concentration into account. Among the studied factors, the performance temperature played the most vital role in η and D regulation. In particular, however, multi-objective optimization by DF explored the degree to which one should be careful about manipulation of assembling and operational parameters in the way maximization of performance of a co-sensitized dye solar cell.     

Synthesis and photovoltaic properties of main chain polymeric metal complexes containing 1,10‐phenanthroline metal complexes conjugating alkyl fluorene or alkoxy benzene by C═C bridge for dye‐sensitized solar cells

Four main chain polymeric metal complexes (P1–P4) based on 1,10‐phenanthroline metal complexes via the Heck coupling have been synthesized and characterized by Fourier transform infrared spectroscopy, ¹H NMR, UV–Vis absorption, photoluminescence spectroscopy, gel permeation chromatography, thermogravimetric analysis, differential scanning calorimetry, elemental analysis, and cyclic voltammetry. To investigate their photovoltaic properties, the dye‐sensitized solar cells based on these polymers dyes are studied, under the illumination of AM 1.5G, 100 mW/cm². The study results show the four polymers exhibit good thermally stable and the solar cells based on them have good device performance, and the maximum power conversion efficiency is up to 0.735% for the solar cells based on P3 with a short‐circuit current (J_sc) of 1.68 mA/cm² and an open‐circuit voltage (V_oc) of 0.62 V. Copyright © 2012 John Wiley & Sons, Ltd.