Heterostructures based on nanodispersed TiO2 and binary systems TiO2-CdTe, TiO2-Cu(In,Ga)Se2 sensitized by polymethyn dye, as photocatalysts of redox processes
{"title":"Heterostructures based on nanodispersed TiO2 and binary systems TiO2-CdTe, TiO2-Cu(In,Ga)Se2 sensitized by polymethyn dye, as photocatalysts of redox processes","authors":"I. Kobasa","doi":"10.31861/chem-2019-819-04","DOIUrl":null,"url":null,"abstract":"New light-sensitive heterostructures of semiconductors (TiO2, TiO2-CdTe, TiO2-Cu(In,Ga)Se2) sensitized with an anionic polymethine dye with three conjugated chromophores have been developed. Based on the analysis of the results of spectral, electrochemical and energy characteristics of the studied dye, the possibility of its use as an effective sensitizer of these semiconductor materials is shown. It was found that the deposition of the dye on TiO2 leads to both batochromic and hypsochromic shifts of long wavelength absorption bands, the values of which depend on the dye content in the heterostructure. This leads to a redistribution of the intensities of the absorption bands, they expand and cover almost the entire part of the visible and near-IR regions of the spectrum. This feature of the created heterostructure allows to increase the efficiency of their photocatalytic action through the use of light quanta of a wide energy range. The results of the analysis of the absorption spectra of heterostructures testify to the significant influence of semiconductors on the electronic system of dye molecules. As a result, the angle between the directions of the chromophores changes. The antibate dependence of the degree of conformational changes on the amount of dye in the heterostructure is revealed. This indicates a decrease in the interaction with the semiconductor with increasing concentration and explains the decrease in the photocatalytic activity of heterostructures at a significant content of sensitizer. Using the method of cyclic voltammetry, for the first time the oxidation and reduction potentials of the investigated polymethine dye were determined. The values of HOMO and LUMO energy levels are calculated, a forecast is made regarding the possibility of their use as sensitizers of the studied semiconductors and the creation of highly efficient redox systems. The photocatalytic activity of heterostructures in the reactions of reduction of methylene blue and oxidation of iodide ions under irradiation with light absorbed by a semiconductor and a sensitizer has been revealed. Based on the analysis of energy parameters of electronic processes, the scheme of this photocatalytic transformation is proposed and substantiated.","PeriodicalId":9913,"journal":{"name":"Chernivtsi University Scientific Herald. Chemistry","volume":"571 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chernivtsi University Scientific Herald. Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31861/chem-2019-819-04","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
New light-sensitive heterostructures of semiconductors (TiO2, TiO2-CdTe, TiO2-Cu(In,Ga)Se2) sensitized with an anionic polymethine dye with three conjugated chromophores have been developed. Based on the analysis of the results of spectral, electrochemical and energy characteristics of the studied dye, the possibility of its use as an effective sensitizer of these semiconductor materials is shown. It was found that the deposition of the dye on TiO2 leads to both batochromic and hypsochromic shifts of long wavelength absorption bands, the values of which depend on the dye content in the heterostructure. This leads to a redistribution of the intensities of the absorption bands, they expand and cover almost the entire part of the visible and near-IR regions of the spectrum. This feature of the created heterostructure allows to increase the efficiency of their photocatalytic action through the use of light quanta of a wide energy range. The results of the analysis of the absorption spectra of heterostructures testify to the significant influence of semiconductors on the electronic system of dye molecules. As a result, the angle between the directions of the chromophores changes. The antibate dependence of the degree of conformational changes on the amount of dye in the heterostructure is revealed. This indicates a decrease in the interaction with the semiconductor with increasing concentration and explains the decrease in the photocatalytic activity of heterostructures at a significant content of sensitizer. Using the method of cyclic voltammetry, for the first time the oxidation and reduction potentials of the investigated polymethine dye were determined. The values of HOMO and LUMO energy levels are calculated, a forecast is made regarding the possibility of their use as sensitizers of the studied semiconductors and the creation of highly efficient redox systems. The photocatalytic activity of heterostructures in the reactions of reduction of methylene blue and oxidation of iodide ions under irradiation with light absorbed by a semiconductor and a sensitizer has been revealed. Based on the analysis of energy parameters of electronic processes, the scheme of this photocatalytic transformation is proposed and substantiated.
基于纳米分散TiO2的异质结构和聚甲基染料敏化TiO2- cdte、TiO2- cu (In,Ga)Se2二元体系作为氧化还原过程光催化剂
采用阴离子聚甲基染料对具有三种共轭发色团的半导体材料(TiO2、TiO2- cdte、TiO2- cu (In,Ga)Se2)进行了敏化处理。通过对所研究染料的光谱、电化学和能量特性的分析,指出了其作为半导体材料的有效敏化剂的可能性。研究发现,在TiO2上沉积染料会导致长波吸收带的色移和次色移,其值取决于异质结构中染料的含量。这导致了吸收带强度的重新分配,它们扩展并覆盖了光谱中可见和近红外区域的几乎整个部分。这种异质结构的特性允许通过使用宽能量范围的光量子来提高其光催化作用的效率。异质结构的吸收光谱分析结果证明了半导体对染料分子电子系统的显著影响。结果,发色团方向之间的角度发生了变化。揭示了异质结构中染料含量对构象变化程度的反作用。这表明随着浓度的增加,与半导体的相互作用减少,并解释了在显着含量的敏化剂下异质结构的光催化活性下降。采用循环伏安法首次测定了所研究的聚甲基染料的氧化还原电位。计算了HOMO和LUMO能级的值,预测了它们作为所研究的半导体的敏化剂和高效氧化还原体系的创建的可能性。揭示了异质结构在半导体和敏化剂吸收光照射下对亚甲基蓝还原和碘离子氧化反应的光催化活性。在分析电子过程能量参数的基础上,提出并证实了该光催化转化方案。