Absorption spectra response of XRQA radiochromic film to x-ray radiation

Gafchromic XRQA, radiochromic film is a high sensitivity auto developing x-ray analysis films designed and available for kilovoltage x-ray, dose and QA assessment applications. The film is designed for reflective analysis with a yellow transparent top filter and white opaque backing materials. This allows the film to be visually inspected for colour changes with a higher level of contrast than clear coated radiochromic films such as Gafchromic EBT version 1. The spectral absorption properties in the visible wavelengths have been investigated and results show two main peaks in absorption located at 636 nm and 585 nm. These peaks are located in the same position as EBT Gafchromic film highlighting a similar chemical monomer/polymer for radiation sensitivity. A much higher sensitivity however is found at kilovoltage energies with an average 1.55 OD units per 20 cGy irradiation variation measured at 636 nm using 150 kVp x-rays. This is compared to approximately 0.12 OD units per 20 cGy measured at 636 nm for EBT film at 6 MV x-ray energy. That is, the XRQA film is more than 10 times more sensitive than EBT1 film. The visual colour change is enhanced by the yellow polyester coating. However this does not affect the absorption spectra properties in the red region of analysis which is the main area for use using desktop scanners in reflection mode.     

Leuco crystal violet/poly(vinyl butyral) thin film as a high-dose dosimeter

A polyvinyl butyral film incorporating a radiochromic leuco crystal violet dye (LCV) and a UV-absorber of tinuvin-P has been investigated as a high-dose dosimetry for ⁶⁰Co radiation processing in the dose range of 1–100 kGy. Upon γ-ray exposure, the prepared film undergoes visual color change to deep purple color characterized with an absorption band peaking at 594 nm with a shoulder around 552 nm. The response of films stored in dark place at room temperature overall a period of 55 days exhibited good stability, that the increase in response of irradiated and unirradiated films did not exceed 2% and 4%, respectively overall this storage period. The results indicate that no further protection of films from laboratory fluorescent light during the measurement of irradiated film is required. The effect of temperature and relative humidity on the performance of film during irradiation and the overall uncertainty associated with absorbed dose monitoring were investigated in the present study.     

Influence of high-energy X-ray irradiation on the optical properties of tetraphenylporphyrin thin films

Tetraphenylporphyrin (TPP) thermally evaporated films were irradiated by different doses (0.5–2.5 kGy) of X-ray with energy 6 MeV. The optical properties for TPP were investigated using spectrophotometric measurements of the transmittance and reflectance at normal incidence of light in the wavelength range from 200 to 1100 nm. The absorption spectra recorded in the UV-VIS region of spectra showed different absorption bands, namely four Q-bands in the visible region of the spectrum and a more intense band termed as the Soret band in the near-UV region of the spectrum. Two other bands labeled N and M appear in the UV region. The Soret band showed Davydov splitting. Increasing X-ray irradiation dose influences the optical properties of TPP films. All absorption bands show a continuous blue shift in position and a decrease in intensity with increasing X-ray dose. At 2.5 kGy the B, N, and M bands disappeared. The reduction in the absorbency was calculated as a function of X-ray dose. The energy gap was determined and the type of optical transition was found to be an indirect allowed transition.     

Excellent UV absorption in spin-coated thin films of oleic acid modified zinc oxide nanorods embedded in Polyvinyl alcohol

The aim of the study is to investigate the optical properties of spin-coated, highly transparent nanocomposite films of oleic acid modified ZnO (Zinc oxide) nanorods embedded in Polyvinyl alcohol (PVA) matrix. Pristine and oleic acid (OA) modified ZnO nanorods have been prepared by wet chemical synthesis and are characterized by X-ray diffraction, FESEM, TEM and FT–IR spectroscopy techniques. The optical properties of ZnO/PVA films are studied using UV–visible absorption and Photoluminescence (PL) spectroscopy. The results show that the optical absorption of the films in the UV region is quite high and more than 95% absorption is observed in films prepared from OA modified ZnO nanorods. The excellent UV absorption at around 300 nm offers prospects of applications of these films as efficient UV filters in this wavelength region. The PL spectrum of pristine ZnO nanorods shows almost white light emission whereas OA modified ZnO nanorods have a more intense peak centered in the blue region. The PL emission of OA modified ZnO/PVA film shows appreciable increase in intensity compared to the film obtained with pristine ZnO. The surface modification of ZnO by the polymer matrix removes defect states within ZnO and facilitates sharp near band edge PL emission at 364 nm.     

Dispersion studies and electronic transitions in nickel phthalocyanine thin films

Thin films of the organic semiconductor nickel phthalocyanine (NiPc) are structurally investigated using X-ray diffraction and infrared light absorption. The optical absorption and dispersion studies of nickel phthalocyanine were investigated using spectrophotometric measurements of transmittance and reflectance at normal incidence in the wavelength range 190–2100 nm. The absorption spectra recorded in the UV-VIS region show two well-defined absorption bands of the phthacyanine molecules, namely, the Soret and the Q-band. The Davydove splitting of the main absorption peak in the metal phthalocyanines correlates with the relative tendencies of the metal to out-of-plane bonding. The refractive index n as well as the absorption index k were calculated and showed an independent of the film thickness in the film thicknesses range 400–770 nm. The refractive index n showed an anomalous dispersion in the absorption region as well as normal dispersion in the transparent region. Some of the important optical absorption such as the molar extinction coefficient, the oscillator strength, the electric dipole strength have been evaluated. The analysis of the spectral behavior of the absorption coefficient α in the absorption region revealed two indirect allowed transitions with corresponding energies 2.77±0.03 and 1.66±0.02 eV. An energy band diagram has been proposed to account for the optical transitions of NiPc thin film. All previous parameters were as well obtained for films annealed at 523 K for 2 h. Discussion of the obtained results and their comparison with the previously published data are also given.     

Spectral response of radiochromic gel detector in the near-ultraviolet region (200–400 nm)

Tissue-equivalent radiochromic gel detector is sensitive in the regions of ultraviolet radiation (UVR) and gamma and X-rays. This study aims to investigate the spectral response and other optical properties of the ferrous sulphate, xylenol orange and gelatin (FXG) radiochromic gel dosimeter at particular UVR wavelengths. A total of nine monochromatic wavelengths were selected in the range of 240–400 nm with an increment of 20 nm. The FXG spectral response was estimated from the variation of spectral absorbance at 560 nm resulting from 1 h exposure to UVR beam at each chosen wavelength. Experimental results show that the FXG responsivity depends on the wavelength of the radiation and the optical path in the gel material. UVC and UVB photons have relatively higher photochemical effect than UVA; however, UVA penetration is deeper. Investigations showed that the FXG gel response is relatively constant between 240 and 320 nm, but it varies rapidly with wavelength in the UVA range and takes a minimal value at 360 nm. UVR spectral absorbance curves for different gel sample thicknesses were examined. The experiment showed that 6 mm of neutral gelatin or FXG gel samples was capable of absorbing >99.7% of the beam in the UV range of 240–290 nm.     

Characterization of the gafchromic EBT3 films for dose distribution measurements in stereotactic radiotherapy

Radiochromic film dosimetry is a promising technique, but at this time there are some artefacts, including non-uniformity, energy dependence and scanner artefacts. Accurate dosimetry with radiochromic films requires characterizing the film as well as the scanning and analysis procedures. In this work, the performance of the EBT3 films in combination with the EPSON Dual Lens Perfection V700 scanner for dose distribution measurements in stereotactic radiotherapy has been evaluated. It has been shown that it was necessary to perform 20 blank scans to obtain the stability of the scanner. In order to reduce the uncertainties due to the non-uniformity of the scan field, it was then decided to use the 12 × 12 cm² central part of the scanner bed. Regarding EBT3 films, intra-sheet and inter-sheet uniformity of unexposed EBT3 films in terms of pixel value has been found to be respectively 0.27% (1 SD) and 0.15% (1 SD). No significant energy dependence has been observed above 30 keV and no angular dependence has been found.     

Energy response of the new EBT2 radiochromic film to x-ray radiation

Gafchromic EBT2, Radiochromic film is assessed for its change in optical density response to x-ray radiation over a broad energy range, from low energy kilovoltage to megavoltage x-rays. A small energy dependence was found with variations in the change in optical density when scanned in the red component of a desktop scanner light source per unit dose of 6.5% from 50 kVp to 10 MV. This produces a slightly smaller and thus even more energy independent film than its predecessor, EBT film whose response varied by 7.7% over the same energy range. The energy response peaked at 100 kVp with a 5% over response compared to 6 MV x-rays and the minimum response found at both 50 kVp and 250 kVp being a 1.5% under response. It should be noted that the shape of the energy dependence response curve increases from 50 kVp up to 100 kVp followed by a decrease through to higher energies whilst the original EBT was found to increase in response from 50 kVp through to 10 MV. A reflected net optical density change of 0.215 ± 0.006 OD for the first Gray of radiation was found for EBT2 analysed in reflection mode at 6 MV x-ray energy. The minimal energy dependence of the EBT2 film provides further enhancement compared to EBT for its accuracy with respect to spectral changes in the beam to measure beams such as IMRT where complex field and multileaf collimator configurations exist causing small spectral changes to occur over the treatment field or at depth where spectral changes also occur.     

Skin dose assessment in unmodulated and intensity-modulated radiation fields with film dosimetry

Superficial dose from 6- and 18-MV photon beams has been studied by measuring surface dose and shallow build-up dose using radiographic film EDR2, radiochromic film EBT2 and plane-parallel chamber. Measurements have been made for intensity- and non-intensity-modulated beams.The results show that the surface dose was found to be 19.8% and 10% of maximum dose in unmodulated fields for 6 and 18 MV photon beams, respectively. The study further showed that intensity modulation decreased surface dose by 1.1% and 0.7% for the same field size at 6 and 18 MV, respectively, and surface dose was dropped by magnetically sweeping contaminating electrons. EDR2 and EBT2 films show in good agreement in shallow build-up region.This study demonstrated the capability of EDR2 film, in addition to radiochromic film, to measure surface and build-up dose in case of treatment planning system uncertainties with regard to skin toxicity or shallow target coverage.     

一种新型辐射变色膜的γ射线辐照研究

报道了以高聚物为载体，以有机染料及添加剂为变色指示剂体系，制备一种辐射变色膜。这种辐射变色膜为无色透明固体薄膜，经60Co γ射线辐照后，其颜色变为蓝色。辐照后样品的紫外-可见吸收光谱表明，在可见光区其最强吸收峰出现在624 nm附近。在10～90 kGy的剂量范围内，不含添加剂的辐射变色膜的光密度变化与吸收剂量呈线性关系，而含有添加剂的辐射变色膜对γ射线辐照的响应在50 kGy时就达到饱和。同时还探索了该体系辐照效应的化学反应机理。     

Quantitative analysis of UV excitation bands for red emissions in Pr-doped CaTiO3, SrTiO3 and BaTiO3 phosphors by peak fitting

A quantitative spectral analysis of the ultraviolet (UV) broad excitation bands, which are located in the range 300-400 nm, for red emissions at around 610 nm in Pr-doped CaTiO₃, SrTiO₃:Al and BaTiO₃:Mg phosphors has been carried out using a peak fitting technique. The obtained results demonstrate that the UV broad band of CaTiO₃:Pr consists of four primary excitation bands centered around 330, 335, 365 and 380 nm and those of both SrTiO₃:Al and BaTiO₃:Mg consist of three primary bands centered around 310, 345 and 370 nm. Based on the behavior patterns and the values of the respective primary excitation bands’ parameters, i.e. center gravity (λ_top), maximum height (I_max) and full-width at half-maximum (FWHM), the UV-to-red relaxation processes in these titanate phosphors can be explained to be essentially the same, except for the existence of an additional relaxation pathway via electron-trap states in CaTiO₃:Pr, which gives a characteristic shape of its UV excitation spectrum in the wavelength range of >360 nm.     

Characterization of Gafchromic EBT3 films for ultraviolet radiation dosimetry

A newly released processless Gafchromic EBT3 film was investigated for its response to ultraviolet radiation (UVR) at three different wavelengths: 365 (UVA), 302 (UVB) and 254 nm (UVC). The change in the film's optical density was dependent on the radiance exposure and UV wavelength and was found to correlate with the UV intensity. The dynamic range of the EBT3 films is ～5 to ～60 J/cm² for UVA and UVB and ～5 to ～300 J/cm² for UVC. The dose sensitivity of EBT3 films for UVA and UVB radiation was approximately 10 times higher than that for UVC radiation. The results indicate the suitability of EBT3 films for quantitative and qualitative measurements of UVR exposure.     

The morphology and optical properties of Cr-doped ZnO films grown using the magnetron co-sputtering method

Undoped ZnO and Zn_0.9Cr_0.1O films were prepared on Al₂O₃ (0 0 0 1) substrates using the magnetron co-sputtering technique. X-ray diffraction scans show that all films exhibit nearly single-phase wurtzite structure with c-axis orientation. Both chromium doping and growth ambient have a significant impact on the lattice constants and nucleation processes in ZnO film. A large quantity of subgrains (10 nm in size) has been observed on Zn_0.9Cr_0.1O film grown under Ar + O₂, while irregular plateau-like grains 40-50 nm in size were observed on Zn_0.9Cr_0.1O film grown under Ar + N₂. The ultraviolet-visible transmittance and optical bandgap of all films were also examined. The photoluminescence spectra of all films exhibit a broad emission located around 400 nm, which is composed of one weak ultraviolet luminescence and another rather intense near-violet one, as determined by Gaussian peak fitting. The near-violet emission centered on 400 nm might originate from the electron transition between the band tail state levels of surface defects and/or lattice imperfection in the ZnO film.     

紫外增强Lumogen薄膜旋涂法制备及其性能表征

Lumogen薄膜用于固态硅基探测器件CCD紫外增强具有显著的成本和工艺优势。研究旋涂法制备Lumogen薄膜的CCD紫外增强技术,通过对薄膜的光谱分析得到优化的制备工艺。制备的薄膜在可见光波段透过率较高,对紫外波段的光具有较强的吸收,其发射峰位于525 nm,并且激发谱较宽, 涵盖200～400 nm。实验结果表明使用旋涂法制备的紫外增强薄膜,能将紫外光转化为可见光,并且在增强紫外响应的同时,不削弱可见波段的响应,是一种有效增强固态检测器紫外响应的紫外增强薄膜。     

One-pot synthesis of oleic acid-capped cadmium chalcogenides (CdE: E = Se,Te) nano-crystals

Surface-capped CdSe and CdTe nano-crystals (NCs) have been synthesized using cadmium acetate, oleic acid and respective tri-octylphosphine chalcogenide (TOPE; E = Se/Te) in diphenyl ether (DPE). Well-dispersed CdSe particles showed two absorption bands at the region of 431–34 and 458–60 nm in optical absorption study. A band-edge emission resulted at 515 nm with an excitation energy of 400 nm, in its photoluminescence (PL) spectrum. Similarly, UV–visible absorption study of CdTe revealed an absorption band at <700 nm. The broadened X-ray diffraction (XRD) pattern showed that at higher reaction temperature cubic CdSe but hexagonal CdTe can be obtained with crystallite size of <10 nm. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) revealed that agglomerated particles are of spherical nature. The inter-planar spacing in CdTe was measured to be 0.406 nm, a characteristic of (100) lattice plane in hexagonal CdTe. X-ray photoelectron spectroscopy (XPS) showed that CdSe NCs have better air stability stable than CdTe. Presence of organic moiety around the semiconductor particles was confirmed by infra-red (IR) spectroscopy.     

Synthesis of nanocrystalline CdS thin film by SILAR and their characterization

Cadmium sulphide (CdS) thin film was prepared by successive ion layer adsorption and reaction (SILAR) technique using ammonium sulphide as anionic precursor. Characterization techniques of XRD, SEM, TEM, FTIR and EDX were utilized to study the microstructure of the films. Structural characterization by x-ray diffraction reveals the polycrystalline nature of the films. Cubic structure is revealed from X-ray diffraction and selected area diffraction (SAD) patterns. The particle size estimated using X-ray line broadening method is approximately 7 nm. Instrumental broadening was taken into account while particle size estimation. TEM shows CdS nanoparticles in the range 5–15 nm. Elemental mapping using EFTEM reveals good stoichiometric composition of CdS. Characteristic stretching vibration mode of CdS was observed in the absorption band of FTIR spectrum. Optical absorption study exhibits a distinct blue shift in band gap energy value of about 2.56 eV which confirms the size quantization.     

Characterization and optimization of EBT2 radiochromic films dosimetry system for precise measurements of output factors in small fields used in radiotherapy

The accurate determination of absorbed dose in small photon beams, especially for stereotactic radiation therapy, is a difficult task with commercially available detectors. As these small fields are characterized by high dose gradients, a lack of lateral particle equilibrium and a variation of energy spectra with beam sizes, a dosimeter with high resolution, tissue-equivalence and high precision is required. The new radiochromic film EBT2, which meets these criteria, was fully characterized in Institut de Radioprotection et Sûreté Nucléaire (IRSN) for this application. This type of film was tested with the reading system EPSON Dual Lens Perfection V700 flatbed scanner in transmission mode. Warm-up effects of the scanner were studied as well as the influence of the scanner light. Uniformity of unirradiated and irradiated EBT2 films in terms of pixel value was found to be respectively 0.3% (1 SD) and 0.5% (1 SD). An original, accurate and efficient radiochromic film dosimetry protocol was established. The overall uncertainty for dose measurement with EBT2 films using this protocol was estimated at less than 2% (1 SD). Encouraging measurements of output factors were performed on a Novalis system.     

Structural and optical properties of chromotrope 2R thin films of different thicknesses

Chromotrope 2R (CHR) films of different thicknesses have been prepared using spin coater. The material has been characterized using FT-IR, DTA and X-ray diffraction. The XRD of the material in powder and thin film forms showed polycrystalline structure with triclinic phase. Preferred orientation at the (1 1 4) plane is observed for the deposited films. Initial indexing of the XRD pattern was performed using “Crystalfire” computer program. Miller indices, h k l, values for each diffraction line in X-ray diffraction (XRD) spectrum were calculated and indexed for the first time. The DTA thermograms of CHR powder have been recorded in the temperature range 25–350 °C with different heating rates. The spectra of the infra-red absorption allow characterization of vibration modes for the powder and thin film. The effect of film thickness on the optical properties has been studied in the UV-visible-NIR regions. The films show high transmittance exceeding 0.90 in the NIR region λ > 800 nm. The intensity of the absorption peaks for λ < 800 nm are enhanced as the film thickness increase. The absorption bands are attributed to the (π–π*) and (n–π*) molecular transitions. The optical properties have been analyzed according to the single-oscillator model and the dispersion energy parameters as well as the free charge carrier concentration have been determined. The optical energy gap as well as the oscillator strength and electric dipole strength have been calculated.     

Degradation and protection of polyaniline from exposure to ultraviolet radiation

The effect of UV radiation on both pure and additive-containing polyaniline thin films is described. Experimental investigations included optical transmittance spectroscopy and electrical conductivity measurements. Exposure to UV radiation in the range of 380 to 400 nm was seen to increase film transmittance by 4% through photobleaching. Different gas ambients were employed for this experiment and progressively more photobleaching was observed for nitrogen, air and oxygen atmospheres. This effect arises due to the destruction of quinoid and benzenoid chromophores on the polymer backbone. Concomitantly, a decrease in film resistivity was also observed and this can be attributed to increased oxidative doping of the film material. The addition of controlled amounts of Tinuvin 213—an ultraviolet absorber (UVA) material—was seen to reduce the UV-induced degradation of polyaniline thin films by absorption of UV photons through regenerative intramolecular photolysis.     

Modelling of optical absorption of silver NP’s produced by UV radiation embedded in mesostructured silica films

Hexagonal mesostructured films containing silver ions were obtained by sol–gel method. Brij 58 was used to produce channels into the film, which house these ions. The films were exposure to UV radiation to produced silver metallic nanoparticles. The presence of the metallic nanoparticles was determined by infrared spectroscopy and optical absorption. Besides, these nanoparticles and core–shell structures of silver–silver oxide nanoparticles were identified by high-resolution transmission electronic microscopy. From these measurements, the obtained size range for silver nanoparticles was 6.1 nm. The absorption spectrum located at 440 nm was modelled and well fitted with the Gans theory considering refractive index higher than the one coming from host matrix. This index is explained because the silver oxide shell modifies the local surrounding medium of the metallic nanoparticles.