1,720,952 research outputs found
Vacuum-Referred Binding Energies of Bismuth and Lanthanide Levels in LiTaO<sub>3</sub> Perovskite: Toward Designing Energy Storage Phosphor for Anti-Counterfeiting, X-Ray Imaging, and Mechanoluminescence
Discovering UV-light or X-ray charged afterglow and storage phosphors with high charge carrier storage capacity remains challenging. Herein, a method is proposed by combining vacuum referred binding energy (VRBE) diagram construction and optimization of dopants’ concentration and compound synthesis. The refined chemical shift model, optical spectroscopy, and thermoluminescence will be combined to construct the VRBE diagram of LiTaO3 with the lanthanide and bismuth charge transition levels. Based on the constructed VRBE diagram of LiTaO3, Bi3+, and/or Ln3+ (Ln = Tb or Pr) doped LiTaO3 will be studied. By combining Bi3+ with Tb3+, Pr3+, or Bi3+ itself, Bi3+ emerges to act as a ≈0.62 eV deep electron trap, while Tb3+, Pr3+, or Bi3+ acts as about 1.5 eV deep hole capturing and recombination centres. The VRBE in the Bi2+ 2P1/2 ground state will be derived by thermoluminescence study. Proof-of-concept X-ray imaging, compression force distribution monitoring, and color-tailoring for anti-counterfeiting will be demonstrated by using the developed Bi3+ and/or Ln3+ doped LiTaO3. This work promotes the understanding of trap level locations and on the trapping and release processes of charge carriers in Bi3+ and/or lanthanides doped inorganic compounds for rational design of new afterglow and storage phosphors.Green Open Access added to TU Delft Institutional Repository ‘You share, we take care!’ – Taverne project https://www.openaccess.nl/en/you-share-we-take-care Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.RST/Luminescence Material
Versatile and High-Performance LiTaO<sub>3</sub>:Tb<sup>3+</sup>, Gd<sup>3+</sup> Perovskite for Multimode Anti-counterfeiting, Flexible X-Ray Imaging, Continuous Stress Sensing, and Non-Real-Time Recording
Multimode luminescence relates to how charge carriers are transported and recombined in response to various physical excitations. It shows promising applications in many fields like advanced anti-counterfeiting, information storage and encryption. Enabling a stable single compound with multimode luminescence is a unique technology but still remains a challenge. Herein, a versatile and high-performance energy storage LiTaO3:0.01Tb3+,xGd3+ perovskite is discovered by utilizing the interplay of electron-trapping defect levels and hole-trapping Tb3+. It combines an excellent charge carrier storage capacity (≈7 and 12 times higher than state-of-the-art BaFBr(I):Eu2+ and Al2O3:C), >1200 h storage duration, >40 h afterglow, efficient optically stimulated luminescence, persistent mechanoluminescence, and force-induced charge carrier storage features. Particularly, it well responds to various stimuli channels, i.e., wide-range X-rays to 850 nm infrared photons, thermal activation, mechanical force grinding, or compression. To elucidate this multimode luminescence, charge carrier trapping and release processes in LiTaO3:0.01Tb3+,xGd3+ with various physical stimulations will be unraveled by combining the vacuum-referred binding diagram construction, spectroscopy, thermoluminescence, and mechanoluminescence techniques. The versatile and high-performance LiTaO3:0.01Tb3+,xGd3+ enables promising proof-of-concept multimode luminescence applications in advanced anti-counterfeiting, flexible X-ray imaging, continuous compression force sensing, and non-real-time recording.Green Open Access added to TU Delft Institutional Repository 'You share, we take care!' - Taverne project https://www.openaccess.nl/en/you-share-we-take-care Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.RST/Luminescence Material
Designing LiTaO<sub>3</sub>:Ln<sup>3+</sup>,Eu<sup>3+</sup> (Ln = Tb or Pr) perovskite dosimeter with excellent charge carrier storage capacity and stability for anti-counterfeiting and flexible X-ray imaging
Developing X-ray charged dosimeters with excellent charge carrier storage capacity and stability is challenging. Such energy storage dosimeters have fascinating use in developing novel applications, for instance, in radiation detection, advanced multimode anti-counterfeiting, and flexible X-ray imaging of curved objects. Herein, novel LiTaO3:Ln3+,Eu3+ (Ln = Tb or Pr) perovskite dosimeters are reported by combining the vacuum referred binding energy (VRBE) diagram of LiTaO3 and the optimization of dopant's concentration and compound synthesis condition. Based on the VRBE diagram prediction, charge carrier capturing and de-trapping processes in Eu3+ and/or Ln3+ (Ln = Tb or Pr) doped LiTaO3 will be studied to unravel the role of Eu3+ as a good electron trapping centre and to discover a record storage phosphor. The ratios of the thermoluminescence intensity of the optimized LiTaO3:0.005Tb3+,0.001Eu3+ to that of the state-of-the-art BaFBr(I):Eu2+, Al2O3:C, or NaLuF4:Tb3+ are 5.2, 8.8, or 2.8, respectively. The charge carriers can be stored more than 1000 h in LiTaO3:0.005Tb3+,0.001Eu3+. Proof-of-concept anti-counterfeiting application will be demonstrated by combining the colour-tailorable photoluminescence, afterglow, thermally, or optically stimulated luminescence in LiTaO3:0.005Tb3+,xEu3+ and LiTaO3:0.005Pr3+,0.001Eu3+. Multimode anti-counterfeiting application will be proposed by combining a high absolute X-ray scintillation light yield of 19000 ± 1800 ph/MeV of LiTaO3:0.005Tb3+,0.001Eu3+. Proof-of-concept flexible X-ray imaging application will be demonstrated by using the optimized LiTaO3:0.005Tb3+, 0.001Eu3+ dispersed in a silicone gel film.Green Open Access added to TU Delft Institutional Repository ‘You share, we take care!’ – Taverne project https://www.openaccess.nl/en/you-share-we-take-care Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.RST/Luminescence Material
Bi<sup>3+</sup> acting both as an electron and as a hole trap in La-, Y-, and LuPO<sub>4</sub>
The vacuum referred binding energy (VRBE)-guided design of Bi3+-based storage and afterglow materials together with charge carrier trapping processes is explored with a study on bismuth- and lanthanide-doped rare earth ortho-phosphates. By combining Bi3+ with the shallow hole trap of Tb3+ or Pr3+, Bi3+ appears to act as a deep electron trap and as a hole recombination center in YPO4. Combining Bi3+ with the deep electron trap of Tm3+, Sm3+, Yb3+, or Eu3+, Bi3+ appears to act as a shallow hole trap in YPO4. Here recombination is also realized by means of hole release instead of more commonly reported electron release. Holes are released from Bi4+ and then recombine through the valence band with the electrons trapped at Ln2+ to produce Ln3+ 4f-4f emission. Lu3+ was introduced into YPO4 to engineer the valence band (VB) energy and to tailor the hole trap depth of Bi3+ in Y1-xLuxPO4 solid solutions. The results show that with increasing x the VRBE at the valence band top moves downward and the hole trap depth of Bi3+ increases. With a deep understanding of the Bi2+ and Bi3+ trap level locations and on the charge carrier trapping process, this work broadens the avenue to explore new persistent luminescence and storage materials using Bi3+ both as electron and hole traps.Accepted Author ManuscriptRST/Fundamental Aspects of Materials and Energ
Wide Range X-Ray to Infrared Photon Detection and Energy Storage in LiTaO<sub>3</sub>:Bi<sup>3+</sup>,Dy<sup>3+</sup> Perovskite
It is challenging to obtain a material that can detect photons ranging from X-rays to infrared light. Such materials have promising use to develop advanced applications like in information storage, anticounterfeiting, or X-ray imaging. This article reports on such a material; LiTaO3:xBi3+,yDy3+ perovskite phosphor. Experimental spectroscopy, thermoluminescence, and vacuum referred binding energy diagram (VRBE) construction are combined to study the trapping processes of charge carriers. The VRBEs in the ground or excited states of Bi3+ and Bi2+ are discussed. Bi3+ emerges to act as a ≈1.3 eV deep hole capturing center and it may possibly also act as a 0.80 ± 0.5 eV deep electron trapping center. A linear relation between the amount of stored charge carriers and a photochromic phenomenon both induced by X-rays or 254 nm UV-light charging appears. The stored charge carriers in LiTaO3:xBi3+,yDy3+ are removed by heating or with an optically stimulated process with 365 nm UV light to 850 nm infrared laser. More than 3 or 40 h of Bi3+ and Dy3+ based white afterglow is measurable in LiTaO3:0.005Bi3+,0.004Dy3+ after exposure to X-rays or 254 nm UV light. Proof-of-concept light detection applications like 2D information storage and anticounterfeiting or X-ray imaging are demonstrated by using the phtotochromic and white afterglow LiTaO3:xBi3+,yDy3+ phosphors.Green Open Access added to TU Delft Institutional Repository ‘You share, we take care!’ – Taverne project https://www.openaccess.nl/en/you-share-we-take-care Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.RST/Luminescence Material
LiTaO<sub>3</sub>:Bi<sup>3+</sup>,Tb<sup>3+</sup>,Ga<sup>3+</sup>,Ge<sup>4+</sup>: A Smart Perovskite with High Charge Carrier Storage Capacity for X-Ray Imaging, Stress Sensing, and Non-Real-Time Recording
Developing X-ray or UV-light charged storage and mechanoluminescence (ML) materials with high charge carrier storage capacity is challenging. Such materials have promising utilization in developing new applications, for example, in flexible X-ray imaging, stress sensing, or non-real-time recording. Herein, the study reports on such materials; Bi3+, Tb3+, Ga3+, or Ge4+ doped LiTaO3 perovskite storage and ML phosphors. Their photoluminescence, thermoluminescence (TL), and ML properties are studied. The charge carrier trapping and release processes in the Bi3+, Tb3+, Ga3+, or Ge4+ doped LiTaO3 are explained by using the constructed vacuum referred binding energy diagram of LiTaO3 including the energy level locations of unintended defects, Tb3+, Bi3+, and Bi2+. The ratio of the TL intensity after X-ray charging of the optimized LiTaO3:0.005Bi3+,0.006Tb3+,0.05Ga3+, or LiTaO3:0.005Bi3+,0.006Tb3+,0.05Ge4+ to that of the state-of-the-art BaFBr(I):Eu2+ is ≈1.2 and 2.7, respectively. Force induced charge carrier storage phenomena is studied in the Tb3+, Bi3+, Ga3+, or Ge4+ doped LiTaO3. Proof-of-concept compression force distribution sensing and X-ray imaging is demonstrated by using optimized LiTaO3:0.005Bi3+,0.006Tb3+,0.05Ga3+ dispersed in a hard epoxy resin disc and in a silicone gel film. Proof-of-concept color-tailorable ML for anti-counterfeiting is demonstrated by admixing commercial ZnS:Cu+,Mn2+ with optimized LiTaO3:0.005Bi3+,0.006Tb3+,0.05Ge4+ in an epoxy resin disc.Green Open Access added to TU Delft Institutional Repository ‘You share, we take care!’ – Taverne project https://www.openaccess.nl/en/you-share-we-take-care Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.RST/Luminescence Material
Charge carrier trapping processes in lanthanide doped La-, Gd-, Y-, and LuPO4
Various methods for deliberate design electron and hole trapping materials are explored with a study on double lanthanide doped rare earth ortho phosphates. Cerium acts as recombination center while lanthanide codopants as electron trapping centers in LaPO4:0.005Ce3+,0.005Ln3+. The electron trap depth generated by lanthanide codopants can be tailored by the choice of lanthanide, and for fixed set of lanthanide dopants like in Gd1-xLaxPO4:0.005Ce3+,0.005Ho3+ solid solutions by changing x leading to conduction band (CB) engineering. Here, the electrons liberated from Ho2+ recombine through the conduction band at Ce4+ to yield Ce3+ 5d-4f emission. In contrast, samarium, europium and ytterbium are recombination centers, while Tb3+ and Pr3+ act as hole trapping centers in double lanthanide doped YPO4. For Tb3+ and Pr3+ codopants recombination is realized via hole release rather than the more common reported electron release. The holes recombine via the valence band with the electrons trapped at Yb2+, Sm2+, or Eu2+ to generate 4f-4f luminescence from Yb3+, Sm3+, or Eu3+. Lu3+ was introduced in YPO4 to tailor the valence band (VB) energy and to tune the hole trap depths of Tb3+ and Pr3+ in Y1-xLuxPO4:0.005Ln3+ solid solutions. Our results promote the deliberate design electron and hole trapping materials from deep understanding of trap level locations and on the transport and trapping processes of charge carriers.RST/Fundamental Aspects of Materials and Energ
Going Beyond Counting First Authors in Author Co-citation Analysis
The present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Variations on the Author
“Variations on the Author” discusses two of Eduardo Coutinho’s recent films (Um Dia na Vida, from 2010, and Últimas Conversas, posthumously released in 2015) and their contribution to the general question of documentary authorship. The director’s filmography is characterized by a consistent yet self-effacing form of authorial self-inscription: Coutinho often features as an interviewer that rather than express opinions propels discourses; an interviewer that is good at listening. This mode of self-inscription characterizes him as an author who is not expressive but who is nonetheless markedly present on the screen. In Um Dia na Vida, however, Coutinho is completely absent form the image, while Últimas Conversas, on the contrary, includes a confessional prologue that moves the director from the margins to the center of his films. This article examines the ways in which these works stand out in the filmography of a director who offers new insights into the notion of cinematic authorship
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