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21.
Gwan-Hyoung Lee 《Journal of luminescence》2011,131(12):2606-2611
The correlation between the crystal structure and luminescent properties of Eu3+-doped metal tungstate phosphors for white LEDs was investigated. Red-emitting A4−3x(WO4)2:Eux3+ (A=Li, Na, K) and B(4−3x)/2(WO4)2:Eux3+ (B=Mg, Ca, Sr) phosphors were synthesized by solid-state reactions. The findings confirmed that these phosphors exhibited a strong absorption in the near UV to green range, due to the intra-configurational 4f-4f electron transition of Eu3+ ions. The high doping concentration of Eu3+ enhanced the absorption of near UV light and red emission without any detectable concentration quenching. Based on the results of a Rietveld refinement, it was attributed to the unique crystal structure. In the crystal structure of the Eu3+-doped metal tungstate phosphor, the critical energy transfer distance is larger than 5 Å so that exchange interactions between Eu3+ ions would occur with difficulty, even at a high doping concentration. The energy transfer between Eu3+ ions, which causes a decrease in red emission with increasing concentration of Eu3+, appears to be due to electric multi-polar interactions. In addition, the Eu-O distance in the host lattice affected the shape of emission spectrum by splitting of emission peak at the 5D0→7F2 transition of Eu3+. 相似文献
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文章首先介绍了发光二极管(LED)的内量子效率、外量子效率的基本概念和提高量子效率的基本方法,接着对LED外延的结构和方法做了简要介绍.文章的第三和第四部分则着重介绍了提高内、外量子效率的外延方法,这些方法包括外延结构的优化,侧向外延生长,SiC和GaN衬底的生长,AlInGaN四元系有源区生长,非极性面、半极性面的外延,表面粗化结构生长,图形化二次外延结构.图形化蓝宝石衬底上的外延,提高载流子注入效率的结构和组分设计.文章的第五部分则介绍了基于可靠性和成本考虑的其他新型外延结构,第六部分介绍了提高LED 相似文献
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Laetitia Hackel Elise Rotureau Aoife Morrin Jos Paulo Pinheiro 《Molecules (Basel, Switzerland)》2021,26(18)
Electrochemical stripping techniques are interesting candidates for carrying out onsite speciation of environmentally relevant trace metals due to the existing low-cost portable instrumentation available and the low detection limits that can be achieved. In this work, we describe the initial analytical technique method development by quantifying the total metal concentrations using Stripping Chronopotentiometry (SCP). Carbon paste screen-printed electrodes were modified with thin films of mercury and used to quantify sub-nanomolar concentrations of lead and cadmium and sub-micromolar concentrations of zinc in river water. Low detection limits of 0.06 nM for Pb(II) and 0.04 nM for Cd(II) were obtained by the standard addition method using a SCP deposition time of 180 s. The SCP results obtained for Pb(II) and Cd(II) agreed with those of inductively coupled plasma mass spectrometry (ICP-MS). The coupling of SCP with screen-printed electrodes opens up excellent potential for the development of onsite speciation of trace metals. Due to the low analysis throughput obtained for the standard addition method, we also propose a new, more rapid screening Cd(II) internal standard methodology to significantly increase the number of samples that can be analyzed per day. 相似文献
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《Electroanalysis》2017,29(12):2863-2872
Fullerene Black (FB) and Extracted Fullerene Black (EFB) were used in modified screen‐printed electrodes producing electrochemical transducers (FB‐SPEs and EFB‐SPEs). A complete electrochemical study was performed and the best results are obtained working with FB‐SPEs, especially in terms of: 1. improved electron‐transfer kinetic mechanisms and 2. sensitivity and selectivity toward Acetaminophen (Ac) and Guanine (G). These latter represent two important electro‐active targets to quantify in medicine field application, because: Ac is a preferred alternative (as analgesic‐antipyretic agent) to aspirin, particularly for patients who cannot tolerate aspirin; the oxidation signal of G is useful for the fabrication of emerging analytical tools, such as DNA chipsand user‐friendly diagnostic devices. Ac and G are quantify by using FB‐SPEs electrochemical devices, with an extended linearity (1–300 μM for Ac; 0.1–300 μM for G), an excellent sensitivity (2.82 μA μM−1 cm−2 in the case of Ac; and 0.183 μA μM−1 cm−2 in the case of G), a low detection limit (0.01 μM for Ac; 0.005 μM for G), a very good reproducibility (both: intra‐; inter‐electrodes reproducibility RSD % ranging from 0.3–0.5 for Ac; and 0.50–0.85 for G) and a very fast response time (6 s for Ac; 5 s in the case of G). In addition, high selectivity is obtained at FB‐SPEs, meaning that the FB‐SPEs electrochemical transducers are suitable to simultaneously quantify Ac and G in real samples, having several different (highly concentrated) interference. 相似文献
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Novel conjugated silole‐containing polyfluorenes, with green‐ and red‐emissive siloles on the backbone of the blue‐emissive polyfluorene are synthesized for white light electroluminescence (EL) from a single polymer with simultaneous red, green, and blue (RGB) emission. The CIE coordinates (0.33, 0.36) of the white light EL spectra are very close to that for pure white light (0.33, 0.33). The EL spectra are also quite stable at different applied voltages or brightness. The relative intensities for the three RGB peaks, at 450, 505, and 574 nm, were 0.94, 1, and 0.97, respectively, which demonstrates a balanced simultaneous RGB emission. A maximum luminous efficiency of 2.03 cd · A−1 for a brightness of 344 cd · m−2, and a luminous efficiency of 1.86 cd · A−1 for a more practical brightness of 2 703 cd · m−2, were achieved.
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《中国化学会会志》2018,65(9):1082-1089
In this work, a screen‐printed carbon electrode (SPCE) was modified with a cobalt/porous silicon (Co@PSi) nanocomposite powder to develop a nonenzymatic sensor for the detection of hydrogen peroxide. The Co@PSi nanocomposite was synthesized through the chemical reaction between silicon powder in a HF/HNO3 solution and cobalt cations. In this process, cobalt nanoparticles were anchored on the porous silicon. The structure and morphology of the synthesized nanocomposite were investigated by X‐ray diffraction, Fourier transform infrared spectroscopy, X‐ray photoemission spectroscopy, energy dispersive X‐ray spectroscopy, and field‐emission scanning electron microscopy. The constructed nonenzymatic, screen‐printed sensors based on the Co@PSi nanocomposite showed perfect electrocatalytic oxidation response to hydrogen peroxide over the range 1–170 and 170–3,770 μmol/L with the limit of detection of 0.8 μmol/L. In addition, the Co@PSi‐SPCE sensor exhibited good selectivity for the determination of H2O2 in the presence of common interfering species including glucose, ascorbic acid, uric acid, dopamine, nitrate, and nitrite ions. The constructed electrochemical sensor was successfully used for the determination of H2O2 in real samples. 相似文献