Pressure-Induced Remarkable Spectral Red-Shift in Mn2+ -Activated NaY9 (SiO4 )6 O2 Red-Emitting Phosphors for High-Sensitive Optical Manometry.

To settle the low sensitivity of luminescent manometers, the Mn2+ -activated NaY9 (SiO4 )6 O2 red-emitting phosphors with splendid pressure sensing performances are developed. Excited by 408 nm, the resulting products emit bright red emission originating from 4 T1 (4 G) → 6 A1 transition of Mn2+ , in which the optimal concentration of the activator ion is ≈1 mol%. Moreover, the admirable thermal stability of the developed phosphors is studied and confirmed by the temperature-dependent emission spectra, based on which the activation energy is derived to be 0.275 eV. By analyzing the pressure-dependent Raman spectra, the structural stability of the synthesized compounds at extreme conditions is verified. Furthermore, the designed phosphors exhibit remarkable spectral red-shift at elevated pressure. Especially, as pressure increases from 0.75 to 7.16 GPa, the emission band centroid shifts from 617.2 to 663.4 nm, resulting in a high sensitivity (dλ/dP) of 7.00 nm GPa-1 , whereas the full width at half maximum (FWHM) increases from 83.0 to 110.6 nm, leading to the ultra-high sensitivity (dFWHM/dP) of 10.13 nm GPa-1 . These achievements manifest that the designed red-emitting phosphors are appropriate for ultrasensitive optical manometry. More importantly, the developed manometer is a current global leader in sensitivity, when operating in the band-width mode, that is, FWHM.

Frontiers of Deep-Red Emission of Mn4+ Ions with Ruddlesden-Popper Perovskites.

It is well-known that the chemical composition of the host material significantly affects the spectroscopic performance of transition metal ions. However, it is worth noting that also the structure and symmetry of crystallographic sites play significant roles in transition metal ion luminescence. In this study, we demonstrate three perovskite structures of strontium titanate forming so-called Ruddlesden-Popper phases doped with Mn4+ ions. The observed reduction in the average Ti4+-O2- distance in the series SrTiO3-Sr2TiO4-Sr3Ti2O7 allowed for a record-breaking shift in the spectral position of Mn4+ emission band with a maximum of around 734 nm and led to an improvement of the already impressive thermometric performance of SrTiO3:Mn4+ in ratiometric and lifetime-based approaches. This research encourages a further search for structures that, with the help of the developed correlations between structural and optical properties, could lead to the discovery of phosphors beyond the limits established so far.

Mn5+-activated Ca6Ba(PO4)4O near-infrared phosphor and its application in luminescence thermometry.

The near-infrared luminescence of Ca6Ba(PO4)4O:Mn5+ is demonstrated and explained. When excited into the broad and strong absorption band that spans the 500-1000 nm spectral range, this phosphor provides an ultranarrow (FWHM = 5 nm) emission centered at 1140 nm that originates from a spin-forbidden 1E → 3A2 transition with a 37.5% internal quantum efficiency and an excited-state lifetime of about 350 µs. We derived the crystal field and Racah parameters and calculated the appropriate Tanabe-Sugano diagram for this phosphor. We found that 1E emission quenches due to the thermally-assisted cross-over with the 3T2 state and that the relatively high Debye temperature of 783 K of Ca6Ba(PO4)4O facilitates efficient emission. Since Ca6Ba(PO4)4O also provides efficient yellow emission of the Eu2+ dopant, we calculated and explained its electronic band structure, the partial and total density of states, effective Mulliken charges of all ions, elastic constants, Debye temperature, and vibrational spectra. Finally, we demonstrated the application of phosphor in a luminescence intensity ratio thermometry and obtained a relative sensitivity of 1.92%K-1 and a temperature resolution of 0.2 K in the range of physiological temperatures.

Influence of the Synthesis Conditions on the Morphology and Thermometric Properties of the Lifetime-Based Luminescent Thermometers in YPO4:Yb3+,Nd3+ Nanocrystals.

An increase in the accuracy of remote temperature readout using luminescent thermometry is determined, among other things, by the relative sensitivity of the thermometer. Therefore, to increase the sensitivity, intensive work is carried out to optimize the host material composition and select the luminescent ions accordingly. However, the role of nanocrystal morphology in thermometric performance is often neglected. This paper presents a systematic study determining the role of synthesis parameters of the solvothermal method on the morphology of YPO4:Yb3+,Nd3+ nanocrystals and their effect on the lifetime of Yb3+ ion-based luminescent thermometer performance. It was shown that by changing the RE3+:(PO4)3- ratio and the concentration of Nd3+ ions, the size, shape, and aggregation level of the nanocrystals can be modified changing the thermometric parameters of the luminescent thermometer. The highest relative sensitivity was obtained for the low RE3+:(PO4)3- ratio and 1% Nd3+ ion concentration.

Quantitative Comparison of the Light-to-Heat Conversion Efficiency in Nanomaterials Suitable for Photothermal Therapy.

Functional colloidal nanoparticles capable of converting between various energy types are finding an increasing number of applications. One of the relevant examples concerns light-to-heat-converting colloidal nanoparticles that may be useful for localized photothermal therapy of cancers. Unfortunately, quantitative comparison and ranking of nanoheaters are not straightforward as materials of different compositions and structures have different photophysical and chemical properties and may interact differently with the biological environment. In terms of photophysical properties, the most relevant information to rank these nanoheaters is the light-to-heat conversion efficiency, which, along with information on the absorption capacity of the material, can be used to directly compare materials. In this work, we evaluate the light-to-heat conversion properties of 17 different nanoheaters belonging to different groups (plasmonic, semiconductor, lanthanide-doped nanocrystals, carbon nanocrystals, and metal oxides). We conclude that the light-to-heat conversion efficiency alone is not meaningful enough as many materials have similar conversion efficiencies─in the range of 80-99%─while they significantly differ in their extinction coefficient. We therefore constructed their qualitative ranking based on the external conversion efficiency, which takes into account the conventionally defined light-to-heat conversion efficiency and its absorption capacity. This ranking demonstrated the differences between the samples more meaningfully. Among the studied systems, the top-ranking materials were black porous silicon and CuS nanocrystals. These results allow us to select the most favorable materials for photo-based theranostics and set a new standard in the characterization of nanoheaters.

Correction: Synthesis and characterizations of YZ-BDC:Eu3+,Tb3+ nanothermometers for luminescence-based temperature sensing.

[This corrects the article DOI: 10.1039/D2RA01759H.].

Synthesis and characterizations of YZ-BDC:Eu3+,Tb3+ nanothermometers for luminescence-based temperature sensing.

In the present work, nanothermometers based on amorphous zirconium metal-organic frameworks co-doped with rare-earth ions (YZ-BDC:Eu3+,Tb3+ nanothermometers) with sizes of about 10-30 nm were successfully synthesized via a microwave-assisted hydrothermal method at 120 °C for 15 min. The determined BET surfaces area, total pore volume and average pore diameter were ∼530 m2 g-1, 0.45 cm3 g-1 and 3.4 nm, respectively. Based on Fourier transform infrared spectroscopy (FTIR) and simultaneous thermal analysis (STA) results, the formation process of carboxylic acid salts and the molecular formula of the samples have been proposed. The thermometric properties of Zr-BDC:Eu3+,Tb3+ nanothermometers and their Y3+ ion co-doped counterparts (YZ-BDC:Eu3+,Tb3+) measured in the 133-573 K temperature range were compared. Moreover, the temperature-dependent CIE(x, y) chromaticity coordinates and emission color of the samples were also determined. As the temperature increased from 133 to 573 K, the emission color of Zr-BDC:Eu3+,Tb3+ nanothermometers without the presence of Y3+ ions changed from orange to red, while for YZ-BDC:Eu3+,Tb3+ nanothermometers, the emission color changed from yellow to orange, due to the strong effect of the presence of Y3+ ions on the luminescence intensity of Eu3+ and Tb3+ ions. The maximum relative sensitivity (S Rmax) in both materials was close to 0.5%/K, however, the temperature range of their occurrence was significantly shifted toward higher temperatures due to doping with Y3+ ions. The obtained results showed that doping with Y3+ ions not only enables the modulation of the useful temperature range with high relative sensitivity, but also provides improved thermal stability.

Boltzmann-distribution-dominated persistent luminescence ratiometric thermometry in NaYF4:Pr3.

A novel, to the best of our knowledge, optical temperature measurement method is proposed, i.e., persistent luminescence intensity ratio (PLIR) thermometry. The PLIR thermometry relies on the micro-sized NaYF4:Pr3+ material that can emit persistent luminescence (PersL) uninterruptedly after being charged by x ray irradiation. The 3P1→3H5 and 3P0→3H5 PersL transitions, locating separately at ∼ 522 and 538 nm, have been confirmed to follow the Boltzmann distribution. The emitting intensity ratio of this pair of PersL lines is thus found to be a good indicator of the variation of temperature. Our work is expected to enrich the optical temperature sensing family.

Self-referenced method for the Judd-Ofelt parametrisation of the Eu3+ excitation spectrum.

Judd-Ofelt theory is a cornerstone of lanthanides' spectroscopy given that it describes 4fn emissions and absorptions of lanthanide ions using only three intensity parameters. A self-referenced technique for computing Judd-Ofelt intensity parameters from the excitation spectra of Eu3+-activated luminescent materials is presented in this study along with an explanation of the parametrisation procedure and free user-friendly web application. It uses the integrated intensities of the 7F0 → 5D2, 7F0 → 5D4, and 7F0 → 5L6 transitions in the excitation spectrum for estimation and the integrated intensity of the 7F0 → 5D1 magnetic dipole transition for calibration. This approach facilitates an effortless derivation of the Ω6 intensity parameter, which is challenging to compute precisely by Krupke's parametrisation of the emission spectrum and, therefore, often omitted in published research papers. Compared to the parametrisation of absorption spectra, the described method is more accurate, can be applied to any material form, and requires a single excitation spectrum.

Standardization of Methodology of Light-to-Heat Conversion Efficiency Determination for Colloidal Nanoheaters.

Localized photothermal therapy (PTT) has been demonstrated to be a promising method of combating cancer, that additionally synergistically enhances other treatment modalities such as photodynamic therapy or chemotherapy. PTT exploits nanoparticles (called nanoheaters), that upon proper biofunctionalization may target cancerous tissues, and under light stimulation may convert the energy of photons to heat, leading to local overheating and treatment of cancerous cells. Despite extensive work, there is, however, no agreement on how to accurately and quantitatively compare light-to-heat conversion efficiency (ηQ) and rank the nanoheating performances of various groups of nanomaterials. This disagreement is highly problematic because the obtained ηQ values, measured with various methods, differ significantly for similar nanomaterials. In this work, we experimentally review existing optical setups, methods, and physical models used to evaluate ηQ. In order to draw a binding conclusion, we cross-check and critically evaluate the same Au@SiO2 sample in various experimental conditions. This critical study let us additionally compare and understand the influence of the other experimental factors, such as stirring, data recording and analysis, and assumptions on the effective mass of the system, in order to determine ηQ in a most straightforward and reproducible way. Our goal is therefore to contribute to the understanding, standardization, and reliable evaluation of ηQ measurements, aiming to accurately rank various nanoheater platforms.

Highly NIR-emitting ytterbium complexes containing 2-(tosylaminobenzylidene)-N-benzoylhydrazone anions: structure in solution and use for bioimaging.

Solution behaviour in DMSO using 1D and 2D NMR spectroscopy was performed for lanthanide complexes Ln(L)(HL) and Ln(HL)2Cl, containing non-macrocyclic 2-(tosylamino)-benzylidene-N-benzoylhydrazone (H2L), and the structure of [Yb(L)]+ cation in solution was determined. Based on the NMR data, the possibility to obtain novel complexes containing [Ln(L)2]- was predicted, which was successfully synthesized, and the crystal structure of K(C2H5OH)3[Yb(L)2] was determined. Thanks to its high quantum yield of NIR luminescence (1.3 ± 0.2%), high absorption, low toxicity, and the stability of its anion against dissociation in DMSO, K(H2O)3[Yb(L)2] was successfully used for bioimaging.

Gallato Zirconium (IV) Phtalocyanine Complex Conjugated with SiO2 Nanocarrier as a Photoactive Drug for Photodynamic Therapy of Atheromatic Plaque.

A new conjugate of gallato zirconium (IV) phthalocyanine complexes (PcZrGallate) has been obtained from alkilamino-modified SiO2 nanocarriers (SiO2-(CH2)3-NH2NPs), which may potentially be used in photodynamic therapy of atherosclerosis. Its structure and morphology have been investigated. The photochemical properties of the composite material has been characterized. in saline environments when exposed to different light sources Reactive oxygen species (ROS) generation in DMSO suspension under near IR irradiation was evaluated. The PcZrGallate-SiO2 conjugate has been found to induce a cytotoxic effect on macrophages after IR irradiation, which did not correspond to ROS production. It was found that SiO2 as a carrier helps the photosensitizer to enter into the macrophages, a type of cells that play a key role in the development of atheroma. These properties of the novel conjugate may make it useful in the photodynamic therapy of coronary artery disease.

Excited State Absorption for Ratiometric Thermal Imaging.

Luminescence thermometry, an alternative to thermal imaging using the thermovision technique, requires the development of new approaches and a thorough understanding of the physical phenomena involved, in order to improve the temperature readout parameters. A phenomenon that has recently been shown to cause an extremely strong increase in the emission intensity for the temperature elevation is the thermally induced excited state absorption. This work demonstrates that taking advantage of the strong thermal dependence of the thermally induced excited state absorption process, the limitation associated with the two thermally coupled excited levels usually involved in the ratiometric temperature readout can be overcome, improving the thermometric properties of the luminescent thermometer. The same excitation wavelength was used to induce the emission resulting from the thermally induced excited state absorption of the Tb3+ ions and ground-state absorption of the other type of co-dopant ions causing the opposite nature of the thermal dependence of their emission intensities. Moreover, thanks to the strong color changes exhibited by the phosphors, it was possible to demonstrate the applicability of the proposed approach for through-object 2D thermal imaging of a microelectronic printed circuit board covered with a glass plate using an ordinary commercial digital camera, where the thermovision camera fails.

All near-infrared multiparametric luminescence thermometry using Er3+, Yb3+-doped YAG nanoparticles.

This paper presents four new temperature readout approaches to luminescence nanothermometry in spectral regions of biological transparency demonstrated on Yb3+/Er3+-doped yttrium aluminum garnet nanoparticles. Under the 10 638 cm-1 excitation, down-shifting near infrared emissions (>10 000 cm-1) are identified as those originating from Yb3+ ions' 2F5/2 → 2F7/2 (∼9709 cm-1) and Er3+ ions' 4I13/2 → 4I15/2 (∼6494 cm-1) electronic transitions and used for 4 conceptually different luminescence thermometry approaches. Observed variations in luminescence parameters with temperature offered an exceptional base for studying multiparametric temperature readouts. These include the temperature-dependence of: (i) intensity ratio between emissions from Stark components of Er3+ 4I13/2 level; (ii) intensity ratio between emissions of Yb3+ (2F5/2 → 2F7/2 transition) and Er3+ (4I13/2 → 4I15/2 transition); (iii) band shift and bandwidth and (iv) lifetime of the Yb3+ emission (2F5/2 → 2F7/2 transition) with maximal sensitivities of 1% K-1, 0.8% K-1, 0.09 cm-1 K-1, 0.46% K-1 and 0.86% K-1, respectively. The multimodal temperature readout provided by this material enables its application in different luminescence thermometry setups as well as improved the reliability of the temperature sensing by the cross-validation between measurements.

The Effect of pH on the Size of Silver Nanoparticles Obtained in the Reduction Reaction with Citric and Malic Acids.

In colloidal methods, the morphology of nanoparticles (size and shape) as well as their stability can be controlled by changing the concentration of the substrate, stabilizer, adding inorganic salts, changing the reducer/substrate molar ratio, and changing the pH and reaction time. The synthesis of silver nanoparticles was carried out according to the modified Lee and Meisel method in a wide pH range (from 2.0 to 11.0) using citric acid and malic acid, without adding any additives or stabilizers. Keeping the same reaction conditions as the concentration of acid and silver ions, temperature, and heating time, it was possible to determine the relationship between the reaction pH, the type of acid, and the size of the silver nanoparticles formed. Obtained colloids were analyzed by UV-Vis spectroscopy and investigated by means of Transmission Electron Microscope (TEM). The study showed that the colloids reduced with citric acid and malic acid are stable over time for a minimum of seven weeks. We observed that reactions occurred for citric acid from pH 6.0 to 11.0 and for malic acid from pH 7.0 to 11.0. The average size of the quasi-spherical nanoparticles changed with pH due to the increase of reaction rate.

Cr3+ based nanocrystalline luminescent thermometers operating in a temporal domain.

Cr3+ doped nanocrystals were examined as a noncontact temperature sensor in a lifetime-based approach. The impact of both the analysis protocols and host materials on the lifetime-based approach was systematically investigated. Temperature-dependent luminescence decay curves were analyzed according to three different procedures (average lifetime approach, double exponential fit and time-gated ratiometric approach). The advantages and drawbacks of each method are discussed. Additionally, the thermal sensitivities derived from the average lifetime approach and the double exponential fit revealed a strong dependence of the thermal sensitivity of the Cr3+ doped nanocrystals on the crystal field strength. In these cases, it was found that the long metal-oxygen distances in the host materials improve the thermal sensitivity of the system. This work reveals the importance of both host materials and analysis procedures in the lifetime thermal sensitivity of Cr3+ doped nanocrystals and opens up an avenue towards their future optimization.

Synergy between NIR luminescence and thermal emission toward highly sensitive NIR operating emissive thermometry.

There are many figures of merit, which determine suitability of luminescent thermometers for practical applications. These include thermal sensitivity, thermal accuracy as well as ease and cost effectivness of technical implementation. A novel contactless emission thermometer is proposed, which takes advantage of the coexistence of photoluminescence from Nd3+ doping ions and black body emission in transparent Nd3+ doped-oxyfluorotellurite glass host matrix. The opposite temperature dependent emission from these two phenomena, enables to achieve exceptionally high relative sensitivity SR = 8.2%/°C at 220 °C. This enables to develop new type of emissive noncontact temperature sensors.

Thermochromic Luminescent Nanomaterials Based on Mn4+/Tb3+ Codoping for Temperature Imaging with Digital Cameras.

A new thermographic nanocrystalline Sr4Al14O25:Mn4+,Tb3+ phosphor was developed, and the concentrations of both dopants and the synthesis conditions were optimized. The combination of the thermally quenched luminescence from the Mn4+ ions to the almost temperature-independent emission from Tb3+ provides a sensitive luminescent thermometer (SR = 2.8%/°C at 150 °C) with strong emission color variability. In addition, a figure of merit for this luminescence thermochromism was proposed, as the relative sensitivities of the x and y CIE coordinates, which for this phosphor reaches at 150 °C SR(x) = 0.6%/°C and SR(y) = 0.4%/°C, respectively. Noncontact thermal imaging was demonstrated with this phosphor using a single consumer digital camera and exploiting the ratio of red (R) and green (G) channels of the RGB images, thereby confirming the high application potential of Sr4Al14O25:Mn4+,Tb3+ nanocrystals for thermal sensing and mapping.

Fabrication and characterization of up-converting ß-NaYF4:Er3+,Yb3+@NaYF4 core-shell nanoparticles for temperature sensing applications.

This paper presents the use of soft template method to synthesize core and core-shell up-converting nanoparticles usefull for temperature sensing applications. Based on the stock solutions of core ß-NaYF4:Er3+,Yb3+ nanoparticles and involving soft template method without any additional process of surface functionalization, it is possible to directly design the core-shell ß-NaYF4:Er3+,Yb3+@NaYF4 nanoparticles, which can be perfectly dispersed in cyclohexane and surfactants like oleic acid (OA), triethanolamine (TEA) or Cetyltrimethylammonium bromide (CTAB). The morphological, crystalline and elemental characteristics of samples were investigated by Field Emission Scanning Electron Microscopy, X-Ray Diffraction, High Resolution Transmission Electron Microscopy, Selected Area Electron Diffraction patterns and Energy-Dispersive X-Ray Spectroscopy (EDX) measurements. The results showed that the synthesized NaYF4:Er3+,Yb3+@NaYF4 core-shell nanoparticles have roughly spherical shape, pure hexagonal ß phase with core size of about 35 ± 5 nm and shell thickness of about 40 ± 5 nm. It has been shown that the coating of the ß-NaYF4:Er3+,Yb3+ core with NaYF4 shell layer enables to enhance the green upconversion (UC) emission intensities in respect to red one. Under 976 nm excitation, the synthesized ß-NaYF4:2%Er3+,19%Yb3+@NaYF4 core-shell nanoparticles revealed three strong emission bands at 520 nm, 545 nm and 650 nm corresponding to 2H11/2, 4S3/2 and 4F9/2 to 4I15/2 transitions of Er3+ ions with the lifetimes of 215, 193 and 474 µs, respectively. The calculated CIE chromaticity coordinates proved that the emission colour of core-shell nanoparticles was changed from red into yellowish green upon increasing the power density of the 976 nm laser from 0.73 to 9.95 W/cm2. The calculated slopes indicated that in the ß-NaYF4:2%Er3+,19%Yb3+@NaYF4 core-shell nanoparticles, two-photon and three-photon UC processes took place simultaneously. Although the former one is similar as in the case of ß-NaYF4:Er3+,Yb3+ bare core nanoparticles, the latter one, three-photon UC process for green emission occurs, due to cross relaxation processes of two Er3+ ions only within nanoparticles with core-shell architecture. Moreover, the energy difference between the 2H11/2 and 4S3/2 levels and associated constant of NaYF4@NaYF4 host lattice were determined and they reached ~ 813 cm-1 and 14.27 (r2 = 0.998), respectively. In order to investigate the suitability of nanoparticles for optical temperature sensing, the emission spectra were measured in a wide temperature range from 158 to 298 K. An exceptionally high value of relative sensitivity was obtained at 158 K and it amounted to 4.25% K-1. Further temperature increase resulted in gradual decrease of relative sensitivity, however, it maintained a high value > 1% K-1 in the entire analyzed temperature range.