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Upconversion detectors monolithically combining a detection unit and a light emitting unit, enables light detection and visualization in a compact structure, promising great advances in miniaturized multifunctional optoelectronics. The detection range of upconversion detectors usually covers a broadband spectrum, limiting their use in spectroscopic fields. This work investigates two wavelength‐selective upconversion detectors made with organic semiconductors to realize narrowband near‐infrared (NIR) light detection and visualization dual function. Two non‐fullerene‐based NIR‐sensitive bulk‐heterojunctions (BHJs) are exploited to make wavelength‐selective upconversion detectors, achieving peak sensitivity at 860 and 890 nm, with full width at half maximum of 125 and 170 nm, respectively. Each NIR‐sensitive BHJ comprises a donor polymer and a non‐fullerene acceptor, both of which are selectively sensitive to NIR light. The cumulative analysis of the optical properties of the absorber and current–voltage characteristics of the device indicates that the wavelength selectivity stems mainly from the wavelength‐dependent absorption. In particular, the upconversion detectors exhibit wavelength‐selective electronic and optical dual‐readouts, which are appealing for miniaturized spectroscopic applications, including health monitoring, optical communication, and microbead imaging, paving the way for practical applications. [ABSTRACT FROM AUTHOR]

The lack of viable solid‐state annihilators is one of the greatest hurdles in perovskite‐sensitized triplet–triplet annihilation upconversion (UC). Unfavorable singlet and triplet energy surfaces in the solid state have limited the successful implementation of many conventional solution‐based annihilators. To date, rubrene is still the best‐performing annihilator; however, this comes at the cost of a limited apparent anti‐Stokes shift. To this point, anthracene derivatives are promising candidates to increase the apparent anti‐Stokes shift. The well‐known green glowstick dye 9,10‐(bisphenylethynyl)anthracene (BPEA) and its chlorinated derivatives have already shown promise in solution‐based UC applications. Due to favorable band alignment of the perovskite and triplet energy levels of BPEA, it is conceivable that a wide variety of BPEA derivatives can be compatible with the perovskite‐based UC system. Here, the properties of the parent molecule BPEA and its derivatives 1‐chloro‐9,10‐(bisphenylethynyl)anthracene and 2‐chloro‐9,10‐(bisphenylethynyl)anthracene are investigated. Despite similar optical properties in solution, the different molecules exhibit vastly different properties in thin films. UC studies in lead halide perovskite/BPEA bilayer devices demonstrate the importance of intermolecular coupling on the resulting properties of the upconverted emission. [ABSTRACT FROM AUTHOR]

Triplet‐triplet annihilation upconversion (TTA‐UC) technology could convert low‐energy light into high‐energy light, and it is a very promising one of the upconversion technologies due to its non‐coherent excitation light, low required excitation optical power density and sensitizer/annihilator flexible adjustability. The application of TTA‐UC into photocatalysis could not only broaden the range of solar energy spectrum utilization, but also bring mild reaction conditions and higher product yields via avoiding the side reaction. However, the detailed catalytic mechanism of TTA‐UC is unclear. Therefore, in this review, we summarized and classified TTA‐UC photocatalytic chemical reactions in terms of mechanism. [ABSTRACT FROM AUTHOR]

The commonly used automotive head‐up display (HUD) technology is confronted with the problems of poor stability in organic resin counterpart and the unsatisfactory display effect of projection lighting source. To solve these issues, developing state‐of‐the‐art materials and designing new HUD schemes with a wide color gamut is of necessity. Herein, a series of pure red/green/blue (R/G/B) upconverting (UC) nano‐glass‐ceramics (GCs) containing lanthanide‐doped NaLuF4 nanocrystals (NCs) are synthesized in a cost‐effective, environment‐friendly, and scalable manner, simultaneously achieving high crystallinity (≈45.44%) and high transparency (>80%). Yb3+ is chosen as the sensitizer to Tm3+ (blue UC)/Ho3+ (green UC), due to its large absorption cross section from ground state 2F7/2 to excited state 2F5/2; meanwhile Er3+, Tm3+ co‐doped into NCs can obtain pure red UC emission via promoting the population of Er3+ red‐emitting 4F9/2 state. Consequently, the as‐prepared materials exhibit high R/G/B color purity of > 80% owing to the energy transfer between different lanthanide ions (Yb3+, Tm3+, Ho3+, and Er3+) upon 980 nm near‐infrared (NIR) laser excitation, and possess superior thermal reversibility/water resistivity. Remarkably, two unprecedented HUD prototypes are constructed to demonstrate the application feasibility of developed pure R/G/B UC GCs. [ABSTRACT FROM AUTHOR]

Ligands combining two lateral bis‐pyridyl‐phosphonated‐pyclens were synthesized, using a flexible linear pegylated linker (L2) or a bulkier K22 crown‐ether (L3). A functionalized pyridyl‐phosphonated‐pyclen (L1) was also prepared as a mononuclear analogue. Coordination behavior of lanthanide cations was studied via NMR titration with Lu for L1, and UV/Vis and luminescence spectroscopy with Yb for L2/L3. Strong coordination of two Yb atoms enabled isolation and spectroscopic characterization of dinuclear complexes in H2O and D2O. Excited state lifetime analysis at 980 nm revealed strong protection of Yb cations, with no coordinated water molecule. Upon titration of the isolated dinuclear Yb complexes with Tb cations, cooperative upconversion (UC) sensitization of Tb in the visible was observed upon excitation of Yb at 980 nm in D2O. In the absence of Tb, the Yb complexes also exhibited cooperative luminescence with a weak emission band around 500 nm upon NIR Yb excitation. Efficient UC with Tb was only observed after thermal treatment, suggesting a slow kinetic of formation of the UC species. [Yb2TbL3] showed weak Tb centered UC emission, while the dinuclear complex of L2 displayed more intense UC emission up to two equivalents of Tb, forming [(Yb2L2)Tbx] (x=1–2), with the tetranuclear heterometallic complex being the most intense emitter. Log‐Log plot analysis confirmed the two‐photon nature of the UC process. [ABSTRACT FROM AUTHOR]

Triplet–triplet annihilation (TTA), or triplet fusion, is a biexcitonic process in which two triplet‐excited molecules can combine their energy to promote one into an excited singlet state. To alleviate the dependence of the TTA rate and yield on triplet diffusion in both solid and solution environments, intramolecular TTA (intra‐TTA) has been recently proposed in conjugated molecular systems able to hold multiple triplet excitons simultaneously. Developing from the previous demonstration of TTA performance enhancement in sensitized upconversion solutions, here similar improvements in triplet harvesting in solid‐state films are reported under electrical excitation in organic light emitting diodes (OLEDs). At low dye concentration and low current densities, the intra‐TTA active OLED shows a +40% improved external quantum efficiency with respect to the reference device, and a TTA spin‐statistical factor f 4DPA of 0.4, close to that determined in fluid solution for the individual chromophore (0.45). These results therefore indicate the utility of this molecular design strategy across a wider range of TTA applications, and with particular utility in the further development of low‐power TTA‐enhanced OLEDs. [ABSTRACT FROM AUTHOR]

In this semi‐quantitative study, laser crystal microparticles which are potentially capable of generating mid‐infrared (MIR) light are incorporated into MIR transmitting optical fibers using a volumetric interface doping technique that combines interface doping with volumetric doping. Using confocal microscopy with a refractive index matching fluid, the Er:YAP microcrystals (MCs) inside the tellurite glass fiber are observed based on the detection of the green upconversion fluorescence emission of Er3+ ions, produced under excitation at 976 nm and localized at the central region within the fiber. The key outcome from this proof‐of‐concept study is that MC particles that are fused with the glass during the fiber drawing process survived heat treatment because the MC particles are exposed for a short time to a glass fluid with high viscosity of ≈105 Pa.s, which prevented the glass from exerting a dissolution effect. The survival of the MCs demonstrated the viability of the doping technique for fabricating fibers with exotic crystal‐glass combinations for applications including good refractive index matching across the pump and lasing bands of rare earth ions. This latter parameter provides significant particle size flexibility whilst minimizing additional loss from scattering especially at MIR wavelengths where the MC diameter‐to‐wavelength ratio becomes smaller. [ABSTRACT FROM AUTHOR]

Hexagonal Er3+/Yb3+ co‐doped LaZrTa3O11 (LZTO) phosphor was prepared by molten salt synthesis with B2O3 flux. Holding temperature, holding time, solute and solvent ratio were regulated. The green upconversion luminescence (UCL) integral intensity of the optimal sample can reach 29.2% of β‐NaYF4:Er3+/Yb3+ under 980 nm laser excitation. This outstanding pure green UCL is due to the low phonon energy, Er3+/Yb3+ monolayer (2D) distribution, asymmetry of Er3+/Yb3+ doped lattice sites, and low oxygen vacancy. The maximum relative temperature sensitivity attains 0.01221 K−1 at 303 K by employing luminescence intensity ratio (LIR) technique. LZTO:Er3+/Yb3+ phosphor can be used in temperature sensing. [ABSTRACT FROM AUTHOR]

Despite the remarkable luminescent properties and temperature sensing capabilities of lanthanide materials, their photothermal effect in practical temperature measurement systems presents a major challenge to sensing reliability. Herein, taking Pr3+ as a typical exemplar, the influence of excitation wavelength and excitation approach on temperature sensing is systematically examined. The pulsed laser excitation method is identified as an efficient tactic to restrain the self‐heating of luminescence materials. In accordance with this principle, it is discovered that diverse excitation wavelengths give rise to alterations in the internal energy transport channels and further impact the temperature sensing performance. The 980 nm pulsed laser can result in the non‐thermal coupling occupying states of 3P0/3P1, which are recognized as thermal coupling energy levels in the conventional concept, and yield a relative sensitivity (Sr) performance more than three times superior to that of down‐shifting‐based sensing. The work provides a comprehensive analytical solution for achieving highly sensitive and stable temperature sensing based on excitation wavelength and working mode strategies. [ABSTRACT FROM AUTHOR]

Upconversion (UC) process involves diverse energy levels and photoluminescence modes, however, it faces the challenge of concentration quenching of the doped lanthanide ions with multiple luminescence centers. Herein, Yb3+/Ho3+ and Yb3+/Tm3+ are heavily codoped into the lead‐free halide double perovskite single crystal Cs2NaErCl6, enabling the controlled energy transfer UC process, and accordingly, the UC materials exhibit anti‐concentration‐quenching owing to the defect tolerance characters. Depending on different doping couples, the UC materials show green and red emissions under the 980 nm laser excitations. Moreover, the green‐to‐red emission ratio in Yb3+/Tm3+ codoped Cs2NaErCl6 changes dynamically with the increasing pumping intensity due to the different sensitivities of the excited energy levels. This study provides a renewed direction of the lanthanide ions heavily‐doped halide double perovskites toward UC materials and facilitates the development of new smart luminescence materials for optical information storage applications. [ABSTRACT FROM AUTHOR]

Lanthanide‐doped nanoparticles (NPs) exhibit temperature‐dependent luminescence, enabling the design of luminescent nanothermometers for industrial and medical applications. This research demonstrates the temperature‐sensing properties of NaYF4:7.5%Er3+@NaYF4 and NaErF4@NaYF4 NPs, which have a hexagonal shape and average size of 17 nm. Their core@shell structure is confirmed using high‐resolution transmission electron microscopy, and they exhibit intense upconversion (UC) emission under 1532 nm excitation in H2O and D2O colloids. The recorded spectra show Er3+ emission bands with varying intensity ratios depending on the Er3+ concentration, chosen solvent, and temperature. The spectroscopic properties of the studied NPs allow for their excitation and observation of emission within biological windows, which makes them useful for bio‐related applications. The emission of prepared NPs is analyzed as a function of temperature from 298 up to 358/363 K in H2O and D2O. The ratios for thermally‐coupled levels  and non‐TCLs and their relative sensitivities are studied. For the high dopant concentration sample in water, the O─H vibrations and blue shift in the absorption spectrum lead to a record relative sensitivity of 2.50% K−1 (at 363 K) for the 2H11/2/4I11/2 ratio. The use of synthesized NPs for bioimaging under 1550 nm excitation is also demonstrated to observe their accumulation in the guts of Daphnia magna. [ABSTRACT FROM AUTHOR]

Visible‐to‐ultraviolet (UV) upconversion provides a fascinating strategy to achieve deep UV emission through readily accessible visible light. However, the intensity of deep UV emission obtained through visible‐to‐UV upconversion progress is still far from satisfactory, severely constraining its practical applications. Herein, a novel class of praseodymium ion (Pr3+)‐doped rare‐earth oxyhalides (YOCl, YOBr, and LuOBr) to achieve efficient upconverted deep UV emission in the spectral range of 250–350 nm is developed. The upconverted UV emission intensity of LuOBr:Pr3+ is determined to be 56.7 times stronger than that of the well‐established Lu7O6F9:Pr3+. When employed as a photon‐converter to activate photocatalytic water splitting reactions, upconverted deep UV emission enables H2 generation under visible light (λ > 420 nm) excitation from a xenon lamp. The efficient deep UV upconversion stems from tuning 4f15d1 state of Pr3+ by oxyhalide constituent which both facilitates the absorption of excitation photons in long‐lived intermediate 4f2 states and suppress the probability of nonradiative relaxation from 4f15d1 state. These findings not only provide new insights into a mechanistic understanding of the host effect on upconversion process but also make a breakthrough in developing efficient deep upconversion materials that will expand their further applications. [ABSTRACT FROM AUTHOR]

Lanthanide‐doped upconversion nanoparticles (UCNPs) have attractive emission properties but suffer from weak light‐absorbing capacities and thereby relatively low brightnesses. This motivates using strongly absorbing dye molecules as antennas and sensitizers. However, despite much effort, understanding of this dye‐UCNP interplay is still limited. Major sensitization mechanisms are still under discussion, largely because there is a lack of effective means to observe key factors such as dark state transitions within the dyes. Here, a combined spectroscopic procedure is established to systematically investigate the photophysics behind the dye‐UCNP interaction, embracing fluorescence‐based transient‐state excitation‐modulation, lifetime and correlation spectroscopy, and spectrofluorometry/spectrophotometry. With this procedure the heptamethine cyanine dye IR806, a typical UCNP sensitizer is studied, its photophysical model is established, its photophysics in UCL‐sensitization‐related environments is deciphered, and the energy transfer from the IR806 singlet excited state to Yb3+ (UCNP sensitizer ion) can be identified as the dominant sensitization mechanism. These studies suggest that IR806 can form non‐emissive H‐aggregates at the nanoparticle surfaces, which can be dissociated after certain light excitation duration (typically>100 µs). Moreover, buildup of a non‐fluorescent, photo‐redox state of IR806 after longer irradiation times (10–100 ms) can deleteriously affect its UCL sensitization effect, inferring an optimal excitation duration for dye‐sensitized UCNPs, relevant for, e.g., optical imaging applications. [ABSTRACT FROM AUTHOR]

Triplet‐triplet annihilation upconversion (TTA‐UC) is a photophysical process in which two low‐energy photons are converted into one higher‐energy photon. This type of upconversion requires two species: a sensitizer that absorbs low‐energy light and transfers its energy to an annihilator, which emits higher‐energy light after TTA. In spite of the multitude of applications of TTA‐UC, few families of annihilators have been explored. In this work, we show dipyrrolonaphthyridinediones (DPNDs) can act as annihilators in TTA‐UC. We found that structural changes to DPND dramatically increase its upconversion quantum yield (UCQY). Our optimized DPND annihilator demonstrates a high maximum internal UCQY of 9.4 %, outperforming the UCQY of commonly used near‐infrared‐to‐visible annihilator rubrene by almost double. [ABSTRACT FROM AUTHOR]

The exploration of photon avalanching (PA) luminescence in different lanthanide emitters has profound implications in plentiful frontier applications. However, studies for universal mechanisms at the nanoscale to exhibit giant nonlinear responses in various avalanching emitters are limited. Here, record‐breaking nonlinear responses up to 60th‐order in high‐lying emitting levels of various emitters at room temperature are generated by proposing a universal mechanism named energy relay‐mediated photon avalanche (enrePA). By harnessing energy from the avalanching nano‐engine through the energy relay of Yb3+ ions, the brightness of blue emissions from Tm3+ and Ho3+ can be enhanced with giant optical nonlinearity up to 60th and 38th order, respectively. Further incorporating gadolinium‐based systems, more emitters (Tb3+, Eu3+, Dy3+, Nd3+) can be activated with extreme optical nonlinearities up to 48th‐order. By expanding PA into the full‐spectrum range, the enrePA mechanism opens exciting avenues for flexible and high‐efficiency PA modulation in multilayer nanostructures, enabling the applicability of PA in more technologies such as super‐resolution imaging, lithography, and optical detection. [ABSTRACT FROM AUTHOR]

Based on the previous optimal concentration of Er3+/Yb3+/Mo4+ co‐doped BiTa7O19 (BTO) samples, Sc3+ or Sb is planned to be doped into BTO:Er3+/Yb3+/Mo4+ for further improving the upconversion luminescence (UCL) intensity under 980‐nm laser excitation. A series of BTO:Er3+/Yb3+/Mo4+/Sc3+ and BTO:Er3+/Yb3+/Mo4+/Sb samples are prepared by high‐temperature solid‐phase sintering method. The microstructure and UCL properties are investigated by X‐ray diffraction, Raman, X‐ray photoelectron spectroscopy (XPS), diffuse reflection, and luminescence spectrum. The green UCL intensity of BTO:Er3+/Yb3+/Mo4+/Sb is little better than that of BTO:Er3+/Yb3+/Mo4+/Sc3+, which reaches 2.40 times than that of β‐NaYF4:Er3+/Yb3+. XPS results show that Sc is 3+, Mo is 4+, and Sb is 3+ and 5+. Raman spectra show that BTO:Er3+/Yb3+/Mo4+/Sb has lower phonon energy and more disorder than BTO:Er3+/Yb3+/Mo4+/Sc3+. The maximum relative temperature sensitivity is got as 0.01012 K−1 at 303 K based on luminescence intensity ratio technology. BTO:Er3+/Yb3+/Mo4+/Sb has outstanding pure green UCL intensity, which can be applied to luminescence display and temperature sensing. [ABSTRACT FROM AUTHOR]

The demand for highly sensitive methods of pathogen detection drives the development of new diagnostic assays. While nucleic acid amplification methods such as PCR are very sensitive and remain widely used, they may be limited in complex sample matrices due to the presence of polymerase inhibitors. On the other hand, the direct detection of nucleic acids by DNA hybridization assays is simple but typically less sensitive. This work combines a branched DNA (bDNA) hybridization assay with upconversion nanoparticle (UCNP) labels to enhance the sensitivity of DNA detection. The anti‐Stokes emission of UCNP labels enables measurements without optical background interference. The bDNA assay relies on a series of oligonucleotide probes creating a branched structure with several binding sites for biotinylated amplification probes and streptavidin‐conjugated UCNPs. Several configurations of the bDNA assay are investigated to achieve the highest signal amplification and the lowest background signal. The optimal configuration of bDNA assay yields a limit of detection (LOD) of 5.9 × 104 cfu mL−1 for the target DNA of the bacteriophage M13. The upconversion‐linked bDNA assay is easily adaptable to other target DNAs by adjusting the oligonucleotide probes. [ABSTRACT FROM AUTHOR]

Despite recent advancements in inorganic and organic phosphors, creating monodisperse afterglow nanocomposites (NCs) remains challenging due to the complexities of wet chemistry synthesis. Inspired by nanoinclusions in opal, we introduce a novel SiO2‐mediated carbon dot (CD) doping method for fabricating monodisperse, multifunctional afterglow NCs. This method involves growing a SiO2 shell matrix on monodisperse nanoparticles (NPs) and doping CDs into the SiO2 shell under hydrothermal conditions. Our approach preserves the monodispersity of the parent NP@SiO2 NCs while activating a green afterglow in the doped CDs with an impressive lifetime of 1.26 s. Additionally, this method is highly versatile, allowing for various core and dopant combinations to finely tune the afterglow through core‐to‐CD or CD‐to‐dye energy transfer. Our findings significantly enhance the potential of SiO2 coatings, transforming them from merely enhancing the biocompatibility of NCs to serving as a versatile matrix for emitters, facilitating afterglow generation and paving the way for new applications. [ABSTRACT FROM AUTHOR]

Alkali‐metal‐based yttrium fluoride host (AY1‒xF4:xEu3+; A: Li/Na/K) nanophosphors were developed using co‐precipitation method. Phase analysis and emission spectral behavior were established for the said nanophosphors. The highest emission observed for NaYF4 doped with Eu3+ was then optimized to achieve maximum photoluminescence (PL) emission for varied dopant amount. The downconversion and upconversion PL studies revealed pure red emission under n‐ultraviolet and infrared excitations. The CIE coordinates are observed to be lie in the red hue of the CIE diagram. The PL decay curves reported to study lifetime of the emitting state and to identify quantum efficiency using Auzel's model for the said nanophosphor. Thermal stability was also evaluated from temperature‐sensitive luminescent spectra. The studies conducted on AYF4:.05Eu3+ (A: Li/Na/K) nanophosphors contemplates that NaYF4 nanophosphors doped with Eu3+ ions are best suited for biophotonic applications as the later one show relatively high emission. [ABSTRACT FROM AUTHOR]

The spatially resolvable multicolored microrods have potential applications in many fields. However, achieving spatially resolved multicolor luminescence tuning on the microrod with a fixed composition remains a daunting challenge. Herein, a strategy is proposed that allows for the tuning of spatially resolved, multicolored upconversion (UC) luminescence (UCL) along a 1D heterogeneous microrod by modifying the pulse width of an external laser. NaYbF4:1 % Ho is identified as an UCL color‐adjustable material, exhibiting pulse width‐dependent multicolored UCL, resulting in a significant regulation of the red/green (R/G) ratio from 0.1 to 10.3 as the pulse width is varied from 0.1 to 10 ms. Such variability can be ascribed to differences in the number of photons incident upon the microrod throughout the period necessary for the UC process to occur. Additionally, NaYbF4:1 %Tm and NaYF4:20 %Yb,1 %Ho are employed as materials that emit blue and green light, respectively, with their UCL colors largely unaffected by changes in the pulse width. Subsequently, a tip‐modified epitaxial growth method is utilized to integrate both UCL color‐adjustable and non‐adjustable segments within the same microrod. Comparing with single‐color or fixed multicolor microrods, our developed multisegmented emissive color adjustable 1D heterogeneous microrods have unique optical characteristics and can carry more optical information. [ABSTRACT FROM AUTHOR]

This work presents a novel paradigm for upconversion‐assisted ferroelectric photovoltaic devices. The system comprises a ferroelectric active layer (BiFeO3), an upconverter layer (Yb; Er‐doped ZnO), a conductive ITO‐coated glass substrate, and a reflective coating (Al) at the rear end of the glass substrate. The photovoltaic efficiency of the single‐layer BFO was found to be 0.71%. With the prescribed device model, the total solar efficiency of BiFeO3 improved significantly and touched solar conversion efficiency of 2.21%. This model's projection widens the future perspectives of device performance in emerging photovoltaic technology, mainly perovskite‐based solar cells. [ABSTRACT FROM AUTHOR]

Recent reports of upconversion and white light emission from graphitic particles warrant an explanation of the physics behind the process. A model is offered, wherein the upconversion is facilitated by photoinduced electronic structure modification allowing for multiphoton processes. As per the prediction of the model, it is experimentally shown that graphite upconverts infrared light centered around 1.31 μm (0.95 eV) to broadband white light centered around 0.85 μm (1.46 eV). The results suggest that upconversion from shortwave infrared (≈3 μm, 0.45 eV) to visible region may be possible. The experiments show that the population dynamics of the electronic states involved in this upconversion process occur in the timescale of milliseconds. [ABSTRACT FROM AUTHOR]

Circularly polarized luminescence (CPL)‐active materials are increasingly recognized for their potential applications such as 3D imaging, data storage, and optoelectronic devices. Typically, CPL materials have required high‐energy (HE) photons for excitation to emit low‐energy (LE) circularly polarized light, a process known as downshifting CPL (DSCPL). However, the emergence of upconverted CPL (UCCPL), where the absorption of multi LE photons results in the emission of a single HE photon with circular polarization, has recently attracted considerable attention. This minireview highlights the intricate relationship between upconversion and CPL phenomena. During upconversion, the dissymmetry factor (glum) value can be improved in certain systems. Additionally, the integration of both LE and HE photons in upconversion‐downshifting‐synergistic systems offers avenues for dual‐excitation or dual‐emission CPL functionalities. More in detail, the emerging UCCPL based on various photon upconversion mechanisms and their synergy with DSCPL are introduced. Additionally, several examples that demonstrate the applications of UCCPL are presented to highlight the future opportunities. [ABSTRACT FROM AUTHOR]

MicroRNAs (miRNAs) are promising biomarkers especially for early‐stage cancer diagnostics, but the implementation of miRNA‐based diagnostic tests is still hindered by the limitations of current analytical methods. The small size, low concentrations in biofluids and high sequence homology of miRNAs are challenges for assay development. Currently, most of the sensitive detection methods rely on enzymatic amplification steps, which complicate the analysis and can lead to biases in quantitation. Therefore, there is an increasing need to develop enzyme‐free detection methods that are sensitive, specific and user‐friendly. In this study, a simple direct hybridization assay for the DNA analogue of miR‐20a was developed. The assay is based on upconverting nanoparticle labels, which enable ultrasensitive detection, and hairpin structured probes, which provide additional hybridization stability due to base stacking. The limit of detection was 0.73 fM with plasma recoveries between 76 % and 111 %, demonstrating that the assay could be used for direct detection of miRNAs from complex sample matrices without isolation of RNA. Due to the simplicity and the excellent sensitivity for an amplification‐free method, the assay has a great potential for miRNA‐based clinical applications. [ABSTRACT FROM AUTHOR]

Pressure‐induced performance enhancement of a given material is an emerging phenomenon, however, among the various known examples very few enhanced properties can retain to ambient conditions. Both new structural mechanism and new material systems are the key challenge to achieve recoverable properties via pressure treatment. Herein, an "Er‐rich" erbium oxyfluoride ErOF is reported with retainable enhanced upconversion (UC) emission by high pressure treatment. The UC emission increases to more than twice the intensity of its pristine state, and followed by additional improvement to 5.1‐fold increase by heat treatment at 100 °C. The site symmetry breaking of Er3+ ions along with the crystal phase transition from R3¯$\bar{3}$m to Pnma, revealed by X‐ray diffraction, is believed to be the underlying reasons for the enhanced UC emission after release. Further, high‐resolution transmission electron microscopy (HRTEM) study reveals that the defects relieved with heat treatment might account for the UC emission enhancement in the released sample. Time‐resolved spectra and I‐P curves are measured comparatively to further illustrate the intrinsic mechanism of UC processes. The findings open up a window to advance UC performance through structure optimization by pressure engineering, thus facilitating its potential applications under ambient conditions. [ABSTRACT FROM AUTHOR]

Alkaline zirconium fluorides (AxZryFx+y, A = Li, Na, and K), featuring unique crystallographic structures, have recently emerged as a class of attractive hosts for fabricating lanthanide (Ln3+)‐doped upconversion nanocrystals (UCNCs) that exhibited distinct morphology, upconversion luminescence (UCL) performance, and physicochemical property. In this paper, for the first time the controlled preparation of Yb3+/Er3+‐doped UCNCs is reported based on the trigonal Cs2ZrF6 host, leading to tunable morphology and size of the resulting UCNCs by varying the reaction temperature and time. By further incorporating Na+ ions into the Cs2ZrF6 crystal lattice, sub‐10 nm Yb3+/Er3+/Na+ tridoped UCNCs with highly improved crystallinity and thus greatly enhanced UCL intensity are obtained. Moreover, these resulting UCNCs display abnormal thermal enhancement of UCL over a temperature range from 333 to 493 K, enabling the fabrication of supersensitive luminescent nanothermometers for temperature sensing. Based on the luminescence intensity ratio of two nonthermally coupled levels (i.e., 4F9/2 and 2H11/2) of Er3+, the as‐prepared Cs2ZrF6:Yb/Er/Na UCNCs exhibit an extremely large absolute sensitivity of 177.3% K−1 and a considerably high relative sensitivity of 1.52% K−1 at 333 K. These results unambiguously demonstrate that Cs2ZrF6 is a suitable host material for preparing small‐sized Ln3+‐doped UCNCs as nanothermometer for high‐performance ratiometric temperature sensing. [ABSTRACT FROM AUTHOR]

Highly transparent inorganic photochromic materials have several promising applications, especially for anti‐counterfeiting application. Enriching and enhancing the luminescent properties of perovskite by doping transition metals and rare earth elements into the host is a feasible and attractive route. Codoping of Mn2+ and Er3+ can realize novel anti‐counterfeiting properties with upconversion emission and photochromic ability within a double perovskite structure of Cs2AgInCl6.The Cs2AgInCl6: Mn2+, Er3+ single crystal can be observed in a reversible color variation from yellow to dark violet by implementing under 365, 520 nm illumination or thermal treatment. In addition, the crystal emits red and green light under the excitation of 365 nm ultraviolet and 980 nm laser, respectively. The introduction of Mn2+ endowed Cs2AgInCl6 with photochromic ability, and Mn2+ acted as a bridge for energy transfer from host excitons to Er3+, facilitating emission in the visible region. Er3+ achieve upconversion luminescence in the material through its abundant energy levels and acting synergistically with Mn2+. Herein, the Cs2AgInCl6:Mn2+, Er3+ combines various optical properties and has applications for specific anti‐counterfeiting demands. [ABSTRACT FROM AUTHOR]

Cyclometalated iridium (Ir) complexes demonstrate impressive capabilities across a range of fields, including biology and photocatalysis, due to their tunable optical characteristics and structure flexibility. However, generating upconversion luminescence of Ir complexes under near‐infrared light excitation is challenging. Herein, by employing lanthanide‐doped upconversion nanoparticles (UCNPs) as the sensitizer, a new strategy is demonstrated to gain upconversion luminescence of Ir complexes via triplet energy transfer. This design relies on a rationally designed hybrid of core‐shell structured NaYbF4:Tb@NaTbF4 UCNPs and new Ir phosphonate complexes, in which UCNPs can migrate upconverted energy to the surface of nanoparticles through Tb3+‐mediated energy migration and then sensitize the upconversion luminescence of Ir complexes upon 980 nm excitation. Both experimental and theoretical investigations highlight the significance of triplet energy transfer from excited Tb3+ ions to the triplet state of Ir complexes in the sensitization of upconversion luminescence of Ir complexes. These findings may open exciting avenues for fabricating hybrid Ir materials with new functions and driving the development of UCNP‐based nanomaterials. [ABSTRACT FROM AUTHOR]

Upconversion (UC) phosphors exhibiting luminescence color tuning (LCT) through variations in infrared excitation intensity offer great potential for high‐security anti‐counterfeiting applications. However, the current LCT capability is limited to high excitation intensities, hindering developments of non‐invasive counterfeit detection. In this study, two orders of magnitude reduction are achieved in excitation intensities for LCT in YF3:Yb/Er, accomplished by attaining an unprecedentedly efficient three‐photon excited red emission for mixing with the two‐photon excited green emission. To enable this breakthrough, deoxygenation techniques are employed during sample preparations, which surprisingly prevent concentration quenching of Yb3+ ions, facilitating efficient three‐photon excitation of the red emission for Yb3+ concentrations ≥ 30% even at excitation intensities as low as 10 mW cm−2. At excitation intensities of 100 mW cm−2, the three‐photon excitation contributes to 91–94% of the red emission, resulting in an 11–17‐fold increase in the red‐to‐green intensity ratio. This low‐excitation‐induced LCT, shifting from green to orange, showcases its potential for anti‐counterfeiting. Furthermore, present YF3:Yb/Er phosphors demonstrate an impressive UC quantum yield of 7.8%, surpassing the popular NaYF4:Yb/Er phosphor (5.6%) under the same excitation intensity of 31.8 W cm−2. These findings represent a significant advancement in highly efficient UC fluoride phosphors, promising diverse applications across various fields. [ABSTRACT FROM AUTHOR]

The development of blue/green/red tricolor upconversion (UC) phosphors under invisible light irradiation has attracted significant interest in emerging applications such as anti‐counterfeiting, three‐dimensional (3D) optical data storage, and solid‐state 3D displays. In this study, a series of LiYO2:RE3+,Yb3+ (RE = Tm, Ho, Eu) phosphors are successfully prepared via first precipitation process followed by calcination, and completely optimized for efficient tricolor UC luminescence with 980 nm laser excitation. Mechanisms involving two‐ or three‐photon absorption processes and low‐phonon‐energy‐suppressed multi‐phonon relaxation have been proposed for Ho3+(Eu3+)/Yb3+ and Tm3+/Yb3+ codoping, respectively. In addition, the RE3+ (Yb3+) concentration‐induced phase transition of the LiYO2 host is discussed for interesting possibilities in spectral regulation. Based on the broad color gamut achieved by the tricolor UC phosphor mixture, homochromatic and polychromatic metamerisms are experimentally fabricated via screen printing for high‐level anti‐counterfeiting and information security. Moreover, for a proof‐of‐concept demonstration, prototypes of 3D optical data storage and volumetric displays are constructed by embedding tricolor UC mixtures and their 3D printed patterns in polydimethylsiloxane. It is believed that the continuous exploration of tricolor UC under invisible light excitation for metamerism anti‐counterfeiting and 3D displays can promote the development of high‐level information security and advanced volumetric display technologies. [ABSTRACT FROM AUTHOR]

The luminescence properties of erbium and yttrium co‐doped cadmium difluoride with three different concentrations of yttrium were investigated. First, we synthesized single crystal samples with good optical quality using the Bridgman technique. From the optical absorption spectra, recorded at room temperature, both in the ultraviolet–visible and infrared spectral ranges, Judd–Ofelt analysis was performed based on yttrium concentrations to predict the radiative properties of Er3+ luminescent ions. For the 10% optimum concentration of yttrium, a detailed photoluminescence investigation was carried out. We mainly explored green, red, and near‐infrared fluorescence under different excitation wavelengths and presented their highlight spectroscopic characteristics. The desired transitions had relatively high emission cross‐sections both under visible and near‐infrared excitation. Optical gain followed a similar trend. Furthermore, the dynamic fluorescence study showed a significant increase in the measured lifetime under an 800 nm infrared excitation. The upconversion process under an 800 nm excitation produced quantum efficiency greater than 100% due to the contribution of more than one energy transfer mechanism. [ABSTRACT FROM AUTHOR]

Preclinical studies of nanoparticles for pulmonary therapeutics are often performed on 2D cell cultures or in vitro models that do not include a mucus barrier. However, the mucus layer lining the lungs is an essential barrier for drugs to permeate in order to exert a therapeutic effect. Herein, the role of surface coating of lanthanide‐doped upconverting nanoparticles (UCNPs) and their interaction with the mucus barrier are explored using a patient‐derived 3D cell culture model. The upconverted emissions from the UCNPs are used to track them throughout the 3D model and study their localization as a function of administration time and mucus thickness. Positively charged, ligand‐free, and negatively charged, supported lipid bilayer‐coated UCNPs are evaluated. A substantial difference in the residence time in mucus and mucociliary clearance of each type of UCNP is observed in a realistic and relevant model. As such, these results underscore the need for preclinical investigations in tissue models, especially with respect to the surface properties of the nanoparticles under study. [ABSTRACT FROM AUTHOR]

Optically upconverted materials that are capable of converting long‐wavelength low‐energy photons into short‐wavelength high‐energy light have found their applications over a broad spectrum of fields, like light‐emitting diodes (LEDs), displays, bio‐detection, etc. Despite the great advances in exploring the conventional near‐infrared‐to‐visible or even near‐infrared‐to‐ ultraviolet upconverted materials, the visible‐to‐ultraviolet‐C counterparts are far from being desired. Here, a new triple‐responsive material is introduced, i.e., Pr3+‐doped Li2SrGeO4. It has the ability to absorb the visible photons at ≈450 nm from LEDs, laser diodes (LDs), and even sunlight and emit the ultraviolet‐C (UVC) light covering the 240–280 nm wavelength range. Considering the unique characteristics of the UVC photon, the promising applications of the material are further demonstrated in several scenarios, including static/dynamic labeling under the excitation of a 450 nm LED, information encryption under excitation of sunlight, and sterilization under excitation of a 450 nm LD. The work enriches the library of optically upconverted visible‐to‐UVC materials and widens the application scenarios of these materials. [ABSTRACT FROM AUTHOR]

Recent advances reveal that due to the cross‐relaxation restriction, impressive upconversion (UC) enhancement (≈100‐folds) can be achieved in cryogenic Er3+‐rich core‐inert shell nanostructures (e.g., NaErF4@NaYF4), which opens up exciting opportunities in diverse frontier applications. However, further promotion of UC intensity is still highly desired, in which the rational design of nanostructures can play a key role. Herein, it is demonstrated that adopting an active shell design will constantly benefit the UC within a wide temperature range (40–300 K). Specifically, through constructing the luminescent core@active shell@inert shell sandwich nanostructure (e.g., NaErF4@NaYbF4@NaYF4), 8.3–73‐folds UC enhancement will be achieved (taking the corresponding core@inert shell structures as competitors). Moreover, from spectral‐domain and time‐domain spectroscopic experiments, the relevant UC enhancement is convincingly attributed to a temperature‐dependent energy injection process (from the active shell to the luminescent core). More interestingly, the unique property of the material makes a temperature‐induced high‐level encryption application possible, which is obtained by employing the nanomaterials on a quick response (QR) code. These results not only deepen the UC mechanism in multi‐layer nanostructures, but also introduce an expanded dimension (via low temperatures) in information security. [ABSTRACT FROM AUTHOR]

With the development of ultra‐fast optical technology, the nonlinear interaction between light and matter has attracted great attention. Upconversion laser generation through multiphoton absorption (MPA) enables numerous critical applications such as quantum signal processing, biophotonics, and 3D microfabrication. Herein, an ultra‐low threshold single‐mode four‐photon absorption (4PA) upconversion lasing at room‐temperature (RT) by constructing a strong‐coupling microcavity is demonstrated. The planar microcavity significantly enhances the 4PA nonlinear interaction, which facilitates the obtainment of low‐threshold upconversion lasing with an excellent output divergence angle and beam quality. In addition, the temporal dynamic mechanism and polarization characteristics of single‐mode upconversion lasing are also comprehensively discussed. The work provides a feasible approach to fabricate a low‐threshold single‐mode upconversion laser through high‐order nonlinear MPA processes. [ABSTRACT FROM AUTHOR]

Tin oxide (SnO2) nanocrystalline powders doped with erbium ion (Er3+) in different molar ratios (0, 3, 5, and 7 mol%) were prepared using a solid‐state reaction technique. These samples were characterized by X‐ray diffraction (XRD), scanning electron microscopy (SEM), ultraviolet‐visible absorption, visible upconversion, and near‐infrared luminescence techniques. XRD analysis revealed the tetragonal rutile structure of SnO2 and the average crystallite size was about 32 nm. From Tauc's plots, it was confirmed that the substitution of Er3+ ions into the SnO2 host lattice resulted in the narrowing its band gap. Optical absorption bands at 520 and 654 nm correspond to the 4f electron transitions of Er3+ further confirming visible light absorption. Infrared luminescence spectra showed a broad band centred at 1536 nm which is assigned to the 4I13/2 → 4I15/2 transition of Er3+. Visible upconverted emission spectra under 980 nm excitation exhibit a strong red luminescence with a main peak at 672 nm which is attributed to the 4F9/2 → 4I15/2 transition of Er3+. Power‐dependent upconversion spectra confirmed that two photons participated in the upconversion mechanism. Enhancement in the intensities of both visible and infrared luminescence was observed when raising the concentration. The results pave the way for the potential applications of these nanocrystalline powders in energy harvesting applications such as infrared light upconverting layer in solar cells, light emitting diodes, infrared broadband sources and amplifiers, and biological labelling. [ABSTRACT FROM AUTHOR]

Optical encryption shows great potential in meeting the growing demand for advanced anti‐counterfeiting in the information age. The development of upconversion luminescence (UCL) materials capable of emitting different colors of light in response to different external stimuli holds great promise in this field. However, the effective realization of multicolor UCL materials usually requires complex structural designs. In this work, orthogonal UCL is achieved in crystals with a simple structure simply by introducing modulator Tm3+ ions to control the photon transition processes between different energy levels of activator Er3+ ions. The obtained crystals emit red and green UCL when excited by 980 nm and 808 nm lasers, respectively. The orthogonal excitation‐emission properties of crystals are shown to be very suitable for high‐level optical encryption, which is important for information security and anti‐counterfeiting. This work provides an effective strategy for obtaining orthogonal UCL in simple structural materials, which will encourage researchers to further explore novel orthogonal UCL materials and their applications, and has important implications for the development of the frontier photonic upconversion fields. [ABSTRACT FROM AUTHOR]

Ho‐based lead‐free double perovskite microcrystals (MCs), Cs2NaHo1‐xYbxCl6, are synthesized and demonstrated to be promising optical temperature sensing materials by understanding the concentration‐dependent upconversion (UC) luminescence mechanisms. By optimizing the dopant concentration, a dominant emission shifting from red to green is successfully achieved in an activator‐rich system. During this process, the red to green emission intensity ratio (R/G) can be changed from 12.5 (pure red light) to 0.14 (pure green light). It is clarified that the cross‐relaxation (CR) process between activator and the energy transfer process between Yb3+ and Ho3+ are the key mechanisms of UC luminescence intensity and R/G ratio variation. Moreover, the intensity of red and green UC emission shows strong dependence on temperature, resulting from the competition between CR and energy transfer in the emission levels. The high‐sensitivity Ho‐based thermometer can be obtained by Cs2NaHo0.99Yb0.01Cl6 MCs with bright red UC luminescence, whose fluorescence intensity ratio thermometer gains maximum relative sensitivities reaching 0.68% K−1 at 400 K. The multicolor UC luminescence quantitative modeling mentioned here is crucial for understanding the concentration‐dependence UC luminescence characteristics and to optimize the design of the Ho‐based thermometer. This study can be an extension of the application range for perovskite UC materials. [ABSTRACT FROM AUTHOR]

In recent years, the remarkable optoelectronic characteristics exhibited by perovskite quantum dots (PQDs) have captured significant attention, which has spurred numerous investigations and novel applications. Nonetheless, the development of solution‐processed upconversion devices (UCDs) has predominantly centered around the utilization of organic materials, 3D perovskite films, and II‐VI quantum dots. In this work, PQDs are utilized for the first time as emission materials to enhance UCD performance. The stability of PQDs, synergistic coverage effect between PQDs and hole‐transporting layers (HTLs), and the interfaces of CGL/HTL are investigated in an attempt to identify the primary factor affecting UCD performance. The optimized UCD incorporating with effective TAPC HTLs demonstrate a maximum luminance of 463.9 cd m−2 at 520 nm (biased at 12 V and irradiated under 785 nm NIR light) accompanied by significant current gains of 167 times (at 3.4 V) and a noteworthy photon‐to‐photon conversion efficiency of 5.68% (at 12 V). The impressive performance is accompanied by a remarkably low turn‐on voltage of 1.4 V and a high leakage voltage of up to 12 V, making the highest record reported for solution‐processed UCDs. [ABSTRACT FROM AUTHOR]

Double perovskite (DP) phosphors attract extensive attention due to their potential applications in the field of optoelectronics. Photochromism‐induced luminescence modulation can extend their application fields. However, designing and preparing DP phosphors with expected photochromic and luminescent properties is still challenging. Herein, the photochromic Ba2YTaO6: Yb3+, Er3+, Co2+ DP with upconversion luminescence properties is developed. The color of the sample turns from white to pink upon 254 nm UV light irradiation, which is fast fading upon 473 nm laser illumination. The mechanism of photochromism is related to the formation of color centers, and the doping of Co2+ ions is crucial for the improvement of photochromism, which is from the increasing of traps depth, the oxygen vacancies, and the carrier concentration of the matrix caused by Co2+ doping. The upconversion luminescence of Er3+ ions can be reversibly modulated by the photochromic effect, exhibiting excellent reproducibility and high stability. The potential application of photochromic Ba2YTaO6: Yb3+, Er3+, Co2+ phosphor is demonstrated in the field of anticounterfeiting and three‐dimensional (3D) artwork. This work not only offers insight into the photochromic mechanism of DP but also presents guidance for developing other photochromic DP phosphors. [ABSTRACT FROM AUTHOR]

Wavelength conversion based on hybrid inorganic–organic sensitized triplet–triplet annihilation upconversion (TTA‐UC) is promising for applications such as photovoltaics, light‐emitting‐diodes, photocatalysis, additive manufacturing, and bioimaging. The efficiency of TTA‐UC depends on the population of triplet excitons involved in triplet energy transfer (TET), the driving force in TET, and the coupling strength between the donor and acceptor. Consequently, achieving highly efficient TTA‐UC necessitates the precise control of the electronic states of inorganic donors. However, conventional covalently bonded nanocrystals (NCs) face significant challenges in this regard. Herein, a novel strategy to exert control over electronic states is proposed, thereby enhancing TET and TTA‐UC by incorporating ionic‐bonded CsPbBr3 and lanthanide Ce3+ ions into composite NCs. These composite‐NCs exhibit high photoluminescence quantum yield, extended single‐exciton lifetime, quantum confinement, and uplifted energy levels. This engineering strategy of electronic states engendered a comprehensive impact, augmenting the population of triplet excitons participating in the TET process, enhancing coupling strength and the driving force, ultimately leading to an unconventional, dopant concentration‐dependent nonlinear enhancement of UC efficiency. This work not only advances fundamental understanding of hybrid TTA‐UC but also opens a door for the creation of other ionic‐bonded composite NCs with tunable functionalities, promising innovations for next‐generation optoelectronic applications. [ABSTRACT FROM AUTHOR]

Photocatalysts capable of harvesting a broad range of the solar spectrum are essential for sustainable chemical transformations and environmental remediation. Herein, we have integrated NIR‐absorbing upconversion nanoparticles (UCNP) with UV‐Vis absorbing conjugated porous organic polymer (POP) through the in situ multicomponent C−C coupling to fabricate a UC−POP nanocomposite. The light‐harvesting ability of UC−POP is further augmented by loading plasmonic gold nanoparticles (AuNP) into UC−POP. A three‐times enhancement in the upconversion luminescence is observed upon the incorporation of AuNP in UC−POP, subsequently boosting the photocatalytic activity of UC−POP−Au. The spectroscopic and photoelectrochemical investigations infer the enhanced photocatalytic oxidation of thioethers, including mustard gas simulant by UC−POP−Au compared to POP and UC−POP due to the facile electron‐hole pair generation, suppressed exciton recombination, and efficient charge carrier migration. Thus, the unique design strategy of combining plasmonic and upconversion nanoparticles with a conjugated porous organic polymer opens up new vistas towards artificial light harvesting. [ABSTRACT FROM AUTHOR]

Local optical field modulation using plasmonic materials or photonic crystals provides a powerful strategy for enhancing upconversion emission of lanthanide-doped upconversion nanocrystals (UCNPs). However, it is restricted to static UC enhancement and the corresponding dynamic modulation of UC is yet to be reported, limiting its practical applications in information devices. Here, a dynamic UC modulation system is reported through electric stimulation by integrating UCNPs with electrically sensitive WO3_x plasmonic photonic crystals (PPCs). The tunable emission enhancement of UCNPs varying from five to 26 folds is achieved in WO3_x PPCs/UCNPs hybrids through external electric stimulation within +1.6 and _1.6 V. It stems from the reversible control of the photonic bandgaps and localized surface plasmon resonance of WO3_x PPCs, ascribed to the variation of refractive index and oxygen vacancy of WO3_x, induced by the reversible change of atomic ratio of W5+ to W6+ under different applied voltages. Moreover, the electrically triggered information encryption devices are developed, employing a programmable logic gate array based on WO3_x PPCs/UCNPs with the ability to convert information-encrypted electrical signals into visible patterns. These observations offer a new attempt to manipulate the UC and will simulate the new applications in the display and optical storage devices. [ABSTRACT FROM AUTHOR]

Image contrast is often limited by background autofluorescence in steady‐state bioimaging microscopy. Upconversion bioimaging can overcome this by shifting the emission lifetime and wavelength beyond the autofluorescence window. Here we demonstrate the first example of triplet‐triplet annihilation upconversion (TTA‐UC) based lifetime imaging microscopy. A new class of ultra‐small nanoparticle (NP) probes based on TTA‐UC chromophores encapsulated in an organic–inorganic host has been synthesised. The NPs exhibit bright UC emission (400–500 nm) in aerated aqueous media with a UC lifetime of ≈1 μs, excellent colloidal stability and little cytotoxicity. Proof‐of‐concept demonstration of TTA‐UC lifetime imaging using these NPs shows that the long‐lived anti‐Stokes emission is easily discriminable from typical autofluorescence. Moreover, fluctuations in the UC lifetime can be used to map local oxygen diffusion across the subcellular structure. Our TTA‐UC NPs are highly promising stains for lifetime imaging microscopy, affording excellent image contrast and potential for oxygen mapping that is ripe for further exploitation. [ABSTRACT FROM AUTHOR]

The narrow range of solar light absorption facilitated by the photoactive organic dyes has been restricting the significant development, and large‐scale applications of dye‐sensitized solar cells (DSSC). The major problem that limits the power conversion efficiency (PCE) of DSSC is the limitations of the organic dyes (light absorbers in DSSC) to absorb beyond the visible region of solar spectrum that resulting in lower PCE (≈13%) as compared with the commercialized technologies. Hence, the focus on developing efficient strategies to harvest the ultraviolet and infrared light regions of the solar spectrum and effective conversion into the absorption limit of dyes and thereby increasing the device performance and stability is the emerging technological development in DSSCs. Rare earth ion‐doped upconversion (UC) and downconversion (DC) phosphors are the most promising solutions for the prevalent issues of the liquid junction solar cells. This review will focus on the emerging strategies for the PCE enhancement of DSSC with UC and DC materials. An exclusive review on the facile approach of simultaneous usage of both the UC and DC phosphors and the effective positioning of these spectral conversion phosphors, to achieve highly stable DSSCs with superior PCE is provided. [ABSTRACT FROM AUTHOR]

Although the chemistry of macrocyclic arenes has seen rapid development in recent years, the synthesis of new macrocyclic arenes from aromatic rings with no directing groups remains a challenge. In this work, a new macrocyclic arene, naphth[4]arene (NA[4]A), composed of four naphthalene rings bridged by methylene groups, was synthesized using macrocycle‐to‐macrocycle conversion. NA[4]A shows 1,3‐alternate and 1,2‐alternate conformations in the solid state, which can be selectively obtained. By supramolecular co‐assembly of NA[4]A and 1,2,4,5‐tetracyanobenzene (TCNB) in different concentrations and temperatures, two conformation‐dependent crystalline luminescent co‐assemblies 1,2‐NTC and 1,3‐NTC can be selectively prepared. Interestingly, the two charge‐transfer crystalline assemblies containing NA[4]A with different conformations show bright yellow and green fluorescence, and also display high photoluminescence quantum yields (PLQYs) of 45 % and 43 %. Furthermore, they exhibit color‐tunable two‐photon excited upconversion emission. [ABSTRACT FROM AUTHOR]

The clinical administration of biophotonic approaches, such as photodynamic therapy (PDT), is impeded by the low penetration of visible light in biological tissues. The cooperation of infrared (IR) light with deeper penetration and implantable IR‐to‐visible upconversion materials and devices establishes an effective strategy to generate visible light in deep tissue. In this work, a wirelessly powered upconversion waveguide‐based light source is reported for PDT‐based in vivo cancer treatments in deep tissue. Combining microscale IR‐to‐visible upconversion device arrays and a biocompatible waveguide, the implant exhibits enhanced IR transmission in biological environments and generates upconverted red emission in the target region at a depth >10 mm. The red illumination activates a photosensitizer in 5‐aminolevulinic acid (5‐ALA)‐based PDT treatment, inducing massive apoptosis (>60% cell death) of tumor cells. After implanted in tumor‐bearing mice, the waveguides enable chronic operation for more than two weeks and reveal ideal anti‐tumor efficacies in the PDT process. Finally, the biocompatible waveguide can be retrieved from the tissue, leaving minimal traces after treatments. Such a waveguide implant represents a prospective technique to realize optical‐based biological modulations and medical treatments within the body. [ABSTRACT FROM AUTHOR]

Materials based on organic chromophores and lanthanides able to transform low‐energy photons, specifically near‐infrared (NIR) photons, into higher energy photons to eventually lead to long‐lived sensitized emission of the dye are highly desirable. Cooperative sensitization (CS) upconversion has only been accomplished for lanthanide‐based clusters. We used here the eosin Y (EOS) dianion and Yb3+ (EOS‐Yb), and demonstrate the efficient CS emission of the dye after NIR excitation. Remarkably, the EOS dianion emission exhibits a nearly linear dependence on the EOS‐Yb concentration and a quadratic dependence on the laser power density. The emission is non‐sensitive to oxygen and its lifetime lasts about 1.76 μs and 12 μs in DMSO and DMSO‐d6, respectively. Moreover, the effect of temperature (293–363 K range) on the EOS‐Yb 1H NMR spectroscopic shifts demonstrates the reversible dynamic nature of the material. [ABSTRACT FROM AUTHOR]

In this study, we attempted to improve the quantum yield of upconversion nanoparticles to achieve high efficiency of amyloid fibril decomposition cascade induced by near‐infrared‐active upconversion nanoparticles complexed with photosensitizers. The effects of the solvothermal reaction time on the crystalline phase of polyethylenimine‐coated NaYF4 : Yb3+/Er3+ were studied, while maintaining constant reaction temperature and concentration of the dopants Yb3+ and Er3+. We found that an increased reaction time resulted in the conversion of the crystalline phase from the cubic α‐ to hexagonal β‐forms with a higher upconversion quantum yield. In addition, the prolonged reaction time effectively increased the ratio of green (2H11/2 and 4S3/2→4I15/2) to red (4F9/2→4I15/2) emissions, increasing the 1O2 generation via photosensitization to approximately 10 times that of conventional ones. Consequently, the efficiency of the amyloid fibril decomposition cascade induced by upconversion nanoparticles complexed with photosensitizers was improved. [ABSTRACT FROM AUTHOR]

β‐NaYF4 nanocrystals are a popular class of optical materials. They can be doped with optically active lanthanide ions and shaped into core‐multi‐shell geometries with controlled dopant distributions. Here, we follow the synthesis of β‐NaYF4 nanocrystals from α‐NaYF4 precursor particles using in situ small‐angle and wide‐angle X‐ray scattering and ex situ electron microscopy. We observe an evolution from a unimodal particle size distribution to bimodal, and eventually back to unimodal. The final size distribution is narrower in absolute numbers than the initial distribution. These peculiar growth dynamics happen in large part before the α‐to‐β phase transformation. We propose that the splitting of the size distribution is caused by variations in the reactivity of α‐NaYF4 precursor particles, potentially due to inter‐particle differences in stoichiometry. Rate equation modeling confirms that a continuous distribution of reactivities can result in the observed particle growth dynamics. [ABSTRACT FROM AUTHOR]