Near-infrared Research Articles

Cr3+-doped Na2CaSn2Ge3O12 garnet showing broadband near-infrared emission at 820 nm with zero thermal quenching and near-unity quantum yield

The continually advancing near-infrared (NIR) phosphor-converted light-emitting diode (pc-LED) hold pivotal significance in optical imaging and NIR spectroscopy. Cr3+-doped garnet broadband NIR phosphors have attracted considerable attention owing to their high optical performance enabled by the rigid structure. Nonetheless, the emission wavelength is severely restricted, and longer wavelength emissions usually result in inferior quantum efficiency and poor luminescence stability. In this work, the concurrent reconstruction of dodecahedral and octahedral sites by introducing [Na+-Sn4+]C unit in the framework of Na2CaSn2Ge3O12 garnet contributes to the Cr3+ broadband NIR emission spanning 700–1200 nm, with a peak at 820 nm. Utilizing a charge compensation strategy via Ta5+ codoping largely boosts the internal quantum efficiency (IQE) of Na2CaSn2Ge3O12:Cr3+ from 93.06 % up to 95.04 %. Trap-mediated energy compensation is proposed to achieve a record-breaking zero-thermal-quenching behavior (99.39 %@423 K) of Cr3+-doped garnet with such a longer wavelength emission. The encapsulated prototype broadband NIR pc–LED gives rise to an overwhelming NIR output power of 590.9 mW@1300 mA and a photoconversion efficiency (PCE) of 32.62 % at 30 mA, rendering exceptional performance in night vision, detection, and NIR imaging applications.

A “performance-inheritance” strategy for achieving hydrophilic/hydrophobic fluorescent biomass-derived carbon dots through simple solvothermal treatments

It remains a challenge to obtain hydrophilic/hydrophobic materials with promising biocompatibility and environmental compatibility by simple methods. Herein, we designed a “performance-inheritance” strategy and for the first time constructed hydrophilic/hydrophobic fluorescent spirulina-derived carbon dots (CDs) through simple solvothermal treatments. The contact angle of hydrophobic CDs with near-infrared (NIR) fluorescence is 110°, while hydrophilic CDs with blue fluorescence is 19°. We further revealed that the NIR luminescence is derived from the chlorophyll structure, while blue fluorescence is from the surface states. Based on the hydrophilicity/hydrophobicity of CDs, a ratiometric sensor was constructed to detect water content in organic solutions. In addition, CDs with NIR emission have low toxicity and good biocompatibility, making them efficient probes for bioimaging. This strategy provides a simple method for the high value-added conversion of algae and a new perspective for the “design-preparation-application” of biomass-derived CDs with specific properties.

Direct near-infrared laser ignition of CL-20 by introducing DATNBI as a bi-functional additive: Energetic photosensitizer and self-assembly stimulator

The ignition strategy of energetic materials using low-energy near-infrared (NIR) laser has garnered significant attention due to its enhanced safety and reliability. This study explores the use of a relatively photosensitive but mechanical insensitive energetic material, DATNBI, to facilitate the self-assembly of nano-CL-20 crystals into polycrystalline particles though solvothermal induction, yielding a rough structure conducive to NIR laser ignition. The findings demonstrate that by adjusting the content of DATNBI, it is possible to achieve micro-nano controllable spherical CL-20/DATNBI (C/D) particles, with CL-20 as the primary component and DATNBI as the auxiliary component. The incorporation of DATNBI and the rough surface structure enhance the light absorption of C/D particles in the NIR band. Additionally, the unique synergistic effect between CL-20 and DATNBI during thermal decomposition further promotes NIR laser ignition. As expected, the C/D particles achieved self-sustained combustion and exhibited excellent combustion performance under a 1064 nm laser, which is challenging to be achieved with raw CL-20 or raw DATNBI. Furthermore, the relatively insensitive DATNBI and spherical structure reduced the impact sensitivity of the C/D particles. This multifunctional material strategy, integrating energy, safety environment-friendliness, and laser ignition performance, offers a novel approach for laser ignition of energetic materials.

Magneto-optic properties of highly Dy3+-doped GeO2-B2O3 glasses for NIR optical applications

Recent progress in the development of optical communication and high power laser systems in the near-infrared (NIR) region (1.5 to 2.0 μm) increased the demand for magneto-optic (MO) devices employing MO materials. These MO materials are required with lower optical absorption coefficients and higher Verdet constants at spectral range of interest. In this study, two series of highly Dy3+-doped GeO2–B2O3 glasses with and without P2O5 were fabricated using a simple melt-quenching technique. The glasses were characterized through various techniques (Raman, UV–VIS-NIR, and DTA) for the evaluation of characteristic properties with respect to the Dy2O3 concentration and glass composition. Faraday rotation measurement was carried out at 1550 nm to quantify the Verdet constant of the glasses. The Verdet constant values were found to increase linearly with increasing Dy3+ concentration for both the glass systems. The increase in Dy3+ concentration and, consequently, the number of unpaired electrons, leads to an increase in the Verdet constant. The GeO2-B2O3 glass doped with 30 mol% of Dy2O3 exhibited the highest Verdet constant of −5.36 rad/(T⋅m) at 1550 nm. The glasses exhibited a good optical transparency (>70 %) in the region covering from 400 to 2400 nm. The thermo-physical, optical, and polarizability properties of both glass systems were also investigated. The results indicate that the highly Dy3+-doped glasses are attractive for magneto-optics at 1550 nm.

Integrating Multisource Data and Machine Learning for Supraglacial Lake Detection: Implications for Environmental Management and Sustainable Development Goals in High Mountainous Regions

The accurate detection and monitoring of supraglacial lakes in high mountainous regions are crucial for understanding their dynamic nature and implications for environmental management and sustainable development goals. In this study, we propose a novel approach that integrates multisource data and machine learning techniques for supra-glacial lake detection in the Passu Batura glacier of the Hunza Basin, Pakistan. We extract pertinent features or parameters by leveraging multisource datasets such as radar backscatter intensity VH and VV parameters from Sentinel-1 Ground Range Detected (GRD) data, near-infrared (NIR), NDWI_green, NDWI_blue parameters from Sentinel-2 Multi-spectral Instrument(MSI) data, and surface slope, aspect, and elevation parameters from topographic data. The entire dataset is partitioned into training and testing sets, with machine learning models including the artificial neural network (ANN), the support vector machine (SVM), logistic regression (LR), random forest (RF), and K-nearest neighbour (KNN) trained on the training data (70%). Accuracy assessment employs testing data and involves the evaluation of metrics such as ROC curves and confusion matrices. The best-performing model, ANN, is validated against manually digitized lake polygons derived from Sentinel-2 and Google Earth Pro imagery. Furthermore, the digitized lake polygons are used to analyze glacial lake dynamics from 2016 to 2022. Key findings of this research presented that the NDWI_green, Sigma0_VH, and elevation are the most significant predictors in detecting supra-glacial lakes. Among the various trained and evaluated models, the Artificial Neural Network (ANN) achieved the highest performance (accuracy: 95%, AUC: 0.99) and accurately mapped supra-glacial lakes regardless of their small size. The findings have significant implications for understanding glacial lake behavior in the context of climate change and informing future research and monitoring efforts.

A novel Cr3+-doped MgGaBO4 phosphor: expanding the horizons in plant illumination

Near-infrared (NIR) spectroscopy technology has demonstrated unparalleled efficacy in night vision, iris authentication, plant illumination, food inspection, and various other domains. Nonetheless, the quest for novel phosphors exhibiting superior luminescent efficiency and enduring thermal stability persists as a formidable obstacle. In this study, phosphors MgGaBO4: Cr3+, Al3+ were successfully synthesized by high-temperature solid-phase reaction method. Firstly, starting from MgGaBO4: Cr3+, the crystal field environment around Cr3+ ions was modulated by replacing Ga3+ with Al3+ to further improve the luminescence performance of the phosphor. The emission peak wavelength of MgGaBO4: 0.0075Cr3+,0.005Al3+ phosphor was about 756 nm, the full width at half-maximum (FWHM) was about 174 nm under the blue light excitation of 440 nm. In addition, the luminescence intensity at 100 °C remains at 77.41% of that at room temperature. Finally, the excellent moisture resistance of this phosphor was demonstrated. This work not only introduces a novel broadband NIR phosphor with promising application potential in advanced agricultural lighting but also proposes a synergistic enhancement strategy for effectively improving the performance of broadband NIR phosphor-converted LED light sources.

Biodegradable Citrate‐Based Polymers Enable 5D Monitoring of Implant Evolution

AbstractBiodegradable tissue engineering scaffolds have garnered increasing interest for their role in providing mechanical support, promoting tissue regeneration, and eliminating the need for removal. However, the in vivo degradation processes remain challenging to track. Here, a novel biodegradable polymer, N‐methyldiethanolamine (MDEA) and Gadolinium(III) diethylenetriamine pentaacetate (Gd‐DTPA) modified biodegradable photoluminescent polymers (BPLPMGd), which combines near‐infrared (NIR) fluorescence and magnetic resonance (MR) dual‐modality imaging are introduced to monitor scaffold degradation in vivo. The chemical structure of BPLPMGd is characterized and its dual‐imaging properties in vitro are evaluated. Subsequently, non‐invasive dual‐modality imaging to track the degradation of implanted BPLPMGd scaffolds is performed in a rat model, comparing these results with histological data. This approach reveals that BPLPMGd enables reliable non‐invasive tracking of the degradation, where NIR fluorescence imaging offers a qualitative and quantitative analysis of scaffold mass loss, total volume and solid content changes, while magnetic resonance imaging (MRI) details structural and morphological changes, allowing for 5D monitoring of implant degradation, including 3D structure, location, mass, volume, and geometry. The combination of these imaging modalities provides a comprehensive view of scaffold degradation, where the synergistic use of both yields results greater than either modality alone, offering unprecedented 5D information of implantable devices. This innovative approach has potential applications in regenerative engineering and beyond.

Quasi-single-crystal Tin Halide Perovskite Films with High Structural Integrity for Near-infrared Imaging Array enabling Hidden Object Recognition.

Near-infrared (NIR) image sensors based on solution-processed thin film are gaining prominence in various applications, including security detection, remote sensing, medical imaging, and environmental monitoring, owing to superior penetration capabilities of NIR light. However, the reported perovskite image sensors suffer from limited resolution and performance due to poor structural integrity, bioincompatibility, and constrained response wavelength range from lead-based perovskite materials employed. In this study, we present non-toxic quasi-single-crystal (QSC) CH(NH2)2SnI3 (FASnI3) perovskite films, prepared via a simple spin-coating technique, that demonstrate high structural integrity and effective NIR response. Through a series of in situ characterizations, we reveal that the orderly growth mode of QSC-FASnI3 perovskite films enables a more oriented crystal growth with reduced trap and grain boundaries. Consequently, self-powered NIR photodetector based on QSC-FASnI3 films exhibited large detectivity over 1013 Jones in the NIR range (780-890 nm). Ultimately, due to the high structural integrity, the high-resolution 64 × 64 (4096) pixels NIR imaging array, exhibiting reduced photo and dark response non-uniformity value, was fabricated on the thin-film transistors (TFT) backplanes, enabling ultraweak NIR light (63 nW cm-2) real-time imaging, fingerprint imaging, and hidden object recognition. This work pioneers the application of lead-free perovskite for high-resolution NIR imaging arrays.

Achieving Flat Ultra‐Broadband NIR Emission in Cr3+ Doped Garnet‐Type Phosphors Enabled by Structural Regulation Toward Multi‐Functional Spectroscopy Applications

AbstractCr3+‐activated near‐infrared (NIR) emitting phosphors are considered as one of the most potential light‐conversion materials for NIR phosphor converted light‐emitting diodes (NIR pc‐LEDs). However, it is still a challenge for a single Cr3+ ion to achieve a flat ultra‐broadband emission toward multi‐functional spectroscopy applications. Herein, a chemical unit co‐substituting strategy is utilized to regulate the crystallographic occupancy of Cr3+ ions, and a flat ultra‐broadband NIR emission is successfully realized with a record emission wavelength of 915 nm in garnet‐type phosphors Ca3Sc2‐xHfxAlxSi3‐xO12: yCr3+ (0 ≤ x ≤ 1, 0.02 ≤ y ≤ 0.06), together with a large full width at half maximum (FWHM) regulation from 130 to 250 nm. The relation between the site occupation of Cr3+ ions in disordered [CaO8], [(Sc, Hf)O6] and [(Si, Al)O4] polyhedrons and the corresponding NIR emission are clarified by carefully evaluating the structural evolution, Raman spectra, electron paramagnetic resonance and time‐resolved emission lifetime spectra of Cr3+ ions. The corresponding crystal field strength of Cr3+ ions is investigated to further clarify the multi‐sites induced flat broadband NIR emission. Finally, a blue light pumped NIR pc‐LED is fabricated with a total output power of 37.58 mW and photoelectric conversion efficiency (PCE) of 13.67%@100 mA, which realizes the multi‐functional applications in night vision imaging, non‐destructive detection and palmprint vein recognition for assistant medical treatment.

Detection of Illicit Conservation Treatments in Sea Bass (Dicentrarchus labrax): Application and Data Integration of NIR Spectrometers

Global fish and seafood consumption is increasing annually, frequently leading to the emergence of food fraud, mainly related to mislabeling and adulteration like, for example, the use of illicit/unauthorized food additives to mask or delay fish spoilage. Among the available diagnostic tools for control purposes, spectroscopic techniques have often been proposed to identify these kinds of illicit practices in fish and seafood products. The presented study aims to test two cheap and portable near infrared (NIR) spectrometers, a handheld MicroNIR and a pocket-sized SCiO, to uncover use of the illicit food additive Cafodos, a mixture of sodium citrate and hydrogen peroxide used to preserve some fish characteristics (like smell, color, na dtexture). The NIR spectroscopy in combination with chemometric approaches, allowed the successfully classification of (81–100%) samples of sea bass (Dicentrarchus labrax) treated with Cafodos. The study highlights the potential of this technique that, by not requiring pre-treatment of samples with further reagents, is cheaper and safer for the environment. In conclusion, the study confirmed the potential of portable devices for rapid NIR spectroscopy analysis to identify food fraud and ensure consumer safety.

Hot spots around Sagittarius A*. Joint fits to astrometry and polarimetry

Observations of Sagittarius A* ( in the near-infrared (NIR) show irregular flaring activity. Flares coincide with the astrometric rotation of the brightness centroid and with looping patterns in fractional linear polarization. These signatures can be explained with a model of a bright hot spot, transiently orbiting the black hole. We extend the capabilities of the existing algorithms to perform parameter estimation and model comparison in the Bayesian framework using NIR observations from the GRAVITY instrument, and simultaneously fitting the astrometric and polarimetric data. Using the numerical radiative transfer code we defined several geometric models describing a hot spot orbiting Sgr A*, threaded with a magnetic field, and emitting synchrotron radiation. We then explored the posterior space of our models with a nested sampling code We used Bayesian evidence to make comparisons between the models. We have used 11 models to sharpen our understanding of the importance of various aspects of the orbital model, such as non-Keplerian motion, hot-spot size, and off-equatorial orbit. All considered models converge to realizations that fit the data well, but the equatorial super-Keplerian model is favoured by the currently available NIR dataset. We have inferred an inclination of $ deg, which corroborates previous estimates, a preferred period of $ minutes, and an orbital radius of $ gravitational radii with the orbital velocity of $ times the Keplerian value. A hot spot with a diameter smaller than 5 gravitational radii is favoured. Black hole spin is not constrained well.

Rationally Designed G-Quadruplex Selective "Turn-On" NIR Fluorescent Probe with Large Stokes Shift for Nucleic Acid Research-Based Applications.

Guanine-rich DNA/RNA sequences can form Hoogsteen bonds to adopt noncanonical secondary structures called G-quadruplexes, and these have been associated with diverse cellular processes. There has been considerable research interest in the design of G4-interacting ligands for cellular probing of the G4 structure and understanding its associated biological function. Most of the fluorescent G4 ligands either do not have significant selectivity over other nucleic acid structures, have high Stokes shift, or are not in the near-infrared (NIR) region, which limits its cellular visualization. The current work involves the rational design and synthesis of NIR fluorescent probes comprising a (Z)-1-methyl-2-((3-methylbenzo[d]thiazol-2(3H)-ylidene)methyl)quinolin-1-ium scaffold. Among the designed molecules, 4a exhibited far-red fluorescence (λmax = 680 nm) with large Stokes shift (∼182 nm) upon selective binding to human telomeric G-quadruplexes. The dye 4a does not disturb the conformation and stability of G-quadruplexes, thereby making it suitable for nucleic acid research based applications. Interestingly, 4a showed remarkable selectivity over single- and double-stranded structures in contrast to a commercially available quadruplex binding probe, Thiazole orange (TO). The molecular docking studies indicate that 4a binds at the groove region of the telomeric DNA G-quadruplex through π-π stacking interactions with the quinoline and amine-substituted phenyl ring and with the phosphate backbone through anion-π interactions with the benzothiazole ring. The designed molecule 4a has interesting photophysical properties, cell permeability, and biocompatibility with minimal cytotoxicity. Fluorescence imaging studies in live HeLa cells showed that probe 4a binds to the transient population of the DNA G-quadruplex in the nucleus and RNA quadruplexes in the cytoplasm. In brief, G-quadruplex NIR fluorescent probe 4a with a higher signal/noise ratio has significant potential for cellular imaging studies and thus opens avenues to decipher the biological pathways for better understanding of G-quadruplex biology.

Developing Screen-Printing Processes for Silver Electrodes Towards All-Solution Coating Processes for Solar Cells

In recent years, third-generation solar cells have experienced a remarkable growth in efficiency, making them a highly promising alternative energy solution. Currently, high-efficiency solar cells often use top electrodes fabricated by thermal evaporation, which rely on high-cost and high energy-consumption vacuum equipment, raising significant concerns for mass production. This study develops a method for fabricating silver electrodes using the screen-printing process, aiming to achieve solar cell production through an all-solution coating process. By selecting appropriate blocking-layer materials and optimizing the process, we have achieved device efficiencies for organic photovoltaics (OPVs) with screen-printed silver electrodes comparable to those with silver electrodes fabricated by thermal evaporation. Furthermore, we developed a method to cure the silver ink using near-infrared (NIR) annealing, significantly reducing the curing time from 30 min with hot air annealing to just 5 s. Additionally, by employing sheet-to-sheet (S2S) slot-die coating, we scaled up the device area and completed module development, successfully verifying stability in ambient air. We have also extended the application of screen-printed silver electrodes to perovskite solar cells (PSCs).

Combining NIR spectroscopy with chemometrics for discriminating naturally ripened banana and calcium carbide ripened banana

Calcium carbide is prohibited as a fruit ripening agent in many countries due to its harmful effects. Current methods for detecting calcium carbide in fruit involve time-consuming and destructive chemical analysis techniques, necessitating the need for non-destructive and rapid detection techniques. This study combined near infrared (NIR) spectroscopy with chemometrics to detect two banana varieties ripened with calcium carbide in different forms when they are peeled or unpeeled. Sixteen linear discriminant analysis (LDA) models were developed with high average classification accuracies for classifying banana based on the mode used to ripen banana, type of carbide treatment and the duration of soaking banana in carbide solution. Banana colour was predicted with partial least squared regression (PLSR) models with R2CV > 0.74, RMSECV and <5.4 and RPD close to 3. NIR coupled with chemometrics has good potential as a technique for detecting carbide ripened banana even if the banana is peeled or not.

NIR-Guided Coating Optimization of Omega-3 Fatty Acid Mini Soft Capsules with Pitavastatin and Ezetimibe

Background: This study aimed to optimize the coating process of Omega-3 fatty acid (OM3-FA) mini soft capsules containing the active pharmaceutical ingredients (APIs) pitavastatin and ezetimibe using near-infrared (NIR) spectroscopy for in-process monitoring. Cardiovascular disease treatments benefit from combining OM3-FA with lipid-lowering agents, but formulating such combinations in mini soft capsules presents challenges in maintaining stability and mechanical integrity. Methods: The coating process was developed using a pan coater and real-time NIR monitoring to ensure uniformity and quality. NIR spectroscopy enabled precise control of coating thickness, ensuring consistent drug distribution across the capsule surface. Results: The optimized process minimized OM3-FA oxidation and preserved the mechanical integrity of the capsules, as confirmed by texture analysis and in-vitro dissolution testing. This integration of NIR spectroscopy as a process analytical technology (PAT) significantly improved coating quality control, resulting in a stable and effective combination therapy for pitavastatin and ezetimibe in a mini soft capsule form. Conclusion: This approach offers an efficient solution for enhancing patient adherence in cardiovascular disease management. The application of NIR spectroscopy for real-time monitoring highlights its broader significance in pharmaceutical manufacturing, where it can serve as a versatile tool for ensuring product quality and optimizing production efficiency in diverse formulation processes. By incorporating NIR-based PAT, manufacturers can not only achieve product-specific improvements but also establish a foundation for continuous manufacturing and automated quality assurance systems, ultimately contributing to a more streamlined and robust production environment.

Multifunctional nanoplatform with near-infrared triggered nitric-oxide release for enhanced tumor ferroptosis

Ferroptosis has emerged as a promising strategy for cancer treatment. Nevertheless, the efficiency of ferroptosis-mediated therapy remains a challenge due to high glutathione (GSH) levels and insufficient endogenous hydrogen peroxide in the tumor microenvironment. Herein, we presented a nitric-oxide (NO) boost-GSH depletion strategy for enhanced ferroptosis therapy through a multifunctional nanoplatform with near-infrared (NIR) triggered NO release. The nanoplatform, IS@ATF, was designed that self-assembled by loading the NO donor L-arginine (L-Arg), ferroptosis inducer sorafenib (SRF), and indocyanine green (ICG) onto tannic acid (TA)-Fe3+‒metal-phenolic networks (MPNs) modified with hydroxyethyl starch. Inside the tumor, SRF could inhibit GSH biosynthesis, impair the activation of glutathione peroxidase 4, and disrupt the ferroptosis defensive system. In conjunction with TA-Fe3+‒MPNs, which has cascaded Fenton catalytic activity, it could navigate the lethal ferroptosis to cancer cells. Upon NIR laser irradiation, the ICG-generated ROS oxidated L-Arg to a substantial quantity of NO, which further depleted the intracellular GSH and caused LPO accumulation, enhancing cell ferroptosis. Moreover, ICG also serves as a photothermal agent that can produce hyperthermia when exposed to irradiation, further potentiating ferroptosis therapy. In addition, the nanoplatform showed significantly improved tumor therapeutic efficacy and anti-metastasis efficiency. This work thus demonstrated that utilizing NO boost-GSH depletion to enhance ferroptosis induction is a feasible and promising strategy for cancer treatment.Graphical abstract

Chiral plasmonic-dielectric coupling enables strong near-infrared chiroptical responses from helicoidal core-shell nanoparticles

Helicoid plasmonic nanoparticles with intrinsic chirality are an emerging class of artificial chiral materials with tailorable properties. The ability to extend their chiroplasmonic responses to the near-infrared (NIR) range is critically important for biomedical and nanophotonic applications, yet the rational design of such materials remains challenging. Herein, a strategy employing chiral plasmon-dielectric coupling is proposed to manipulate the chiroptical responses into the NIR region with high optical anisotropy. Through this strategy, the helicoid Au@Cu2O nanoparticles with structural chirality are designed and synthesized with tunable and enriched NIR chiroptical responses. Specially, a high optical anisotropy (g-factor) with a value of 0.35 is achieved in the NIR region, and multi-band chiroptical behaviors are observed. Spectral and electromagnetic simulations elucidate that strong coupling between chiroplasmonic core and chiral dielectric shell with high refractive index contributes to the rich and strong chiroptical responses, which are related to the interplay between various emerged and enhanced electric and magnetic multipolar resonance modes proved by multipole expansion analysis. Moreover, the helicoid Au@Cu2O nanoparticles display greater polarization rotation capability than the helicoid Au nanoparticles. This work offers mechanistic insights into chiral plasmon-dielectric coupling and suggests a general approach of creating NIR chiroplasmonic materials.

Glacier Cover Estimation: a Multitemporal Retrospective Analysis of the Uruashraju Snow-capped Mountain (Ancash)

Objectives: To estimate the evolution of the glacier cover of the Uruashraju snow-capped mountain (Áncash, Peru) between the years 2014 and 2024, Theoretical framework: The research is framed in the context of climate change, specifically in the reduction of tropical glaciers. Andean glaciers are key indicators of global warming, and their retreat affects the availability of water resources, impacting sectors such as agriculture, human consumption and local biodiversity. Method: A cartographic analysis of satellite images obtained through the "Landsat 8-9 OLI/TIRS C2 L2" mission for the years 2014, 2016, 2018, 2020, 2022 and 2024 was used. The images were downloaded from the USGS Earth Explorer platform and selected from the months of July to maintain temporal homogeneity. The spatial resolution used was 30 meters in visible, near infrared (NIR) and shortwave infrared (SWIR) bands. Results and discussion: The results reveal a significant reduction of 37.28% in the glacier surface of the Uruashraju snow-capped mountain between 2014 and 2024. Despite some periods of temporary stabilization, the general trend is one of retreat due to climate change. This phenomenon affects water availability and poses risks for essential activities such as agriculture. Implications of the research: The research highlights the urgent need to take measures to mitigate the effects of climate change on Andean glaciers, since their loss compromises the water and economic security of local communities that depend on glacial resources. Originality/Value: This study offers a detailed and updated analysis of the evolution of glacier cover on the Uruashraju snow-capped mountain, providing relevant data for water resource planning and climate change adaptation strategies in the Andean region.

Two-Dimensional MXene (Ti3C2Tx)-based Nano-Photosensitizers for Enhanced Photothermal Ablation of Tumor Cells

Cancer remains one of the leading causes of death globally, accounting for approximately one in every six deaths. Traditional cancer therapies, including surgery, chemotherapy, chemoimmunotherapy, and radiation, face numerous challenges and limitations. In this context, we explore the advantages of photothermal therapy (PTT) using two-dimensional (2D) MXene-based nanocomposites for cancer treatment. MXenes, composed of abundant and non-toxic elements, such as titanium (Ti), carbon (C), fluorine (F), and oxygen (O), demonstrate low toxicity and are promising candidates in photothermal cancer therapies. Their ultrathin planar nanostructure, high photothermal conversion efficiency, strong near-infrared (NIR) responsiveness, and chemically modifiable surfaces enhance their therapeutic potential. Recent innovations include the development of folic acid-functionalized Au@c-Ti3C2 nanostructures, a skin-mountable electrostimulation patch (eT-patch), ionic gels containing MXene (Ti3C2Tx), and composite scaffolds made of MXene, collagen, silk fibroin, and quercetin. These MXene-based photosensitive compounds offer efficient targeting and selective treatment of cancer cells, highlighting their significant role in advancing cancer therapies.

Pyro-phototronic Effect Enhanced Self-Powered Photoresponse in Lead-Free Hybrid Perovskite.

Pyro-phototronic effect (PPE) can significantly boost the performance of hybrid perovskite (HPs) photodetectors due to the effective modulation of photogenerated charge carrier separations, transportation, and extraction. However, there are few reports on the application of PPE in lead-free HPs. Herein, a polar lead-free HP (1,3-BMACH)BiBr5 [1,3-BMACH = 1,3-bis(aminomethyl)cyclohexane] is synthesized and realized broadband self-powered photoresponse from X-rays to near-infrared (NIR) through the PPE. Particularly, this light-induced PPE in lead-free HPs breaks the limitation of the optical band gap, making them suitable for broadband self-powered photodetection. Under 405 nm illumination, compared with a purely photovoltaic system, Iphoto+pyro is boosted by 3100%, and R and D* are both enhanced by 260% after coupled PPE. It is particularly interesting that an obvious X-ray-induced PPE phenomenon is also observed, which endows (1,3-BMACH)BiBr5 with a high sensitivity of 154 μC Gy-1 cm-2 and a low detection limit of 307 nGy s-1 under the self-powered mode. The implementation of light-induced PPE from X-rays to NIR in lead-free HPs provides a new approach for constructing environmentally friendly, broadband, and self-powered optoelectronic devices in the future.