White Light Illumination Research Articles

Tetraphenylethene-Based Molecular Cage with Coenzyme FAD: Conformationally Isomeric Complexation toward Photocatalysis-Assisted Photodynamic Therapy.

Flavin adenine dinucleotide (FAD), serving as a light-absorbing coenzyme factor, can undergo conformationally isomeric complexation within different enzymes to form various enzyme-coenzyme complexes, which exhibit photocatalytic functions that play a crucial role in physiological processes. Constructing an artificial photofunctional system using FAD or its derivatives can not only develop biocompatible photocatalytic systems with excellent activities but also further enhance our understanding of the role of FAD in biological systems. Here, we demonstrate a supramolecular approach for constructing an artificial enzyme-coenzyme-type host-guest complex with photoinduced catalytic function in water. First, we have designed and synthesized a water-soluble tetraphenylethene (TPE)-based octacationic molecular cage (1) with a large and flexible cavity, which can adaptively encapsulate with two FAD molecules with "U-shaped" conformation (uFAD) to form a 1:2 host-guest complex (1⊃uFAD2) in water. Second, based on the conformationally isomeric complexation of FAD within 1, the 1⊃uFAD2 complex facilitates electron and energy transfers to molecular oxygen upon the white-light illumination, efficiently producing reactive oxygen species (ROS) such as superoxide radical (O2•-) and singlet oxygen (1O2). To our knowledge, the 1⊃uFAD2 complex acts as a photocatalyst to achieve the highest turnover frequency (TOF) of 35.6 min-1 for the photocatalytic oxidation reaction of NADH via a photoinduced superoxide radical catalysis mechanism in an aqueous medium. At last, combining the cytotoxic effects of ROS and the disruption of the intracellular redox balance involving NADH, 1⊃uFAD2 as a supramolecular photosensitizer displays an excellent oxygen-independent photocatalysis-assisted photodynamic therapy in hypoxic tumors.

Blue Light-Emitting Diodes Based on Pure Bromide Perovskites.

Blue perovskite light-emitting diodes (LEDs) are essential for the creation of full-color displays and white-light illumination, and some significant progress is made in recent years. However, most high-performance blue perovskite LEDs are currently based on mixed-halide perovskites and suffer from unstable spectra due to inevitable halide phase segregation, which is unfavorable for the application of blue perovskite LEDs. In contrast, blue emissions from pure bromide perovskites generally exhibit stable spectra (consistent emission peak positions and spectral shapes) and are worthy of attention. In this review, the recent advances in blue LEDs based on pure bromide perovskites according to different strategies are classified and summarized. Moreover, the challenges related to poor charge injection, high defect-state density, lack of high-performance in the deeper blue region, and inferior operational stability are addressed. Finally, an outlook is provided on feasible future research directions for highly bright, efficient, and stable blue perovskite LEDs.

Scalable Multistep Imprinting of Multiplexed Optical Anti-counterfeiting Patterns with Hierarchical Structures.

Multiplexed optical techniques with multichannel patterns provide powerful strategies for high-capacity anti-counterfeiting. However, it is still a big challenge to meet the demands of achieving high encryption levels, excellent readability, and simple preparation simultaneously. Herein, we use a multistep imprinting technique, leveraging surface work-hardening to massively produce multiplexed encrypted patterns with hierarchical structures. These patterns with coupled nano- and microstructures can be instantaneously decoded into different pieces of information at different view angles under white light illumination. By incorporating perpendicular nano- and microgratings, we achieve four-channel encoded patterns, enhancing anti-counterfeiting capacity. This versatile method works on various metal/polymer materials, offering high-density information storage, direct visibility, broad material compatibility, and low-cost mass production. Our high-performance anti-counterfeiting patterns show significant potential in real-world applications.

Charge separation in a copper(I) donor-chromophore-acceptor assembly for both photoanode and photocathode sensitization.

A copper(I) donor-chromophore-acceptor triad bearing 1,8-napthalenemonoimide as the electron acceptor and triphenylamine as the electron donor was synthesized. Photophysical and electrochemical characterization suggest stepwise photoinduced charge separation upon excitation of the copper(I)-based metal-to-ligand charge transfer (MLCT) transition. Analyses of femtosecond transient absorption data of the triad show that intersystem crossing from the 1MLCT to the 3MLCT state is followed by two electron-transfer steps with time constants of 20 ps and 722 ps yielding a presumed final charge-separated state with a radical cation on the donor and radical anion on the acceptor that has an 18 ns lifetime in acetonitrile. Finally, this triad was anchored onto n-type (ZnO) and p-type (NiO) semiconductor surfaces to construct a photoanode and photocathode respectively. Successful photocurrent generation from both electrodes upon white light illumination confirms the potential utilization of such systems in dye-sensitized photoelectrochemical cells.

Modulation the carrier separation mechanism of CdS photoanode: From vacancy to crystal phase transformation

The photoelectrochemical (PEC) water splitting performance is conventionally limited by the process of photogenerated carrier separation and transport. This work provides an innovative strategy by combination of the spin-polarized electric field and homogeneous junction to address this critical issue. In this work, it finds that a spin-polarized electric field can be fabricated in the CdS photoanode with cubic phase by S vacancy intervention. Furthermore, after controlling the annealing temperature to reach 500 °C, cubic phase CdS photoanode translates to hexagonal phase by localized, forming a homogeneous junction CdS photoanode. By the synergy, the optimized CdS photoanode achieves a photocurrent density exceeding ∼5.0 mA/cm2 for hydrogen evolution under 100 mW/cm2 white light illumination, a 2.4-fold improvement over the performance of the unoptimized photoanodes. Thus, this work provides a novel method to regulation of the photogenerated carrier separation and transport processes for sulfur-based semiconductor photoelectrodes.

Camphor-Based CVD Graphene Integrating CsPbBr3 Quantum Dots for High-Temperature Endurance, High Flexibility, and Fast Optical Switch Photodetection

Photodetectors (PDs) based on camphor-based CVD graphene integrating CsPbBr3 quantum dots (QDs) have been fabricated on mica substrates successfully, showing temperature resistant, foldable, and fast response properties. The graphene synthesized from eco-friendly camphor was transferred onto mica substrates, and then the CsPbBr3 QDs were coated onto the graphene surface to form CsPbBr3 QDs/graphene composition on a flexible mica substrate. According to the Raman spectrum, the structure of camphor-based CVD graphene is multilayer. The photoresponse of CsPbBr3 QDs/graphene composition was revealed by temperature-dependent (ranging from 300 K to 523 K) I-V measurements with/without white light illumination (light intensity: 112 mW/cm2). To highlight the temperature resistance of PDs based on CsPbBr3 QDs/graphene composition, a photo-to-dark current ratio (PDCR) of at 5 V is estimated at different temperatures. The PDCR of the CsPbBr3 QDs/graphene composition-based PD decreased from 3.2 to 0.74 with increasing temperature from 300 K to 523 K. Moreover, after 0 to 300 bending cycles, the vibration of PDCR value at 5 V is small (from 4.3 to 3.7), showing the high flexibility of the CsPbBr3 QDs/graphene composition-based PD. Furthermore, we found that the rise and fall times of the CsPbBr3 QDs/graphene composition-based PDs when we switched the illumination source ON and OFF are ~ 2 and ~1 ms, respectively, indicating fast optical switch behavior. In this study, camphor-based CVD graphene incorporating CsPbBr3 QDs composition-based PD is demonstrated to exhibit high-temperature resistance, high flexibility, and fast response photodetection.Keywords: Camphor, graphene, CsPbBr3 quantum dots, flexible photodetectors

Narrow-band imaging to enhance intraneural dissection in head and neck schwannoma surgery: a quantitative evaluation

ObjectiveThe objective of this study was to assess the utility of narrow-band imaging (NBI) for improving intraneural dissection during gross total resection of head and neck schwannoma. Specifically, we aimed to quantitatively evaluate whether NBI can enhance the identification of pseudocapsule and true capsule within the tumor. MethodsNine schwannoma surgery cases conducted between February 2018 and October 2022 were retrospectively analyzed. The surgical procedures followed established principles with a specific focus on utilizing NBI to distinguish between the pseudocapsule and true capsule. Intraneural dissection was performed by searching for a tumor surface with a fascicle-free window, followed by longitudinal incision of the pseudocapsule. NBI was used to distinguish between the pseudocapsule and true capsule. Surgical views were captured under both white light (WL) illumination and NBI for further analysis. The brightness and contrast of the pseudocapsule and true capsule were quantitatively measured using ImageJ and were compared. ResultsUnder NBI, the pseudocapsule consistently appeared greenish-gray, whereas the true capsule exhibited a white appearance. Quantitative analysis revealed a statistically significant difference (p < 0.0001) in brightness between the pseudocapsule (mean grayscale value 52.1, 95%CI; 46.4–75.3) and true tumor capsule (mean grayscale value 120.8, 95%CI; 155.7–109.0) under NBI. Conversely, there was no statistically significant difference in the brightness of these structures under WL (p = 0.2067). NBI also showed significantly higher contrast between the two structures than did WL (contrast 73.6, 95%CI; 53.1–89.5 vs. 30.9, 95%CI; 1.0–47.5, p = 0.0034). Further spectral analysis revealed that the most substantial difference in brightness between the pseudocapsule and the true tumor capsule was observed in the red spectrum, with a difference in brightness of −0.6 (95%CI; −16.8–14.8) under WL and 83.5 (95%CI; 50.3–100.0) under NBI (p < 0.0001). ConclusionNBI proved to be a valuable tool for enhancing the identification of pseudocapsule and true capsule during intraneural dissection in head and neck schwannoma surgery. The improved contrast and membrane visibility offered by NBI might have the potential to reduce postoperative neurological deficits and improve surgical outcomes. Further research is warranted to validate our findings and explore the broader applications of NBI in schwannoma surgery.

One-step synthesis of O, P co-doped g-C3N4 under air for photocatalytic reduction of uranium

The photocatalytic reduction of uranium from nuclear wastewater represents a promising method for both uranium extraction and environmental remediation. This approach facilitates the recovery of uranium resources for the nuclear industry while addressing environmental pollution. Despite significant research advancements, there remains a need for cost-effective and environmentally friendly catalytic materials. In this context, we present a two non-metal O, P co-doped g-C3N4 (OPCN) synthesized via a simple one-step thermo-polymerization in air. OPCN demonstrates a high uranium reduction efficiency of 94.9 % under white LED light illumination. Even after five cycles, OPCN maintained a reduction efficiency of 81.7 %, highlighting its stability and reusability. Additionally, OPCN also performs effectively in uranium reduction under natural sunlight and exhibits impressive antimicrobial properties. These features position OPCN as a promising candidate for practical environmental applications.

Sulfur-doped carbon dots and g-C3N4 composite with thermally activated delayed fluorescence for white-light illumination and anticounterfeiting

Long-lived afterglow materials have attracted considerable interest in the fields of information security and illumination. Herein, a novel carbon dot (CD)-based thermally activated delayed fluorescence (TADF) material was synthesized by embedding sulfur-doped CDs (SCDs) into a graphitic carbon nitride matrix. The formation of covalent bonds between the matrix and SCDs enhances the stabilization of the triplet state in the composite, effectively suppressing nonradiative transitions. This stabilization, coupled with the effects of sulfur doping and covalent bonding, reduces the singlet–triplet splitting energy in the composite, thereby facilitating reverse intersystem crossing and resulting in TADF emission. This composite material has been successfully employed in the development of three types of CD-based white light–emitting diodes (WLEDs) excited by blue light. These WLEDs exhibit color temperatures of 7641, 5590, and 3215 K, with CIE coordinates of (0.30, 0.29), (0.33, 0.30), and (0.42, 0.40), respectively. The corresponding values of the color rendering index are recorded as 81.86, 90.13, and 75.07. In addition, this research provides a brief demonstration of the potential of the composite in information encryption and visible-light encryption applications. Furthermore, this study contributes to the advancement of CD utilization in the WLED field, promoting the development of next-generation CD-based WLEDs with exceptional properties.

Absolute thickness field measurement on curved axisymmetric thin free films with monochromatic light

The thickness of thin films is a key parameter to understand their thinning dynamics and stability. Thickness measurements are commonly performed using interferometry. White light illumination allows us to measure the absolute thickness, but is limited to small thicknesses (&amp;lt;2μm) or is restricted to a point with a spectrometer. Monochromatic light gives access to a broader range of thicknesses but solely in a relative manner unless a reference thickness is known. These methods are extensively used to quantify the thickness profiles of flat soap films. In contrast, they are applied to curved interfaces (bubbles) only in a few specific cases, mainly due to the complexity arising from the curvature as the optical path depends on the position. In this paper, we elucidate the influence of the curvature and show that it can be used to measure the entire and absolute thickness profiles using monochromatic light. We demonstrate the validity of the method on soap bubbles, antibubbles, and catenoid soap films. This cost-effective technique is adapted to quantitatively study the thin film dynamics in these geometries.

Identification of exfoliated monolayer hexagonal boron nitride films with a digital color camera under white light illumination

Optical microscopy with white light illumination has been employed when obtaining exfoliated monolayer hexagonal boron nitride (1L hBN) films from a large number of randomly placed films on a substrate. However, real-time observation of 1L hBN using a color camera under white light illumination remains challenging since hBN is transparent in the visible wavelength range. The poor optical constant of 1L hBN films in microphotographs is significantly improved using a Si substrate coated with a SiN x thin-film (SiN x /Si). When observing hBN thin films on SiN x /Si using a color digital camera in an optical microscope under white light illumination, the clarity of the captured color images depends on the thickness of the SiN x film (d). For real-time direct observation, the d was optimized based on quantitative chromatic studies tailored to Bayer filters of a color image sensor. Through image simulation, it was determined that the color difference between 1L hBN and the bare substrate is maximized at d = 59 or 70 nm, which was experimentally verified. The SiN x /Si with optimized d values visualized 1L hBN films without requiring significant contrast enhancement via image processing under white light illumination in real-time. Furthermore, the captured color photographs facilitate the reliable determination of the number of layers in few-layer hBN films using the contrast of the green channel of the images.

Complete polarization state generator composed of one fixed polarizer and two rotating retarders

We discuss all possible responses of a linearly polarized light passing through two linear retarders. Based on this theory, a complete polarization state generator (PSG) composed of a fixed polarizer and two rotating retarders is proposed. The restriction on the phase retardances of the two retarders is given, and the procedures to determine the orientations of the two retarders to generate any pre-specified elliptical polarization state are presented. Compared with the traditional PSG, our design has the advantage that the working wavelength can be selected in a rather broad range. At the same time, our system only requires two normal linear retarders, and is thus cheaper than the PSG composed of achromatic or variable retarders. In addition, by selecting the retardance values of the two retarders, our complete PSG can also be designed to show a good broadband property, such as generating a specific polarization for an extended range of wavelengths under white light illumination. Finally, the comprehensive analysis of a linearly polarized light passing through two linear retarders presented in our paper is also inspiring for the design of other related systems.

Fabrication and high photoresponse performance of a La-doped HfO2 thin film-based UV photodiode

The ability to detect ultraviolet light is crucial for various applications such as energy harvesting, environmental monitoring, sensing, and ultraviolet astronomy. In this paper, we determined the photoelectric properties of a photodiode based on an interfacial layer of a La-doped HfO2 (HfLaO) thin film. We carried out several tests to analyze the electrical behavior and photoresponse of the Au/HLO/p-Si photodiode under ultraviolet (UV) and white light illumination and in the dark. The chemical composition, surface morphology, cross-sectional thickness, optical properties, and crystalline structure of the HfLaO (HLO) film prepared by the sol-gel method were characterized. We found that the prepared photodiode exhibited excellent repeatability and stability. Moreover, the photocurrent increased with increasing UV light intensity. When the UV light intensity was 23.5 mW/cm2, the photocurrent reached 700 μA and remained unsaturated at a 7 V bias voltage. Moreover, we systematically analyzed the changes in the energy bands and carriers under dark and ultraviolet light conditions to further understand the working mechanism of the photodiode. Overall, the Au/HLO/p-Si photodiode had excellent ultraviolet detector performance and could be a strong candidate for optoelectronic applications.

Dual-Band Photomultiplication-Type Organic Photodetectors with Ultrahigh Signal-to-Noise Ratios.

A series of dual-band photomultiplication (PM)-type organic photodetectors (OPDs) were fabricated by employing a donor(s)/acceptor (100:1, wt/wt) mixed layer and an ultrathin Y6 layer as the active layers, as well as by using PNDIT-F3N as an interfacial layer near the indium tin oxide (ITO) electrode. The dual-band PM-type OPDs exhibit the response range of 330-650 nm under forward bias and the response range of 650-850 nm under reverse bias. The tunable spectral response range of dual-band PM-type OPDs under forward or reverse bias can be explained well from the trapped electron distribution near the electrodes. The dark current density (JD) of the dual-band PM-type OPDs can be efficiently suppressed by employing PNDIT-F3N as the anode interfacial layer and the special active layers with hole-only transport characteristics. The light current density (JL) of the dual-band PM-type OPDs can be slightly increased by incorporating wide-bandgap polymer P-TPDs with relatively large hole mobility (μh) in the active layers. The signal-to-noise ratios of the optimized dual-band PM-type OPDs reach 100,980 under -50 V bias and white light illumination with an intensity of 1.0 mW·cm-2, benefiting from the ultralow JD by employing wide-bandgap PNDIT-F3N as the anode interfacial buffer layer and the increased JL by incorporating appropriate P-TPD in the active layers.

A Cu-based metal-organic frameworks-modified BiOCl heterojunction for enhanced photodegradation of rhodamine B

Environmental pollution caused by organic dyes has attracted increasing attention and prompts people to develop an effective treating method. Photocatalysis isregarded as one of the most promising treatment methodsowing to low cost, flexibility, and high efficiency. Herein, we reported a copper-based metal–organic frameworks (Cu-MOF) modified BiOCl heterojunction Cu-MOF/BiOCl (CMB) to treat organic dye rhodamine B (RhB) under white light illumination. The optimal photodegradation efficiency is shown to be 97 % within 40 min, exhibiting a higher photocatalytic ability than individual BiOCl and Cu-MOF. The enhanced photocatalytic activity is attributed to the formation of CMB heterojunction improving the visible light utilization efficiency and promoting significantly the separation/transfer of carriers. This study highlights the importance of combining narrow band gap nanomaterial with wide counterpart in environmental remediation.

Particle Detection in Free-Falling Nanoliter Droplets.

Sorting and dispensing distinct numbers of cellular aggregates enables the creation of three-dimensional (3D) in vitro models that replicate in vivo tissues, such as tumor tissue, with realistic metabolic properties. One method for creating these models involves utilizing Drop-on-Demand (DoD) dispensing of individual Multicellular Spheroids (MCSs) according to material jetting processes. In the DoD approach, a droplet dispenser ejects droplets containing these MCSs. For the reliable printing of tissue models, the exact number of dispensed MCSs must be determined. Current systems are designed to detect MCSs in the nozzle region prior to the dispensing process. However, due to surface effects, in some cases the spheroids that are detected adhere to the nozzle and are not dispensed with the droplet as expected. In contrast, detection that is carried out only after the droplet has been ejected is not affected by this issue. This work presents a system that can detect micrometer-sized synthetic or biological particles within free-falling droplets with a volume of about 30 nanoliters. Different illumination modalities and detection algorithms were tested. For a glare point projection-based approach, detection accuracies of an average of 95% were achieved for polymer particles and MCF-7 spheroids with diameters above 75 μm. For smaller particles the detection accuracy was still in the range of 70%. An approach with diffuse white light illumination demonstrated an improvement for the detection of small opaque particles. Accuracies up to 96% were achieved using this concept. This makes the two demonstrated methods suitable for improving the accuracy and quality control of particle detection in droplets for Drop-on-Demand techniques and for bioprinting.

Peptide-AIE Nanofibers Functionalized Sutures with Antimicrobial Activity and Subcutaneous Traceability.

As one of the most widely used medical devices, sutures face challenges related to surgical site infections (SSIs) and lack of subcutaneous traceability. In the present study, a facile and effective approach using peptide-AIE nanofibers (NFs-K18) to create fluorescent-traceable antimicrobial sutures, which have been applied to four commercially available sutures is developed. The functionalized sutures of PGAS-NFs-K18 and PGLAS-NFs-K18 exhibit fluorescence with excellent penetration from 4mm chicken breasts. They also demonstrate remarkable stability after 24h of white light illumination and threading through chicken breasts 10 times. These sutures efficiently generate ROS, resulting in significant suppression of four clinical bacteria, with the highest antimicrobial rate of ≈100%. Moreover, the sutures exhibit favorable hemocompatibility and biocompatibility. In vivo experiments demonstrate that the optimized PGLAS-NFs-K18 suture displays potent antimicrobial activity against MRSA, effectively inhibiting inflammation and promoting tissue healing in both skin wound and abdominal wall wound models, outperforming the commercially available Coated VICRYL Plus Antibacterial suture. Importantly, PGLAS-NFs-K18 exhibits sensitive subcutaneous traceability, allowing for accurate in situ monitoring of its degradation. It is believed that this straightforward strategy offers a new pathway for inhibiting SSIs and monitoring the status of sutures.

Bright Bifacial White-Light Illumination by Highly Deformable Electroluminescent Devices Based on Transparent Ionic-Hydrogel Electrodes and Quantum-Dot Color Conversion.

Deformable alternating-current electroluminescent (ACEL) devices are of increasing interest because of their potential to drive innovation in soft optoelectronics. Despite the research focus on efficient white ACEL devices, achieving deformable devices with high luminance remains difficult. In this study, this challenge is addressed by fabricating white ACEL devices using color-conversion materials, transparent and durable hydrogel electrodes, and high-k nanoparticles. The incorporation of quantum dots enables the highly efficient generation of red and green light through the color conversion of blue electroluminescence. Although the ionic-hydrogel electrode provides high toughness, excellent light transmittance, and superior conductivity, the luminance of the device is remarkably enhanced by the incorporation of a high-k dielectric, BaTiO3. The fabricated ACEL device uniformly emits very bright white light (489cdm-2) with a high color-rendering index (91) from both the top and bottom. The soft and tough characteristics of the device allow seamless operation in various deformed states, including bending, twisting, and stretching up to 400%, providing a promising platform for applications in a wide array of soft optoelectronics.

Rational Design of Nitride Phosphor-In-Glass with Robust Stability and Photoluminescence Performance.

Phosphor-in-glass represents a promising avenue for merging the luminous efficiency of high-quality phosphor and the thermal stability of a glass matrix. Undoubtedly, the glass matrix system and its preparation are pivotal factors in achieving high stability and preserving the original performance of embedded phosphor particles. In contrast to the well-established commercial Y3Al5O12:Ce3+ oxide phosphor, red nitride phosphor, which plays a critical role in high-quality lighting, exhibits greater structural instability during the high-temperature synthesis of inorganic glasses. A telluride glass with a refractive index (RI = 2.15@615 nm) akin to that of nitride phosphor (∼2.19) has been devised, demonstrating high efficiency in photon utilization. The lower glass-transition temperature plays a crucial role in safeguarding phosphor particles against erosion resulting from exposure to high-temperature melts. Phosphor-in-glass retains 93% of the quantum efficiency observed for pure phosphor. The assembled white light-emitting diodes module has precise color tuning capabilities, achieving an optimal color rendering index of 93.7, a luminous efficacy of 80.4 lm/W, and a correlated color temperature of 5850 K. These outcomes hold potential for advancing the realm of inorganic package and high-quality white light illumination.

Viscosity-modulated intramolecular excitation energy transfer for mitochondria-targeted sensing and photokilling

Viscosity is a key parameter of mitochondria that related to several diseases. To design a probe acting as both the mitochondria-targeted viscosity sensor and photosensitizer is meaningful for diagnosis and therapies. Herein, we report a ratiometric viscosity sensor with dual-emission mediated by excitation energy transfer (EET) effect, which can detect the mitochondrial viscosity and serve as an efficient photosensitizer to eradicate cancer cells. The probe comprises of a blue-emitting imidazole moiety as the energy donor and a green-emitting boron dipyrromethene (BODIPY) core as the energy acceptor, respectively. Via viscosity-modulated EET effect, the dual-emissive probe can sensitively detect the medium viscosity in a ratiometric model. Directed by imidazole as the targeting factor, the probe can specifically accumulate in mitochondria and ratiometrically determine the intracellular viscosity increase induced by Nystatin treatment. Furthermore, it also exhibits light-triggered reactive oxygen species (ROS) generation including singlet oxygen and superoxide radical, which can efficiently kill the cancer cells under white light illumination. Thus, this work provides a versatile and promising candidate for disease diagnosis and phototherapy.