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Developing stable perovskite nanocrystals (NCs) with enhancing luminescent properties holds great importance for future potential applications in optoelectronics. Here, we engaged perovskite NCs in Cu2+ ion-based metal–organic framework (MOF) Cu-BTC (BTC = 1,3,5-benzene tricarboxylate) by physical mixing of MOF with CsPbBr3 NCs in toluene solution. MOF-protected perovskite NCs achieved high photoluminescence quantum yield 96.51% than pristine state CsPbBr3 NCs (51.66%). Along with the improvement in optical properties, the long-term stability of CsPbBr3 NCs in the solution phase also increases considerably upon loading in Cu-BTC MOF. Moreover, the changes in the luminescent intensity of the samples have been observed for 3 months in the solution. After 1 month, pristine CsPbBr3 NCs lose their emission intensity 68% from the initial, while the MOF-protected CsPbBr3 NCs show only a 10% reduction from the initial. These results indicate that the effective passivation of Cu-BTC MOF inhibits the aggregation of NCs, protecting them from the defective atmosphere. The excellent photoluminescence findings provide a new pathway for future optoelectronic applications. [ABSTRACT FROM AUTHOR]

Indium tin oxide (ITO) film, which is the most commonly used transparent conductive film (TCF), has traditionally been believed to be transparent in the visible spectrum but to reflect infrared (IR) light beyond the plasma wavelength (λp). However, our theoretical analysis challenges this notion by demonstrating that an ultrathin ITO TCF that is thinner than the light's penetration depth can overcome the transmission barrier at λp. To validate the theoretical modeling, we have successfully fabricated ultrathin ITO films that, despite having λp ≈ 1 μm, remain transparent from 400 nm to 20 μm. This represents the broadest transparency range ever reported for any In2O3-based TCF. The 10-nm-thick ITO TCFs have high visible transmittance (91.0% at 550 nm), low resistivity (5 × 10−4 Ω cm), and good IR transmittance (averaging 60% over 1.35–18.35 μm). Their IR transparency facilitates radiative cooling of the underlying circuitry. When an operational resistor is enclosed by commercial ITO TCFs that are 140 nm thick, its temperature increases. However, using 10-nm-thick ITO TCFs instead of the commercial ones can completely avoid this temperature rise. Moreover, attaching a silver grid to a 10-nm-thick ITO TCF can reduce the effective sheet resistance to ∼10 Ω/□ at the expense of only ∼3% transmittance. This development paves the way for large-scale applications that require low sheet resistance and far-IR transparency. [ABSTRACT FROM AUTHOR]

Developing stable perovskite nanocrystals (NCs) with enhancing luminescent properties holds great importance for future potential applications in optoelectronics. Here, we engaged perovskite NCs in Cu2+ ion-based metal–organic framework (MOF) Cu-BTC (BTC = 1,3,5-benzene tricarboxylate) by physical mixing of MOF with CsPbBr3 NCs in toluene solution. MOF-protected perovskite NCs achieved high photoluminescence quantum yield 96.51% than pristine state CsPbBr3 NCs (51.66%). Along with the improvement in optical properties, the long-term stability of CsPbBr3 NCs in the solution phase also increases considerably upon loading in Cu-BTC MOF. Moreover, the changes in the luminescent intensity of the samples have been observed for 3 months in the solution. After 1 month, pristine CsPbBr3 NCs lose their emission intensity 68% from the initial, while the MOF-protected CsPbBr3 NCs show only a 10% reduction from the initial. These results indicate that the effective passivation of Cu-BTC MOF inhibits the aggregation of NCs, protecting them from the defective atmosphere. The excellent photoluminescence findings provide a new pathway for future optoelectronic applications. [ABSTRACT FROM AUTHOR]

Gain medium‐doped active optical fibers for optical amplification and long‐range transmission have triggered a lot of researches. Traditional rare‐earth ion‐doped active fibers have non‐adjustable emissions, narrow band luminescence, limited gain enhancement, and other challenges. The unique optical properties of quantum dots (QDs) can further improve the doped optical fibers in the light amplification capacity, temperature sensitivity and to gain a broad‐spectrum coverage and lower laser threshold and other superiorities. However, there are few systematic discussions on the development of the technologies and applications of those QD‐doped optical fibers. In this review, the optical properties, temperature characteristics and optical amplification mechanisms of QD‐doped optical fibers are outlined. Then, the preparation technologies and the applications of QD‐doped optical fibers are highlighted. Additionally, the existing challenges and future development prospects of QD‐doped optical fibers are discussed. [ABSTRACT FROM AUTHOR]

Lead‐free metal halide double perovskites have emerged as promising scintillators owing to their superior optoelectronic properties, low‐cost and solution processability. However, it is still challenging to develop high‐performance flexible X‐ray scintillators based on the B(I)‐site alkali metal modulation in lead‐free double perovskite nanocrystals (NCs). Herein, a series of novel Cs2B(I)GdCl6 (B: Li, Na, K) of double perovskite A2B(I)M(III)X6 NCs structures are successfully synthesized, the optical and scintillator properties of which are significantly sensitive to the B(I)‐site alkali metals with the doping of Sb3+. They showed efficient self‐trapped exciton (STE) emission with high photoluminescence quantum yield (PLQY) and exhibited the highest X‐ray detection limit (86 nGyair s−1) and excellent spatial resolutions (>15 lp mm−1). The femtosecond transient absorption measurement and theoretical analysis further revealed that the B(I)‐site alkali metal fundamentally balanced the exciton–phonon coupling with appropriate STEs formation energy barrier and the electron localization and thus improved the optical and scintillator properties. This B(I)‐site alkali metal engineering offers a strategy to develop bright luminescent double perovskite NCs for X‐ray detection and imaging devices. [ABSTRACT FROM AUTHOR]

Since the discovery of electrochemical coloration phenomenon, electrochromic devices capable of monitoring transmittance, reflectance, and absorption at designated wavelengths have embraced great achievements. The marriage of electrochemistry and optical modulation has infused fascinating properties in electrochromic devices, which find applications in thermal management, display, smart windows, and camouflage. Inspired by the multipronged advancements in electrochemical devices, the incorporation of multivalent metal ions having rich electrochemistry into electrochromic devices is bloomed in recent years. Zinc, distinguished by its high crustal abundance, suitable standard redox potential, and inherent safety, has facilitated the assembly of highly efficient electrochromic devices. Zinc anode-based electrochromic devices with dual-band (visible and near-infrared) tunability, energy retrieval functions, multi-color options, multiple working modes (transmittance mode and reflectance mode), and scalability have been prominently showcased. Here in this review, the birth of zinc anode-based electrochromic devices will be systematically narrated, starting from the discovery of electrochromic phenomenon, to the evolution of electrochromic devices, and to the latest achievements in zinc anode-based electrochromic devices. Additionally, this review delves into the future development trends and perspectives of zinc anode-based electrochromic devices. This review serves as a handbook, which summarizes the history of electrochromism, introduces the physics behind it, highlights the development in zinc anode-based electrochromic devices, and aims to inspire future endeavors into this field, particularly those focused on developing energy-efficient electrochromic devices. [ABSTRACT FROM AUTHOR]

Highlights: [•] TiO2 and ZnO nanomaterials incorporated into sunscreens were evaluated for ROS production. [•] Presented here chemical assays were ideal tools to assess photoactivity of sunscreen pigments. [•] TiO2 was inactive upon UV irradiation; coatings render its surfaces non-reactive. [•] ZnO nanomaterials produced substantial amounts of ROS upon UVA illumination. [•] ZnO in sunscreens is either uncoated or ineffectually coated to limit its intrinsic property. [Copyright &y& Elsevier]

Abstract: Quantum dots nanoparticles have novel optical properties for biomedical applications and electronics, but little is known about their skin permeability and interaction with cells. QD621 are nail-shaped nanoparticles that contain a cadmium/selenide core with a cadmium sulfide shell coated with polyethylene glycol (PEG) and are soluble in water. QD were topically applied to porcine skin flow-through diffusion cells to assess penetration at 1 μM, 2 μM and 10 μM for 24 h. QD were also studied in human epidermal keratinocytes (HEK) to determine cellular uptake, cytotoxicity and inflammatory potential. Confocal microscopy depicted the penetration of QD621 through the uppermost stratum corneum (SC) layers of the epidermis and fluorescence was found primarily in the SC and near hair follicles. QD were found in the intercellular lipid bilayers of the SC by transmission electron microscopy (TEM). Inductively coupled plasma-optical emission spectroscopy (ICP-OES) analysis for cadmium (Cd) and fluorescence for QD both did not detect Cd nor fluorescence signal in the perfusate at any time point or concentration. In HEK, viability decreased significantly (p <0.05) from 1.25 nM to 10nM after 24 h and 48 h. There was a significant increase in IL-6 at 1.25 nM to 10 nM, while IL-8 increased from 2.5nM to 10nM after 24 h and 48 h. TEM of HEK treated with 10 nM of QD621 at 24 h depicted QD in cytoplasmic vacuoles and at the periphery of the cell membranes. These results indicate that porcine skin penetration of QD621 is minimal and limited primarily to the outer SC layers, yet if the skin were damaged allowing direct QD exposure to skin or keratinocytes, an inflammatory response could be initiated. [Copyright &y& Elsevier]

High-quality nanocrystals formed in organic solvents can be completely solubilized in water using amphiphilic copolymers containing poly(ethylene glycol) or PEG. These copolymers are generated using a maleic anhydride coupling scheme that permits the coupling of a wide variety of PEG polymers, both unfunctionalized and functionalized, to hydrophobic tails. Thermogravimetric analysis, size exclusion chromatography, cryogenic transmission electron microscopy, and infrared spectroscopy all indicate that the copolymers effectively coat the nanocrystals surfaces. The composite nanocrystal-polymer assemblies can be targeted to recognize cancer cells with Her2 receptor and are biocompatible if their surface coatings contain PEG. In the particular case of semiconductor nanocrystals (e.g., quantum dots), the materials in water have the same optical spectra as well as quantum yield as those formed initially in organic solutions. [ABSTRACT FROM AUTHOR]

Abstract: Semiconductor nanocrystals are 1–10nm inorganic particles with unique size-dependent optical and electrical properties due to quantum confinement (so they are also called quantum dots). Quantum dots are new types of fluorescent materials for biological labeling with high quantum efficiency, long-term photostability, narrow emission, and continuous absorption spectra. Here, we discuss the recent development in making water-soluble quantum dots and related cytotoxicity for biomedical applications. [Copyright &y& Elsevier]

Abstract: A series of selective hydrogenation reactions, cinnamaldehyde to cinnamyl alcohol, crotonaldehyde to crotyl alcohol, citronellal to citronellol, and o-chloronitrobenzene to o-chloroaniline, were studied over polymer-stabilized nanoscale noble metal colloid catalysts in solutions. Metal cations and metal complex ions significantly affected the catalytic performances of the noble metal colloidal nanocatalysts. Some metal cations increased both the activity and the selectivity of the nanosized catalysts, and metal complex ions exhibited more complicate effects. [Copyright &y& Elsevier]

Abstract: The effects of various physical properties (particle size, shape, surface area, crystal structure, and phase composition) on the photocatalytic performance of nanosized TiO2 were studied through the photodegradation of Congo Red. Kinetic results showed that anatase TiO2 was a superior photocatalyst to rutile TiO2 due to the inherent difference in the two crystal structures. Anatase TiO2 nanorods with predominantly (101) surface exhibited low activity because the non-dissociative adsorption of H2O to this surface retarded the generation of OH required for facile photocatalytic oxidation. It was found for the first time that the shape of TiO2 nanocrystals significantly affected their photocatalytic activities. The previously reported anatase–rutile synergetic effect in commercialized mixed-phase TiO2 (Degussa P25) was not observed in this study, perhaps, due to poor contact between the two phases and the extremely small sizes, as well as the not-optimized phase compositions in the current work. [Copyright &y& Elsevier]

The development of electrochromic materials has opened the door to the development of numerous devices including smart windows, color displays, optical filters, wearable camouflages, among others. Although the current electrochromic devices do not consume energy while maintaining their colored or colorless states, their bistable operation requires external electrical energy to be consumed during switching. To reduce the energy consumption of an electrochromic device, an emerging Zn anode‐based electrochromic device concept was recently introduced to partially retrieve the consumed electrical energy. In this Review, key technological developments and scientific challenges are presented for a broad range of Zn anode‐based electrochromic device configurations with emphasis on the inherent distinctions between the Zn anode‐based and conventional electrochromic devices. Specifically, a comprehensive comparison of the two classes of electrochromic devices in the high‐performance device design is provided. For the electrochromic layer, the methods for obtaining high‐quality electrochromic materials and thin films are reviewed. For the electrolytes, the effect of the dual ion system on the electrochromic performance is discussed. Also, some critical but unresolved issues in the device design and fabrication are discussed. The perspectives and outlook at the end of this Review provide recommendations to improve performance for future electrochromic studies. [ABSTRACT FROM AUTHOR]

Electrolytes have become a research frontier in the electrochromic community owing to their widespread applications in advanced electronic devices especially in electrochromic devices (ECDs). However, traditional ECDs with liquid electrolytes commonly suffer from inflexibility, complicated configurations, and poor electrochromic properties. To achieve solid‐ or flexible‐state ECDs, an alternative method is to employ polymer electrolyte gels, which integrate the virtues of both liquid‐ and solid‐state electrolytes. In this review, first, the device configurations of conventional ECDs are introduced, where the classification of electrolytes for ECDs is comprehensively introduced. Then the current situation and applications of hydrogels for ECDs, where it is expected to reveal the developing trends of hydrogel‐based ECDs are specially reviewed. Finally, the insights on the design methods of hydrogel electrolytes for flexible and efficient ECDs are proposed. [ABSTRACT FROM AUTHOR]

Lead perovskite nanocrystals (PNCs) have shown great potential for optoelectronic device applications due to their excellent optoelectronic properties. However, the application of PNCs is significantly limited due to the inferior stability resulting from the highly dynamic ligands on the surface. Herein, poly(maleic anhydride‐alt‐1‐octadecene) (PMAO) with low molecular weight (Mn = 1911) is synthesized by copolymerization and used as multi‐dentate ligands to prepare CsPbBr3 PNCs via hot injection. The PNCs exhibit excellent water resistance, which maintains fluorescence for 2600 min while conventional PNCs are completely destroyed after 100 min. Density functional theory calculations demonstrate that PMAO as a multi‐dentate ligand has higher adsorption energy to the surface of PNCs. Due to the large amount of extra anhydride structure of PMAO, PMAO‐PNCs are used as a cross‐linking agent to directly prepare flexible films by an in situ one‐step polymerization reaction with 1,3‐bis(3‐aminopropyl) polydimethylsiloxane (PDMS‐NH2). The fluorescent flexible films show great potential for applications including X‐ray imaging scintillators and flexible light‐emitting diodes (LEDs). This study can provide guidance to prepare ultra‐stable PNCs and flexible perovskite films with good stability in a simple and efficient way. [ABSTRACT FROM AUTHOR]

[Display omitted] • Amphiphilic Janus nanosheets were used as carriers to achieve the integration of catalysts and solid emulsifiers for the degradation of azo dyes. • Bifunctional Janus-[BMIM][heteropolyanions] with phenyl side and ionic liquids side were fabricated via an anion-exchange reaction. • Compared with the traditional two-phase catalytic system, the emulsified catalytic degradation exhibited better performance on pollutant removal. • The mechanism of catalytic degradation for methyl orange based on Janus emulsification was investigated. • The Janus emulsion could be easily demulsified and exhibited excellent reusability. Amphiphilic Janus nanosheets with an asymmetric structure of non-polar phenyl side and polar ionic liquid side (1-Butyl-3-methylimidazolium chloride, [BMIM]Cl), denoted as Janus-[BMIM]Cl, were prepared and used as a carrier to achieve the integration of catalyst and emulsifier. Catalytic heteropolyanions (e.g., [PW 12 O 40 ]3-, [PMo 12 O 40 ]3- or [SiW 12 O 40 ]4-) were selectively decorated on the polar side induced by anion-exchange of [BMIM]Cl moieties, Janus catalysts (Janus-[BMIM][heteropolyanions]) were assembled and utilized as an open degradation platform for azo dyes such as methyl orange (MO). Morphology, structure, and properties were characterized by SEM, FT-IR, XPS, UV–Vis, Zeta potential, etc. The inbuilt amphipathy of Janus nanosheets endowed the decolorization process of dyes to perform in the emulsified system. The extremely increased interface coupled with the effective dispersion of catalysts at the interface synergistically improved the catalytic degradation performance. Compared with the decolorization catalyzed in a conventional immiscible system, the removal efficiency of MO achieved in the Janus emulsion greatly improved from 78.6 to 98.2% within 3 h. Besides, the Janus emulsion could be demulsified easily by centrifugation, and the degradation efficiency was still maintained at 93.7% after five cycles. These results provide valuable information for exploring and enriching the applications of Janus functional materials. [ABSTRACT FROM AUTHOR]

Highlights: La3+/Na+ bimetallically doped vanadate, designed for the first time, is promising in many electrochemical applications (e.g., batteries, electrochromics). This is the first report of electrochromic displays employing bimetallically doped vanadate. It is demonstrated for the first time that zinc dendrites and vanadate dissolution are significantly inhibited by employing an aqueous hybrid Zn2+/Na+ electrolyte. Vanadates are a class of the most promising electrochromic materials for displays as their multicolor characteristics. However, the slow switching times and vanadate dissolution issues of recently reported vanadates significantly hinder their diverse practical applications. Herein, novel strategies are developed to design electrochemically stable vanadates having rapid switching times. We show that the interlayer spacing is greatly broadened by introducing sodium and lanthanum ions into V3O8 interlayers, which facilitates the transportation of cations and enhances the electrochemical kinetics. In addition, a hybrid Zn2+/Na+ electrolyte is designed to inhibit vanadate dissolution while significantly accelerating electrochemical kinetics. As a result, our electrochromic displays yield the most rapid switching times in comparison with any reported Zn-vanadate electrochromic displays. It is envisioned that stable vanadate-based electrochromic displays having video speed switching are appearing on the near horizon. [ABSTRACT FROM AUTHOR]

[Display omitted] Non-desirable solar energy absorption and poor charge transfer efficiency are two problems that limit the peroxymonosulfate (PMS) photocatalytic techniques. Herein, a metal-free boron-doped graphdiyne quantum dot (BGDs) modified hollow tubular g-C 3 N 4 photocatalyst (BGD/TCN) was synthesized to activate PMS and achieved effective space separation of carriers for degradation of bisphenol A. With 0.5 mM PMS, the degradation rate of bisphenol A (20 ppm) was 0.0634 min−1, 3.7-fold higher than that of TCN itself. The roles of BGDs in the distribution of electrons and photocatalytic property were well identified by experiments and density functional theory (DFT) calculations. The possible degradation intermediate products of bisphenol A were monitored by mass spectrometer and demonstrated to be nontoxic using ecological structure activity relationship modeling (ECOSAR). Finally, this newly-designed material was successfully applied in actual water bodies, which further renders its promising prospect for actual water remediation. [ABSTRACT FROM AUTHOR]

Vanadium oxides are highly valued as electrochromic materials because of their multicolor capabilities. However, their practical applications have been limited due to challenges such as the dissolution of vanadate into aqueous electrolytes, leading to poor long‐term stability. Herein, a solution is proposed to the vanadate dissolution issue by utilizing a hybrid electrolyte consisting of tetraethylene glycol dimethyl ether (TEGDME) and water. This electrolyte has the unique ability to form a robust cathode electrolyte interface layer on vanadium oxide electrodes. As a proof of concept, zinc‐anode‐based multicolor transparent electrochromic displays are prepared using layered potassium vanadate (K2V6O16·1.5H2O, KVO) with a TEGDME–water hybrid electrolyte. By soaking the KVO electrode in the hybrid electrolyte, it is demonstrated that KVO has remarkable stability against dissolution. Furthermore, it is shown that KVO has superior electrochromic performance compared to sodium vanadate (NaV3O8·1.5H2O, SVO), due to the wide KVO interlayer spacing. Given the enhanced performance of this hybrid electrolyte and KVO cathode material, a zinc‐anode‐based electrochromic display prototype is shown to exhibit compelling performance. As such, this work is expected to be a significant catalyst for accelerating the development of vanadate‐based electrochromic displays. [ABSTRACT FROM AUTHOR]

Colloidal dot-, rod-, and tetrapod-shaped CdTe nanocrystals (NCs) are obtained by varying the precursor concentration and the ligands. Both the dot- and rod-shaped NCs are of zinc-blende phase, whereas the tetrapod-shaped NCs are a mixture of zinc-blende and wurtzite structures. It is proposed that the concentration of stacking faults forming during NCs’ growth plays an important role in the geometry of CdTe NCs. [ABSTRACT FROM AUTHOR]

In the literature, lead halide perovskites are very notable for their degradation in the presence of polar solvents, such as water. In contrast, in this research, it is observed that adding a minor amount of water into the precursor solution can improve the stability and photoluminescence quantum yield of CsPbBr3 nanocrystals through a ligand‐assisted reprecipitation (LARP) method. In this way, the shape and phase transformation from CsPbBr3 nanoplates to CsPbBr3/Cs4PbBr6 nanorods and Cs4PbBr6 nanowires can be controlled with increasing water content in the precursor solution. Upon adding water up to an ideal amount, CsPbBr3 maintains its phase and nanoplate morphology. The key role of water amount for tuning the crystallinity, stability, morphology, optical properties, and phase transformation of cesium lead halide perovskite nanocrystals will be beneficial in the future commercialization of optoelectronics. [ABSTRACT FROM AUTHOR]

Most lead‐free halide double perovskite materials display low photoluminescence quantum yield (PLQY) due to the indirect bandgap or forbidden transition. Doping is an effective strategy to tailor the optical properties of materials. Herein, efficient blue‐emitting Sb3+‐doped Cs2NaInCl6 nanocrystals (NCs) are selected as host, rare‐earth (RE) ions (Sm3+, Eu3+, Tb3+, and Dy3+) are incorporated into the host, and excellent PLQY of 80.1% is obtained. Femtosecond transient absorption measurement found that RE ions not only served as the activator ions but also filled the deep vacancy defects. Anti‐counterfeiting, optical thermometry, and white‐light‐emitting diodes (WLEDs) are exhibited using these RE ions‐doped halide double perovskite NCs. For the optical thermometry based on Sm3+‐doped Cs2NaInCl6:Sb3+ NCs, the maximum relative sensitivity is 0.753% K−1, which is higher than those of most temperature‐sensing materials. Moreover, the WLED fabricated by Sm3+‐doped Cs2NaInCl6:Sb3+ NCs@PMMA displays CIE color coordinates of (0.30, 0.28), a luminous efficiency of 37.5 lm W−1, a CCT of 8035 K, and a CRI over 80, which indicate that Sm3+‐doped Cs2NaInCl6:Sb3+ NCs are promising single‐component white‐light‐emitting phosphors for next‐generation lighting and display technologies. [ABSTRACT FROM AUTHOR]

The Zn anode-based electrochromic energy storage devices (EESDs) provide a promising strategy to overcome the contradiction of electrochromism and energy storage for efficient devices. In this regard, the device configuration can endow the electrochromic devices with superior electrochromic performance and excellent energy recovery efficiencies. [Display omitted] With the emerging demand of multifunctional optoelectronic devices, the integration of electrochromism and energy storage functionalities within a single platform has become a research frontier in the electrochromic community. However, the conventional electrochromic function is inherently contradictory to the energy storage function in electrochromic devices. In this review, we firstly introduced the working principles and device configurations of the rudimentary electrochromic energy storage devices (EESDs), where the origin of the contradiction between electrochromic and energy storage functionalities is comprehensively introduced. We then reviewed the current status and applications of EESDs, where we hope to clearly reveal the developing trends of the EESDs. Finally, we proposed our perspectives on the design strategy of zinc anode-based electrochromic devices for overcoming the contradiction between electrochromism and energy storage of EESDs. [ABSTRACT FROM AUTHOR]

[Display omitted] • PU copolymers based on polysiloxane soft segment and disiloxane chain extender exhibit certain crystallinity and possess shape memory function. • The combined effect of the soft segment and the chain extender leads to partial crystallization of the copolymers. • The unique crystallization kinetics of the typical flexible chain of -(Si-O-Si) x - plays a major role in forming crystalline hard segment domains. Partial crystalline polysiloxane-based polyurethane copolymers were prepared by using hydroxyethoxypropyl capped polydimethylsiloxane (PDMS) as soft segment and α,ω-(bis (hydroxyethylthioether) ethyl)-disiloxane as chain extender. Due to this partial crystalline structure, the copolymer shows fairly good tensile properties and multiple shape deformation property. Repeated tensile tests revealed that stretch led to crystal destruction, and the microstructure of samples became stable after twice stretches. The lost crystallinity got 85.1% recovered upon treated at 60 °C for 1 h. It was proved that partial crystallization properties of the polysiloxane-polyurethane copolymer were from combined effects of polysiloxane soft segment and disiloxane chain extender. This unique crystallization kinetics of -(Si-O-Si) x - structure coexisting in soft and hard segments is regarded as one main reason to form crystalline hard segment domains in a common two-step synthesis. [ABSTRACT FROM AUTHOR]

Wide‐coverage near infrared (NIR) phosphor‐converted LEDs possess promising potential for practical applications, but little is developed towards the efficient and wide‐coverage NIR phosphors. Here, we report the single‐component lanthanide (Ln3+) ions doped Cs2M(In0.95Sb0.05)Cl6 (M=alkali metal) nanocrystals (NCs), exhibiting emission from 850 to 1650 nm with high photoluminescence quantum yield of 20.3 %, which is accomplished by shaping the multiple metal halide octahedra of double perovskite via the simple alkali metal substitution. From Judd‐Ofelt theoretical calculation and spectroscopic investigations, the shaping of metal halide octahedra in Cs2M(In1−xSbx)Cl6 NCs can break the forbidden of f‐f transition of Ln3+, thus increasing their radiative transition rates and simultaneously boosting the energy transfer efficiency from host to Ln3+. Finally, the wide‐coverage NIR LEDs based on Sm3+, Nd3+, Er3+‐tridoped Cs2K0.5Rb0.5(In0.95Sb0.05)Cl6 NCs are fabricated and employed in the multiplex gas sensing and night‐vision application. [ABSTRACT FROM AUTHOR]

Wide‐coverage near infrared (NIR) phosphor‐converted LEDs possess promising potential for practical applications, but little is developed towards the efficient and wide‐coverage NIR phosphors. Here, we report the single‐component lanthanide (Ln3+) ions doped Cs2M(In0.95Sb0.05)Cl6 (M=alkali metal) nanocrystals (NCs), exhibiting emission from 850 to 1650 nm with high photoluminescence quantum yield of 20.3 %, which is accomplished by shaping the multiple metal halide octahedra of double perovskite via the simple alkali metal substitution. From Judd‐Ofelt theoretical calculation and spectroscopic investigations, the shaping of metal halide octahedra in Cs2M(In1−xSbx)Cl6 NCs can break the forbidden of f‐f transition of Ln3+, thus increasing their radiative transition rates and simultaneously boosting the energy transfer efficiency from host to Ln3+. Finally, the wide‐coverage NIR LEDs based on Sm3+, Nd3+, Er3+‐tridoped Cs2K0.5Rb0.5(In0.95Sb0.05)Cl6 NCs are fabricated and employed in the multiplex gas sensing and night‐vision application. [ABSTRACT FROM AUTHOR]

Cobalt-free layered perovskite LnBa 0.5 Sr 0.5 Cu 2 O 5+δ (Ln = Pr and Nd, PBSC and NBSC) powders are prepared using combined citrate and EDTA complexing method. The performance of PBSC and NBSC cathode materials are evaluated for solid oxide fuel cells (SOFCs). Two oxidation states (Cu 2+ /Cu + ) for Cu ions exist in LnBa 0.5 Sr 0.5 Cu 2 O 5+δ oxides. The main valence of Pr ions in PBSC is 3+. The average thermal expansion coefficients (TECs) of PBSC and NBSC are 14.2 and 14.6 × 10 −6 K −1 between 30 and 950 °C, which are similar to the TECs of La 0.9 Sr 0.1 Ga 0.8 Mg 0.2 O 3 − δ (LSGM) intermediate-temperature electrolyte. The electrical conductivity of PBSC is slightly higher than that of NBSC. At 800 °C, the polarization resistance ( R p ) values of the PBSC and NBSC cathodes on the LSGM electrolyte are 0.043 and 0.057 Ω cm 2 , respectively. The electrolyte-supported single cells were prepared by using PBSC and NBSC as cathode, LSGM as electrolyte (300 μm thickness), Ce 0.9 Sm 0.1 O 1.95 (SDC) as interlayer and Ni/SDC as anode. At 850 °C, the maximal power densities are obtained as 681 and 651 mW cm −2 for PBSC and NBSC cathodes. [ABSTRACT FROM AUTHOR]

Dramatic advances in wearable electronics have triggered tremendous demands for wearable power sources. To mitigate the impact of CO2 emission on the environment caused by energy consumption, biomechanical energy harvesting for self‐powered wearable electronics offers a promising solution. The output power of devices largely relies on the surface charge density, where adhesion interfaces generate a higher amount than nonadhesion counterparts, yet unfavorable for wearable devices due to the large detachment force required. Thus, sustaining high surface charge density in an adhesion‐free interface represents a major challenge. Herein, by leveraging intermolecular interactions and solvent evaporation induced phase separation, a nonadhesion interface is successfully realized, minimizing the interfacial adhesion from 20 to 0 kPa. Importantly, benefiting from the induced nano/microscale topography upon phase separation, comparable surface charges are generated at the interface. Consequently, a high‐performance flexible biomechanical energy harvester featuring a record high peak power density of 20.5 W m‐2 Hz‐1 at low matching impedance of 1 MΩ is achieved under a low biomechanical input force of 5 N. The device can power small electronics by harvesting regular or intermittent biomechanical energy and illuminate light‐emitting diodes wired/wirelessly. This work provides a facile strategy for interfacial engineering toward efficient energy harvesting. [ABSTRACT FROM AUTHOR]

Flexible perovskite light‐emitting diodes (LEDs) have been highly expected to realize advanced wearable optoelectronic applications due to the excellent optoelectronic properties of perovskites. However, the poor water and oxygen stability and limited flexibility of perovskites prevent their commercialization and applications in flexible LEDs. Herein, the low‐cost and green biomass materials‐ethyl cellulose (EC) is added in the CsPbI3 nanocrystals (NCs), acting as a cross‐linker between neighboring halide octahedra through hydrogen bonds and PbO coordination bonds. It reduces the defect densities of NCs, leading to improved photoluminescence quantum yield. Simultaneously, the synergistic effect of efficient defect passivation and hydrophobic ether groups of EC significantly improve the environment stability of NCs. Additionally, the favorable flexibility of EC and cross‐linking between EC and perovskite NCs improve the deformation resistance of the perovskite layer with stable photoluminescence and negligible cracks after repeated bending. Consequently, flexible LEDs based on the EC‐passivated CsPbI3 NCs achieved a record external quantum efficiency of 12.1% and significantly enhanced operational stability. Moreover, the flexible LEDs show small luminance degradation after bending for 1000 cycles at a radius of 3 mm, and still retain high performance even after repeatedly bending at an ultrasmall bending radius of 1 mm. [ABSTRACT FROM AUTHOR]

[Display omitted] • Acidic IL-based liposomes of poly[MimA11, A11][heteropolyanions] were fabricated to achieve efficient catalytic degradation of methyl orange. • Uniformly arranged IL units provided anchor points for the attachment of catalytic heteropolyanions through anion exchange. • Isotropic enrichment of catalysts, combined with the emulsion-like interface, synergistically enhanced the catalytic degradation activity. • Poly[MimA11, A11][heteropolyanions] displayed excellent regeneration and reusability. Amphiphilic ionic liquids (ILs) with an imidazole head and two undecene tails (abbreviated as [MimV 11 , V 11 ]Br) were synthesized through alkylation reaction. They were utilized as lipoid monomers for constructing an isotropic catalytic degradation platform of azo dyes. The spherical structure of this IL-based liposome was reinforced by cross-linking polymerization of the olefin tails. The imidazole groups served as anchor points for attaching catalytic heteropolyanions (such as [PW 12 O 40 ]3-, [PMo 12 O 40 ]3-) to the liposomal vehicle. Furthermore, the arrangement of these linkers on the liposome surface facilitated the trapping and enrichment of the catalytic species. Consequently, a series of isotropic catalysts decorated with heteropolyanions (poly[MimA 11 , A 11 ][heteropolyanions]) were prepared through anion exchange, where sufficiently exposed heteropolyanions maximized the catalytic degradation activity. The morphology, structure, and properties of the catalysts were confirmed using SEM, TEM, FTIR, XPS, UV–vis, and GC–MS. Experimental results found that poly[MimA 11 , A 11 ][PW 12 O 40 ] was the optimal catalyst, achieving a removal efficiency of 97.2% for methyl orange (MO) within 3 h. The intermediates involved in the reaction were analyzed to propose the degradation pathway of MO. Moreover, this kind of solid catalyst could be recovered by centrifugation, and its degradation efficiency remained above 91% even after five cycles. This research provides valuable insights for expanding the applications of IL-functionalized materials. [ABSTRACT FROM AUTHOR]

The article discusses various reports published within the issue including one on synthesis of single crystalline ZnTe hierarchical nanostructures and another on the synthesis of CdSe and CdTe quantum dots.

Plasmon stimulation represents an appealing way to modulate enzyme mimic functions, but utilization efficiency of plasmon excitation remains relatively low. To overcome this drawback, a heterojunction composite based on graphdiyne nanowalls wrapped hollow copper sulfide nanocubes (CuS@GDY) with strong localized surface plasmon resonance (LSPR) response in the near‐infrared (NIR) region is developed. This nanozyme can concurrently harvest LSPR induced hot carriers and produce photothermal effects, resulting in dramatically increased peroxidase‐like activity when exposed to 808 nm light. Both experimental results and theoretical calculations show that the remarkable catalytic performance of CuS@GDY is due to the unique hierarchical structure, narrow bandgap of GDY nanowalls, LSPR effect of CuS nanocages, fast interfacial electron transfer dynamics, and carbon vacancies on CuS@GDY. This plasmonic nanozyme exhibits rapid, efficient, broad‐spectrum antibacterial activity (>99.999%) against diverse pathogens (methicillin‐resistant Staphylococcus aureus, Staphylococcus aureus, and Escherichia coli). This study not only sheds light on the mechanism of the nanozyme‐/photocatalysis coupling process, but also opens up a new avenue for engineering plasmonic NIR light driven nanozymes for rapid synergistic photothermal and photo‐enhanced nanozyme therapy. [ABSTRACT FROM AUTHOR]

Although light‐emitting devices (LEDs) based on metal halide perovskite nanocrystals (PNCs) developed rapidly in recent years, the luminance of pure red LEDs with the Rec. 2020 standard Commission Internationale de l'Eclairage 1931 color coordinates of (0.708, 0.292) cannot meet the requirement of outdoor display. Herein, a facile in situ modification strategy is proposed to prepare the efficiently luminescent CsPb(Br/I)3 PNCs, where metal bromides are used to create a halide‐rich environment and inhibit the formation of nonradiative surface defects. Synchronously, appropriately increased surface ligands improved the effective exciton confinement. Hence, the modified CsPb(Br/I)3 PNCs exhibited a high photoluminescence quantum yield of 92.0%. Additionally, the electrical conductivity is improved due to the increased hole mobility, and the Auger process is inhibited caused by balanced carrier mobilities. Consequently, LEDs based on the modified CsPb(Br/I)3 PNCs exhibited a maximum luminance of 11233 cd m−2 with the pure red color coordinate (0.704, 0.292) and a peak external quantum efficiency value of 13.2%. Furthermore, the luminance reached 5198 cd m−2 under the driving voltage of 4.4 V. This is the first study to realize a pure red PNC LED with high luminance under low bias, which can meet the requirement of outdoor display. [ABSTRACT FROM AUTHOR]

Although light‐emitting devices (LEDs) based on metal halide perovskite nanocrystals (PNCs) developed rapidly in recent years, the luminance of pure red LEDs with the Rec. 2020 standard Commission Internationale de l'Eclairage 1931 color coordinates of (0.708, 0.292) cannot meet the requirement of outdoor display. Herein, a facile in situ modification strategy is proposed to prepare the efficiently luminescent CsPb(Br/I)3 PNCs, where metal bromides are used to create a halide‐rich environment and inhibit the formation of nonradiative surface defects. Synchronously, appropriately increased surface ligands improved the effective exciton confinement. Hence, the modified CsPb(Br/I)3 PNCs exhibited a high photoluminescence quantum yield of 92.0%. Additionally, the electrical conductivity is improved due to the increased hole mobility, and the Auger process is inhibited caused by balanced carrier mobilities. Consequently, LEDs based on the modified CsPb(Br/I)3 PNCs exhibited a maximum luminance of 11233 cd m−2 with the pure red color coordinate (0.704, 0.292) and a peak external quantum efficiency value of 13.2%. Furthermore, the luminance reached 5198 cd m−2 under the driving voltage of 4.4 V. This is the first study to realize a pure red PNC LED with high luminance under low bias, which can meet the requirement of outdoor display. [ABSTRACT FROM AUTHOR]

Graphdiyne supported hemin (Hemin-GDY) nanocomposite is a biomimetic designed 2D peroxidase-like nanozyme that catalyses the decomposition of H 2 O 2 to produce massive highly reactive oxygen species (ROS). This nanozyme exhibits outstanding activity and stability for efficient catalytic degradation of multiple organic pollutants. [Display omitted] Effective electronic interactions between molecular catalysts and supports are critical for heterogeneous enzyme mimics, yet they are frequently neglected in most catalyst designs. Taking the enzyme mimics of hemin immobilized on graphdiyne (Hemin-GDY) as an example, we explicate for the first time the underlying role of GDY as a co-catalyst. Based on the robust conjugation between GDY and hemin, the delocalized π-electrons in GDY act as a ligand for Fe ions so that the orbital interactions including electron transport from GDY → Fe can induce the formation of an electron-rich Fe center and an electron-deficient π-electron conjugated system. This mechanism was validated by electron paramagnetic resonance (EPR), Raman spectroscopy, and DFT calculations. Moreover, both EPR spetra and Lineweaver-Burk plots revealed that Hemin-GDY could efficiently catalyze the decomposition of hydrogen peroxide (H 2 O 2) to produce hydroxyl radical (•OH) and superoxide anion (O 2 •–) by a ping-pong type catalytic mechanism, and particularly, the catalytic activity was increased by 2.3-fold comparing to that of hemin immobilized on graphene (Hemin-GR). In addition, Hemin-GDY with the exceptional activity and stability was demonstrated for efficient catalytic degradation of organic pollutants under acidic conditions. Collectively, this work provides a theoretical basis for the design of GDY supported catalysts and renders great promises of the GDY based enzyme mimics. [ABSTRACT FROM AUTHOR]

0D perovskites have gained much attention in recent years due to their fascinating properties derived from their peculiar structure with isolated metal halide octahedra or metal halide clusters. However, the systematic discussion on the crystal and electronic structure of 0D perovskites to further understand their photophysical characteristics and the comprehensive overview of 0D perovskites for their further applications are still lacking. In this review, the unique crystal and electronic structure of 0D perovskites and their diverse properties are comprehensively analyzed, including large bandgaps, high exciton binding energy, and largely Stokes‐shifted broadband emissions from self‐trapped excitons. Furthermore, the photoluminescence regulation are discussed. Then, the various synthetic methods for 0D perovskite single crystals, nanocrystals, and thin films are comprehensively summarized. Finally, the emerging applications of 0D perovskites to light‐emitting diodes, solar cells, detectors, and some others are illustrated, and the outlook on future research in the field is also provided. [ABSTRACT FROM AUTHOR]

Highlights: A reversible Zn2+ insertion in anatase TiO2 nanocrystals is reported for the first time. This is the first report regarding TiO2 for zinc-anode-based electrochromic devices, which will subsequently broaden its applications to zinc-ion electrochemical cells. A prototype device based on the TiO2 nanocrystals delivers a high optical modulation, fast response times, and robust electrochemical stability.Zinc-anode-based electrochromic devices (ZECDs) are emerging as the next-generation energy-efficient transparent electronics. We report anatase W-doped TiO2 nanocrystals (NCs) as a Zn2+ active electrochromic material. It demonstrates that the W doping in TiO2 highly reduces the Zn2+ intercalation energy, thus triggering the electrochromism. The prototype ZECDs based on W-doped TiO2 NCs deliver a high optical modulation (66% at 550 nm), fast spectral response times (9/2.7 s at 550 nm for coloration/bleaching), and good electrochemical stability (8.2% optical modulation loss after 1000 cycles). [ABSTRACT FROM AUTHOR]

The unbalanced charge transport is always a key influencing factor on the device performance of quantum dot light-emitting diodes (QLEDs), particularly for the blue QLEDs due to their large optical band gap. Here, a method of electron transport layer (ETL) doping was developed to regulate the energy levels and the carrier mobility of the ETL, which resulted in more balanced charge injection, transport and recombination in the blue emitting CdZnS/ZnS core/shell QLEDs. Consequently, an enhanced performance of blue QLEDs was achieved by modulating the charge balance through ETL doping. The maximum external quantum efficiency and luminance was dramatically increased from 2.2% to 7.3% and from 3786 cd m−2 to 9108 cd m−2, respectively. The results illustrate that charge transport layer doping is a simple and effective strategy to regulate the charge injection barrier and carrier mobility of QLEDs. [ABSTRACT FROM AUTHOR]

Pd-based nanostructures have high catalytic activity and good light trapping ability for photothermal catalysis. In this work, PdFe nanosheets (NSs) were synthesized through a hydrothermal method and efficiently catalyzed ethylene glycol electrooxidation reaction (EGOR). Under the irradiation of light, the mass activity of EGOR enhanced 1.78 times (from 4.02 to 7.17 A mg−1) comparing with no light, which was 18 times higher than commercial Pd/C. The high activity is attributed to the combination of high photothermal conversion efficiency and the exposure of high energy facet (111) of PdFe NSs. The effects of Pd/Fe ratio, light intensity, and wavelength were investigated. [ABSTRACT FROM AUTHOR]

Lead‐based halide perovskites have received great attention in light‐emitting applications due to their excellent properties, including high photoluminescence quantum yield (PLQY), tunable emission wavelength, and facile solution preparation. In spite of excellent characteristics, the presence of toxic element lead directly obstructs their further commercial development. Hence, exploiting lead‐free halide perovskite materials with superior properties is urgent and necessary. In this review, the deep‐seated reasons that benefit light emission for halide perovskites, which help to develop lead‐free halide perovskites with excellent performance, are first emphasized. Recent advances in lead‐free halide perovskite materials (single crystals, thin films, and nanocrystals with different dimensionalities) from synthesis, crystal structures, optical and optoelectronic properties to applications are then systematically summarized. In particular, phosphor‐converted LEDs and electroluminescent LEDs using lead‐free halide perovskites are fully examined. Ultimately, based on current development of lead‐free halide perovskites, the future directions of lead‐free halide perovskites in terms of materials and light‐emitting devices are discussed. [ABSTRACT FROM AUTHOR]

Hydrogel electrolytes are a promising advancement in electrochromic devices, as they combine the benefits of liquid- and solid-state electrolytes. They offer good performance in transparency, conductivities, flexibility, and interfacial stabilities. These electrolytes have a wide range of applications, including electrochromic wearable devices, smart windows, displays, and batteries. The article provides more details on this topic and is authored by Yadong Yang, William W. Yu, Haizeng Li, and their colleagues. William W. Yu is a professor at Shandong University with research interests in various nanomaterials and technologies, while Haizeng Li is a professor at Shandong University focusing on electrochromic devices, wearable electronics, energy storage, and radiative heat transfer. [Extracted from the article]

Background. Comprehensive information on determinants and patterns of use and spending for ambulatory physical therapy services is needed to inform health planning and policy decisions. Most research in the literature on this topic is limited to specific payers, age groups, and conditions. Objective. The purpose of this study was to examine factors associated with the resource intensity of physical therapy episodes for adults in the United States as measured by number of visits and expenses per visit. Design. This study was a secondary analysis of longitudinal survey data from the Medical Expenditure Panel Survey (MEPS) panels 9, 10, and 11. Methods. An analytic file was created based on data from the longitudinal data files for 3 MEPS panels and the annual office-based and hospital outpatient event files. A total of 1,377 episodes of physical therapy care were identified. Variation in both the total number of visits per episode and expenses per visit was examined by fitting regression models to evaluate the effects of selected independent variables classified into 4 categories: episode-level variables, demographic characteristics, geographic variables, and health status indicators. Results. Average total expenses per episode (in 2007 dollars) were $1,184 (median$651), with an average number of visits per episode of 9.6 (median=6.0) and average expenses per visit of $130 (median=$95). Significant variation by geographic characteristics, sex, and one comorbid condition (high blood pressure) was found in the number of visits model. In the expenditures model, expenses per visit were associated with age/insurance coverage, setting (hospital outpatient versus office based), primary condition category, and mental health status. Limitations. Limitations include limited sample sizes of physical therapy users and lack of detailed clinical information. Conclusions. Variability in the resource intensity of physical therapy episodes is influenced to some degree by nonclinical variables. [ABSTRACT FROM AUTHOR]

A series of finely dispersed poly(vinyl-2-pyrrolidone)- stabilized platinum colloidal nanocatalysts (PVP-Pt) were prepared and characterized by TEM. Hydrogenation of monochlorobenzene (MCB) was carried out in a batch mode using hydrogen over PVP-Ptat298 K and atmospheric pressure. The product consisted of benzene and cyclohexane during the reaction, and nearly 100% selectivity to cyclohexane could be obtained at ∼100% conversion of MCB. The catalytic performance of the PVP-Pt colloids is dependent on the preparation conditions. The small amount of the stabilizing polymer (PVP) in the preparation of colloidal platinum could not protect the platinum colloid commendably, but the large amount of PVP hindered the contact of reactant with catalyst surface and the desorption of product Extra PVP added in the reaction system has some inhibiting effect on the reaction activity, and also resulting in some decrease in selectivity to cyclohexane. The reaction was verified to be first order to the concentration of MCB. The polymer-stabilized noble metal nanoparticles could be suitable to be hydrodehalogenation and reduction catalysts forthe remediation of various chloroaromatic compounds in the environment. [ABSTRACT FROM AUTHOR]

• Characterization of the nonlinear refraction coefficient of CsPbBr 1.5 I 1.5 QD. • Investigation of the averaged second-order hyperpolarizability of the perovskite QD. • Analyses of the SSPM diffraction symmetry from the perovskite QD. • Demonstration of the SSPM-mediated all-optical switching. The averaged second-order hyperpolarizability of perovskite (CsPbBr 1.5 I 1.5) quantum dots (QDs) was characterized using the intensity-dependent spatial self-phase modulation (SSPM). The radial intensity variation of the Gaussian beam displayed the diffraction profile of concentric rings at the far-field due to the coherent superposition of transverse wave vectors with characteristic spatial nonlinear phases. The number of concentric rings as a function of input-intensity revealed the nonlinear refraction coefficients of the QDs. The nonlinear refraction coefficient or the real part of third-order nonlinear susceptibility as a function of concentration of QDs characterized the averaged second-order hyperpolarizability which is the nonlinear refraction coefficient of a single perovskite QD. The vertically asymmetric diffraction ring of SSPM indicates the phase distortion of the optical field due to the heat convection. All-optical switching characteristics of perovskite QDs is attributable to the intensity-modulated SSPM. The input intensity of optical switching by the SSPM was estimated to be ~1.05 MW/m2. [ABSTRACT FROM AUTHOR]

Magnetic separations at very low magnetic field gradient (< tesla per meter) can now be applied to diverse problems, such as point-of-use water purification and the simultaneous separation of complex mixture. High-Surface area and monodisperse magnetic (Fe3 O4) nanocrystals (NCs) were shown to respond to low fields in a size-dependent fashion. The particles apparently do not act independently in the separation but rather reversibly aggregate through the resulting high-field gradients present at their surface. Using the high specific surface area of Fe3O4 NCs that were 12 nanometers in diameter, we reduced the mass of waste associated with arsenic removal from water by orders of magnitude. Additionally, the size dependence of magnetic separation permitted mixtures of 4- and 12-nanometers-sized Fe3O4 NCs to be separated by the application of different magnetic fields. [ABSTRACT FROM AUTHOR]

Highlights: A reversible Zn2+ insertion in anatase TiO2 nanocrystals is reported for the first time. This is the first report regarding TiO2 for zinc-anode-based electrochromic devices, which will subsequently broaden its applications to zinc-ion electrochemical cells. A prototype device based on the TiO2 nanocrystals delivers a high optical modulation, fast response times, and robust electrochemical stability.Zinc-anode-based electrochromic devices (ZECDs) are emerging as the next-generation energy-efficient transparent electronics. We report anatase W-doped TiO2 nanocrystals (NCs) as a Zn2+ active electrochromic material. It demonstrates that the W doping in TiO2 highly reduces the Zn2+ intercalation energy, thus triggering the electrochromism. The prototype ZECDs based on W-doped TiO2 NCs deliver a high optical modulation (66% at 550 nm), fast spectral response times (9/2.7 s at 550 nm for coloration/bleaching), and good electrochemical stability (8.2% optical modulation loss after 1000 cycles). [ABSTRACT FROM AUTHOR]

LED light bulbs that simulate solar spectrum were fabricated using CdSe core–shell quantum dots in combination with GaN blue-light chips. They exhibited excellent optical properties such as white CIE coordinates of (0.33, 0.33), high color rendering index (CRI) of 98 and correlated color temperature (CCT) of 5352 K. Moreover, a circuit system was used to control the LEDs so that the lighting spectrum changes with the time in a day to simulate the actual solar spectrum. The results show that the sun-like spectrum smart bulbs not only have good optical properties and high electrical stability, but also can automatically adjust their spectrum according to the time, making the lighting natural. This work makes sun-like lighting conditions for some special environments to promote the application of smart bulbs in smart lighting. [ABSTRACT FROM AUTHOR]

Graphdiyne (GDY) as an emerging carbon nanomaterial has attracted increasing attention because of its uniformly distributed pores, highly π-conjugated, and tunable electronic properties. These excellent characteristics have been widely explored in the fields of energy storage and catalysts, yet there is no report on the development of sensors based on the outstanding optical property of GDY. In this paper, a new sensing mechanism is reported built upon the synergistic effect between inner filter effect and photoinduced electron transfer. We constructed a novel nanosensor based upon the newly-synthesized nanomaterial and demonstrated a sensitive and selective detection for both Fe3+ ion and ascorbic acid, enabling the measurements in real clinical samples. For the first time fluorescent graphdiyne oxide quantum dots (GDYO-QDs) were prepared using a facile ultrasonic protocol and they were characterized with a range of techniques, showing a strong blue-green emission with 14.6% quantum yield. The emission is quenched efficiently by Fe3+ and recovered by ascorbic acid (AA). We have fabricated an off/on fluorescent nanosensors based on this unique property. The nanosensors are able to detect Fe3+ as low as 95 nmol L−1 with a promising dynamic range from 0.25 to 200 μmol L−1. The LOD of AA was 2.5 μmol L−1, with range of 10–500 μmol L−1. It showed a promising capability to detect Fe3+ and AA in serum samples. [ABSTRACT FROM AUTHOR]

2D transition metal carbides, nitrides, and carbonitrides called MXenes show outstanding performance in many applications due to their superior physical and chemical properties. Herein, a ZnO–MXene mixture with different contents of Ti3C2 is applied as electron transport layers (ETLs) and the influence of the Ti3C2 MXene in all‐inorganic metal halide perovskite nanocrystal light‐emitting diodes (perovskite NC LEDs) is explored. The addition of Ti3C2 makes more balanced charge carrier transport in LEDs by changing the energy level structure and electron mobility of ETL. Moreover, lower surface roughness is obtained for the ETL, thus guaranteeing uniform distribution of the perovskite NCs layer and further reducing leakage current. As a result, a 17.4% external quantum efficiency (EQE) with low efficiency roll‐off is achieved with 10% Ti3C2, which is a 22.5% improvement compared to LEDs without Ti3C2. [ABSTRACT FROM AUTHOR]

One‐dimensional semiconductor nanostructures have already been used for a variety of optoelectronic applications. Metal halide perovskites have emerged in recent years as promising high‐performance optoelectronic materials, but reports on 1D nanorods (NRs) of all‐inorganic halide perovskites are still scarce. This work demonstrates a synthetic strategy toward cesium‐based inorganic perovskite NRs by exploiting composition‐controlled crystal phase engineering. It is accomplished for Cd‐rich mixed‐cation CsPb1‐xCdxBr3 nanocrystals, where the initial 1D hexagonal perovskite phase drives the growth of the 1D NRs, as supported by first‐principles calculations. The band gaps of the resulting NRs are tunable by varying the Cd‐content, and the highly uniform CsPb0.08Cd0.92Br3 NRs (with an average length of 84 nm and width of 16 nm) exhibit a true blue‐color emission centered at 460 nm, with a high quantum yield of 48%. Moreover, this work also demonstrates the tunability of the Fermi levels in the films made of CsPb1‐xCdxBr3 alloyed nanocrystals, where samples with highest Cd content show an increase of the electron concentration and a related increase in the conductivity. [ABSTRACT FROM AUTHOR]