White-color organic light-emitting diodes (WOLEDs) have aroused wide interests for future lighting because of low energy consumption in principle, while still suffer from the degradation by Joule heating and polaron-induced quenching under high luminance caused by high current in practical. To obtain high current efficiency, which means high luminance at low current density, tandem WOLEDs with multiple electroluminescence (EL) units connected in series with charge generation layers (CGLs) have been developed. Here we report the improved hybrid tandem WOLED with two EL units, EL1 and EL2, where EL1 and EL2 generate fluorescent blue and phosphorescent yellow emissions from a metal-free material BCzVBi and a Ir-complex (fbi)₂Ir(acac), respectively, with CGL composed of a HATCN/NPB bilayer. The white-light emitting device shows the maximum current efficiency and power efficiency of 60.2 cd/A and 29.6 lm/W, respectively, without out-coupling structure. A low driving voltage of 6.5 V at 1,000 cd/m² is realized, which is an important value because such a luminance is required for actually employed lighting device. The blue emission appears from 5.4 V, and the light color changes from yellowish to bluish white during 5.4 V to 13.4 V, which could be explained by the energy level structures of the device and proved by the J-V characteristics. Additionally, this tandem WOLED also shows photovoltaic effect. This work provides a design of room light source whose color temperature could be tuned through applied voltage when needed, and a display system for low-current operated amorphous Si-TFT due to its high current efficiency.

Circularly polarized light (CPL) features electromagnetic vectors that rotate regularly in a plane perpendicular to the direction of propagation, transmitting optical chirality information that is imperceptible to human beings. CPL can be classified into the left-handed and right-handed circularly polarization light (L-/R-CPL), depending on whether the rotation direction is clockwise or anticlockwise, respectively. The ability to manipulate and characterize CPL is crucial for advancing various optical technologies, making the effective and direct detection of CPL extremely important. Breeding in the hotbed provided by the explosively increased chiral materials with CPL luminescence and strong circular dichroism (CD), CPL detectors are currently experiencing savage growth. Mainstream strategies can be divided into the leverage of photoactive materials with inherent chirality and the integration of chiral metamaterials with nonchiral photoactive materials. In this review, we not only highlight significant material innovations and detector architectures for CPL detection but also address the broader implications of these advancements. We discuss the challenges and future directions in this field, particularly focusing on how these developments could impact existing commodities, such as polarimetric imaging and security communications, and contribute to sustainability in technology through improved detection efficiency. Our goal is to inspire further promising developments in CPL photodetectors and encourage a broader application spectrum.

Blue emitters are highly desired in organic light-emitting diodes (OLEDs), but their electroluminescence efficiencies and roll-offs are always less than satisfactory. In this work, a triazine-based deep-blue emitter (2PhCzTRZ-Cz) is designed and synthesized. It prefers high thermal stability with a decomposition temperature of up to 543 °C, and possesses strong deep-blue photoluminescence. The doped OLEDs using 2PhCzTRZ-Cz as an emitter attain deep-blue lights at 418-424 nm, with high maximum external quantum efficiencies (η_extS) of 4.46-5.68%, maximum luminances of 2,820-7,400 cd m^-2, CIE_y values < 0.1 and small efficiency roll-offs. In addition, multiple-resonance thermally activated delayed fluorescence OLED by using 2PhCzTRZ-Cz as host realizes a high maximum η_ext of 21.5%, significantly higher than those of the device based on traditional mCBP host (12.9%). These outstanding performances demonstrate the great potential of 2PhCzTRZ-Cz as an emitter and host for OLEDs.

Incorporation of two dimensional (2D) materials into a polymer matrix is an efficient way to prepare high performance coatings. Here we report the in-situ mechanical exfoliation of graphite in a mixture of hydroxyethylacrylate terminated polybutadiene urethane (HTPU) prepolymer and reactive diluent. The mixture containing exfoliated graphite nanoplatelets (GN) is directly used to prepare UV cured composite resins (G/HTPU) with various GN concentrations. Various techniques, such as scanning electron microscopy (SEM), Raman, atomic force microscopy (AFM), have been used to characterize the GN, confirming that few-layered GN are obtained after the in-situ mechanical exfoliation. The incorporation of GN exerts little effect on the curing of the coatings with a gelation around 95%, but greatly enhances the elastic modulus. Tafel polarization curves, electrochemical impedance spectroscopy (EIS) and salt-spray testing were conducted to comparatively evaluate the G/HTPU coatings with different GN loadings. The results indicate that the incorporation of GN greatly improves the corrosion resistance of the HTPU UV coatings. The self-corrosion current density (I _corr) and the charge transfer resistance (R _c) of G/HTPU-2 (0.2% GN loading) are greatly reduced to 1.03 × 10^-8 A·cm^-2 and increased by two magnitudes, respectively, compared to those of the parent HTPU coating. Additionally, the G/HTPU-2 coating with thickness of 100 μm can protect galvanized sheet against 0.5 mol/l sulfuric acid for at least 24 h. The practical application in protection of electronics was illustrated by coating the G/HTPU-2 on a standard printed circuit board (PCB, IPC-B-24A). No corrosion was observed after it was immersed in an artificial sweat solution even under open-circuit voltage of 12 V for 72 h and then 24 V for 48 h.

Nitrogen/boron-based multi-resonance thermally activated delayed fluorescence (MR-TADF) materials offer advantages in terms of high photoluminescence quantum yield (PLQY) and narrowband emission, making them highly promising for display applications. Represented by ν-DABNA, diboron MR-TADF materials demonstrate the potential for high-efficiency narrowband emission. However, their large planar structures are susceptible to intermolecular interactions, thus increasing the complexity of device fabrication. In this research, our objective was to enhance the anti-aggregation capabilities of the diboron-based ν-DABNA by incorporating sterically hindered terphenyl groups. We synthesized two luminescent materials, DTPF-ν-DABNA and DTP-ν-DABNA, with intermolecular distances exceeding 4 Å in single-crystal stacking, significantly inhibiting intermolecular interactions. Both materials achieved an external quantum efficiency (EQE) exceeding 30% and full width at half maximum (FWHM) of no more than 22 nm, demonstrating characteristics of high-efficiency narrowband emission. Our research provides a straightforward and practical method to obtain MR-TADF materials with high device efficiency and low sensitivity to doping concentration.

White-color organic light-emitting diodes (WOLEDs) have aroused wide interests for future lighting because of low energy consumption in principle, while still suffer from the degradation by Joule heating and polaron-induced quenching under high luminance caused by high current in practical. To obtain high current efficiency, which means high luminance at low current density, tandem WOLEDs with multiple electroluminescence (EL) units connected in series with charge generation layers (CGLs) have been developed. Here we report the improved hybrid tandem WOLED with two EL units, EL1 and EL2, where EL1 and EL2 generate fluorescent blue and phosphorescent yellow emissions from a metal-free material BCzVBi and a Ir-complex (fbi)₂Ir(acac), respectively, with CGL composed of a HATCN/NPB bilayer. The white-light emitting device shows the maximum current efficiency and power efficiency of 60.2 cd/A and 29.6 lm/W, respectively, without out-coupling structure. A low driving voltage of 6.5 V at 1,000 cd/m² is realized, which is an important value because such a luminance is required for actually employed lighting device. The blue emission appears from 5.4 V, and the light color changes from yellowish to bluish white during 5.4 V to 13.4 V, which could be explained by the energy level structures of the device and proved by the J-V characteristics. Additionally, this tandem WOLED also shows photovoltaic effect. This work provides a design of room light source whose color temperature could be tuned through applied voltage when needed, and a display system for low-current operated amorphous Si-TFT due to its high current efficiency.

Circularly polarized light (CPL) features electromagnetic vectors that rotate regularly in a plane perpendicular to the direction of propagation, transmitting optical chirality information that is imperceptible to human beings. CPL can be classified into the left-handed and right-handed circularly polarization light (L-/R-CPL), depending on whether the rotation direction is clockwise or anticlockwise, respectively. The ability to manipulate and characterize CPL is crucial for advancing various optical technologies, making the effective and direct detection of CPL extremely important. Breeding in the hotbed provided by the explosively increased chiral materials with CPL luminescence and strong circular dichroism (CD), CPL detectors are currently experiencing savage growth. Mainstream strategies can be divided into the leverage of photoactive materials with inherent chirality and the integration of chiral metamaterials with nonchiral photoactive materials. In this review, we not only highlight significant material innovations and detector architectures for CPL detection but also address the broader implications of these advancements. We discuss the challenges and future directions in this field, particularly focusing on how these developments could impact existing commodities, such as polarimetric imaging and security communications, and contribute to sustainability in technology through improved detection efficiency. Our goal is to inspire further promising developments in CPL photodetectors and encourage a broader application spectrum.

Blue emitters are highly desired in organic light-emitting diodes (OLEDs), but their electroluminescence efficiencies and roll-offs are always less than satisfactory. In this work, a triazine-based deep-blue emitter (2PhCzTRZ-Cz) is designed and synthesized. It prefers high thermal stability with a decomposition temperature of up to 543 °C, and possesses strong deep-blue photoluminescence. The doped OLEDs using 2PhCzTRZ-Cz as an emitter attain deep-blue lights at 418-424 nm, with high maximum external quantum efficiencies (η_extS) of 4.46-5.68%, maximum luminances of 2,820-7,400 cd m^-2, CIE_y values < 0.1 and small efficiency roll-offs. In addition, multiple-resonance thermally activated delayed fluorescence OLED by using 2PhCzTRZ-Cz as host realizes a high maximum η_ext of 21.5%, significantly higher than those of the device based on traditional mCBP host (12.9%). These outstanding performances demonstrate the great potential of 2PhCzTRZ-Cz as an emitter and host for OLEDs.

Nitrogen/boron-based multi-resonance thermally activated delayed fluorescence (MR-TADF) materials offer advantages in terms of high photoluminescence quantum yield (PLQY) and narrowband emission, making them highly promising for display applications. Represented by ν-DABNA, diboron MR-TADF materials demonstrate the potential for high-efficiency narrowband emission. However, their large planar structures are susceptible to intermolecular interactions, thus increasing the complexity of device fabrication. In this research, our objective was to enhance the anti-aggregation capabilities of the diboron-based ν-DABNA by incorporating sterically hindered terphenyl groups. We synthesized two luminescent materials, DTPF-ν-DABNA and DTP-ν-DABNA, with intermolecular distances exceeding 4 Å in single-crystal stacking, significantly inhibiting intermolecular interactions. Both materials achieved an external quantum efficiency (EQE) exceeding 30% and full width at half maximum (FWHM) of no more than 22 nm, demonstrating characteristics of high-efficiency narrowband emission. Our research provides a straightforward and practical method to obtain MR-TADF materials with high device efficiency and low sensitivity to doping concentration.

Incorporation of two dimensional (2D) materials into a polymer matrix is an efficient way to prepare high performance coatings. Here we report the in-situ mechanical exfoliation of graphite in a mixture of hydroxyethylacrylate terminated polybutadiene urethane (HTPU) prepolymer and reactive diluent. The mixture containing exfoliated graphite nanoplatelets (GN) is directly used to prepare UV cured composite resins (G/HTPU) with various GN concentrations. Various techniques, such as scanning electron microscopy (SEM), Raman, atomic force microscopy (AFM), have been used to characterize the GN, confirming that few-layered GN are obtained after the in-situ mechanical exfoliation. The incorporation of GN exerts little effect on the curing of the coatings with a gelation around 95%, but greatly enhances the elastic modulus. Tafel polarization curves, electrochemical impedance spectroscopy (EIS) and salt-spray testing were conducted to comparatively evaluate the G/HTPU coatings with different GN loadings. The results indicate that the incorporation of GN greatly improves the corrosion resistance of the HTPU UV coatings. The self-corrosion current density (I _corr) and the charge transfer resistance (R _c) of G/HTPU-2 (0.2% GN loading) are greatly reduced to 1.03 × 10^-8 A·cm^-2 and increased by two magnitudes, respectively, compared to those of the parent HTPU coating. Additionally, the G/HTPU-2 coating with thickness of 100 μm can protect galvanized sheet against 0.5 mol/l sulfuric acid for at least 24 h. The practical application in protection of electronics was illustrated by coating the G/HTPU-2 on a standard printed circuit board (PCB, IPC-B-24A). No corrosion was observed after it was immersed in an artificial sweat solution even under open-circuit voltage of 12 V for 72 h and then 24 V for 48 h.