Photocatalytic reduction of CO₂ to produce valuable fuels or chemicals is a promising CO₂ utilization technology, which is of great significance for carbon emission reduction. The unique features of the UiO series of metal-organic frameworks (MOFs), such as the excellent water and chemical stability, notable structural tunability, broad and adjustable light-harvesting capacity, strong electron-hole separation ability, and high porosity and specific surface area, make them a class of photocatalysts with great potential for the CO₂ reduction reaction (CO₂RR). Significant progress has been made in the development of efficient UiO-based photocatalysts for CO₂RR. This paper provides a summary of recent research advances in UiO-MOFs for photocatalytic CO₂RR. The characteristics, synthesis methods, and modifications of UiO-based materials, along with their photocatalytic performance, are described. Various modification strategies for UiO-MOFs, including band-gap engineering, defect engineering, introduction of metal species, and construction of composite materials, are summarized and discussed. The challenges facing UiO-MOFs in photocatalytic CO₂RR and potential future development directions are also presented. This review is intended to provide insights into CO₂ photoreduction using UiO-based materials and to encourage further research and development in this promising field.

The development of high-performance narrowband red organic light-emitting diodes (OLEDs) has garnered significant attention, offering both exciting opportunities and formidable challenges. In this study, we report the synthesis of a novel red thermally activated delayed fluorescence (TADF) molecule, 10,10',10''-([1,2,4]triazolo[1,5-a][1,3,5]triazine-2,5,7-triyltris(benzene-4,1-diyl))tris(10H-phenoxazine) (TPXZ-TAZTRZ), which integrates a highly electron-deficient triazolotriazine unit as the acceptor and three strongly electron-donating phenoxazine (PXZ) moieties as donors. TPXZ-TAZTRZ exhibits a small singlet-triplet energy gap, enabling a rapid reverse intersystem crossing rate. Additionally, it shows a broad emission spectrum peaking at 634 nm, spanning the yellow-to-red region. These features render TPXZ-TAZTRZ as an ideal TADF sensitizer for narrowband red fluorescent OLEDs. Accordingly, TPXZ-TAZTRZ was employed to sensitize the conventional fluorescent emitter DBP. The resulting TADF-sensitized fluorescence OLEDs (TSF-OLEDs) demonstrated efficient energy transfer from the TADF sensitizer to the emitter, effectively addressing the limitations previous encountered with TADF systems. The devices achieved high-performance pure red emission, with Commission International de l'Éclairage (CIE) coordinates of [0.67, 0.33], an emission peak at 612 nm, a narrow full width at half maximum (FWHM) of 27 nm, and a maximum external quantum efficiency of 16.2%.

High-performance and long-lifetime blue organic light-emitting diodes (OLEDs) are crucial for meeting the demands of advanced display and lighting technologies. Despite high device efficiency has been achieved in blue OLEDs, development of high-performance and long-lifetime blue OLEDs still lag far behind their red/green counterparts due to the presence of long-lived high-energy triplet excitons and polarons. Given the critical role of charge and exciton management in both the emission and degradation processes of OLEDs, this review systematically summarizes strategies for suppressing charge leakage and exciton quenching, as well as for enhancing exciton utilization in blue fluorescent, phosphorescent, and thermally activated delayed fluorescent (TADF) OLEDs. In this context, we further discuss the roles of conventional fluorescent hosts, triplet-triplet annihilation/hot exciton hosts, TADF assistant hosts, phosphorescent assistant hosts, and exciplex/electroplex hosts in regulating charge and exciton dynamics in blue OLEDs. Additionally, the modification of emitting layer materials is highlighted as a key strategy for managing charge and exciton processes in efficient and stable solution-processed blue OLEDs. Based on current insights into the efficiency and operational stability of blue OLEDs, this review proposes feasible charge and exciton management strategies to address the current challenges.

Supercapacitors, renowned for their high-power density, rapid charge/discharge capabilities, and exceptional cycling stability, have emerged as promising solutions for sustainable and efficient energy storage. Among various electrode materials, carbon materials stands out due to its abundance, excellent electrical conductivity, chemical stability and structural versatility. This review explores the design strategies, performance optimization, and the expanding applications of carbon-based electrodes for supercapacitors. We first analyze the key factors that impact the performance of carbon electrodes for supercapacitors, including pore structure, surface chemistry, electrical conductivity and nanoscale architecture. Subsequently, we provide an in-depth analysis of recent advancements in the rational design of carbon materials, focusing on strategies for optimizing pore architecture, functionalizing surfaces, enhancing conductivity and designing nanostructures. By addressing performance limitations, the review highlights strategies that have significantly improved the efficiency of carbon electrodes. Furthermore, we explore the practical applications of carbon-based supercapacitors in wearable electronics, self-powered devices, and implantable systems. Lastly, we discuss the challenges and opportunities associated by carbon-based electrodes from the perspective of electrode design and practical application.