Two-dimensional van der Waals heterostructures with exotic quantum phenomena have garnered a huge surge in the field of optoelectronic devices. Herein, we report spectroscopic evidence of efficient interfacial charge transfers at the interface of a novel 2D/2D V4C3Tx MXene/protonated g-C3N4 (PCN) heterostructured thin film, demonstrating robust photosensitivity and a large exciton activation energy of 139.5 meV. Through temperature-dependent photoluminescence (PL) and time-resolved PL spectroscopy, we unravel the photophysical mechanism driving efficient charge transfer and photosensitivity in V4C3Tx/PCN heterostructures. These heterostructures exhibit superior photosensitivity to white and UV light compared with either PCN or V4C3Tx pristine materials. Additionally, we observed significant PL quenching with unusual negative thermal quenching and extended charge carrier lifetime in the V4C3Tx/PCN heterostructures across a broad temperature range of 70-370 K. Notably, at the elevated temperature of 370 K, the carrier lifetime was enhanced by more than 2-fold, making the heterostructures promising for optoelectronic applications. This work provides critical insight into the charge transfer mechanism between V4C3Tx MXene and PCN, opening a new avenue for rationally designing g-C3N4-based heterostructures for highly photosensitive optoelectronic devices.

In recent decades, vapor sensors have gained substantial attention for their crucial roles in environmental monitoring and pharmaceutical applications. Herein, we introduce a chameleon-inspired colorimetric (CIC) sensor, detailing its design, fabrication, and versatile applications. The sensor seamlessly combines a PEDOT:PSS vapor sensor with a colorimetric display, using thermochromic liquid crystal (TLC). We further explore the electrical characteristics of the CIC sensor when doped with ethylene glycol (EG) and polyvinyl alcohol (PVA). Comparative analyses of resistance change rates for different weight ratios of EG and PVA provide insights into fine-tuning the sensor's responsiveness to varying humidity levels. The CIC sensor's proficiency in measuring ambient humidity is investigated under a voltage input as small as 2.6 V, capturing resistance change rates and colorimetric shifts at relative humidity (RH) levels ranging from 20% to 90%. Notably, the sensor exhibits distinct resistance sensitivities of 9.7 mΩ (0.02% ∆R/R0)/%RH, 0.5 Ω (0.86% ∆R/R0)/%RH, and 5.7 Ω (9.68% ∆R/R0)/%RH at RH 20% to 30%, RH 30% to 80%, and RH 80% to 90%, respectively. Additionally, a linear temperature change is observed with a sensitivity of -0.04 °C/%RH. The sensor also demonstrates a colorimetric temperature sensitivity of -82,036 K/%RH at RH 20% to 30% and -514 K/%RH at RH 30% to 90%, per captured image. Furthermore, real-time measurements of ethanol vapor with varying concentrations showcase the sensor's applicability in gas sensing applications. Overall, we present a comprehensive exploration of the CIC sensor, emphasizing its design flexibility, electrical characteristics, and diverse sensing capabilities. The sensor's potential applications extend to real-time environmental monitoring, highlighting its promising role in various gas sensing fields.

Semiconductor photodetectors, as photoelectric devices using optical-electrical signal conversion for detection, are widely used in various fields such as optical communication, medical imaging, environmental monitoring, military tracking, remote sensing, etc. Compared to the conventional photodetector materials including silicon, III-V semiconductors and metal sulfides, graphitic carbon nitride (g-C3N4) as a metal-free polymeric semiconductor, has many advantages such as low-price, easy preparation, efficient visible light response, and relatively good thermal stability. In the meantime, the polymer characteristics also endow the g-C3N4 with good mechanical properties. Apart from being used for photo(electro)catalysts during the past decades, the potential use of g-C3N4 in photodetectors has attracted great research interests very recently. In this review, we first briefly introduce the structure and properties of g-C3N4 and the key performance parameters of photodetectors. Then, combining the very recent progress, the review focuses on the active materials, fabrication methods and performance enhancement strategies for g-C3N4 based photodetectors. The existing challenges are discussed and the future development of g-C3N4 based photodetectors is also forecasted.

A general method for the direct synthesis of highly homogeneous and dense polymerized carbon nitride (PCN) nanosheet films on F: SnO2 (FTO) is developed. Detailed photoelectrochemical (PEC) water-splitting studies reveal that the as-synthesized PCN films exhibit outstanding performance as photoanode for PEC water-splitting. The optimal PCN photoanode exhibits excellent photocurrent density of 650 µA cm-2 , and monochromatic incident photon-to-electron conversion efficiency (IPCE) value up to 30.55% (λ = 400 nm) and 25.97% (λ = 420 nm) at 1.23 VRHE in 0.1 m KOH electrolyte. More importantly, the PCN photoanode has an excellent hole extraction efficiency of up to 70 ± 3% due to the abundance of active sites provided by the PCN photoanode nanosheet, which promotes the transport rates of OER-relevant species. These PCN films provide a new benchmark for PCN photoanode materials.

Template is frequently studied as a structure-directing agent to tune the nanomorphology of photocatalysts. However, the influences of template on the polymerization of precursors and compositions of the resulting samples are rarely considered. Herein, a biomass carbon-modified graphitic carbon nitride (CCNx) with a thin-layer morphology is synthesized via one-pot surface-assisted polymerization of melamine precursor on organic yeast. The formation of the hydrogen bond between melamine and yeast induces a strong interfacial confinement, giving rise to small-sized CCNx. In addition, the carbon materials derived from yeast dramatically broaden n → π* visible light harvesting, improve electron delocalization, and greatly enhance charge carrier separation. The optimized CCNx presents a much higher photocatalytic hydrogen production rate of 2704 μmol g^-1h^-1 under visible light irradiation (λ ≥ 420 nm), which is nearly 11-fold that of its pristine counterpart. This work realizes the synergistic effect between morphology tunning and composition tailoring by using biomass template, which shows a great potential in developing efficient metal-free photocatalysts.

Achieving intimate particle-to-particle and particle-to-substrate contacts is the first priority for fabricating high-quality photoelectrodes to ensure sufficient visible light absorption and efficient charge separation/transport. To achieve this goal, a seeding strategy is designed to construct a robust carbon nitride (CN) homojunction photoelectrode, in which vaporized precursors are condensed into a compact seeding layer at low temperatures, inducing the further deposition of the top layer. This optimized photoelectrode displays an excellent photocurrent density of 320 μA cm^-2 in 0.1 M NaOH electrolyte at 1.23 V_RHE (V vs reversible hydrogen electrode) under AM 1.5G illumination, with H₂ and O₂ evolution rates of 2.98 and 1.47 μmol h^-1 cm^-2, respectively. Characterizations show that both the robust contact and the homojunction of the double-layered CN film contribute to enhanced photoelectrochemical performance. This work may provide a new strategy for the design of high-performing CN photoelectrodes.

Formulation of heterojunction with remarkable high efficiency by utilizing solar light is promising to synchronously overcome energy and environmental crises. In this concern, hexagonal-borocarbonitride (h-BCN) based Z-schemes have proved potential candidates due to their spatially separated oxidation and reduction sites, robust light-harvesting ability, high charge pair migration and separation, and strong redox ability. H-BCN has emerged as a hotspot in the research field as a metal-free photocatalyst with a tunable bandgap range of 0-5.5 eV. The BCN photocatalyst displayed synergistic benefits of both graphene and boron nitride. Herein, the review demonstrates the current state-of-the-art in the Z-scheme photocatalytic application with a special emphasis on the predominant features of their photoactivity. Initially, fundamental aspects and various synthesis techniques are discussed, including thermal polymerization, template-assisted, and template-free methods. Afterward, the reaction mechanism of direct Z-scheme photocatalysts and indirect Z-scheme (all-solid-state) are highlighted. Moreover, the emerging Step-scheme (S-scheme) systems are briefly deliberated to understand the charge transfer pathway mechanism with an induced internal electric field. This review critically aims to comprehensively summarize the photo-redox applications of various h-BCN-based heterojunction photocatalysts including CO₂ photoreduction, H₂ evolution, and pollutants degradation. Finally, some challenges and future direction of h-BCN-based Z-scheme photocatalyst in environmental remediation are also proposed.

Localized excitons are expected to achieve high-performance electroluminescence and have been widely investigated in GaN-based light-emitting diodes (LEDs). Although carbon nanodot (CD) based LEDs have been achieved with the radiative recombination of electrons and holes, localized excitonic electroluminescence has been not reported before. In this Letter, localized excitonic electroluminescent devices have been fabricated using fluorescent CDs as an active layer. The CDs show strong localized excitonic yellow emission with a fluorescence quantum yield of 76% and Stokes shift of 2.1 eV. The CD-based LEDs present a sub-bandgap turn-on voltage of 2.4 V and a maximum luminance of 60.2 cd m^-2, which is the lowest driving voltage among the CD-based electroluminescent devices. Localized centers trap carriers effectively, resulting in sub-bandgap light emission. The current results manifest that localized excitons may furnish a promising approach to boost the development of CD-based LEDs.

The current study was designed to develop a single-step and simple approach to effectively fabricate three-dimensional raspberry-like In³⁺/NiO hierarchical nanostructures (In³⁺/NiO RLHNSs) as a modifier, which was subsequently characterized by the techniques of X-ray diffraction (XRD), energy dispersive spectrometry (EDS) and field emission scanning electron microscopy (FE-SEM). The new prepared nano-modifier was practically used to co-detect electrochemically sunset yellow and tartrazine dyes. Potent sensitivity and acceptable selectivity were obtained for the produced In³⁺/NiO RLHNSs to co-detect both the food colorants, thus providing oxidation peaks in differential pulse voltammetry (DPV) with a peak potential separation of ca. 190 mV. The results showed a 5.14-fold and 8.07-fold increase in the electrochemical response of our modified electrode to sunset yellow and tartrazine, respectively, compared to the control (the unmodified electrode). Limits of detection of 2.7 and 3.1 nM were calculated for sunset yellow and tartrazine, respectively. The results from the interaction of common food additives showed satisfactory outcomes for the application of this method in determining sunset yellow and tartrazine in several beverage specimens. Other useful documentation was obtained for the production of portable food additive sensors.