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Nitrogen-doped carbon dots (NCDs), exhibiting strong yellow emission in aqueous solution and solid matrices, have been utilized for fabricating heterostructure white electroluminescence devices. These devices consist of nitrogen-doped carbon dots as an emissive layer sandwiched between an organic hole transport layer (PEDOT:PSS) and an array of rutile TiO2 nanorods, acting as an electron transport layer. Under an applied forward bias of 5 V, the device exhibits broadband electroluminescence covering the wavelength range of 390–900 nm, resulting in pure white light emission characteristics at room temperature. The result demonstrates the successful fabrication of all solution-processed, low-cost, eco-friendly NCDs-based LEDs with CIE (Commission Internationale d'Éclairage) coordinate of (0.31, 0.34) and color rendering index (CRI) > 90, which are close to ideal white light emission characteristics. The device functionalities are achieved based on defect-related NIR emission from TiO2 nanorods array and visible emission from nitrogen-doped carbon dots. This result paves a new opportunity to develop low-cost, solution-processed nitrogen-doped carbon dots based on warm White light emitting diodes with high CRI for large-area display and lighting applications. [ABSTRACT FROM AUTHOR]

Utilizing the remarkably high light absorption and long carrier diffusion length of inorganic perovskites, superior performance self‐powered broadband photodetectors using the vertical heterojunction of cesium lead iodide (CsPbI3) nanocrystals (NCs) and zinc oxide (ZnO) films on a flexible platform are reported. Here, the pure cubic or α‐phase of as‐synthesized CsPbI3 NCs facilitate the novelty of the present work in terms of their enhanced structural stability suitable for optical applications. The α‐CsPbI3/ZnO device exhibits superior performance with photoresponsivity of ≈8.2 AW−1, ON/OFF ratio of ≈2.4 × 104, and specific detectivity up to ≈1.4 × 1012 Jones. Furthermore, the piezo‐phototronic effect of ZnO has been exploited to enhance the device performance by utilizing the compressive strain‐induced piezoelectric charges for modulating the generation, separation, and transportation of charge carriers. By introducing an approximate −0.042% compressive strain in the hybrid heterostructure, the enhancement of photocurrent, spectral responsivity, and specific detectivity of the detector by ≈619%, ≈536%, and ≈506%, respectively, under visible light illumination has been successfully achieved. This work not only presents an inventive method for improving the performance of perovskite photodetectors through interface engineering, but it also provides a thorough understanding of the piezo‐phototronic effect on optoelectronic devices. [ABSTRACT FROM AUTHOR]

Although α‐CsPbI3 is regarded as an attractive optical luminophore, it is readily degraded to the optically inactive δ‐phase under ambient conditions. Here, we present a simple approach to revive degraded ("optically sick") α‐CsPbI3 through "medication" with thiol‐containing ligands. The effect of different types of thiols is systematically studied through optical spectroscopy. The structural reconstruction of degraded α‐CsPbI3 nanocrystals to cubic crystals in the presence of thiol‐containing ligands is visualized through high‐resolution transmission electron microscopy and supported by X‐ray diffraction analysis. We found that 1‐dodecanethiol (DSH) effectively revives degraded CsPbI3 and results in high immunity towards moisture and oxygen, hitherto unreported. DSH facilitates the passivation of surface defects and etching of degraded Cs4PbI6 phase, thus reverting them back to the cubic CsPbI3 phase, leading to enhanced PL and environmental stability. [ABSTRACT FROM AUTHOR]

Phosphor-converted LEDs or pc-LEDs, as a solid-state lighting source, are attractive for next-generation display technologies because of their energy savings, and green environmentally friendly nature. Recently, white LEDs are being produced commercially by coating blue LED (440–470 nm) chips with various yellow-emitting phosphors. However, the LEDs produced by this technique often exhibit high correlated color temperature (CCT) and low color rendering index (CRI) values, due to sufficient red spectral components not being present, and thus aren't suitable for commercial grade white illumination. To circumvent this drawback, our work reports for the first time the use of blue and green-emitting nitrogen-functionalized graphene quantum dots (GQDs) coupled with red-emitting CsPbI3 NCs for phosphor-based LED applications. We deployed near-UV to visible excitable red-emitting perovskite CsPbI3 nanocrystals which contribute toward the red spectral component, thus greatly improving the CRI of the LEDs. CsPbI3 nanocrystals are optically excited by nitrogen-functionalized GQD with blue and green emissions in a remote double-layer phosphor stack technique. This double phosphor layer stacking greatly improves both the CRI and luminous efficiency of radiation (LER), which usually has a trade-off in previously reported phosphor stacks. A CCT of ∼5182 K providing daylight white tonality, with superior CRI (∼90%) and ultrahigh LER (∼250 lumens/watt) are reported, which are significantly higher than the established benchmarks. [ABSTRACT FROM AUTHOR]

Synthesis of monodispersed, stable halide, and mixed halide perovskite nanocrystals by hot‐injection approach is still challenging due to the fast reaction kinetics and unrevealed ligand chemistry. The atomic scale imaging of perovskite nanocrystals using transmission electron microscopy (TEM) is also challenging because of their structural degradation due to high electron dose and soft nature of perovskites. Here, a novel technique is proposed to synthesize pure cubic phase, monodispersed, stable CsPbX3 (X = I/Br) nanocrystals by simply modifying ligand chemistry using olive oil, which also leads to realization of tuneable composition mixed halide perovskites by simple physical mixing. Here, the atomic scale images and the probable distribution of Cs, Pb, and I/Br atoms in single halide and mixed halide perovskites via high‐resolution TEM microscopy are presented. The estimated atomic distance (PbPb and PbI/Br) is strongly corroborated with the VESTA structure. Interestingly, the lattice constant (d‐value) of the synthesized nanocrystals is smaller (≈3%) than the theoretical predicted one, leading to a higher phase stability in laboratory ambient conditions (45–55% humidity, 300 K). The theoretical analysis using density functional theory enlightens the understanding of higher stability of CsPbI2Br along with the maximum optical absorption in the visible regime, as a preferable material for the photovoltaic applications. [ABSTRACT FROM AUTHOR]

Full exploitation of two-dimensional (2D) semiconducting MoSe2, an exciting 2D transition-metal dichalcogenide, in optoelectronics is hampered because of dearth of scalable production methods. Here, a redox-mediated green route growth of ultrathin MoSe2 nanosheets and nanocrystals is reported. At solvothermal condition, molybdenum acetate [(CH3COO–)2Mo2+]2 at (+II) oxidation state is employed as the molybdenum source for the first time to grow 2D MoSe2 of 2H phase. Edible olive oil acts as a solvent as well as a ligand to block the growth in the Z direction, leading to the formation of 2D MoSe2. The bottom-up solution-processed method differs distinctly from other available synthesis methods in terms of the 2D MoSe2 nanosheet growth of the semiconducting phase (2H) without using any template or any external reducing agent. Evolution of MoSe2 nanosheets is systematically studied by X-ray diffraction and Raman spectroscopy with the variation of the reaction temperature and the reaction time. Prolonged sonication and gradient centrifugations enable in obtaining MoSe2 nanocrystals of different sizes. Tuneable optical properties and temperature-dependent emissions of MoSe2 nanocrystals and nanosheets are studied by UV–visible and photoluminescence spectroscopies. Finally, we have fabricated a photoconductive device which shows broadband visible light detection, demonstrating the potential use of bottom-up solution-processed semiconducting MoSe2 in broadband photodetection applications. [ABSTRACT FROM AUTHOR]

The synthesis of single‐crystalline β‐CsPbI3 perovskite nanorods (NRs) using a colloidal process is reported, exhibiting their improved photostability under 45–55% humidity. The crystal structure of CsPbI3 NRs films is investigated using Rietveld refined X‐ray diffraction (XRD) patterns to determine crystallographic parameters and the phase transformation from orthorhombic (γ‐CsPbI3) to tetragonal (β‐CsPbI3) on annealing at 150 °C. Atomic resolution transmission electron microscopy images are utilized to determine the probable atomic distribution of Cs, Pb, and I atoms in a single β‐phase CsPbI3 NR, in agreement with the XRD structure and selected area electron diffraction pattern, indicating the growth of single crystalline β‐CsPbI3 NR. The calculation of the electronic band structure of tetragonal β‐CsPbI3 using density functional theory (DFT) reveals a direct transition with a lower band gap and a higher absorption coefficient in the solar spectrum, as compared to its γ‐phase. An air‐stable (45–55% humidity) inverted perovskite solar cell, employing β‐CsPbI3 NRs without any encapsulation, yields an efficiency of 7.3% with 78% enhancement over the γ‐phase, showing its potential for future low cost photovoltaic devices. [ABSTRACT FROM AUTHOR]