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Summary The inferior light extraction efficiency (LEE), which is generally less than 20%, based on optical modeling, and the difficulty in achieving white emission are the two main challenges in the metal-halide-perovskite light-emitting diode (PeLED) field. Herein, we report a simple and efficient approach to construct high-performance white PeLEDs with much-enhanced LEE by coupling a blue PeLED with a layer of red perovskite nanocrystal (PeNC) down-converter through a rationally designed multilayer semitransparent electrode (LiF/Al/Ag/LiF). The red PeNC layer allows the extraction of the trapped waveguide mode and surface plasmon polariton mode in a blue PeLED and converts them to red emission, resulting in over 50% LEE improvement. Simultaneously, the complementary emission spectrum of blue photons and down-converting red photons contributes to a white PeLED with a high external quantum efficiency and luminance of more than 12% and approximately 2,000 cd m−2, respectively, which represent state-of-the-art results in this field.

Despite demonstrating higher photoluminescence quantum yield and better ambient and operational stability than organic–inorganic hybrid perovskites, all-inorganic perovskites encounter the problem of inferior film quality and interfacial electrical properties, which limits the resultant device performance. In this study, three polymers, P4a–c, bearing distinct pendant groups based on a similar conjugated group are synthesized and employed as an interlayer to modify the PEDOT:PSS/CsPbBr3 interface. Due to the pendant design, P4a–c possess deep-lying HOMO levels and high transparency across the visible range. The different structures of the pendant groups in P4a–c are shown to result in their different propensity in energy-level modulation and solid-state aggregation, which plays a non-trivial role in affecting the resulting device performance. Due to the more appropriate energy levels and better regulation of CsPbBr3 crystals, P4c with a polar bridge moiety is shown to better mediate the performance of the derived device. The P4c-mediated PeLED delivers six times enhanced luminance (Lmax, ∼36 000 cd m−2) and 3.6 times enhanced external quantum efficiency (EQE, 2.16%) as compared to the control device (∼6000 cd m−2, 0.60%). Notably, all the devices using P4a–c interlayers deliver a lower turn-on voltage than the control device, clearly revealing the positive role of P4a–c interlayers on diminishing the barrier across the associated interface to improve charge injection efficiency.

Gas hydrate is a nonstoichiometric crystalline material. It is attracting more and more attention not only because natural gas hydrate is a potential energy resource, but also because hydrate-based technologies can be potentially applied to the industry of energy and environment such as energy storage, carbon sequestration, etc. The nucleation mechanism of gas hydrate is a key issue in studying reservoir formation of natural gas hydrate and the kinetic properties of gas hydrate as an energy-storage media. Molecular dynamics simulation can provide microscopic insights into molecular-scale understanding of hydrate nucleation. In this review, the advances on the study of heterogeneous hydrate nucleation by molecular dynamics simulation are summarized, with a specific focus on the factors affecting nucleation processes. The interfacial energy barrier for nucleation will be lowered by molecular structure of interfacial water between hydrate and solid substrate. The interface and surface properties of solid substrate, including hydrophilicity and hydrophobicity, surface roughness, layer-accumulated adsorption potential, crystallinity and surface layer-charge are also recognized as being associated with the process of hydrate nucleation by influencing the dynamics of gas and water molecules. In case of hydrate nucleation in confined pore space, confinement effect, pore size and elasticity are identified as the controlling factors.

Quasi-2D perovskites have long been considered to have favorable "energy funnel/cascade" structures and excellent optical properties compared with their 3D counterparts. However, most quasi-2D perovskite light-emitting diodes (PeLEDs) exhibit high external quantum efficiency (EQE) but unsatisfactory operating stability due to Auger recombination induced by high current density. Herein, a synergetic dual-additive strategy is adopted to prepare perovskite films with low defect density and high environmental stability by using 18-crown-6 and poly(ethylene glycol) methyl ether acrylate (MPEG-MAA) as the additives. The dual additives containing COC bonds can not only effectively reduce the perovskite defects but also destroy the self-aggregation of organic ligands, inducing the formation of perovskite nanocrystals with quasi-core/shell structure. After thermal annealing, the MPEG-MAA with its CC bond can be polymerized to obtain a comb-like polymer, further protecting the passivated perovskite nanocrystals against water and oxygen. Finally, state-of-the-art green PeLEDs with a normal EQE of 25.2% and a maximum EQE of 28.1% are achieved, and the operating lifetime (T50 ) of the device in air environment is over ten times increased, providing a novel and effective strategy to make high efficiency and long operating lifetime PeLEDs.

A high-performance monolithic perovskite/organic tandem solar cell based on the integration of a large bandgap CsPbI2Br inorganic perovskite front cell with a narrow bandgap PM6:Y6-based or PTB7-Th:O6T-4F-based bulk-heterojunction organic rear cell is demonstrated. Large bandgap inorganic perovskites are well suited candidates for the front cell due to their excellent optoelectronic properties and broad absorption for visible light, they also possess smaller voltage loss (Eloss) and higher external quantum efficiency (EQE) response when compare to their organic counterparts with approximate bandgap. Low bandgap organic solar cells offer potentially better stability and absorption tunability compared with the Sn-based perovskite counterparts, making them be good candidates for the rear cell of the tandem cells. As a result, the best power conversion efficiency (PCE) of the perovskite/organic tandem cell presented in this work reaches over 18%. In addition, based on the photovoltaic performance parameters (EQE, fill factor (FF), Eloss) that have already been achieved in state-of-the-art organic and perovskite solar cells, we further evaluate the potential PCE of the perovskite/organic tandem cells, showing a maximum calculated PCE of over 31% when the bandgaps of the subcells are optimized. This work paves the way for the development of hybrid tandem solar cells with promising performance.

Summary Low-band-gap metal halide perovskite semiconductor based on mixed Sn/Pb is a key component to realize high-efficiency tandem perovskite solar cells. However, the mixed perovskites are unstable in air due to the oxidation of Sn2+. To overcome the stability problem, we introduced N-(3-aminopropyl)-2-pyrrolidinone into the CH3NH3Sn0.5Pb0.5IxCl3-x thin film. The carbonyl group on the molecule interacts with Sn2+/Pb2+ by Lewis acid coordination, forming vertically oriented 2D layered perovskite. The 2D phase is seamlessly connected to the bulk perovskite crystal, with a lattice coherently extending across the two phases. Based on this 2D/3D hybrid structure, we assembled low-band-gap Sn-based perovskite solar cells with power conversion efficiency greater than 12%. The best device was among the most stable Sn-based organic-inorganic hybrid perovskite solar cells to date, keeping 90% of its initial performance at ambient condition without encapsulation, and more than 70% under continuous illumination in an N2-filled glovebox for over 1 month., Graphical Abstract, Highlights • The 2D perovskite lattice is seamlessly connected to the 3D perovskite lattice • Polymorphs of 2D perovskite were directly observed in a single perovskite film • The best device is among the most stable Sn-based perovskite solar cells to date, Materials Science; Optical Materials; Energy Materials

The accurate prediction of surface solar irradiance is of great significance for the generation of photovoltaic power. Surface solar irradiance is affected by many random mutation factors, which means that there are great challenges faced in short-term prediction. In Northwest China, there are abundant solar energy resources and large desert areas, which have broad prospects for the development of photovoltaic (PV) systems. For the desert areas in Northwest China, where meteorological stations are scarce, satellite remote sensing data are extremely precious exploration data. In this paper, we present a model using FY-4A satellite images to forecast (up to 15–180 min ahead) global horizontal solar irradiance (GHI), at a 15 min temporal resolution in desert areas under different sky conditions, and compare it with the persistence model (SP). The spatial resolution of the FY-4A satellite images we used was 1 km × 1 km. Particle image velocimetry (PIV) was used to derive the cloud motion vector (CMV) field from the satellite cloud images. The accuracy of the forecast model was evaluated by the ground observed GHI data. The results showed that the normalized root mean square error (nRMSE) ranged from 18.9% to 21.6% and the normalized mean bias error (nMBE) ranged from 3.2% to 4.9% for time horizons from 15 to 180 min under all sky conditions. Compared with the SP model, the nRMSE value was reduced by about 6%, 8%, and 14% with the time horizons of 60, 120, and 180 min, respectively.

In recent years, substantial progress has been made in developing perovskite light-emitting diodes with near-infrared, red and green emissions and over 20% external quantum efficiency. However, the development of perovskite light-emitting diodes with blue emission remains a great challenge, which retards further development of full-color displays and white-light illumination based on perovskite emissive materials. Here, firstly, through composition and dimensional engineering, we prepare quasi-two-dimensional perovskite thin films with improved blue emission, taking advantages of reduced trap density and enhanced photoluminescence quantum yield. Secondly, we find a vertically non-uniform distribution of perovskite crystals in the PEDOT:PSS/perovskite hybrid film. Through modulating the position of the recombination zone, we activate the majority of quasi-two-dimensional perovskite crystals, and thus demonstrate the most efficient blue perovskite light-emitting diode to date with emission peak at 480 nm, record luminance of 3780 cd m−2 and record external quantum efficiency of 5.7%., Halide perovskite based light-emitting diodes attracted intensive research interest recently but the efficiency of blue diodes is much lower than the green and red ones. Here Li et al. push up the efficiency of blue diodes through composition engineering and vertical morphology control.

Methylammonium (MA)-free perovskite solar cells (PVSCs) have obtained great attention recently, owing to their superior stability. However, there are still gaps in efficiency between MA-free PVSCs and MA-containing counterparts. Their stability still needs to be further enhanced for meeting commercial standards, especially the illumination stability. Here, we incorporate Zn2+ into perovskite thin films to passivate defects, successfully achieving a champion efficiency of 20.7% and reinforcing the stability of MA-free FA0.9Cs0.1PbI3 PVSCs. This study reveals that Zn-doping can increase the grain size and contribute to modulate the crystallization process. Moreover, it is found that most of the Zn2+ aggregates at the grain boundaries passivating defects and, thus, effectively restrain the non-radiative recombination in the PVSCs. These findings provide a new way of realizing highly efficient and stable PVSCs.

Inspired by the photosynthesis process of natural plants, multifunctional transistors based on natural biomaterial chlorophyll and organic semiconductors (OSCs) are reported. Functions as photodetectors (PDs) and light-stimulated synaptic transistors (LSSTs) can be switched by gate voltage. As PDs, the devices exhibit ultrahigh photoresponsivity up to 2 × 106 A W-1 , detectivity of 6 × 1015 Jones, and Iphoto /Idark ratio of 2.7 × 106 , which make them among the best reported organic PDs. As LSSTs, important synaptic functions similar to biological synapses are demonstrated, together with a dynamic learning and forgetting process and image-processing function. Significantly, benefiting from the ultrahigh photosensitivity of chlorophyll, the lowest operating voltage and energy consumption of the LSSTs can be 10-5 V and 0.25 fJ, respectively. The devices also exhibit high flexibility and long-term air stability. This work provides a new guide for developing organic electronics based on natural biomaterials.

Almost all highly efficient perovskite solar cells (PVSCs) with power conversion efficiencies (PCEs) of greater than 22% currently contain the thermally unstable methylammonium (MA) molecule. MA-free perovskites are an intrinsically more stable optoelectronic material for use in solar cells but compromise the performance of PVSCs with relatively large energy loss. Here, the open-circuit voltage (Voc ) deficit is circumvented by the incorporation of β-guanidinopropionic acid (β-GUA) molecules into an MA-free bulk perovskite, which facilitates the formation of quasi-2D structure with face-on orientation. The 2D/3D hybrid perovskites embed at the grain boundaries of the 3D bulk perovskites and are distributed through half the thickness of the film, which effectively passivates defects and minimizes energy loss of the PVSCs through reduced charge recombination rates and enhanced charge extraction efficiencies. A PCE of 22.2% (certified efficiency of 21.5%) is achieved and the operational stability of the MA-free PVSCs is improved.

In the past few years, substantial progress has been made in perovskite light-emitting devices. Both pure green and infrared thin-film perovskite light-emitting devices with external quantum efficiency over 20% have been successfully achieved. However, pure-red and blue thin-film perovskite light-emitting diodes still suffer from inferior efficiency. Therefore, the development of efficient and stable thin-film perovskite light-emitting diodes with pure-red and blue emissions is urgently needed for possible applications as a new display technology and solid-state lighting. Here, we demonstrate an efficient light-emitting diode with pure-red emission based on polymer-assisted in situ growth of high-quality all-inorganic CsPbBr0.6I2.4 perovskite nanocrystal films with homogenous distribution of nanocrystals with size 20–30 nm. With this method, we can dramatically reduce the formation temperature of CsPbBr0.6I2.4 and stabilize its perovskite phase. Eventually, we successfully demonstrate a pure-red-emission ...

In this letter, a vertical GaN p-n junction diode with high-K/low-K compound dielectric structure (GaN CD-VGD) is proposed. The high-K/low-K compound dielectric structure consists of a layer of high dielectric constant and multilayer dielectric layers which have a lower dielectric constant, and these compound dielectric layers formed along the current flow direction. Compared with a conventional p-n diode, the edge electric field will be suppressed due to the effects of high-K passivation. And a new electric field peak will be introduced in the p-n diodes, because of a discontinuity of electrical field at the interface of high-K and low-K layer. Therefore the distribution of electric field in p-n diodes will become more uniform and an enhancement of breakdown voltage can be achieved. A best trade-off breakdown voltage (BV) and on-resistance (R on ) have been obtained by optimizing device parameters including dielectric layer situation, length and width. Numerical simulation demonstrate that GaN CD-VGD with a BV of 10650V and a Ron of 5.83 mΩ-cm2, resulting in a figure-of-merit (V B 2/R on ) of 19 GW/cm2.