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Compared with the rapid development of red and green perovskite light-emitting diodes (PeLEDs), the improvement of the device performance is urgent for blue PeLEDs. Herein, we developed a creative method to incorporate Cl- into quasi-2D perovskite films via dynamic processing, by mixing two main strategies of mixed-Cl/Br perovskites and quasi-2D perovskites. With methylammonium chloride (MACl) treating the perovskite film, the devices presented excellent spectral stability owing to the effective suppression of non-radiative recombination. Consequently, CsPbBr3 : PEABr-based PeLEDs exhibited a maximum external quantum efficiency of 1.74% with a bright luminance of 537 cd m−2. The redshift of the emitting luminescence (EL) peak was no more than 2 nm around 477 nm. The findings in this work will help develop other new routes for pure blue PeLEDs with ideal spectral stability.

Defects easily form in organic-inorganic hybrid perovskite (CH3NH3PbX3) absorber layers acting as recombination centers which reduce the performance of solar cells. Therefore, defect passivation is an efficient method to improve the performance of solar cells. Herein, ethylamine alcohol chlorides is introduced into perovskite films to passivate defects. The hydroxyl group and ammonium group in ethylamine alcohol chlorides can interact with halogen in MAPbIxCl3-x to form hydrogen bonds suppressing ion migration. In addition, the crosslinking neighbouring perovskite grains through hydrogen bonds can also improve the perovskite grain size and film coverage. The data demonstrate that the obvious reduction of the defect concentration via defect passivation contributes to an enhancement of the open-circuit voltage from 0.87 V to 0.92 V and the device efficiency from 14.52% to 16.97%.

A light-emitting organic solar cell (LE-OSC) with electroluminescence (EL) and photovoltaic (PV) properties is successfully fabricated by connecting the EL and PV units using a MoO(3):Al co-evaporation interfacial layer, which has suitable work function and good transmittance. PV and EL units are fabricated based on poly(3-hexylthiophene) (P3HT)-indene-C(60) bisadduct (IC(60)BA) blends, and 4,4′-bis (N-carbazolyl) biphenyl-factris (2-phenylpyridine) iridium (Ir(ppy)(3)), respectively. The work function and the transmittance of the MoO(3):Al co-evaporation are measured and adjusted by the ultraviolet photoelectron spectroscopy and the optical spectrophotometer to obtain the better bi-functional device performance. The forward- and reverse-biased current density-voltage characteristics in dark and under illumination are evaluated to better understand the operational mechanism of the LE-OSCs. A maximum luminance of 1550 cd/m(2) under forward bias and a power conversion efficiency of 0.24% under illumination (100 mW/cm(2)) are achieved in optimized LE-OSCs. The proposed device structure is expected to provide valuable information in the film conditions for understanding the polymer blends internal conditions and meliorating the film qualities. [Image: see text]

Interface strains and lattice distortion are inevitable issues during perovskite crystallization. Silane as a coupling agent is a popular connector to enhance the compatibility between inorganic and organic materials in semiconductor devices. Herein, a protonated amine silane coupling agent (PASCA-Br) interlayer between TiO2 and perovskite layers is adopted to directionally grasp both of them by forming the structural component of a lattice unit. The pillowy alkyl ammonium bromide terminals at the upper side of the interlayer provide well-matched growth sites for the perovskite, leading to mitigated interface strain and ensuing lattice distortion; meanwhile, its superior chemical compatibility presents an ideal effect on healing the under-coordinated Pb atoms and halogen vacancies of bare perovskite crystals. The PASCA-Br interlayer also serves as a mechanical buffer layer, inducing less cracked perovskite film when bending. The developed molecular-level flexible interlayer provides a promising interfacial engineering for perovskite solar cells and their flexible application.

Wearable devices are mainly based on plastic substrates, such as polyethylene terephthalate and polyethylene naphthalate, which causes environmental pollution after use due to the long decomposition periods. This work reports on the fabrication of a biodegradable and biocompatible transparent conductive electrode derived from bamboo for flexible perovskite solar cells. The conductive bioelectrode exhibits extremely flexible and light-weight properties. After bending 3000 times at a 4 mm curvature radius or even undergoing a crumpling test, it still shows excellent electrical performance and negligible decay. The performance of the bamboo-based bioelectrode perovskite solar cell exhibits a record power conversion efficiency (PCE) of 11.68%, showing the highest efficiency among all reported biomass-based perovskite solar cells. It is remarkable that this flexible device has a highly bendable mechanical stability, maintaining over 70% of its original PCE during 1000 bending cycles at a 4 mm curvature radius. This work paves the way for perovskite solar cells toward comfortable and environmentally friendly wearable devices.

Semiconductor nanomaterials with controlled morphologies and architectures are of critical importance for high-performance optoelectronic devices. However, the fabrication of such nanomaterials on polymer-based flexible electrodes is particularly challenging due to degradation of the flexible electrodes at a high temperature. Here we report the fabrication of nickel oxide nanopillar arrays (NiO x NaPAs) on a flexible electrode by vapor deposition, which enables highly efficient perovskite solar cells (PSCs). The NiO x NaPAs exhibit an enhanced light transmittance for light harvesting, prohibit exciton recombination, promote irradiation-generated hole transport and collection, and facilitate the formation of large perovskite grains. These advantageous features result in a high efficiency of 20% and 17% for the rigid and flexible PSCs, respectively. Additionally, the NaPAs show no cracking after 500 times of bending, consistent with the mechanic simulation results. This robust fabrication opens a new opportunity for the fabrication of a large area of high-performance flexible optoelectronic devices.

Poly(3,4-ethylene dioxythiophene):poly(4-styrenesulfonate) (PEDOT:PSS) is a widely utilized hole-transporting material (HTM) in planar photovoltaic devices, such as organic solar cells (OSCs) and perovskite solar cells (PSCs). However, the hygroscopic nature of PEDOT:PSS aqueous dispersions may restrict their future application. Therefore, it is necessary to develop other effective and stable HTMs to achieve high-performance photovoltaic devices. Herein, we demonstrate a facile route to deposit solution-processed MoO3, GeO2, V2O5 and CrO3 thin films as hole-transporting layers by directly dissolving their commercial powders in deionized water. Among these, the solution-processed V2O5 (sV2O5) film exhibited the highest work function of 5.2 eV, and the best hydrophobicity, with a contact angle of 77.2°. The sV2O5-based OSCs and PSCs presented power conversion efficiencies (PCEs) of 8.36% and 14.13%, respectively. Notably, the PEDOT:PSS V2O5 composite HTM based device obtained a maximum PCE of 18.03% with a Voc exceeding 1.0 V. These aqueous-solution-processed HTMs have potential applications in green and low-cost photovoltaic devices by virtue of their simple and ecofriendly preparations.

Organic-inorganic metal halide perovskites have drawn the interest of scientific community due to their suitable optoelectronic properties and high solar cell efficiency. In this report, we demonstrated, for the first time, the application of Cs2CO3 - doped TiO2 as an efficient electron-transporting layer (ETL) in PSCs. Remarkably, the optimized Cs2CO3-doped TiO2 films exhibited improved wetting properties which assisted the deposition of perovskite films and improved the TiO2/perovskite interface by lowering the work function. With X-ray diffraction studies, better crystalline of the perovskite films could be found in the doped devices. Solar cells prepared with the Cs2CO3-doped TiO2 as ETL resulted in a 19% efficiency performance and improved stability.

Interface engineering is an efficient method for improving the performance of planar perovskite solar cells (PSCs). In this paper, the performance of PSCs was improved significantly by introducing 4,7-diphenyl-1,10-phenanthroline (Bphen) doped with bis(2-methyldibenzo-[f,h]quinoxaline) (Ir(MDQ)2(acac)) to modify the interface between perovskite (CH3NH3PbI3−xClx)/PCBM (phenyl-C61-butyric acid methyl ester) and an Ag electrode. The power conversion efficiency (PCE) was enhanced up to 15.87%, compared with 10.77% for the reference device without interlayer modification. It was found that the enhanced PCE was attributed to the better interface contact between the perovskite and Ag cathode. A suitable interface roughness is beneficial for reducing the leakage current and the probability of carrier recombination, resulting in an enhanced fill factor and thus improved device efficiency.

New fabrication techniques for solution-processed organic photovoltaics are more and more desirable due to greater demand for affordable method to make large area. Different from traditional spin-coating, here, we report a new fabrication technique inspired by “liquid-chalk”. Solution can be added into liquid-chalk, and is almost all coated on the devices, while spin-coating will waste most of solution. In addition, large area could be easily achieved with it. Meanwhile, the thickness and roughness could be adjusted by optimizing speed, time of annealing and amount of the solution added. We demonstrated solar cells based on liquid-chalk-coated perovskite photoactive layer (CH3NH3PbI3) exhibit comparatively high power con-version efficiency (PCE) of 14.83% on average. A champion PCE of 16.04% was attained. Similarly, applying the method in pure inorganic system (CsPbBrI2), we also successfully fabricated devices with a highest PCE of 9.17%. The results indicate that using liquid-chalk to coat is an effective new way to fabricate perovskite solar cells, and also an ideal method to make large-area and flexible devices.

A facile strategy was developed to simultaneously improve the performance and stability of perovskite solar cells (PSCs). It involves the dissolution of an ultranarrow bandgap material, (2,2′-((2Z,2′Z)-(((4,4,9,9-tetrakis (4-hexylphenyl)-4,9-dihydro-s-indaceno [1,2-b:5,6-b′] dithiophene-2,7-diyl) bis (4-((2-ethylhexyl) oxy) thiophene-5,2-diyl))bis(methanylylidene))bis(5,6-difluoro-3-oxo-2,3-dihydro-1H-indene-2,1-diylidene)) dimalononitrile (IEICO-4F)), in chlorobenzene (antisolvent), the use of the solution in the treatment of perovskite films during spin-coating, and the fabrication of solar cells using the treated perovskite films. IEICO-4F formed a charge transfer bridge at the perovskite/Spiro-OMeTAD interface and improved the charge extraction and transport. Furthermore, the addition of IEICO-4F facilitated the crystallization, improved the surface morphology, and enhanced the passivation of trap sites of perovskite films. Meanwhile, a reliable power conversion efficiency exceeding 20% for CH3NH3PbI3-based cells and 15.72% for CsPbBrI2-based all-inorganic PSCs was realized. These values surpass those of the control devices (i.e., 18.66% and 13.30%, respectively).

We report oxygen vacancies (OVs) rich hexagonal ReO3 nanostructured electrocatalysts for efficient hydrogen generation. Through a simple argon plasma exposure, OVs are introduced into the ReO3 nanoparticles (NP) and nanosheets to enhance electrocatalytic activities with decreasing overpotentails from 157 mV and 178 mV to 138 mV and 145 mV at the current density of 10 mA cm-2, respectively. As-processed OVs rich ReO3 NP exhibit a good stability during electrochemical measurements for 20 h in acidic electrolyte. The huge active surface area, abundant OVs and excellent conductivity contribute to the performance according to the experimental data. Further theoretical calculations show that the abundant OVs adsorb H with lower Gibbs free energy facilitating hydrogen evolution.

The underlayer plays an important role for organic–inorganic hybrid perovskite formation and charge transport in perovskite solar cells (PSCs). Here, we employ a classical organic small molecule, 5,6,11,12-tetraphenyltetracene (rubrene), as the underlayer of perovskite films to achieve 15.83% of power conversion efficiency with remarkable moisture tolerance exposed to the atmosphere. Experiments demonstrate rubrene hydrophobic underlayer not only drives the crystalline grain growth of high quality perovskite, but also contributes to the moisture tolerance of PSCs. Moreover, the matching energy level of the desirable underlayer is conductive to extracting holes and blocking electrons at anode in PSCs. This introduction of organic small molecule into PSCs provides alternative materials for interface optimization, as well as platform for flexible and wearable solar cells.

The authors developed a seed-mediated method by GeO2 nano-particles (NPs) for growing crystal perovskite films. Poly(3,4-ethylene dioxythiophene):poly(4-styrenesulfonate) (PEDOT:PSS)-GeO2 composite films can act as an efficient underlayer for the growth of crystal perovskite films. GeO2 NPs are regarded as the growing sites of crystal nucleus of the perovskites. Superior quality of perovskite films are achieved by tuning the size of the GeO2 NPs, which results in a power conversion efficiency as high as 16.77%. The seed-mediated growing route on perovskite crystallization also gives a hint to seek other nano-particle materials for fabricating highly efficient and stable perovskite solar cells in the future.

Due to the good photocatalytic activity, the TiO2@CNTs thin film is highly desirable to apply to the self-cleaning glass for green intelligent building. Here, the TiO2@CNTs thin film has been successfully achieved by polymer-assisted approach of an aqueous chemical solution method. The polymer, polyethylenimine, aims to combine the Ti4+ with CNTs for film formation of TiO2@CNTs. The resultant thin film was uniform, highly transparent, and super-hydrophilic. Owing to fast electron transport and effectively hindering electron-hole recombination, the TiO2@CNTs thin film has nearly twofold photocatalytic performance than pure TiO2. The TiO2@CNTs thin films show a good application for self-cleaning glasses. Electronic supplementary material The online version of this article (doi:10.1186/s11671-016-1674-4) contains supplementary material, which is available to authorized users.