Infrared photodetectors based on single-layer CVD-grown graphene and PbS quantum dots, which are fabricated by solution processing, show ultrahigh responsivities of up to 10(7) A/W under infrared light illumination. The devices fabricated on flexible plastic substrates have excellent bending stability. The photoresponse is attributed to the field-effect doping in graphene films induced by negative charges generated in the quantum dots.

Poor stability of organic–inorganic halide perovskite materials in humid condition has hindered the success of perovskite solar cells in real applications since controlled atmosphere is required for device fabrication and operation, and there is a lack of effective solutions to this problem until now. Here we report the use of lead (II) thiocyanate (Pb(SCN)2) precursor in preparing perovskite solar cells in ambient air. High-quality CH3NH3PbI3−x(SCN)x perovskite films can be readily prepared even when the relative humidity exceeds 70%. Under optimized processing conditions, we obtain devices with an average power conversion efficiency of 13.49% and the maximum efficiency over 15%. In comparison with typical CH3NH3PbI3-based devices, these solar cells without encapsulation show greatly improved stability in humid air, which is attributed to the incorporation of thiocyanate ions in the crystal lattice. The findings pave a way for realizing efficient and stable perovskite solar cells in ambient atmosphere.

Semitransparent perovskite solar cells are prepared by laminating graphene transparent electrodes on the top for the first time. The device performance is optimized by improving the conductivity of the graphene electrodes and the contact between the graphene and the perovskite active layers during the lamination process. The devices show high power conversion efficiencies when they are illuminated from both sides.

With a certified efficiency as high as 25.2%, perovskite has taken the crown as the highest efficiency thin film solar cell material. Unfortunately, serious instability issues must be resolved before perovskite solar cells (PSCs) are commercialized. Aided by theoretical calculation, an appropriate multifunctional molecule, 2,2‐difluoropropanediamide (DFPDA), is selected to ameliorate all the instability issues. Specifically, the carbonyl groups in DFPDA form chemical bonds with Pb2+ and passivate under‐coordinated Pb2+ defects. Consequently, the perovskite crystallization rate is reduced and high‐quality films are produced with fewer defects. The amino groups not only bind with iodide to suppress ion migration but also increase the electron density on the carbonyl groups to further enhance their passivation effect. Furthermore, the fluorine groups in DFPDA form both an effective barrier on the perovskite to improve its moisture stability and a bridge between the perovskite and HTL for effective charge transport. In addition, they show an effective doping effect in the HTL to improve its carrier mobility. With the help of the combined effects of these groups in DFPDA, the PSCs with DFPDA additive achieve a champion efficiency of 22.21% and a substantially improved stability against moisture, heat, and light.

Organolead halide perovskites have emerged as the most promising materials for various optoelectronic devices, especially solar cells, because of their excellent optoelectronic properties. Here, we present the first report of low-voltage high-gain phototransistors based on perovskite/organic-semiconductor vertical heterojunctions, which show ultrahigh responsivities of ~109A W–1 and specific detectivities of ~1014 Jones in a broadband region from the ultraviolet to the near infrared. The high sensitivity of the devices is attributed to a pronounced photogating effect that is mainly due to the long carrier lifetimes and strong light absorption in the perovskite material. In addition, flexible perovskite photodetectors have been successfully prepared via a solution process and show high sensitivity as well as excellent flexibility and bending durability. The high performance and facile solution-based fabrication of the perovskite/organic-semiconductor phototransistors indicate their promise for potential application for ultrasensitive broadband photodetection.

Cesium‐based inorganic perovskites, such as CsPbI2Br, are promising candidates for photovoltaic applications owing to their exceptional optoelectronic properties and outstanding thermal stability. However, the power conversion efficiency of CsPbI2Br perovskite solar cells (PSCs) is still lower than those of hybrid PSCs and inorganic CsPbI3 PSCs. In this work, passivation and n‐type doping by adding CaCl2 to CsPbI2Br is demonstrated. The crystallinity of the CsPbI2Br perovskite film is enhanced, and the trap density is suppressed after adding CaCl2. In addition, the Fermi level of the CsPbI2Br is changed by the added CaCl2 to show heavy n‐type doping. As a result, the optimized CsPbI2Br PSC shows a highest open circuit voltage of 1.32 V and a record efficiency of 16.79%. Meanwhile, high air stability is demonstrated for a CsPbI2Br PSC with 90% of the initial efficiency remaining after more than 1000 h aging in air.

A single-layer graphene film with high conductance and transparency was realized by effective chemical doping. The conductance of single-layer graphene was increased for more than 400% when it was doped with Au nanoparticles and poly(3,4-ethylenedioxythiophene): poly(styrene sulfonic acid). Then semitransparent organic solar cells based on poly(3-hexylthiophene) (P3HT) and phenyl-C61-butyric acid methyl ester (PCBM) were fabricated with single-layer graphene and indium tin oxide (ITO) as the top and bottom electrodes, respectively. The performance of the devices was optimized by tuning the active layer thickness and doping the single-layer graphene electrodes. The maximum efficiency of 2.7% was observed in the devices with the area of 20 mm(2) illuminated from graphene electrode under the AM1.5 solar simulator. It is notable that all of the devices showed higher efficiency from the graphene than ITO side, which was attributed to the better transmittance of the graphene electrodes. In addition, the influence of the active area of the organic solar cell on its photovoltaic performance was studied. We found that, when the active areas increased from 6 to 50 mm(2), the power conversion efficiencies decreased from 3% to 2.3% because of the increased series resistances and the decreased edge effect of the devices.

Package-free flexible organic solar cells are fabricated with multilayer graphene as top transparent electrodes, which show the highest power conversion efficiency of about 3.2% and excellent flexibility and bending stability. The devices also show good air stability, indicating that multilayer graphene is a promising environmental barrier that can protect the organic solar cells from air contamination.