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Three functionalized thienopyrazines (TPs), TP‐MN (1), TP‐CA (2), and TPT‐MN (3) were designed and synthesized as self‐assembled monolayers (SAMs) deposited on the NiOx film for tin‐perovskite solar cells (TPSCs). Thermal, optical, electrochemical, morphological, crystallinity, hole mobility, and charge recombination properties, as well as DFT‐derived energy levels with electrostatic surface potential mapping of these SAMs, have been thoroughly investigated and discussed. The structure of the TP‐MN (1) single crystal was successfully grown and analyzed to support the uniform SAM produced on the ITO/NiOx substrate. When we used NiOx as HTM in TPSC, the device showed poor performance. To improve the efficiency of TPSC, we utilized a combination of new organic SAMs with NiOx as HTM, the TPSC device exhibited the highest PCE of 7.7 % for TP‐MN (1). Hence, the designed NiOx/TP‐MN (1) acts as a new model system for the development of efficient SAM‐based TPSC. To the best of our knowledge, the combination of organic SAMs with anchoring CN/CN or CN/COOH groups and NiOx as HTM for TPSC has never been reported elsewhere. The TPSC device based on the NiOx/TP‐MN bilayer exhibits great enduring stability for performance, retaining ~80 % of its original value for shelf storage over 4000 h. [ABSTRACT FROM AUTHOR]

A new series of triphenylamine (TPA)‐functionalized isomeric polythiophenes are developed as hole transporting materials (HTM) for inverted tin‐based perovskite solar cells (TPSCs). Bithiophene (BT) is first functionalized with two TPA (electron donor; D) at 3 and 5 positions to give two structural isomeric compounds (3BT2D and 5BT2D). The functionalized BT2Ds are then coupled with 3,3′‐bis(tetradecylthio)‐2,2′‐bithiophene (SBT‐14)/3,3′‐ditetradecyl‐2,2′‐bithiophene (BT‐14) to produce structural isomeric polythiophenes (1‐4), which are compared to conventional poly[N,N″‐bis(4‐butylphenyl)‐N,N″‐bis(phenyl)‐benzidine] (poly‐TPD) as HTMs for TPSCs. With the appropriate alignment of energy levels with regard to the perovskite layer, the TPA‐functionalized polymers‐based TPSCs exhibit enhanced operational stability and efficiency. Moreover, the long thiotetradecyl chain in SBT‐14 with intramolecular S(alkyl)∙∙∙S(thio) interactions restricts the molecular rotation and has a strong impact on the molecular solubility and wettability of the film during device fabrication. Among all the polymers studied, TPSCs fabricated with 3‐SBT‐BT2D polymer exhibit the highest hole mobility as well as the slowest charge recombination and achieve the highest power conversion efficiency of 8.6%, with great long‐term stability for the performance retaining ≈90% of its initial values for shelf storage over 4000 h, which is the best efficiency for non‐PEDOT:PSS‐based TPSCs ever reported. [ABSTRACT FROM AUTHOR]

We report a simple strategy to grow a novel cobalt nickel vanadium oxide (CoxNiVyOz) nanocomposite on bare and reduced-graphene-oxide (rGO)-coated nickel foam (Ni foam) substrates. In this way, the synthesized graphene oxide is coated on Ni foam, and reduced electrochemically with a negative voltage to prepare a more conductive rGO-coated Ni foam substrate. The fabricated electrodes were characterized with a field-emission scanning electron microscope (FESEM), energy-dispersive X-ray spectra (EDX), X-ray photoelectron spectra (XPS), and Fourier-transform infrared (FTIR) spectra. The electrochemical performance of these CoxNiVyOz-based electrode materials deposited on rGO-coated Ni foam substrate exhibited superior specific capacitance 701.08 F/g, which is more than twice that of a sample coated on bare Ni foam (300.31 F/g) under the same experimental conditions at current density 2 A/g. Our work highlights the effect of covering the Ni foam surface with a rGO film to expedite the specific capacity of the supercapacitors. Despite the slightly decreased stability of a CoxNiVyOz-based electrode coated on a Ni foam@rGO substrate, the facile synthesis, large specific capacitance, and preservation of 92% of the initial capacitance, even after running 5500 cyclic voltammetric (CV) scans, indicate that the CoxNiVyOz-based electrode is a promising candidate for high-performance energy-storage devices. [ABSTRACT FROM AUTHOR]

Tin perovskite solar cells (TPSCs) were developed by adding the co-cations acetamidinium (AC) and rubidium (Rb) in varied proportions based on the FASnI 3 structure (E1). We found that adding 10% AC and 3% Rb can optimize the device (E1AC10Rb3) to attain an efficiency of power conversion of 14.5% with great shelf- and light-soaking stability. The films at varied AC and Rb proportions were characterized using XPS, SEM, AFM, GIWAXS, XRD, TOPAS, TOF-SIMS, UV-vis, PL, TCSPC, and femtosecond TAS techniques to show the excellent optoelectronic properties of the E1AC10Rb3 film in comparison to those of the other films. AC was found to have the effect of passivating the vacancy defects on the surface and near the bottom of the film, while Rb plays a pivotal role in passivating the bottom interface between perovskite and PEDOT:PSS. Therefore, the E1AC10Rb3 device with a band gap of 1.43 eV becomes a promising candidate as a narrow band gap device for tandem lead-free perovskite solar cell development.

Perovskites doped with chlorine (Cl - ), which are usually fabricated using the solution process, can effectively improve the stability and carrier mobility. Compared with the low tolerance of the solution process that relies mostly on personal skill, thermal evaporation is an important method for large-scale production of perovskite solar cells but the production cost is high. In this study, the sandwich evaporation-solvent annealing (SE-SA) method is proposed. Using sandwich evaporation with a low-cost chamber of the sandwich evaporation technique (SET) made in the laboratory and with the help of DMSO steam-assisted crystallization, we have successfully produced chlorine-containing perovskite solar cells with a high crystallinity and a high efficiency of 15.1% with V oc = 0.98 V, J sc = 21.94 mA/cm 2 , FF = 74.29%, and R s = 3.66 Ω·cm 2 , which can greatly reduce the production cost. It is worth mentioning that all the processes are carried out outside a glove box, which makes it possible for large-scale production of chlorine-containing perovskite solar cells by evaporation.