Researchers developed a perovskite solar cell with high power-conversion efficiency (>20%) and intense electroluminescence yield (0.5%).

Perovskite solar cells (PSC) with efficiencies > 20% have only been realized with highly expensive archetype organic hole transporting materials that can impede the large-scale deployment of PSC. Here we demonstrate PSCs achieving stabilized efficiencies of 20.3% with CuSCN as hole electron extraction layer. We developed a new method for the solution deposition of compact and highly conformal CuSCN layers that afford fast carrier extraction and collection. We also show that the notorious instability of CuSCN based PSCs is not associated with the CuSCN/perovskite interface but rather originates from the CuSCN/Au contact. By introducing a thin spacer layer between CuSCN and gold layers, the PSCs retained >95% of their initial efficiency after aging for 500 h under full-sun illumination at 60 °C, and >85% of their initial efficiency after aging at 85 °C for 1000 h. Importantly, under both continuous illumination and thermal stress, CuSCN based devices surpass the stability of spiro-OMeTAD based PSCs.One Sentence Summary: A record performance displayed by operationally stable perovskite solar cells employing all-inorganic charge extraction layers was realized after introducing a simple dynamic approach for the deposition of thin and conformal CuSCN layer onto perovskite layer and a thin spacer layer between CuSCN and gold layers, which will foster their large scale deployment.The prominence of organic-inorganic perovskite solar cells (PSC) can be credited to the unprecedented advancement in the power conversion efficiencies (PCEs), realized mostly by tailoring the formation and composition of the absorber layer (1,2). Certified PCEs >20% have been obtained while retaining the electron selective TiO 2 layer and by using either spiroOMeTAD [2,2′,7,7′-tetrakis(N,N-di-p-methoxyphenyl-amine)9,9′-spirobifluorene] or a polymerbased PTTA (poly-triarylamine) as the hole-transporting material (HTM) (2,3). However, the cost of these HTMs is prohibitively high for large-scale applications and the long-term operational and thermal instability seems to be associated with the archetype organic HTMs or their ingredients (4). One of the strategies to combat the issues of cost and instability could be the use of inexpensive inorganic hole extraction layers similar to the use of TiO 2 as an electron transporting material (5). However, obtaining stable PCEs >20% with PSCs using inorganic 2 HTMs, such as NiO, CuI, Cs 2 SnI 6 , and CuSCN when subjected to light soaking under realistic operational conditions, i.e., at maximum power point and 60°C has remained a challenge (6-9).The realization of efficiencies > 20% using PSCs with inorganic HTMs remains undoubtedly a key goal to foster the large-scale deployment of PSC. Among various inorganic hole transporting materials, CuSCN is an extremely cheap, abundant p-type semiconductor, that exhibits high hole mobility, a good thermal stability and a well-aligned work function (10). The CuSCN is intrinsically p-doped and transmits light across the entire visible and near infrared spect...

Although β-CsPbI3 has a bandgap favorable for application in tandem solar cells, depositing and stabilizing β-CsPbI3 experimentally has remained a challenge. We obtained highly crystalline β-CsPbI3 films with an extended spectral response and enhanced phase stability. Synchrotron-based x-ray scattering revealed the presence of highly oriented β-CsPbI3 grains, and sensitive elemental analyses—including inductively coupled plasma mass spectrometry and time-of-flight secondary ion mass spectrometry—confirmed their all-inorganic composition. We further mitigated the effects of cracks and pinholes in the perovskite layer by surface treating with choline iodide, which increased the charge-carrier lifetime and improved the energy-level alignment between the β-CsPbI3 absorber layer and carrier-selective contacts. The perovskite solar cells made from the treated material have highly reproducible and stable efficiencies reaching 18.4% under 45 ± 5°C ambient conditions.

In the past few years, organic-inorganic halide perovskites have rapidly emerged as promising materials for photovoltaic applications, but simultaneously achieving high performance and long-term stability has proved challenging. Here, we show a one-step solution-processing strategy using phosphonic acid ammonium additives that results in efficient perovskite solar cells with enhanced stability. We modify the surface of methylammonium lead triiodide (CH3NH3PbI3) perovskite by spin-coating its precursor solution in the presence of butylphosphonic acid 4-ammonium chloride. Morphological, structural and elemental analyses show that the phosphonic acid ammonium additive acts as a crosslink between neighbouring grains in the perovskite structure, through strong hydrogen bonding of the -PO(OH)2 and -NH3(+) terminal groups to the perovskite surface. The additives facilitate the incorporation of the perovskite within a mesoporous TiO2 scaffold, as well as the growth of a uniform perovskite layer at the surface, enhancing the material's photovoltaic performance from 8.8 to 16.7% as well as its resistance to moisture.

Preventing the degradation of metal perovskite solar cells (PSCs) by humid air poses a substantial challenge for their future deployment. We introduce here a two-dimensional (2D) A2PbI4 perovskite layer using pentafluorophenylethylammonium (FEA) as a fluoroarene cation inserted between the 3D light-harvesting perovskite film and the hole-transporting material (HTM). The perfluorinated benzene moiety confers an ultrahydrophobic character to the spacer layer, protecting the perovskite light-harvesting material from ambient moisture while mitigating ionic diffusion in the device. Unsealed 3D/2D PSCs retain 90% of their efficiency during photovoltaic operation for 1000 hours in humid air under simulated sunlight. Remarkably, the 2D layer also enhances interfacial hole extraction, suppressing nonradiative carrier recombination and enabling a power conversion efficiency (PCE) >22%, the highest reported for 3D/2D architectures. Our new approach provides water- and heat-resistant operationally stable PSCs with a record-level PCE.