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Nickel oxide (NiOx) is a promising hole-selective contact to produce efficient inverted p-i-n structured perovskite solar cells (PSCs) due to its high carrier mobility and high transparency. However, the light-induced degradation of the NiOx–perovskite heterojunction is the main factor limiting its long-term operational lifetime. In this study, we used the time-resolved mass spectrometry technique to clarify the degradation mechanism of the NiOx-formamidinium–methylammonium iodide perovskite (a common composition for high-performance PSCs) heterojunction under operational conditions, and observed that (1) oxidation of iodide and generation of free protons under 1-sun illumination, (2) formation of volatile hydrogen cyanide, methyliodide, and ammonia at elevated temperatures, and (3) a condensation reaction between the organic components under a high vapor pressure. To eliminate these multi-step photochemical reactions, we constructed an aprotic trimethylsulfonium bromide (TMSBr) buffer layer at the NiOx/perovskite interface, which enables excellent photo-thermal stability, a matched lattice parameter with the perovskite crystal, and robust trap-passivation ability. Inverted PSCs stabilized with the TMSBr buffer layer reached the maximum efficiency of 22.1% and retained 82.8% of the initial value after continuous operation for 2000 hours under AM1.5G light illumination, which translates into a T80 lifetime of 2310 hours that is among the highest operational lifetimes for NiOx-based PSCs.

Ionic liquids and poly(ionic liquid)s act as bulk and/or passivation agents when used as additives in methylammonium-free lead perovskites, leading to devices showing enhanced power conversion efficiencies, reduced hysteresis and improved stability.

The carrier-type of the emerging photovoltaic Sb2Se3 was evaluated for both thin films and bulk crystals via a range of complementary techniques. X-ray photoelectron spectroscopy (XPS), hot probe, Hall effect, and surface photovoltage spectroscopy showed films and crystals synthesized from the Sb2Se3 granulate material to be n-type with chlorine identified as an unintentional n-type dopant via secondary ion mass spectrometry analysis. The validity of chlorine as a dopant was confirmed by the synthesis of intrinsic crystals from metallic precursors and subsequent deliberate n-type doping by the addition of MgCl2. Chlorine was also shown to be a substitutional n-type shallow dopant by density functional theory calculations. TiO2/Sb2Se3 n–n isotype heterojunction solar cells with 7.3% efficiency are subsequently demonstrated, with band alignment analyzed via XPS.

CCBY Antimony selenide (Sb$_2$Se$_3$) is an emerging chalcogenide photovoltaic absorber material that has been the subject of increasing interest in recent years, demonstrating rapid efficiency increases with a material that is simple, abundant, and stable. This paper examines the material from both a theoretical and practical standpoint. The theoretical viability of Sb$_2$Se$_3$ as a solar photovoltaic material is assessed and the maximum spectroscopically limited performance is estimated, with a 200 nm film expected to be capable of achieving a photon conversion efficiency of up to 28.2%. By adapting an existing CdTe close-spaced sublimation (CSS) process, Sb$_2$Se$_3$ material with large rhubarb-like grains is produced and solar cells are fabricated. We show that the established CdS window layer is unsuitable for use with CSS, due to intermixing during higher temperature processing. Substituting CdS with the more stable TiO$_2$, a power conversion efficiency of 5.5% and an open-circuit voltage V$_oc$ of 0.45 V are achieved; the voltage exceeding current champion devices. This paper demonstrates the potential of CSS for scalable Sb$_2$Se$_3$ deposition and highlights the promise of Sb$_2$Se$_3$ as an abundant and low-toxicity material for solar applications.

Alternatives to lead- and tin-based perovskites for photovoltaics and optoelectronics are sought that do not suffer from the disadvantages of toxicity and low device efficiency of present-day materials. Here we report a study of the double perovskite Cs2TeI6, which we have synthesized in the thin film form for the first time. Exhaustive trials concluded that spin coating CsI and TeI4 using an antisolvent method produced uniform films, confirmed as Cs2TeI6 by XRD with Rietveld analysis. They were stable up to 250 °C and had an optical band gap of ∼1.5 eV, absorption coefficients of ∼6 × 104 cm-1, carrier lifetimes of ∼2.6 ns (unpassivated 200 nm film), a work function of 4.95 eV, and a p-type surface conductivity. Vibrational modes probed by Raman and FTIR spectroscopy showed resonances qualitatively consistent with DFT Phonopy-calculated spectra, offering another route for phase confirmation. It was concluded that the material is a candidate for further study as a potential optoelectronic or photovoltaic material.

We investigated the formation of photovoltaic (PV) devices using direct n-Si/MAPI (methylammonium lead tri-iodide) two-sided heterojunctions for the first time (as a possible alternative to two-terminal tandem devices) in which charge might be generated and collected from both the Si and MAPI. Test structures were used to establish that the n-Si/MAPI junction was photoactive and that spiro-OMeTAD acted as a “pinhole blocking” layer in n-Si/MAPI devices. Two-terminal “substrate” geometry devices comprising Al/n-Si/MAPI/spiro-OMeTAD/Au were fabricated and the effects of changing the thickness of the semitransparent gold electrode and the silicon resistivity were investigated. External quantum efficiency and capacitance–voltage measurements determined that the junction was one-sided in the silicon—and that the majority of the photocurrent was generated in the silicon, with there being a sharp cutoff in photoresponse above the MAPI bandgap. Construction of band diagrams indicated the presence of an upward valence band spike of up to 0.5 eV at the n-Si/MAPI interface that could impede carrier flow. Evidence for hole accumulation at this feature was seen in both Kelvin-probe transients and from unusual features in both current–voltage and capacitance–voltage measurements. The devices achieved a hysteresis-free best power conversion efficiency of 2.08%, V OC 0.46 V, J SC 11.77 mA/cm2, and FF 38.4%, demonstrating for the first time that it is possible to create a heterojunction PV device directly between the MAPI and n-Si. Further prospects for two-sided n-Si/MAPI heterojunctions are also discussed.

Combining a perovskite top cell with a conventional passivated emitter and rear cell PERC silicon bottom cell in a monolithically integrated tandem device is an economically attractive solution to boost the power conversion efficiency PCE of silicon single junction technology. Proof of concept perovskite silicon tandem solar cells using high temperature stable bottom cells featuring a polycrystalline silicon on oxide POLO front junction and a PERC type passivated rear side with local aluminum p contacts are reported. For this PERC POLO cell, a process flow that is compatible with industrial, mainstream PERC technology is implemented. Top and bottom cells are connected via a tin doped indium oxide recombination layer. The recombination layer formation on the POLO front junction of the bottom cell is optimized by postdeposition annealing and mitigation of sputter damage. The perovskite top cell is monolithically integrated in a p amp; 8722;i amp; 8722;n junction device architecture. Proof of concept tandem cells demonstrate a PCE of up to 21.3 . Based on the experimental findings and supporting optical simulations, major performance enhancements by process and layer optimization are identified and a PCE potential of 29.5 for these perovskite silicon tandem solar cells with PERC like bottom cell technology is estimated

Incorporation of CdSe layers into CdTe thin film solar cells has recently emerged as a route to improve cell performance. It has been suggested that the formation of lower band gap CdTe(1-x)Se(x) phases following Se diffusion induces bandgap grading which may increase the carrier lifetime and thereby open circuit voltage. In this study we investigate the impact of CdSe incorporation on CdTe solar cell performance. We demonstrate that the standard CdS/CdTe device architecture is incompatible with Se incorporation, owing to large optical losses. An alternative cell structure with an oxide partner layer replacing the CdS with SnO2/CdSe/CdTe is developed, leading to cell efficiencies of > 13.5%. The differences in processing required for effective selenium incorporation are investigated with performance improvements resulting from additional post-growth annealing. Finally, other oxides such as TiO2, ZnO and FTO are demonstrated to be unsuitable partner layers but highlight that the choice of partner layer is key to further improving the performance.

In this manuscript, the inorganic perovskite CsPbI2Br is investigated as a photovoltaic material that offers higher stability than the organic-inorganic hybrid perovskite materials. It is demonstrated that CsPbI2Br does not irreversibly degrade to its component salts as in the case of methylammonium lead iodide but instead is induced (by water vapor) to transform from its metastable brown cubic (1.92 eV band gap) phase to a yellow phase having a higher band gap (2.85 eV). This is easily reversed by heating to 350 °C in a dry environment. Similarly, exposure of unencapsulated photovoltaic devices to water vapor causes current (JSC) loss as the absorber transforms to its more transparent (yellow) form, but this is also reversible by moderate heating, with over 100% recovery of the original device performance. NMR and thermal analysis show that the high band gap yellow phase does not contain detectable levels of water, implying that water induces the transformation but is not incorporated as a major component. Performances of devices with best efficiencies of 9.08% (VOC = 1.05 V, JSC = 12.7 mA cm-2 and FF = 68.4%) using a device structure comprising glass/ITO/c-TiO2/CsPbI2Br/Spiro-OMeTAD/Au are presented, and further results demonstrating the dependence of the performance on the preparation temperature of the solution processed CsPbI2Br films are shown. We conclude that encapsulation of CsPbI2Br to exclude water vapor should be sufficient to stabilize the cubic brown phase, making the material of interest for use in practical PV devices.

In this manuscript, the inorganic perovskite CsPbI

Guidance Document 25/2010, suggests sediment and biota are the most suitable matrices for the trend monitoring purpose, because they integrate the pollution over time and space. So, from 2005 to 2014, the sediment and biota concentrations of heavy metals (As, Cd, Cr, Hg, Ni, Pb) were analysed in the Vallona Lagoon (northern Adriatic Sea, Italy), widely used for intensive and extensive bivalve farming. The contamination levels in sediment and biota were compared with Environmental Quality Standard (EQS) and threshold levels (TL) for human health. The results identified critical issues related to Cd in sediment samples as well as to Hg and Pb in biota which were not only ascribable to the physiological and seasonal variability of organisms. The Cr and Ni levels in sediment were higher than the EQS. However, the concentration increases at biota stations close to sites where EQS excesses were observed in sediment were not verified.

The Decision No. 2455/2001/EC of the European Parliament and Council established a list of harmful and priority substances whose release into the aquatic environment should be eliminated or progressively reduced. Evaluation of the accumulation of these substances in sediment and organisms tissues is an aid in the assessment of the aquatic environment. Total concentrations and the fractionation of selected metals (Cd, Pb and Hg) in four sediment samples taken from two Italian ports, and their accumulation in Mytilus galloprovincialis Lam. tissues were measured. The investigation reveals differences in the accumulation pattern of metals in the mussel tissues corresponding to sediments characterized by different metal mobility. The metal concentrations frequently have been found to be greater than quality standards for Italian marine sediments (Ministerial Decree no. 367/03). Lead and Cd are mainly associated with the mobile fraction of sediment and show greater bioaccumulation in mussel samples, whe...

Fluorine-doped tin oxide (F-SnO 2 ) nanoparticles were prepared via the “benzyl alcohol route” assisted by microwave radiation. The samples were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD) and impedance spectroscopy. The synthesized F-SnO 2 nanoparticles showed a high degree of crystallinity and rather uniform size and shape. They were used as sensing layer in resistive sensors and their sensing properties towards H 2 were tested. The developed sensor showed high sensitivity upon exposure to H 2 gas, in the concentration range 0 – 4% in air, and extremely fast response and recovery time.