DL-Serine Hydrazide Hydrochloride Multiple-site Synergy Induced Effective and Stable Formamidine-Rich Perovskite Solar Cells.

The efficiency and stability of solar cells are two key indicators that determine for the commercial feasibility of photovoltaic devices. Formamidine-cesium perovskite has been extensively investigated since its excellent thermal stability and has great potential in achieving high power conversion efficiency. However, during the aging process, especially under light conditions, formamidine-rich perovskites are prone to produce iodine, and the escape of iodine is one of the important factors leading to device degradation. Here, DL-Serine Hydrazide Hydrochloride containing the reducing group is introduced into the precursor solution of formamidine-cesium perovskite, which achieves multiple-site passivation. Hydrazine reacts with iodine to reduce it to iodine ions, inhibiting the escape of iodine. In addition, carbonyl groups and uncoordinated lead ions form coordination bonds to reduce defects. In the end, the perovskite solar cell with DL-Serine Hydrazide Hydrochloride added achieves a champion efficiency of 22.22%, and maintains 85.88% of the initial efficiency after continuous exposure under 1 sun for 7000 s at a relative humidity of ≈40%. Additionally, DL-Serine Hydrazide Hydrochloride added device shows good stability in air environments with relative humidity of 50%-60%. DL-Serine Hydrazide Hydrochloride improves the stability of formamidine-rich perovskite solar cells and provides a low-cost strategy for commercial development.

Unlocking the Ambient Temperature Effect on FA-Based Perovskites Crystallization by In Situ Optical Method.

Multiple cation-composited perovskites are demonstrated as a promising approach to improving the performance and stability of perovskite solar cells (PSCs). However, recipes developed for fabricating high-performance perovskites in laboratories are always not transferable in large-scale production, as perovskite crystallization is highly sensitive to processing conditions. Here, using an in situ optical method, the ambient temperature effect on the crystallization process in multiple cation-composited perovskites is investigated. It is found that the typical solvent-coordinated intermediate phase in methylammonium lead iodide (MAPbI3 ) is absent in formamidinium lead iodide (FAPbI3 ), and nucleation is almost completed in FAPbI3 right after spin-coating. Interestingly, it is found that there is noticeable nuclei aggregation in Formamidinium (FA)-based perovskites even during the spin-coating process, which is usually only observed during the annealing in MAPbI3 . Such aggregation is further promoted at a higher ambient temperature or in higher FA content. Instead of the general belief of stress release-induced crack formation, it is proposed that the origin of the cracks in FA-based perovskites is due to the aggregation-induced solute depletion effect. This work reveals the limiting factors for achieving high-quality FA-based perovskite films and helps to unlock the existing narrow processing window for future large-scale production.

Simultaneous removal of Cr(III) and V(V) and enhanced synthesis of high-grade rutile TiO2 based on sodium carbonate decomposition.

Rutile TiO2 is widely applied as the raw material to produce titanium dioxide and titanium sponge, whereas the Cr (III) and V (V) impurities in rutile TiO2 significantly affect the performance of related products. In the present work, the sodium carbonate decomposition treatment on Panzhihua titanium slag was attempted, to improve the preparation process of rutile TiO2 with high crystallinity and simultaneously reduce the chromium (Cr) and vanadium (V) content as hazardous elements. Effects of sodium carbonate decomposition treatment on the crystal composition, microstructure of rutile TiO2 were determined using XRD, SEM and Raman characterization. The recovery of Cr(III) and V(V) was achieved through leaching the roasted titanium slag by dilute sulfuric acid, with the chromium and vanadium content in the residue decreasing up to 0.03 % and 0.04 %, respectively, followed by the final product rutile TiO2 was produced by the leaching residue calcined at 1323.15 K with a duration time of 120 min, with 85.56 % of TiO2 grade. The work highlights the feasibility of synchronously preparing rutile TiO2 and removing hazardous Cr (III) and V (V) impurities from titanium slag using sodium carbonate decomposition.

Microwave absorption properties of steelmaking dusts: effects of temperature on the dielectric constant (ε') and loss factor (ε'') at 1064 MHz and 2423 MHz.

The microwave absorption properties of a material depend largely on the dielectric properties of the material being heated. Therefore, the influences of temperature on the dielectric constant (ε'), loss factor (ε''), loss tangent (tan δ d) and penetration depth (D P) of steelmaking dust at frequencies of 1064 MHz and 2423 MHz were measured. Three steelmaking dust samples were studied. The effects of temperature on the dielectric properties of the samples were insignificant at temperatures below 600 °C. However, above this temperature, a rapid rise in the values of the dielectric properties of the samples was observed. Comparing the thermogravimetric analysis and differential scanning calorimetry (TGA-DSC) results and mass spectra (MS) of the dusts with their dielectric properties revealed that the changes in the dielectric values of the dusts were associated with the thermal decomposition of calcium carbonate and the release of CO/CO2 gases. Furthermore, the increase in the electrical conductivity of the samples at high temperature resulted in increased dielectric values. The behavior of the loss tangent of the samples with increasing temperature coincided with the behavior of the loss factor. The penetration depth decreased with an increase in temperature at both frequencies, while an increase in the dielectric properties caused a significant decrease in the penetration depth. The results indicated that steelmaking dusts have good microwave absorbing properties owing to their carbon and iron oxide contents.

Improving hydrocarbon yield via catalytic fast co-pyrolysis of biomass and plastic over ceria and HZSM-5: An analytical pyrolyzer analysis.

The excessive oxygen content in biomass obstructs the production of high-quality bio-oils. In this work, we developed a tandem catalytic bed (TCB) of CeO2 and HZSM-5 in an analytical pyrolyzer to enhance the hydrocarbon production from co-pyrolysis of corn stover (CS) and LDPE. Results indicated that CeO2 could remove oxygen from acids, aldehydes and methoxy phenols, producing a maximum yield of hydrocarbons of 85% and highest selectivity of monocyclic aromatics of 73% in the TCB. The addition of LDPE exhibited a near-complete elimination of oxygenates, leaving hydrocarbons as the overwhelming products. With increasing LDPE proportion, the yield of aliphatics and the selectivity of BTX kept increasing. An optimum H/Ceff of 0.7 was superior to that reported in literature. Mechanisms consisting of deoxygenation, Diels-Alder reactions, hydrocarbon pool and hydrogen transfer reactions were discussed extensively. Our findings provide an efficient method to produce high-quality biofuels from renewable biomass resources.