Investigations of S-nZVI/AC composites for hexavalent chromium (Cr(VI)) elimination: synthesis and application.

Sulfidated nano zero-valent iron supported by activated carbon (S-nZVI/AC) composites were synthesized via liquid phase reduction method, and then they were used for Cr(VI) elimination. Characterization results showed that Fe0 was the main component, besides, iron oxides and iron sulfides were also detected. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) results showed that S-nZVI nanoparticles were homogeneously distributed on the surfaces of AC. The influences of S/Fe ratio, C/Fe ratio, pH value, reaction temperature and co-existed ions (Cl-, SO42-, PO43- and NO3-) on Cr(VI) removal performances were investigated. Furthermore, the corresponding mechanisms were also discussed. The S-nZVI/AC composites exhibited good aging-resistance performances that Cr(VI) removal efficiency still maintained at 83.1% after being sealed in water for seven days, and they also had satisfying cycling stabilities that Cr(VI) removal efficiency only decreased less than 10% after four cycles. The good performances of S-nZVI/AC composites for Cr(VI) removal are attributed to the protection effect of iron sulfides and immobilization effect of AC, making S-nZVI/AC as a promising candidate for Cr(VI) elimination in effluents.

A Coplanar π-Extended Quinoxaline Based Hole-Transporting Material Enabling over 21 % Efficiency for Dopant-Free Perovskite Solar Cells.

Developing dopant-free hole transporting materials (HTMs) is of vital importance for addressing the notorious stability issue of perovskite solar cells (PSCs). However, efficient dopant-free HTMs are scarce. Herein, we improve the performance of dopant-free HTMs featuring with a quinoxaline core via rational π-extension. Upon incorporating rotatable or chemically fixed thienyl substitutes on the pyrazine ring, the resulting molecular HTMs TQ3 and TQ4 show completely different molecular arrangement as well as charge transporting capabilities. Comparing with TQ3, the coplanar π-extended quinoxaline based TQ4 endows enriched intermolecular interactions and stronger π-π stacking, thus achieving a higher hole mobility of 2.08×10-4  cm2 V-1 s-1 . It also shows matched energy levels and high thermal stability for application in PSCs. Planar n-i-p structured PSCs employing dopant-free TQ4 as HTM exhibits power conversion efficiency (PCE) over 21 % with excellent long-term stability.

Minimizing buried interfacial defects for efficient inverted perovskite solar cells.

Controlling the perovskite morphology and defects at the buried perovskite-substrate interface is challenging for inverted perovskite solar cells. In this work, we report an amphiphilic molecular hole transporter, (2-(4-(bis(4-methoxyphenyl)amino)phenyl)-1-cyanovinyl)phosphonic acid, that features a multifunctional cyanovinyl phosphonic acid group and forms a superwetting underlayer for perovskite deposition, which enables high-quality perovskite films with minimized defects at the buried interface. The resulting perovskite film has a photoluminescence quantum yield of 17% and a Shockley-Read-Hall lifetime of nearly 7 microseconds and achieved a certified power conversion efficiency (PCE) of 25.4% with an open-circuit voltage of 1.21 volts and a fill factor of 84.7%. In addition, 1-square centimeter cells and 10-square centimeter minimodules show PCEs of 23.4 and 22.0%, respectively. Encapsulated modules exhibited high stability under both operational and damp heat test conditions.

Efficient and Stable Methylammonium-Free Tin-Lead Perovskite Solar Cells with Hexaazatrinaphthylene-Based Hole-Transporting Materials.

Incorporating non-aqueous hole-transporting materials (HTMs) to replace the widely used PEDOT:PSS is favorable for improving the stability of tin-lead perovskite solar cells (Sn-Pb PSCs). Herein, hexaazatrinaphthylene (HATNA) is found to be a promising HTM building block for Sn-Pb PSCs. By introducing triphenylamine (TPA) and methoxy-triphenylamine into the HATNA core, molecular energy levels and surface wettability can be well regulated, and a high hole mobility and thermal stability can be maintained. Moreover, a homogeneous Sn-Pb perovskite film with low Sn4+ contents and vertically orientated grains can be prepared on the substrate TPA-HATNA. Compared with PEDOT:PSS, the optimal TPA-HATNA-based methylammonium-free device enables a 70 mV increase in VOC, delivering a remarkable PCE exceeding 18% (certified 16.4%). Impressively, the TPA-HATNA-based devices without encapsulation retain 90% efficiency after aging for 600 min under maximum-power-point tracking. Our work provides alternative HTMs for boosting the performance of Sn-Pb PSCs.