High-Efficiency Perovskite Solar Cells with Improved Interfacial Charge Extraction by Bridging Molecules.

The interface between the perovskite layer and electron transporting layer is a critical determinate for the performance and stability of perovskite solar cells (PSCs). The heterogeneity of the interface critically affects the carrier dynamics at the buried interface. To address this, a bridging molecule, (2-aminoethyl)phosphonic acid (AEP), is introduced for the modification of SnO2/perovskite buried interface in n-i-p structure PSCs. The phosphonic acid group strongly bonds to the SnO2 surface, effectively suppressing the surface carrier traps and leakage current, and uniforming the surface potential. Meanwhile, the amino group influences the growth of perovskite film, resulting in higher crystallinity, phase purity, and fewer defects. Furthermore, the bridging molecules facilitate the charge extraction at the interface, as indicated by the femtosecond transient reflection (fs-TR) spectroscopy, leading to champion power conversion efficiency (PCE) of 26.40% (certified 25.98%) for PSCs. Additionally, the strengthened interface enables improved operational durability of ≈1400 h for the unencapsulated PSCs under ISOS-L-1I protocol.

Realizing Stable Perovskite Solar Cells with Efficiency Exceeding 25.6% Through Crystallization Kinetics and Spatial Orientation Regulation.

Organic-inorganic hybrid perovskites have emerged as highly promising candidates for photovoltaic applications, owing to the exceptional optoelectronic properties and low cost. Nonetheless, the performance and stability of solar cells suffer from the defect states of perovskite films aroused by non-optically active phases and non-centralized crystal orientation. Herein, a versatile organic molecule, Hydantoin, to modulate the crystallization of perovskite, is developed. Benefiting from the diverse functional groups, more spatially oriented perovskite films with high crystallinity are formed. This enhancement is accompanied by a conspicuous reduction in defect density, yielding efficiency of 25.66% (certified 25.15%), with superb environmental stability. Notably, under the standard measurement conditions (ISOS-L-1I), the maximum power point (MPP) output maintains 96.8% of the initial efficiency for 1600 h and exhibits excellent ion migration suppression. The synergistic regulation of crystallization and spatial orientation offers novel avenues for propelling perovskite solar cell (PSC) development.

Multifunctional Additive CdAc2 for Efficient Perovskite-Based Solar Cells.

Polycrystalline perovskite films fabricated on flexible and textured substrates often are highly defective, leading to poor performance of perovskite devices. Finding substrate-tolerant perovskite fabrication strategies is therefore paramount. Herein, this study shows that adding a small amount of Cadmium Acetate (CdAc2 ) in the PbI2 precursor solution results in nano-hole array films and improves the diffusion of organic salts in PbI2 and promotes favorable crystal orientation and suppresses non-radiative recombination. Polycrystalline perovskite films on the flexible substrate with ultra-long carrier lifetimes exceeding 6 µs are achieved. Eventually, a power conversion efficiency (PCE) of 22.78% is obtained for single-junction flexible perovskite solar cells (FPSCs). Furthermore, it is found that the strategy is also applicable for textured tandem solar cells. A champion PCE of 29.25% (0.5003 cm2 ) is demonstrated for perovskite/silicon tandem solar cells (TSCs) with CdAc2 . Moreover, the un-encapsulated TSCs maintains 109.78% of its initial efficiency after 300 h operational at 45 °C in a  nitrogen atmosphere. This study provides a facile strategy for achieving high-efficiency perovskite-based solar cells.

Secondary Anti-Solvent Treatment for Efficient 2D Dion-Jacobson Perovskite Solar Cells.

Surface defects-mediated nonradiative recombination plays a critical role in the performance and stability of perovskite solar cells (PSCs) and surface post-treatment is widely used for efficient PSCs. However, the commonly used surface passivation strategies are one-off and the passivation defect ability is limited, which can only solve part of the defects in the topmost surface area. Here, a secondary anti-solvent strategy is proposed to further reduce surface defects based on conventional surface passivation for the first time. Based on this, the crystallization quality of 2D Dion-Jacobson perovskite is enhanced and the surface defects density is further reduced by nearly two orders. In addition, a gradient structure of perovskite with n = 2 phases located at the top of the film and 3D-like phases located at the bottom of the film can also be obtained. The modulated perovskite film boosts the efficiency of 2D perovskites (n = 5) up to 19.55%. This strategy is also very useful in other anti-solvent processed perovskite dipping systems, which paves a promising avenue for minimizing surface defects toward highly efficient perovskite devices.

CsPbCl3 -Cluster-Widened Bandgap and Inhibited Phase Segregation in a Wide-Bandgap Perovskite and its Application to NiOx -Based Perovskite/Silicon Tandem Solar Cells.

Nickel oxide (NiOx ) is an attractive hole-transport material for efficient and stable p-i-n metal-halide perovskite solar cells (PSCs). However, an undesirable redox reaction occurs at the NiOx /perovskite interface, which results in a low open-circuit voltage (VOC ), instability, and phase separation of the NiOx -based wide-bandgap perovskite (Br > 20%). In order to simultaneously address the abovementioned phase separation problem and redox chemistry at the perovskite/NiOx interface, the bandgap is widened from 1.64 to 1.67 eV by adding inorganic CsPbCl3 -clusters (3 mol%) to the Cs22 Br15 perovskite precursor solution. Moreover, adding extra 2 mol% CsCl enriches the NiOx /perovskite interface with Cl, thereby preventing the redox reaction at the interface, while controlling the Br content to within 15% improves the photostability of the wide-bandgap perovskite. Consequently, the power conversion efficiency (PCE) of a single-junction p-i-n PSC increases from 17.82% to 19.76%, which leads to the fabrication of highly efficient monolithic p-i-n-type NiOx -based perovskite/silicon tandem solar cells with PCEs of up to 27.26% (certified PCE: 27.15%). The perovskite to an n-i-p-type perovskite/silicon tandem solar cell is also applied to deliver a VOC of 1.93 V and a final efficiency of 25.5%. These findings provide critical insight into the fabrication of highly efficient and stable wide-bandgap perovskites.

Novel Three-Dimensional Graphene-Like Networks Loaded with Fe3O4 Nanoparticles for Efficient Microwave Absorption.

A novel three-dimensional graphene-like networks material (3D-GLN) exhibiting the hierarchical porous structure was fabricated with a large-scale preparation method by employing an ion exchange resin as a carbon precursor. 3D-GLN was first studied as the effective microwave absorbing material. As indicated from the results of the electromagnetic parameter tests, and the minimum reflection loss (RL) of the 3D-GLN reached -34.75 dB at the frequency of 11.7 GHz. To enhance the absorption performance of the nonmagnetic 3D-GLN, the magnetic Fe3O4 nanoparticles were loaded on the surface of the 3D-GLN by using the hydrothermal method to develop the 3D-GLN/Fe3O4 hybrid. The hybrid exhibited the prominent absorbing properties. Under the matching thickness of 3.0 mm, the minimum RL value of hybrid reached -46.8 dB at 11.8 GHz. In addition, under the thickness range of 2.0-5.5 mm, the effective absorption bandwidth (RL < 10 dB) was 13.0 GHz, which covered part of the C-band and the entire X-band, as well as the entire Ku-band. The significant microwave absorption could be attributed to the special 3D network structure exhibited by the hybrid and the synergistic effect exerted by the graphene and the Fe3O4 nanoparticles. As revealed from the results, the 3D-GLN/Fe3O4 hybrid could be a novel microwave absorber with promising applications.

Quasi-Heteroface Perovskite Solar Cells.

Perovskite solar cells (PSCs) have attracted unprecedented attention due to their rapidly rising photoelectric conversion efficiency (PCE). In order to further improve the PCE of PSCs, new possible optimization path needs to be found. Here, quasi-heteroface PSCs (QHF-PSCs) is designed by a double-layer perovskite film. Such brand new PSCs have good carrier separation capabilities, effectively suppress the nonradiative recombination of the PSCs, and thus greatly improve the open-circuit voltage and PCE. The root cause of the performance improvement is the benefit from the additional built-in electric field, which is confirmed by measuring the external quantum efficiency under applied electric field and Kelvin probe force microscope. Meanwhile, an intermediate band gap perovskite layer can be obtained simply by combining a wide band gap perovskite layer with a narrow band gap perovskite layer. Tunability of the band gap is obtained by varying the film thicknesses of the narrow and wide band gap layers. This phenomenon is quite different from traditional inorganic solar cells, whose band gap is determined only by the narrowest band gap layer. It is believed that these QHF-PSCs will be an effective strategy to further enhance PCE in PSCs and provide basis to further understand and develop the perovskite materials platform.