High defect tolerance ß-CsSnI3 perovskite light-emitting diodes.

All-inorganic lead-free CsSnI3 has shown promising potential in optoelectronic applications, particularly in near-infrared perovskite light-emitting diodes (Pero-LEDs). However, non-radiative recombination induced by defects hinders the optoelectronic properties of CsSnI3-based Pero-LEDs, limiting their potential applications. Here, we uncovered that ß-CsSnI3 exhibits higher defect tolerance compared to orthorhombic γ-CsSnI3, offering a potential for enhancing the emission efficiency. We further reported on the deposition and stabilization of highly crystalline ß-CsSnI3 films with the assistance of cesium formate to suppress electron-phonon scattering and reduce nonradiative recombination. This leads to an enhanced photoluminescence quantum yield up to ∼10%. As a result, near-infrared LEDs based on ß-CsSnI3 emitters are achieved with a peak external quantum efficiency of 1.81% and excellent stability under a high current injection of 1.0 A cm-2.

Regulating The Electronic Configuration of Low-Dimensional Hybrid Perovskites via Organic Cations for Self-Powered Ultraviolet Photodetectors.

Ultraviolet photodetectors (UPDs) based on low-dimensional halide perovskites have undergone rapid development. Here, regulation of the electronic configuration of low-dimensional hybrid perovskites are reported via organic cations for self-powered UPDs. For the first time, it is determine that the rational design of organic cation phenyl alkylammonium can effectively prevent phonon scattering thus increasing charge carrier extraction in low dimensional lead chlorine perovskite thin-films. As a result, the exciton-binding energy can be reduced to 62.91 meV in (PMA)2 PbCl4 perovskite films with a charge-carrier mobility of 0.335 cm2  V-1  s-1 . The fabricated (PMA)2 PbCl4 -based self-powered UPDs has achieved a high detectivity of 6.32 × 1013 jones with a low noise current of 0.35 pA Hz-1/2 under zero bias. A further demonstration of images with high UV to visible light rejection ratio under weak-light illumination of 70 nW cm-2 highlights the feasible potential application of low-dimensional perovskite.

Progress and Challenges Toward Effective Flexible Perovskite Solar Cells.

The demand for building-integrated photovoltaics and portable energy systems based on flexible photovoltaic technology such as perovskite embedded with exceptional flexibility and a superior power-to-mass ratio is enormous. The photoactive layer, i.e., the perovskite thin film, as a critical component of flexible perovskite solar cells (F-PSCs), still faces long-term stability issues when deformation occurs due to encountering temperature changes that also affect intrinsic rigidity. This literature investigation summarizes the main factors responsible for the rapid destruction of F-PSCs. We focus on long-term mechanical stability of F-PSCs together with the recent research protocols for improving this performance. Furthermore, we specify the progress in F-PSCs concerning precise design strategies of the functional layer to enhance the flexural endurance of perovskite films, such as internal stress engineering, grain boundary modification, self-healing strategy, and crystallization regulation. The existing challenges of oxygen-moisture stability and advanced encapsulation technologies of F-PSCs are also discussed. As concluding remarks, we propose our viewpoints on the large-scale commercial application of F-PSCs.

Surface Modification in CsPb0.5Sn0.5I2Br Inorganic Perovskite Solar Cells: Effects of Bifunctional Dipolar Molecules on Photovoltaic Performance.

Inorganic tin-lead binary perovskites have piqued the interest of researchers as effective absorbers for thermally stable solar cells. However, the nonradiative recombination originating from the surface undercoordinated Sn2+ cations and the energetic offsets between different layers cause an excessive energy loss and deteriorate the perovskite device's performance. In this study, we investigated two thioamide derivatives that differ only in the polar part connected to their common benzene ring, namely, benzenecarbothioamide and 4-fluorophenylcarbothioamide (F-TBA). These two molecules were implemented as modifiers onto the inorganic tin-lead perovskite (CsPb0.5Sn0.5I2Br) surface in the perovskite solar cells. Modifiers that carry C═S and NH2 functional groups, equipped with lone electron pairs, can autonomously associate with surface Sn2+ through coordination and electrostatic attraction mechanisms. This interaction serves effectively to passivate the surface. In addition, due to the permanent dipole moment of the intermediate layer, an interfacial dipole field appears at the PCBM/CsPb0.5Sn0.5I2Br interface, reducing the electron extraction potential barrier. Consequently, the planar solar cell with an ITO/PEDOT:PSS/CsPb0.5Sn0.5I2Br/PCBM/BCP/Ag layered structure featuring an F-TBA surface post-treatment demonstrated a noteworthy power conversion efficiency of 14.01%. Simultaneously, after being stored for 1000 h in an inert atmosphere glovebox, the non-encapsulated CsPb0.5Sn0.5I2Br solar cells managed to preserve 94% of their original efficiency.

Single-Crystal Nanowire Cesium Tin Triiodide Perovskite Solar Cell.

This work reports for the first time a highly efficient single-crystal cesium tin triiodide (CsSnI3 ) perovskite nanowire solar cell. With a perfect lattice structure, low carrier trap density (≈5 × 1010 cm-3 ), long carrier lifetime (46.7 ns), and excellent carrier mobility (>600 cm2 V-1 s-1 ), single-crystal CsSnI3 perovskite nanowires enable a very attractive feature for flexible perovskite photovoltaics to power active micro-scale electronic devices. Using CsSnI3 single-crystal nanowire in conjunction with highly conductive wide bandgap semiconductors as front-surface-field layers, an unprecedented efficiency of 11.7% under AM 1.5G illumination is achieved. This work demonstrates the feasibility of all-inorganic tin-based perovskite solar cells via crystallinity and device-structure improvement for the high-performance, and thus paves the way for the energy supply to flexible wearable devices in the future.

Fabrication of High-Quality CsPbI3 Perovskite Films with Phosphorus Pentachloride Additive for Highly Stable Solar Cells.

Fully inorganic perovskite cesium lead triiodide (CsPbI3 ) has garnered much attention from researcher for photovoltaic application because of its excellent thermal stability compared with the inorganic-organic hybrid counterparts, along with the potential to serve as the top cell in tandem devices with silicon solar cell. However, the active α-phase cubic CsPbI3 spontaneously tends to transform into the non-perovskite δ-CsPbI3 when subjected to ambient condition. This work proposes an effective method to fabricate high-quality and stable α-phase cubic CsPbI3 films by introducing phosphorus pentachloride (PCl5 ) as an additive. PCl5 acts as colloidal binder for modulating crystallization dynamics of perovskites, resulting in high-quality film and a significantly suppressed phase transition. Finally, highly stable CsPbI3 perovskite solar cells can be achieved with a power conversion efficiency up to 17.85 %, and a long-term stability in N2 filled glove box.

Controlling Quantum-Well Width Distribution and Crystal Orientation in Two-Dimensional Tin Halide Perovskites via a Strong Interlayer Electrostatic Interaction.

Two-dimensional (2D) tin halide perovskites have recently emerged as very promising materials for eco-friendly lead-free photovoltaic devices. However, the fine control of the bulky organic cations orderly embedding into the perovskite structure with a narrow quantum-well width distribution and favorable orientation is rather complicated. In this study, we proposed to introduce the F-substituted phenylethlammonium (PEA) cation (i.e., 4-fluorophenethylammonium FPEA) in 2D tin halide perovskite, which may mitigate phase polydispersity and crystal orientation, thus potentially increasing attainable charge-carrier mobility. A strong interlayer electrostatic attraction between electron-deficient F atoms and its adjacent phenyl rings aligns the crystal structure, working together with the validated dipole interaction. Therefore, the fluorination of organic cation leads to orderly self-assembly of solvated intermediates and promotes vertical crystal orientation. Furthermore, the interlayer electrostatic interaction serves as a supramolecular anchor to stabilize the 2D tin halide perovskite structure. Our work uncovers the effect of interlayer molecular interaction on efficiency and stability, which contributes to the development of stable and efficient low-toxicity perovskite solar cells.

Structure evolution characterization of Anyang anthracites via H2O2 oxidization and HF acidification.

The structural characteristics of the raw coal (AY), the H2O2 oxidized coals (AY-H2O2) and the HF acidized AY-H2O2 (AY-H2O2-HF) were investigated by SEM, X-ray diffraction, Raman and FTIR spectroscopy. The results indicate that the derivative coals show an obvious increase in the aromaticity, crystalline carbon content and hydroxyl content, especially the AY-H2O2-HF. The stacking layer number of crystalline carbon decreases and the aspect ratio (La/Lc) remarkably increases for AY-H2O2 and AY-H2O2-HF. The crystalline layers become much thinner. The particle size of AY-H2O2-HF in width significantly decreases from 1 µm to less than 100 nm. The combination of H2O2 oxidization and HF acidification is effective to reduce the size of the aromatic layers and to increase the reactivity of derivative coals. The process can help us obtain the superfine crystalline carbon materials like graphite structure.