Aminoazanium of A-site Cations in Metal-Free Halide Perovskite Single Crystals to Reduce Thermal Expansion for Efficient X-ray Detection.

Metal-free perovskites (MFPs) have recently become a newcomer in X-ray detection due to their flexibility and low toxicity characteristics. However, their photoelectronic properties and stability should be further improved mainly through materials design. Here, the aminoazanium of DABCO2+ was developed for the preparation of NDABCO-NH4Br3 (NDABCO = N-amino-N'-diazabicyclo[2.2.2]octonium) single crystals (SCs), and its physical properties, intermolecular interactions, and device performance were systematically explored. Notably, NDABCO-NH4Br3 can achieve improved stability by enlarging defect formation energy and inducing abundant intermolecular forces. Moreover, the slight lattice distortion could ensure the weakening electron-phonon coupling for improving carrier transport. In particular, the slight lattice distortion after the long-chain NDABCO2+ introduction could retard thermal expansion for the preparation of high-quality crystals. Finally, the corresponding X-ray detector delivered a moderate sensitivity of 623.3 µC Gyair-1 cm-2. This work provides a novel strategy through rationally designed organic cations to balance the material stability and device performance.

Metal-Free Hydrazinium Halide Perovskitoid Single Crystals for X-ray Detection.

Metal-free perovskitoids (MFPs) with N2H5+ as B-site component possess higher crystal density and hydrogen bonding networks and have been recently expanded into X-ray detection. However, research on this material is in its infancy and lacks an understanding of the function of halide components on physical properties and device performance. Here, N2H5-based MFP single crystals (SCs) with different halides are fabricated, and the influence of halides on the crystal structure, band nature, charge transport characteristics, and final device performance is actively explored. Based on theory and experiments, the tolerance factor and octahedral factor jointly determine the octahedral composition. Further, halides with different electronegativities and ionic radii also affect octahedral distortion and energy band bending, further influencing carrier transport and device performance. Finally, a sensitivity of 1284 µC Gyair-1 cm-2 and low detection limits (LoD) of 5.62 µGyair s-1 were obtained by the Br-based device due to its superior physical properties.

Metal-Free Perovskites for X-Ray Detection.

Metal-free perovskites are a promising class of materials for X-ray detection due to their unique structural, optical, and electrical properties. Here, we first delve into the stoichiometry and geometric argument of metal-free perovskites. Followed, the alternative A/B/X ions and hydrogen-bonding are clearly introduced to further optimize the materials' stability and properties. Finally, we provide a comprehensive overview of their potential applications for flexible X-ray images and prospects for metal-free perovskite development. In conclusion, metal-free perovskite is a promising material for X-ray detection. Its stoichiometric and geometric parameters, ion, and hydrogen bond selection, and application prospects are worthy of further study.

PF6 - Pseudohalides Anion Based Metal-Free Perovskite Single Crystal for Stable X-Ray Detector to Attain Record Sensitivity.

Metal-free perovskites (MFPs) possess excellent photophysical properties of perovskites while avoiding the introduction of toxic metal ions and organic solvents, and have been expanded to X-ray detection. However, iodine-based high-performance MFPs are tended to oxidation, corrosion, and uncontrolled ion migration, resulting in poor material stability and device performance. Herein, the strongly electronegative PF6 - pseudohalide is used to fabricate the large-size MDABCO-NH4 (PF6 )3 (MDBACO = methyl-N'-diazabicyclo[2.2.2]octonium) single crystals (SCs) for solving the problems of iodine ions. After the introduction of PF6 - pseudohalides, the Coulomb interaction and hydrogen bonding strength are enhanced to alleviate the ion-migration and stability problems. Moreover, combined with theoretical calculations, PF6 - pseudohalides increase the ion-migration barrier, and affect the contribution of its components to the energy band for a broadening bandgap. Meanwhile, the improved physical properties, such as large activation energy of ionic migration, high resistivity, and low current drift, further expand its application in low-dose and sensitive X-ray detection. Finally, the X-ray detector based on MDABCO-NH4 (PF6 )3 SCs achieves a sensitivity of 2078 µC Gyair -1 cm-2 (highest among metal-free SCs-based detectors) and the lowest detectable dose rate (16.3 nGyair s-1 ). This work has expanded the selection of MFPs for X-ray detectors and somewhat advanced the development of high-performance devices.

Hydrogen Bonds Strengthened Metal-Free Perovskite for Degradable X-ray Detector with Enhanced Stability, Flexibility and Sensitivity.

Metal-free perovskites (MFPs) with flexible and degradable properties have been adopted in flexible X-ray detection. For now, figuring out the key factors between structure and device performance are critical to guide the design of MFPs. Herein, MPAZE-NH4 I3 ⋅ H2 O was first designed and synthesized with improved structural stability and device performance. Through theoretical calculations, the introducing methyl group benefits modulating tolerance factor, increases dipole moment and strengthens hydrogen bonds. Meanwhile, H2 O increases the hydrogen bond formation sites and synergistically realizes the band nature modulation, ionic migration inhibition and structural stiffness optimization. Spectra analysis also proves that the improved electron-phonon coupling and carrier recombination lifetime contribute to enhanced performance. Finally, a flexible and degradable X-ray detector was fabricated with the highest sensitivity of 740.8 µC Gyair -1 cm-2 and low detection limit (0.14 nGyair s-1 ).

Novel PHA Organic Spacer Increases Interlayer Interactions for High Efficiency in 2D Ruddlesden-Popper CsPbI3 Solar Cells.

The two-dimensional (2D) Ruddlesden-Popper (RP) CsPbI3 with hydrophobic organic spacers can significantly improve the environmental and phase stability of photovoltaic devices by suppressing ion migration and inducing steric hindrance. However, due to the multiple-quantum-well structure, these spacer cations lead to weak interactions in 2D RP CsPbI3, which seriously affect the carrier transport. Here, a novel N-H-group-rich phenylhydrazine spacer, namely, PHA, was developed for 2D RP CsPbI3 perovskite solar cells (PSCs). A series of characterizations confirm that the 2D perovskites using PHA spacers enhanced the N-H···I hydrogen-bonding interaction between the organic spacer cations and the [PbI6]4- inorganic layer and accelerated the crystallization rate of the perovskite film, which was beneficial to the preparation of high-quality films with preferred vertical orientation, large grain size, and dense morphology. Meanwhile, the trap state density of the as-prepared 2D RP perovskite films is significantly reduced to enable efficient charge carrier transport. As a result, the (PHA)2Cs4Pb5I16 PSCs achieved a performance of 16.23% with good environmental stability. This work provides a simple organic spacer selection scheme to realize interaction optimization in 2D RP CsPbI3 to develop efficient and stable PSCs.

Metal-Free PAZE-NH4 X3 ⋠H2 O Perovskite for Flexible Transparent X-ray Detection and Imaging.

Metal-free perovskites are of interest for their chemical diversity and eco-friendly properties, and recently have been used for X-ray detection with superior carrier behavior. However, the size and shape complexity of the organic components results in difficulties in evaluating their stability in high-energy radiation. Herein, we introduce multiple hydrogen-bond metal-free PAZE-NH4 X3 ⋅H2 O perovskite, where H2 O leads to more hydrogen bonds appearing between organic molecules and the perovskite host. As suggested by the theoretical calculations, multiple hydrogen bonds promote stiffness of the lattice, and increase the diffusion barrier to inhibit ionic migration. Then, low trap density, high µτ products and structural flexibility of PAZE-NH4 Br3 ⋅H2 O give a flexible X-ray detector with the highest sensitivity of 3708 µC Gyair -1 cm-2 , ultra-low detection limit of 0.19 µGyair -1 s-1 and superior spatial resolution of 5.0 lp mm-1 .

Ordered Element Distributed C3 N Quantum Dots Manipulated Crystallization Kinetics for 2D CsPbI3 Solar Cells with Ultra-High Performance.

Two-dimensional (2D) CsPbI3 is developed to conquer the phase-stability problem of CsPbI3 by introducing bulky organic cations to produce a steric hindrance effect. However, organic cations also inevitably increase the formation energy and difficulty in crystallization kinetics regulation. Such poor crystallization process modulation of 2D CsPbI3 leads to disordered phase-arrangement, which impedes the transport of photo-generated carriers and worsens device performance. Herein, a type of C3 N quantum dots (QDs) with ordered carbon and nitrogen atoms to manipulate the crystallization process of 2D CsPbI3 for improving the crystallization pathway, phase-arrangement and morphology, is introduced. Combination analyses of theoretical simulation, morphology regulation and femtosecond transient absorption (fs-TA) characterization, show that the C3 N QDs induce the formation of electron-rich regions to adsorb bulky organic cations and provide nucleation sites to realize a bi-directional crystallization process. Meanwhile, the quality of 2D CsPbI3 film is improved with lower trap density, higher surface potential, and compact morphology. As a result, the power conversion efficiency (PCE) of the optimized device (n = 5) boosts to an ultra-high value of 15.63% with strengthened environmental stability. Moreover, the simple C3 N QDs insertion method shows good universality to other bulky organic cations of Ruddlesden-Popper and Dion-Jacobson, providing a good modulation strategy for other optoelectronic devices.

Strategies for Improving the Stability of Tin-Based Perovskite (ASnX3) Solar Cells.

Although lead-based perovskite solar cells (PSCs) are highly efficient, the toxicity of lead (Pb) limits its large-scale commercialization. As such, there is an urgent need to find alternatives. Many studies have examined tin-based PSCs. However, pure tin-based perovskites are easily oxidized in the air or just in glovebox with an ultrasmall amount of oxygen. Such a characteristic makes their performance and stability less ideal compared with those of lead-based perovskites. Herein, how to address the instability of tin-based perovskites is introduced in detail. First, the crystalline structure, optical properties, and sources of instability of tin-based perovskites are summarized. Next, the preparation methods of tin-based perovskite are discussed. Then, various measures for solving the instability problem are explained using four strategies: additive engineering, deoxidizer, partial substitution, and reduced dimensions. Finally, the challenges and prospects are laid out to help researchers develop highly efficient and stable tin-based perovskites in the future.

Unveiling the Effects of Hydrolysis-Derived DMAI/DMAPbI x Intermediate Compound on the Performance of CsPbI3 Solar Cells.

Introducing hydroiodic acid (HI) as a hydrolysis-derived precursor of the intermediate compounds has become an increasingly important issue for fabricating high quality and stable CsPbI3 perovskite solar cells (PSCs). However, the materials composition of the intermediate compounds and their effects on the device performance remain unclear. Here, a series of high-quality intermediate compounds are prepared and it is shown that they consist of DMAI/DMAPbI x . Further characterization of the products show that the main component of this system is still CsPbI3. Most of the dimethylammonium (DMA+) organic component is lost during annealing. Only an ultrasmall amount of DMA+ is doped into the CsPbI3 and its structure is stabilized. Meanwhile, excessive DMA+ forms Lewis acid-base adducts and interactions with Pb2+ on the CsPbI3 surface. This process passivates the CsPbI3 film and decreases the recombination rate. Finally, CsPbI3 film is fabricated with high crystalline, uniform morphology, and excellent stability. Its corresponding PSC exhibits stable property and improved power conversion efficiency (PCE) up to 17.3%.