All-inorganic lead halide perovskites demonstrate improved thermal stability over the organic-inorganic halide perovskites, but the cubic α-CsPbI with the most appropriate bandgap for light harvesting is not structurally stable at room temperature and spontaneously transforms into the undesired orthorhombic δ-CsPbI. Here, we present a new member of black-phase thin films of all-inorganic perovskites for high-efficiency photovoltaics, the orthorhombic γ-CsPbI thin films with intrinsic thermodynamic stability and ideal electronic structure. Exempt from introducing organic ligands or incorporating mixed cations/anions into the crystal lattice, we stabilize the γ-CsPbI thin films by a simple solution process in which a small amount of HO manipulates the size-dependent phase formation through a proton transfer reaction. Theoretical calculations coupled with experiments show that γ-CsPbI with a lower surface free energy becomes thermodynamically preferred over δ-CsPbI at surface areas greater than 8600 m/mol and exhibits comparable optoelectronic properties to α-CsPbI. Consequently, γ-CsPbI-based solar cells display a highly reproducible efficiency of 11.3%, among the highest records for CsPbI thin-film solar cells, with robust stability in ambient atmosphere for months and continuous operating conditions for hours. Our study provides a novel and fundamental perspective to overcome the Achilles' heel of the inorganic lead iodide perovskite and opens it up for high-performance optoelectronic devices.

Hybrid organic/inorganic lead halide perovskites (LHPs) have recently emerged as extremely promising photonic materials. However, the exploration of their optical nonlinearities has been mainly focused on the third- and higher-order nonlinear optical (NLO) effects. Strong second-order NLO responses are hardly expected from ordinary LHPs due to their intrinsic centrosymmetric structures, but are highly desirable for advancing their applications in the next generation integrated photonic circuits. Here we demonstrate the fabrication of a novel noncentrosymmetric LHP material by introducing chiral amines as the organic component. The nanowires grown from this new LHP material crystallize in a noncentrosymmetric P1 space group and demonstrate highly efficient second harmonic generation (SHG) with high polarization ratios and chiroptical NLO effects. Such a chiral perovskite skeleton could provide a new platform for future engineering of optoelectronic functionalities of hybrid perovskite materials.

Complex compositional engineering of mixed halides/mixed cations perovskites has recently fostered a rapid progress in perovskite solar cell technology. Here we demonstrate that when 10% of formamidinium (FA +) is simply added into methylammonium lead iodide (MAPbI 3) a highly crystalline and compositionally uniform perovskite is formed, self-organizing into a stable "quasi-cubic" phase at room temperature. We reached power conversion efficiency of over 20.2%, the highest value reported to date for FA x MA 1−x PbI 3 perovskite.

Graphdiyne is a new carbon allotrope comprising sp‐ and sp2‐hybridized carbon atoms arranged in a 2D layered structure. In this contribution, 2D graphdiyne is demonstrated to exhibit a strong light–matter interaction with high stability to achieve a broadband Kerr nonlinear optical response, which is useful for nonreciprocal light propagation in passive photonic diodes. Furthermore, advantage of the unique Kerr nonlinearity of 2D graphdiyne is taken and a nonreciprocal light propagation device is proposed based on the novel similarity comparison method. Graphdiyne has demonstrated a large nonlinear refractive index in the order of ≈10−5 cm2 W−1, comparing favorably to that of graphene. Based on the strong Kerr nonlinearity of 2D graphdiyne, a nonlinear photonic diode that breaks time‐reversal symmetry is demonstrated to realize the unidirectional excitation of Kerr nonlinearity, which can be regarded as a significant demonstration of a graphdiyne‐based prototypical application in nonlinear photonics and might suggest an important step toward versatile graphdiyne‐based advanced passive photonics devices in the future.

Organic–inorganic metal halide perovskite solar cells (PSCs) have achieved certified power conversion efficiency (PCE) of 25.2% with complex compositional and bandgap engineering. However, the thermal instability of methylammonium (MA) cation can cause the degradation of the perovskite film, remaining a risk for the long‐term stability of the devices. Herein, a unique method is demonstrated to fabricate highly phase‐stable perovskite film without MA by introducing cesium chloride (CsCl) in the double cation (Cs, formamidinium) perovskite precursor. Moreover, due to the suboptimal bandgap of bromide (Br−), the amount of Br− is regulated, leading to high power conversion efficiency. As a result, MA‐free perovskite solar cells achieve remarkable long‐term stability and a PCE of 20.50%, which is one of the best results for MA‐free PSCs. Moreover, the unencapsulated device retains about 80% of the original efficiencies after a 1000 h aging study. These results provide a feasible approach to enhance solar cell stability and performance simultaneously, paving the way for commercializing PSCs.

Oxygen vacancy is intrinsically coupled with magnetic, electronic, and transport properties of transition-metal oxide materials and directly determines their multifunctionality. Here, we demonstrate reversible control of oxygen content by postannealing at temperature lower than 300 °C and realize the reversible metal-insulator transition in epitaxial NdNiO₃ films. Importantly, over 6 orders of magnitude in the resistance modulation and a large change in optical bandgap are demonstrated at room temperature without destroying the parent framework and changing the p-type conductive mechanism. Further study revealed that oxygen vacancies stabilized the insulating phase at room temperature is universal for perovskite nickelate films. Acting as electron donors, oxygen vacancies not only stabilize the insulating phase at room temperature, but also induce a large magnetization of ∼50 emu/cm³ due to the formation of strongly correlated Ni²⁺ t(2g)⁶e(g)² states. The bandgap opening is an order of magnitude larger than that of the thermally driven metal-insulator transition and continuously tunable. Potential application of the newly found insulating phase in photovoltaics has been demonstrated in the nickelate-based heterojunctions. Our discovery opens up new possibilities for strongly correlated perovskite nickelates.

Halide perovskites have emerged as a type of extremely promising material for their diverse chemical and electronic structures along with their brilliant optoelectronic properties. The introduction of chirality into perovskite scaffolds, generating a novel concept of chiral perovskite materials, offers an immense step forward toward the development of smart optoelectronic and spintronic materials and devices. The present Review summarizes recent advances in such an emerging field regarding the design and construction of chiral perovskite materials, along with their optoelectronic performances. In addition, an outlook of future challenges as well as the potential significance of the chiral perovskite family on the optical communication is proposed.

Functionalized imidazolium iodide salts (ionic liquids) modified with CH CHCH , CH CCH, or CH CN groups are applied as dopants in the synthesis of CH NH PbI -type perovskites together with a fumigation step. Notably, a solar cell device prepared from the perovskite film doped with the salt containing the CH CHCH side-chain has a power conversion efficiency of 19.21%, which is the highest efficiency reported for perovskite solar cells involving a fumigation step. However, doping with the imidazolium salts with the CH CCH and CH CN groups result in perovskite layers that lead to solar cell devices with similar or lower power conversion efficiencies than the dopant-free cell.