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Glassy hybrid metal halides have emerged as promising materials in recent years due to their high structural adjustability and low melting points, offering unique merits that overcome the limitations of their crystalline and polycrystalline counterparts as well as other conventional amorphous semiconductors. This review article comprehensively explores the structural characteristics, electronic properties, and chemical coordination of hybrid metal halides, emphasizing their role in the glass transition from the crystalline phase to the amorphous phase. We examine the intrinsic disorder within the amorphous phase that facilitates light transmission and discuss recent advances in device architecture and interface engineering by optimizing the charge transport of glassy hybrid metal halides for high-quality applications. With full theoretical understanding and rational structural design, potential applications in displays, information storage, X-ray imaging, and sensing are highlighted, underscoring the transformative impact of glassy hybrid metal halides in the fields of materials science and information science. [ABSTRACT FROM AUTHOR]

Perovskite interfaces where defects enrich are pivotal for both device efficiency and stability. Herein, a high‐molecular‐weight polyvinyl pyrrolidone (PVP) is proposed as a robust multi‐functional interlayer to engineer the buried interface. Besides the well‐known defect passivation, perovskite crystallization is intriguingly modulated via the formation of hydrogen‐bond‐based polymer‐ammonium intermediates (e.g., PVP‐FA+ or PVP‐MA+, where MA and FA are methylamine and formamidine, respectively). The interaction energies derived from density functional theory calculations (−34.5, −26.8, and −9.9 kcal mol−1 for PVP‐FA+, PVP‐MA+, and PVP‐Pb2+) suggest that PVP predominately interacts with ammonium cations to form the intermediates, thus largely excluding other chemical interactions and retarding the perovskite crystallization. As such, the hydrophilic PVP interlayer leads to spontaneous perovskite spreading yet a counterintuitively similar nucleation density with respect to the hydrophobic poly[bis(4‐phenyl)(2,4,6‐trimethylphenyl)amine] (PTAA), a change of preferred crystal orientation, improved crystallinity, and remarkably suppressed non‐radiative recombination. These conducive effects jointly minimize the open‐circuit voltage loss and give rise to superior power conversion efficiency for small‐area and large‐area devices. [ABSTRACT FROM AUTHOR]

Metal–organic frameworks (MOFs), formed by the coordination of metal nodes and organic linkers, constitute a class of multifunctional materials with unprecedentedly high chemical/structural designability. Through properly harnessing the synergistic interplay between high atomic number nodes and functional linkers, radiation‐responsive MOFs have recently come on the scene, which can convert ionizing radiations (e.g., X‐ray, γ‐ray, β‐ray, α‐particle, and neutron) into electrical charges or visible light. Given the attributes of cost‐effectiveness, robust environmental stability, extensive chemical tunability, and diverse functionalities, cutting‐edge radiation‐responsive MOFs with remarkable electronic and optical properties have emerged as promising substitutes for conventional organic and inorganic radiation‐responsive substances in applications across biomedicine and technology. This review article documents recent advancements in radiation‐responsive MOFs by elucidating the foundational mechanisms governing electronic transport and photon conversion within frameworks through inherent node–linker and host–guest interactions prompted by high‐energy radiation. Furthermore, this review delves into state‐of‐the‐art applications that leverage newly formulated radiation‐responsive MOFs, capitalizing on precisely engineered component interactions to achieve efficient energy absorption, conversion, and emission. The rationale behind these developments is concluded and future opportunities for expanding the research of radiation‐responsive MOFs are simultaneously highlighted. [ABSTRACT FROM AUTHOR]

Copper indium sulfide (CuInS2) is a ternary A(I)B(III)X (VI)2 -type semiconductor featuring a direct bandgap with a high absorption coefficient. In attempts to explore their practical applications, nanoscale CuInS2 has been synthesized with crystal sizes down to the quantum confinement regime. The merits of CuInS2 nanocrystals (NCs) include wide emission tunability, a large Stokes shift, long decay time, and eco-friendliness, making them promising candidates in photoelectronics and photovoltaics. Over the past two decades, advances in wet-chemistry synthesis have achieved rational control over cation–anion reactivity during the preparation of colloidal CuInS2 NCs and post-synthesis cation exchange. The precise nano-synthesis coupled with a series of hybridization strategies has given birth to a library of CuInS2 NCs with highly customizable photophysical properties. This review article focuses on the recent development of CuInS2 NCs enabled by advanced synthetic and hybridization techniques. We show that the state-of-the-art CuInS2 NCs play significant roles in optoelectronic and biomedical applications. [ABSTRACT FROM AUTHOR]