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This study explores the impact of organic cations in bismuth iodide complexes on their memristive behavior in metal-insulator-metal (MIM) type thin-layer devices. The presence of electron-donating and electron withdrawing functional groups (-CN, -CH3, -NH2, and -N(CH3)2) on pyridinium cations induces morphological alterations in crystals, thus influencing the electronic or ionic conductivity of devices comprising sandwiched thin layers (thickness = 200 nm ± 50) between glass/ITO as bottom electrode (~110 nm) and copper (~80 nm) as the top electrode. It was found that the current-voltage (I-V) scans of the devices reveal characteristic pinched hysteresis loops, a distinct signature of memristors. The working voltage windows are significantly influenced by both the types of cation and the dimensionality of ionic fragments (0D or 1D) in the solid-state form. Additionally, the temperature alters the surface area of the I-V loops by affecting resistive switching mechanisms, corresponding log-log plots at three temperatures (-30 °C, room temperature and 150 °C) are fully studied. Given that a memristor can operate as a single synapse without the need for programming, aligning with the requirements of neuromorphic computing, the study investigates long-term depression, potentiation, and spike-time-dependent plasticity-a specific form of the Hebbian learning rule-to mimic biologically synaptic plasticity. Different polar pulses, such as triangle, sawtooth, and square waveforms were employed to generate Hebbian learning rules. The research demonstrates how the shape of the applied pulse series, achieved by overlapping pre- and postpulses at different time scales, in association with the composition and dimensionality of ionic fragments, lead to changes in the synaptic weight percentages of the devices. [ABSTRACT FROM AUTHOR]

This study investigates the impacts of structure and composition on the optical and electronic properties of a series of pyridinium-based bismuth iodide complexes. Organic substrates with various functional groups, such as 4-aminopyridine (4-Ampy), 4-methylpyridine (4-Mepy), 4-dimethylaminopyridine (4-Dmapy), and 4-pyridinecarbonitrile (4-CNpy) with different electron-donating and electron-withdrawing groups at the para position of the pyridine ring were employed. Crystallographic analysis reveals various bismuth iodide structures, including 1D chains and discrete 0D motifs. The optical band gap of these materials, identified via diffuse reflectance spectroscopy (DRS) and verified with density functional theory (DFT) calculations, is influenced by the crystal packing and stabilising interactions. Through a comprehensive analysis, including Hirshfeld surface (HS) and void assessment, the study underscores the influence of noncovalent intermolecular interactions on crystal packing. Spectroscopic evaluations provide insights into electronic interactions, elucidating the role of electron donor and acceptor substituents within the lattice. Thermogravimetric differential thermal analysis (TG–DTA) indicates structural stability up to 250 °C. Linear sweep voltammetry (LSV) reveals significant conductivity in the range of 10–20 mS per pixel at 298.15 K. X-ray absorption spectroscopy (XAS) at the Bi L3 edge indicates a similar oxidation state and electronic environment across all samples, underscoring the role of bismuth centres surrounded by iodides. [ABSTRACT FROM AUTHOR]

This review focuses on the synthesis, properties and selected applications of heavy pnictogen chalcohalides, i.e. compounds of the MQX stoichiometry, where M = As, Sb, and Bi; Q = O, S, Se, and Te; and X = F, Cl, Br and I. The first section focuses on their synthesis and crystal structures, and the second section discusses the electronic structure on the basis of quantum chemical modelling and selected experimental data. Finally, the third section discusses their electrical, photoelectrochemical and photocatalytic properties and applications. In contrast to perovskites, chalcopyrites and kesterites, chalcohalides have attracted relatively less attention, but their structure and properties are well suited for numerous applications. [ABSTRACT FROM AUTHOR]

This study investigates the impacts of structure and composition on the optical and electronic properties of a series of pyridinium-based bismuth iodide complexes. Organic substrates with various functional groups, such as 4-aminopyridine (4-Ampy), 4-methylpyridine (4-Mepy), 4-dimethylaminopyridine (4-Dmapy), and 4-pyridinecarbonitrile (4-CNpy) with different electron-donating and electron-withdrawing groups at the para position of the pyridine ring were employed. Crystallographic analysis reveals various bismuth iodide structures, including 1D chains and discrete 0D motifs. The optical band gap of these materials, identified via diffuse reflectance spectroscopy (DRS) and verified with density functional theory (DFT) calculations, is influenced by the crystal packing and stabilising interactions. Through a comprehensive analysis, including Hirshfeld surface (HS) and void assessment, the study underscores the influence of noncovalent intermolecular interactions on crystal packing. Spectroscopic evaluations provide insights into electronic interactions, elucidating the role of electron donor and acceptor substituents within the lattice. Thermogravimetric differential thermal analysis (TG-DTA) indicates structural stability up to 250 °C. Linear sweep voltammetry (LSV) reveals significant conductivity in the range of 10-20 mS per pixel at 298.15 K. X-ray absorption spectroscopy (XAS) at the Bi L 3 edge indicates a similar oxidation state and electronic environment across all samples, underscoring the role of bismuth centres surrounded by iodides.