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One of the most promising properties of lead halide perovskite nanocrystals (NCs) is their defect tolerance. It is often argued that, due to the electronic structure of the conduction and valence bands, undercoordinated ions can only form localized levels inside or close to the band edges (i.e., shallow traps). However, multiple studies have shown that dangling bonds on surface Br- can still create deep trap states. Here, we argue that the traditional picture of defect tolerance is incomplete and that deep Br- traps can be explained by considering the local environment of the trap states. Using density functional theory calculations, we show that surface Br- sites experience a destabilizing local electrostatic potential that pushes their dangling orbitals into the bandgap. These deep trap states can be electrostatically passivated through the addition of ions that stabilize the dangling orbitals via ionic interactions without covalently binding to the NC surface. These results shed light on the formation of deep traps in perovskite NCs and provide strategies to remove them from the bandgap.

Donor-bridge-acceptor systems based on boron dipyrromethene (BODIPY) are attractive candidates for bio-imagining and sensing applications because of their sensitivity to temperature, micro-viscosity and solvent polarity. The optimization of the properties of such molecular sensors requires a detailed knowledge of the relation between the structure and the photophysical behavior in different environments. In this work we have investigated the excited-state dynamics of three acceptor-donor-acceptor molecules based on benzodithiophene and BODIPY in solvents of different polarities using a combination of ultrafast spectroscopy and DFT-based electronic structure calculations. Transient absorption spectra show that upon photoexcitation an initial excited species with an induced absorption band in the near-infrared regime is formed independent of the solvent polarity. The subsequent photophysical processes strongly depend on the solvent polarity. In non-polar toluene this initial excited state undergoes a structural relaxation leading to a delocalized state with partial charge transfer character, while in the more polar tetrahydrofuran a fully charge separated state is formed. The results clearly show how factors such as donor-acceptor distance and restricted rotational motion by steric hindrance can be used to tune the excited state photophysics to optimize such systems for specific applications.

Switching effects are key elements in the design and characterization of nanoscale molecular electronics systems. They are used to achieve functionality through the transition between different conducting states. In this study, we analyze the presence of switching events in reference molecular systems, which are not designed to have switching behavior, such as oligo(phenylene ethynylene)s and alkanes, using the mechanically controllable break junction technique. These events can be classified in two groups, depending on whether the breaking trace shows exponential decay or plateau-like features before the switch happens. We argue that the former correspond to junctions forming after rupture of the gold atomic point contact, while the latter can be related to a change in the contact geometry of the junction. These results highlight how a proper choice of anchoring group and careful comparison with reference compounds are essential to understanding the origin of switching in molecular break junctions.

A series of three perylenemonoimide-p-oligophenylene-dimethylaniline molecular dyads undergo photoinduced charge separation (CS) with anomalous distance dependence as a function of increasing donor-acceptor (DA) distances. A comprehensive experimental and computational investigation of the photodynamics in the donor-bridge-acceptor (DBA) chromophores reveals a clear demarcation concerning the nature of the CS accessed at shorter (bridgeless) and longer DA distances. At the shortest distance, a strong DA interaction and ground-state charge delocalization populate a hot excited state (ES) with prominent charge transfer (CT) character, via Franck-Condon vertical excitation. The presence of such a CT-polarized hot ES enables a subpicosecond CS in the bridgeless dyad. The incorporation of the p-oligophenylene bridge effectively decouples the donor and the acceptor units in the ground state and consequentially suppresses the CT polarization in the hot ES. Theoretically, this should render a slower CS at longer distances. However, the transient absorption measurement reveals a fast CS process at the longer distance, contrary to the anticipated exponential distance dependence of the CS rates. A closer look into the excited-state dynamics suggests that the hot ES undergoes ultrafast geometry relaxation (τ < 1 ps) to create a relaxed ES. As compared to a decoupled, twisted geometry in the hot ES, the geometry of the relaxed ES exhibits a more planar conformation of the p-oligophenylene bridges. Planarization of the bridge endorses an increased charge delocalization and a prominent CT character in the relaxed ES and forms the origin for the evident fast CS at the longest distance. Thus, the relaxation of the hot ES and the concomitantly enhanced charge delocalization adds a new caveat to the classic nature of distance-dependent CS in artificial DBA chromophores and recommends a cautious treatment of the attenuation factor (β) while discussing anomalous CS trends.

Recently two-dimensional (2D) hybrid organic-inorganic perovskites have attracted a lot of interest as more stable analogues of their three-dimensional counterparts for optoelectronic applications. However, a thorough understanding of the effect that this reduced dimensionality has on dynamical and structural behavior of individual parts of the perovskite is currently lacking. We have used molecular dynamics simulations to investigate the structure and dynamics of 2D Ruddlesden-Popper perovskite with the general formula BA2MAn-1PbnI3n+1, where BA is butylammonium, MA is methylammonium, and n is the number of lead-iodide layers. We discuss the dynamic behavior of both the inorganic and the organic part and compare between the different 2D structures. We show that the rigidness of the inorganic layer markedly increases with the number of lead-iodide layers and that low-temperature structural phase changes accompanied by tilting of the octahedra occurs in some but not all structures. Furthermore, the dynamic behavior of the MA ion is significantly affected by the number of inorganic layers, involving changes both in the reorientation times and in the occurrence of specific preferred orientations.

Structure-property relationships of donor-π-acceptor (D-π-A) type molecular dyad (pp-AD) and triads (pp-ADA and Me-pp-ADA) based on benzodithiophene and BODIPY with biphenyl spacers have been reported. Rotors pp-AD and pp-ADA showed efficient twisted intramolecular charge transfer (TICT) with near infrared (NIR) emissions at ∼712 nm and ∼725 nm with (pseudo-)Stokes shifts of ∼208 nm and ∼221 nm, respectively, and prominent solvatochromism. A structurally similar triad, Me-pp-ADA, with tetramethyl substituents on the BODIPY core instead was TICT inactive and exhibited excitation energy transfer with a transfer efficiency of ∼88% as revealed using steady state emission and transient absorption measurements. Rotors pp-AD and pp-ADA showed NIR emission with an enhancement in intensity with the addition of water in THF solution as well as a pronounced change in emission intensity with temperature and viscosity variations, which justify their utility as temperature and viscosity sensors. Furthermore, the linear correlation of lifetime with fluorescence intensity ratios of the donor and acceptor justifies the rigidochromic behaviour of these rotors.

[Image: see text] Singlet fission (SF) involves the conversion of one excited singlet state into two lower excited triplet states and has received considerable renewed attention over the past decade. This Perspective highlights recent developments and emerging concepts of SF in solid-state crystalline materials. Recent experiments showed the crucial role of vibrational modes in speeding up SF, and theoretical modeling has started to define an optimal energetic landscape and intermolecular orientation of chromophores for highly efficient singlet fission. A critical analysis of these developments leads to directions for future research to eventually find singlet fission chromophores with excellent optoelectronic properties.

The control of local order in polymer semiconductors using non-covalent interactions may be used to engineer materials with interesting combinations of mechanical and optoelectronic properties. To investigate the possibility of preparing n-type polymer semiconductors in which hydrogen bonding plays an important role in structural order and stability, we have used solution-phase polycondensation to incorporate dicyanoperylene bisimide repeat units into an aliphatic polyamide chain backbone. The morphology and thermomechanical characteristics of the resulting polyamides, in which the aliphatic spacer length was varied systematically, were comparable with those of existing semiaromatic engineering polyamides. At the same time, the charge carrier mobility as determined by pulse-radiolysis time-resolved microwave conductivity measurements was found to be about 10-2 cm2 V-1 s-1, which is similar to that reported for low molecular weight perylene bisimides. Our results hence demonstrate that it is possible to use hydrogen bonding interactions as a means to introduce promising optoelectronic properties into high-performance engineering polymers.

In recent years, a wide range of single-molecule devices has been realized, enabled by technological advances combined with the versatility offered by synthetic chemistry. In particular, single-molecule diodes have attracted significant attention with an ongoing effort to increase the rectification ratio between the forward and reverse current. Various mechanisms have been investigated to improve rectification, either based on molecule-intrinsic properties or by engineering the coupling of the molecule to the electrodes. In this perspective, we first provide an overview of the current experimental approaches reported in literature to achieve rectification at the single-molecule level. We then proceed with our recent efforts in this direction, exploiting the internal structure of multi-site molecules, yielding the highest rectification ratio based on a molecule-intrinsic mechanism. We introduce the theoretical framework for multi-site molecules and infer general design guidelines from this. Based on these guidelines, a series of two-site molecules have been developed and integrated into devices. Using two- and three-terminal mechanically controllable break junction measurements, we show that depending on the on-site energies, which are tunable by chemical design, the devices either exhibit pronounced negative differential conductance, or behave as highly-efficient rectifiers. Finally, we propose a design of a single-molecule diode with a theoretical rectification ratio exceeding a million.

Solution-processed quasi-2D perovskites are promising for stable and efficient solar cells because of their superior environmental stability compared to 3D perovskites and tunable optoelectronic properties. Changing the number of inorganic layers (n) sandwiched between the organic spacers allows for tuning of the bandgap. However, narrowing the phase distribution around a specific n-value is a challenge. In-situ UV–vis–NIR absorption spectroscopy is used to time-resolve the crystallization dynamics of quasi-2D butylammonium-based (BA) perovskites with = 4, processed from N,N-dimethylformamide (DMF) in the presence of different co-solvents. By combining with photoluminescence, transient absorption, and grazing-incidence wide-angle X-ray scattering, the crystallization is correlated to the distribution of phases with different n-values. Infrared spectroscopy and density functional theory reveal that the phase distribution correlates with perovskite precursor—co-solvent interaction energies and that stronger interactions shift the phase distribution towards smaller n-values. Careful tuning of the solvent/co-solvent ratio provides a more homogeneous phase distribution, with highly oriented perovskite crystals and suppressed formation of n = 1–2 phases, providing a power conversion efficiency for BA2MA3Pb4I13 solar cells that increases from 3.5% when processed from DMF to over 11% and 10% when processed from DMF/dimethyl sulfoxide and DMF/N-methyl-2-pyrrolidone mixtures, respectively.

Two light-harvesting antenna molecules were obtained by positioning naphthalene monoimide energy donors at the imide position, instead of the bay positions, of perylene imide energy acceptors. Such rational design resulted in a complete suppression of parasitic intramolecular charge transfer without compromising the desired ultrafast rates of excitation energy transfer.

Layered hybrid perovskites comprising adamantyl spacer (A) cations based on the A2FAn−1PbnI3n+1(n= 1-3, FA = formamidinium) compositions have recently been shown to act as promising materials for photovoltaic applications. While the corresponding perovskite solar cells show performances and stabilities that are superior in comparison to other layered two-dimensional formamidinium-based perovskite solar cells, the underlying reasons for their behaviour are not well understood. We provide a comprehensive investigation of the structural and photophysical properties of this unique class of materials, which is complemented by theoretical analysisviamolecular dynamics simulations and density functional theory calculations. We demonstrate the formation of well-defined structures of lower compositional representatives based onn= 1-2 formulations with (1-adamantyl)methanammonium spacer moieties, whereas higher compositional representatives (n> 2) are shown to consist of mixtures of low-dimensional phases evidenced by grazing incidence X-ray scattering. Furthermore, we reveal high photoconductivities of the corresponding hybrid perovskite materials, which is accompanied by long charge carrier lifetimes. This study thereby unravels features that are relevant for the performance of FA-based low-dimensional hybrid perovskites.

Two-dimensional (2D) hybrid organic-inorganic perovskites are an interesting class of semi-conducting materials. One of their main advantages is the large freedom in the nature of the organic spacer molecules that separates the individual inorganic layers. The nature of the organic layer can significantly affect the structure and dynamics of the 2D material; however, there is currently no clear understanding of the effect of the organic component on the structural parameters. In this work, we have used molecular dynamics simulations to investigate the structure and dynamics of a 2D Ruddlesden-Popper perovskite with a single inorganic layer (n = 1) and varying organic cations. We discuss the dynamic behavior of both the inorganic and the organic part of the materials as well as the interplay between the two and compare the different materials. We show that both aromaticity and the length of the flexible linker between the aromatic unit and the amide have a clear effect on the dynamics of both the organic and the inorganic part of the structures, highlighting the importance of the organic cation in the design of 2D perovskites.

2D layered hybrid perovskites are currently in the spotlight for applications such as solar cells, light-emitting diodes, transistors and photodetectors. The structural freedom of 2D layered perovskites allows for the incorporation of organic cations that can potentially possess properties contributing to the performance of the hybrid as a whole. In this study, we incorporated a benzothieno[3,2-b]benzothiophene (BTBT) alkylammonium cation into the organic layer of a 2D layered lead iodide perovskite. The formation and degradation of this material are discussed in detail. It is shown that the use of a solvent vapour annealing method significantly enhances the absorption, emission and crystallinity of films of this 2D layered perovskite as compared to regular thermal annealing. The photoconductivity of the films was determined using time-resolved microwave conductivity (TRMC) as well as in a device. In both cases, the solvent vapour annealed films show markedly higher photoconductivity than the films obtained using the regular thermal annealing approach. W. T. M. V. G., L. L. and D. V. acknowledge the FWO for the funding of the SBO project PROCEED (FWO-S002019N) and the senior FWO research project G043320N. M. M. is an SB PhD fellow at FWO (Number 1S20118N), R. H. is a PhD in chemistry currently employed as an R&D Project Leader at Agfa and P.-H. D. is a special research fund (BOF) doctoral (PhD) student at UHasselt/IMO. The research leading to these results in the Delft University of Technology has received funding from the European Research Council Horizon 2020 ERC Grant Agreement no. 648433. KVH thanks the Hercules Foundation (AUGE/11/029) and the Special Research Fund (BOF) – UGent (01N03217) for funding.

In this work we demonstrate a novel approach to achieve efficient charge separation in dimensionally and dielectrically confined two-dimensional perovskite materials. Two-dimensional perovskites generally exhibit large exciton binding energies that limit their application in optoelectronic devices that require charge separation such as solar cells, photo-detectors and in photo-catalysis. Here, we show that by incorporating a strongly electron accepting moiety, perylene diimide organic chromophores, on the surface of the two-dimensional perovskite nanoplatelets it is possible to achieve efficient formation of mobile free charge carriers. These free charge carriers are generated with ten times higher yield and lifetimes of tens of microseconds, which is two orders of magnitude longer than without the peryline diimide acceptor. This opens a novel synergistic approach, where the inorganic perovskite layers are combined with functional organic chromophores in the same material to tune the properties for specific applications., Functionalizing two-dimensional (2D) hybrid perovskites with organic chromophores is a novel approach to tune their optoelectronic properties. Here, the authors report efficient charge separation and conduction in 2D hybrid perovskite nanoplatelets by incorporating an electron acceptor chromophore.

Layered hybrid perovskites have emerged as a promising alternative to stabilizing hybrid organic–inorganic perovskite materials, which are predominantly based on Ruddlesden-Popper structures. Formamidinium (FA)-based Dion-Jacobson perovskite analogs are developed that feature bifunctional organic spacers separating the hybrid perovskite slabs by introducing 1,4-phenylenedimethanammonium (PDMA) organic moieties. While these materials demonstrate competitive performances as compared to other FA-based low-dimensional perovskite solar cells, the underlying mechanisms for this behavior remain elusive. Here, the structural complexity and optoelectronic properties of materials featuring (PDMA)FAn–1PbnI3n+1 (n = 1–3) formulations are unraveled using a combination of techniques, including X-ray scattering measurements in conjunction with molecular dynamics simulations and density functional theory calculations. While theoretical calculations suggest that layered Dion-Jacobson perovskite structures are more prominent with the increasing number of inorganic layers (n), this is accompanied with an increase in formation energies that render n > 2 compositions difficult to obtain, in accordance with the experimental evidence. Moreover, the underlying intermolecular interactions and their templating effects on the Dion-Jacobson structure are elucidated, defining the optoelectronic properties. Consequently, despite the challenge to obtain phase-pure n > 1 compositions, time-resolved microwave conductivity measurements reveal high photoconductivities and long charge carrier lifetimes. This comprehensive analysis thereby reveals critical features for advancing layered hybrid perovskite optoelectronics.

Herein we demonstrate the dry synthesis of CsBi3I10 both as a free-standing material and in the form of homogeneous thin films, deposited by thermal vacuum deposition. Chemical and optical characterization shows high thermal stability, phase purity, and photoluminescence centered at 700 nm, corresponding to a bandgap of 1.77 eV. These characteristics make CsBi3I10 a promising low-toxicity material for wide bandgap photovoltaics. Nevertheless, the performance of this material as a semiconductor in solar cells remains rather limited, which can be at least partially ascribed to a low charge carrier mobility, as determined from pulsed-radiolysis time-resolved microwave conductivity. Further developments should focus on understanding and overcoming the current limitations in charge mobility, possibly by compositional tuning through doping and/or alloying, as well as optimizing the thin film morphology which may be another limiting factor. Perovskite Thin-film Photovoltaics (PERTPV) REFERENCIA: 763977 Hetero-structures for Efficient Luminescent Devices (HELD) REFERENCIA: 834431

In this work, we show that the quality of the precursor and the thin film preparation strongly affect the optoelectronic properties of the 2D perovskite BA2PbI4. 2D perovskites with alkylammonium organic cations such as butylammonium (BA) are relatively soft structures that exhibit large dynamic disorder and phase variations. Here we show, by a variety of spectroscopy techniques (steady state absorption, photoluminescence and ultrafast transient absorption), that at temperatures below the phase transition (253 K) the material exhibits excitonic features from the room temperature phase (due to incomplete structural transition) and a broadband emission at 560–600 nm (due to self-trapped excitons) with varied relative intensities depending on the precursors and processing conditions. This suggests that the processing conditions have a large influence on the crystallization and introduction of extrinsic defect impurities directly affecting the optoelectronic properties. Making absolute statements about the properties of BA2PbI4 requires improved control over the materials thin film deposition and a better understanding of the role of the lattice vibrational dynamics and extrinsic defects on the exciton dynamics.

Two-dimensional (2D) hybrid perovskites make up an emerging class of materials for optoelectronic applications in which inorganic octahedral layers are separated by nonconductive large organic cations. This leads to a high-dimensional and dielectric confinement and hence a high exciton binding energy, which severely limits their application in devices in which charge carrier separation is required. In this work, we achieve improved charge separation by replacing nonconductive organic cations with organic charge-transfer complexes consisting of a pyrene donor and a tetracyanoquinodimethane acceptor. Steady-state absorption measurements show that these materials exhibit optical features that match with the absorption of the organic charge-transfer complexes. Using microwave conductivity and femtosecond transient absorption, we show that photoexcitation of these charge-transfer states leads to long-lived mobile charges in the inorganic layers. While the efficiency of charge separation is relatively low, these experiments demonstrate that it is possible to induce charge separation in solid-state 2D perovskites by engineering the organic layer. The research leading to these results at the Delft University of Technology has received funding from European Research Council Horizon 2020 ERC Grant Agreement 648433. The FWO is acknowledged for the funding of the research. W.T.M.V.G. is an SB PhD fellow at FWO (1S17516N). RH. is a special research fund (BOF) doctoral (PhD) student at UHasselt/IMO. The PVopMaat project funded by Interreg Vlaanderen-Nederland is acknowledged for funding. The synthesis of materials and films has been carried out in the context of the Solliance network (www.solliance.eu) and the EnergyVille consortium (http://www.energyville.be), of which Hasselt University is a member.

Polymer semiconductors show unique combinations of mechanical and optoelectronic properties that strongly depend on their microstructure and morphology. Here, we have used a model p-conjugated bithiophene repeat unit to incorporate optoelectronic functionality into an aliphatic polyamide backbone by solution-phase polycondensation. Intermolecular hydrogen bonding between the amide groups ensured stable short-range order in the form of lamellar crystalline domains in the resulting semiaromatic polyamides, which could be processed from the melt and exhibited structural and thermomechanical characteristics comparable with those of existing engineering polyamides. At the same time, however, pulse-radiolysis time-resolved microwave conductivity measurements indicated charge carrier mobilities that were an order of magnitude greater than previously observed in bithiophene-based materials. Our results hence provide a convincing demonstration of the potential of amide hydrogen bonding interactions for obtaining unique combinations of mechanical and optoelectronic properties in thermoplastic polymers.

We report herein a versatile and user-friendly synthetic methodology based on sequential functionalization that enables the synthesis of previously unknown perylene bisimide (PBI) dyes with up to five different substituents attached to the perylene core (e.g., compound 15). The key to the success of our strategy is a highly efficient regiospecific 7-mono- and 7,12-di-phenoxy bay substitution at the "imide-activated" 7- and 12-bay positions of 1,6,7,12-tetrachloroperylene monoimide diester 1. The facile subsequent conversion of the diester groups into an imide group resulted in novel PBIs (e.g., compound 14) with two phenoxy substituents specifically at the 7- and 12-bay positions. This conversion led to the activation of C-1 and C-6 bay positions, and thereafter, the remaining two chlorine atoms were substituted to obtain tetraphenoxy-PBI (compound 15) that has two different imide and three different bay substituents. The methodology provides excellent control over the functionalization pattern, which enables the synthesis of various regioisomeric pairs bearing the same bay substituents. Another important feature of this strategy is the high sensitivity of HOMO-LUMO energies and photoinduced charge transfer toward sequential functionalization. As a result, systematic fluorescence on-off switching has been demonstrated upon subsequent substitution with the electron-donating 4-methoxyphenoxy substituent.

Although methylammonium lead iodide (MAPI) perovskite solar cells have reached efficiencies above 20%, the material is environmentally unstable. Mixing MAPI with lower dimensional (LD) perovskites has been suggested to improve its stability in recent studies. However, the LD-mixed perovskites have lower device performance, likely as a result of limited charge-carrier mobility due to their decreased structural dimensionality. To understand this effect, we mixed large-A-site cation LD perovskites, tert-butylammonium lead iodide, with MAPI, and performed a device performance diagnostics. The results suggested although the charge-carrier lifetime was improved, the mobility decreased by a factor of 20. This contributed to a reduction in device efficiency by 2 orders of magnitude, indicating that mobility plays an important role in 3D/LD perovskite mixtures.

In this contribution we describe a combined experimental and theoretical study of the relation between the molecular structure and the electronic properties of conjugated donor-acceptor type chromophores for light-harvesting applications. A series of model systems was synthesized where a central anthracene (electron donor) is connected to dicyanovinyl units (electron acceptor) through a π-conjugated spacer. The study of the redox and optical properties of these chromophores and of reference compounds without dicyanovinyl units allows us correlate the electronic properties to the presence of the electron withdrawing groups and the molecular conformation. Comparison with calculated electronic structure shows that the construction of chromophores that consist of electron donating and accepting units does not always follow the simple rules that are generally used in the design of such molecules. The results show a subtle relation between the charge transfer character and the geometry of the molecules. In some cases this leads to significant contribution of charge transfer excitation to the absorption spectra of some chromophores while such contributions are completely absent in others.

Perylene diimides (PDIs) are attractive chromophores that exhibit singlet exciton fission (SF) and have several advantages over traditional SF molecules such as tetracene and pentacene; however, their photophysical properties relating to SF have received only limited attention. In this study, we explore how introduction of bulky bromine atoms in the so-called bay-area PDIs, resulting in a nonplanar structure, affects the solid-state packing and efficiency of singlet fission. We found that changes in the molecular packing have a strong effect on the temperature dependent photoluminescence, expressed as an activation energy. These effects are explained in terms of excimer formation for PDIs without bay-area substitution, which competes with singlet fission. Introduction of bromine atoms in the bay-positions strongly disrupts the solid-state packing leading to strongly reduced excitonic interactions. Surprisingly, these relatively amorphous materials with weak electronic coupling exhibit stronger formation of triplet excited states by SF because the competing excimer formation is suppressed here.

Two of the key parameters that characterize the usefulness of organic semiconductors for organic or hybrid organic/inorganic solar cells are the mobility of charges and the diffusion length of excitons. Both parameters are strongly related to the supramolecular organization in the material. In this work we have investigated the relation between the solid-state molecular packing and the exciton diffusion length, charge carrier mobility, and charge carrier separation yield using two perylene diimide (PDI) derivatives which differ in their substitution. We have used the time-resolved microwave photoconductivity technique and measured charge carrier mobilities of 0.32 and 0.02 cm2/(Vs) and determined exciton diffusion lengths of 60 and 18 nm for octyl- and bulky hexylheptyl-imide substituted PDIs, respectively. This diffusion length is independent of substrate type and aggregate domain size. The differences in charge carrier mobility and exciton diffusion length clearly reflect the effect of solid-state packing of PDIs on their optoelectronic properties and show that significant improvements can be obtained by effectively controlling the solid-state packing.

Solution-processed AgBiS2 nanocrystal films are a promising material for nontoxic, earth-abundant solar cells. While solar cells with good device efficiency are demonstrated, so far, hardly anything is known about charge generation, transport, and recombination processes in these films. Here, a photoinduced time-resolved microwave conductivity study on AgBiS2 nanocrystal films is presented. By modeling the experimental data with density-dependent recombination processes, the product of the temperature-dependent electron and hole quantum yield and mobility, and the electron and hole recombination kinetics are determined.

[Image: see text] The rotational dynamics of an organic cation in hybrid halide perovskites is intricately linked to the phase transitions that are known to occur in these materials; however, the exact relation is not clear. We have performed detailed model studies on methylammonium lead iodide and formamidinium lead iodide to unravel the relation between rotational dynamics and phase behavior. We show that the occurrence of the phase transitions is due to a subtle interplay between dipole–dipole interactions between the organic cations, specific (hydrogen bonding) interactions between the organic cation and the lead iodide lattice, and deformation of the lead iodide lattice in reaction to the reduced rotational motion of the organic cations. This combination of factors results in phase transitions at specific temperatures, leading to the formation of large organized domains of dipoles. The latter can have significant effects on the electronic structure of these materials.

Phase‐pure CsSnI3, FASnI3, Cs(PbSn)I3, FA(PbSn)I3 perovskites (FA = formamidinium = HC(NH2)2+) as well as the analogous so‐called vacancy‐ordered double perovskites Cs2SnI6 and FA2SnI6 are mechanochemically synthesized. The addition of SnF2 is found to be crucial for the synthesis of Cs‐containing perovskites but unnecessary for hybrid ones. All compounds show an absorption onset in the near‐infrared (NIR) region, which makes them especially relevant for photovoltaic applications. The addition of Pb(II) and SnF2 is crucial to improve the electronic properties in 3D Sn(II)‐based perovskites, in particular their charge carriers mobility (≈0.2 cm2 Vs−1) which is enhanced upon reduction of the dark carrier conductivity. Stokes‐shifted photoluminescence is observed on dry powders of Sn(II)‐based perovskites, which makes these materials promising for light‐emitting and sensing applications. Thermal stability of all compounds is examined, revealing no significant degradation up to at least 200 °C. This meets the requirements for standard operation conditions of most optoelectronic devices and is potentially compatible with thermal vacuum deposition of polycrystalline thin films.

The synthesis and characterization of different conjugated phthalocyanine–perylenemonoimidebenzimidazole [ZnPc-PBIm(OR)4] and nonconjugated phthalocyanine–perylenediimide [ZnPc-PDI(OR)4] dyads are carried out. UV–vis, 1H NMR, and electrochemistry measurements reveal the interaction between perylene and phthalocyanine moieties in the ground state in the conjugated hybrid and the lack of interaction in the nonconjugated one. Ultrafast transient absorption measurements show that a state with substantial charge-transfer character is formed in both compounds, but the rates for the formation and recombination from this state are much faster for the conjugated compound.

The implementation of next generation ultrathin electronics by applying highly promising dimensionality-dependent physical properties of two-dimensional (2D) semiconductors is ever increasing. In this context, the van der Waals layered semiconductor InSe has proven its potential as photodetecting material with high charge carrier mobility. We have determined the photogeneration charge carrier quantum yield and mobility in atomically thin colloidal InSe nanosheets (inorganic layer thickness 0.8-1.7 nm, mono/double-layers, ≤ 5 nm including ligands) by ultrafast transient terahertz (THz) spectroscopy. A near unity quantum yield of free charge carriers is determined for low photoexcitation density. The charge carrier quantum yield decreases at higher excitation density due to recombination of electrons and holes, leading to the formation of neutral excitons. In the THz frequency domain, we probe a charge mobility as high as 20 ± 2 cm2/(V s). The THz mobility is similar to field-effect transistor mobilities extracted from unmodified exfoliated thin InSe devices. The current work provides the first results on charge carrier dynamics in ultrathin colloidal InSe nanosheets.

Metal halide perovskites such as methylammonium lead iodide (CH3 NH3 PbI3) are generating great excitement due to their outstanding optoelectronic properties, which lend them to application in high-efficiency solar cells and light-emission devices. However, there is currently debate over what drives the second-order electron-hole recombination in these materials. Here, we propose that the bandgap in CH3 NH3 PbI3 has a direct-indirect character. Time-resolved photo-conductance measurements show that generation of free mobile charges is maximized for excitation energies just above the indirect bandgap. Furthermore, we find that second-order electron-hole recombination of photo-excited charges is retarded at lower temperature. These observations are consistent with a slow phonon-assisted recombination pathway via the indirect bandgap. Interestingly, in the low-temperature orthorhombic phase, fast quenching of mobile charges occurs independent of the temperature and photon excitation energy. Our work provides a new framework to understand the optoelectronic properties of metal halide perovskites and analyse spectroscopic data.

The low photovoltaic efficiency of iron pyrite-based solar cells is often related to the presence of sulfur deficiencies. In this paper surfur-rich iron pyrite nanocrystals (FeS2 NCs) are synthesized by the hot injection method and deposited using layer by layer deposition. Optical absorption measurements show substantial sub-bandgap absorption, which is attributed to a sulfur-rich, thin surface layer. Microwave photoconductance measurements show very little signal of films with the original long ligands, while an approximately 100-fold higher signal is observed for films treated with FeCl2 and 1,2-ethanedithiol (EDT) solutions. In mesoporous hybrid systems of FeS2/SnO2 both sub-band-gap and above-band-gap photons lead to electron injection from FeS2 into the SnO2 conduction band. We explain these findings by proposing that pinning of the Fermi level by the surface layer leads to a downward band bending in the direction of the surface within the FeS2 NC. Hence, photoexcited electrons will first move towar...

Recent observations of destructive quantum interference in single-molecule junctions confirm the role played by quantum effects in the electronic conductance properties of molecular systems. We show here that the destructive interference can be turned ON or OFF within the same molecular system by mechanically controlling its conformation. Using a combination of ab-initio calculations and single-molecule conductance measurements, we demonstrate the existence of a quasi-periodic destructive quantum interference pattern along the breaking traces of {\pi}-{\pi} stacked molecular dimers. The detection of these interferences, which are due to opposite signs of the intermolecular electronic couplings, was only made possible by a combination of wavelet transform and higher-order statistical analysis of single-breaking traces. The results demonstrate that it is possible to control the molecular conductance over a few orders of magnitudes and with a sub-angstrom resolution by exploiting the subtle structure-property relationship of {\pi}-{\pi} stack dimers. These large conductance changes may be beneficial for the design of single-molecule electronic components that exploit the intrinsic quantum effects occurring at the molecular scale., Comment: 10 pages, 4 figures

Organic-inorganic hybrid halide perovskites are a promising class of materials for photovoltaic application with reported power efficiencies over ∼22%. However, not much is known about the influence of the organic dipole rotation and phase transitions on charge carrier dynamics. Here, we report substantial changes in mobility and lifetime of charge carriers in CH3NH3PbI3 after the low-temperature tetragonal (β) to orthorhombic (γ) phase transition. By using microwave conductivity measurements, we observed that the mobility and lifetime of ionized charge carriers increase as the temperature decreases and a sudden increment is seen after the β-γ phase transition. For CH3NH3PbI3, the mobility and the half-lifetime increase by a factor of 3-6 compared with the values before the β-γ phase transition. We attribute the considerable change in the dynamics at low temperature to the decrease of the inherent dynamic disorder of the organic cation (CH3NH3 +) inside the perovskite crystal structure.

Directing energy and charge transfer processes in light-harvesting antenna systems is quintessential for optimizing the efficiency of molecular devices for artificial photosynthesis. In this work, we report a novel synthetic method to construct two regioisomeric antenna molecules (1-D2A2 and 7-D2A2), in which the 4-(n-butylamino)naphthalene monoimide energy and electron donor is attached to the perylene monoimide diester (PMIDE) acceptor at the 1- and 7-bay positions, respectively. The non-symmetric structure of PMIDE renders a polarized distribution of the frontier molecular orbitals along the long axis of this acceptor moiety, which differentiates the electron coupling between the donor, attached at either the 1- or the 7-position, and the acceptor. We demonstrate that directional control of the photo-driven charge transfer process has been obtained by engineering the molecular structure of the light-harvesting antenna molecules.