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By combining X-ray absorption fine structure and X-ray diffraction measurements with density functional and molecular dynamics simulations, we study the structure of a set of AgxBi1&minus, xS2 nanoparticles, a materials system of considerable current interest for photovoltaics. An apparent contradiction between the evidence provided by X-ray absorption and diffraction measurements is solved by means of the simulations. We find that disorder in the cation sublattice induces strong local distortions, leading to the appearance of short Ag&ndash, S bonds, the overall lattice symmetry remaining close to hexagonal.

We report on a nanomechanical engineering method to monitor matter growth in real time via e-beam electromechanical coupling. This method relies on the exceptional mass sensing capabilities of nanomechanical resonators. Focused electron beam-induced deposition (FEBID) is employed to selectively grow platinum particles at the free end of singly clamped nanotube cantilevers. The electron beam has two functions: it allows both to grow material on the nanotube and to track in real time the deposited mass by probing the noise-driven mechanical resonance of the nanotube. On the one hand, this detection method is highly effective as it can resolve mass deposition with a resolution in the zeptogram range; on the other hand, this method is simple to use and readily available to a wide range of potential users because it can be operated in existing commercial FEBID systems without making any modification. The presented method allows one to engineer hybrid nanomechanical resonators with precisely tailored functionalities. It also appears as a new tool for studying the growth dynamics of ultrathin nanostructures, opening new opportunities for investigating so far out-of-reach physics of FEBID and related methods., This work is supported by the ERC advanced Grant 692876, ERC PoC Grant 862149, the Foundation Cellex, the CERCA Programme, AGAUR, Severo Ochoa (SEV-2015−0522), the Grants FIS2015-69831-P, RTI2018-097953-B-I00, MAT2017- 82970-C2-1-R, and MAT2017-82970-C2-2-R of MINECO, the Fondo Europeo de Desarrollo Regional (FEDER), and the project E13_17R from Aragon Regional Government (Construyendo Europa desde Aragon). P.V. acknowledges support from the ERC starting Grant 758794 “Q-ROOT”.

The use of photothermal sensitizers to facilitate the sintering of polymer powders is rapidly becoming a pivotal additive manufacturing technology, impacting multiple sectors of industry. However, conventional carbon-based sensitizers can only produce black or gray objects. To create white or colorful prints with this method, visibly transparent equivalents are needed. Here, we address this problem by designing resonant photothermal sensitizers made of plasmonic nanoparticles that strongly absorb in the near-infrared, while only minimally interacting with visible light. Gold nanorods were coated with silica before being mixed with polyamide powders to create stable colorful nanocomposite powders. At resonance, these composites showed greatly improved light-to-heat conversion compared with equivalent composites using the industry standard carbon black as a sensitizer and could be sintered using low-power light sources. Furthermore, they appear much whiter and can produce brightly colored 3D objects when mixed with dyes. Our results open a new route to utilize plasmonic nanoparticles to produce colorful and functional 3D-printed objects.

Doping colloidal quantum dots (CQDs) with aliovalent cations is a promising, yet underexplored, approach to control the optoelectronic properties in CQDs. In CQD doping, kinetics determine whether a dopant element will incorporate into the host crystal structure, while thermodynamics dictate the mechanism of dopant incorporation. Here, we show that those mechanisms can be readily monitored by simple optical measurements and XRD studies in CQD ensembles. Based on this, we outline the critical role of dopant solubility limit in CQD doping, bridging the gap between nanocrystalline and bulk semiconductors. Finally, we present a combined simulation and X-ray absorption fine structure (XAFS) data study to shed new insights on the origin of charge compensation upon doping in CQD materials that has, thus far, limited high doping efficacy, even under efficient dopant incorporation schemes.

We report on a nanomechanical engineering method to monitor matter growth in real time via e-beam electromechanical coupling. This method relies on the exceptional mass sensing capabilities of nanomechanical resonators. Focused electron beam-induced deposition (FEBID) is employed to selectively grow platinum particles at the free end of singly clamped nanotube cantilevers. The electron beam has two functions: it allows both to grow material on the nanotube and to track in real time the deposited mass by probing the noise-driven mechanical resonance of the nanotube. On the one hand, this detection method is highly effective as it can resolve mass deposition with a resolution in the zeptogram range; on the other hand, this method is simple to use and readily available to a wide range of potential users because it can be operated in existing commercial FEBID systems without making any modification. The presented method allows one to engineer hybrid nanomechanical resonators with precisely tailored functionalities. It also appears as a new tool for studying the growth dynamics of ultrathin nanostructures, opening new opportunities for investigating so far out-of-reach physics of FEBID and related methods.

Lead halide perovskite nanocrystals (NCs) are currently emerging as one of the most interesting solution-processed semiconductors because they possess high photoluminescence quantum yield (PLQY) and color tunability through anion exchange reactions or quantum confinement. Here, we show efficient solar cells based on mixed-halide (CsPbBrI2) NCs obtained via anion exchange reactions under ambient conditions. We performed anion exchange reactions in concentrated NC solutions with I–, thus inducing a PL red shift up to 676 nm and obtaining a high PLQY in film (65%). Solar cell devices operating in the wavelength range 350–660 nm were fabricated in air with two different deposition methods. The solar cells display a photoconversion efficiency of 5.3% and open circuit voltage (Voc) up to 1.31 V, among the highest reported for perovskite-based solar cells with band gap below 2 eV, clearly demonstrating the potential of this material.

Colloidal quantum dot (CQD) light-emitting diodes (LEDs) deliver a compelling performance in the visible, yet infrared CQD LEDs underperform their visible-emitting counterparts, largely due to their low photoluminescence quantum efficiency. Here we employ a ternary blend of CQD thin film that comprises a binary host matrix that serves to electronically passivate as well as to cater for an efficient and balanced carrier supply to the emitting quantum dot species. In doing so, we report infrared PbS CQD LEDs with an external quantum efficiency of ~7.9% and a power conversion efficiency of ~9.3%, thanks to their very low density of trap states, on the order of 1014 cm−3, and very high photoluminescence quantum efficiency in electrically conductive quantum dot solids of more than 60%. When these blend devices operate as solar cells they deliver an open circuit voltage that approaches their radiative limit thanks to the synergistic effect of the reduced trap-state density and the density of state modification in the nanocomposite. PbS quantum dot ternary blends enable the realization of high-efficiency colloidal quantum dot infrared light-emitting diodes

AgBiS2 nanocrystals offer a route to solution-processed environmentally friendly solar cells.

Over the last several years tremendous progress has been made in incorporating colloidal quantum dot (CQD) solids as photoactive components in optoelectronic devices. A large part of this progress is associated with significant advancements made in controlling the electronic doping of CQD solids. Today, a variety of strategies exists towards that purpose; this Minireview aims to survey the major published works in this subject. Additional attention is given to the many challenges associated with the task of doping CQDs, as well as to the realization of optoelectronic functionalities and applications upon successful light and heavy electronic doping of CQD solids.

Two-terminal tandem cell architectures are believed to be an effective way to further improve the power conversion efficiency in solution processed photovoltaics. To design an efficient tandem solar cell, two key issues need to be considered. First, subcells with well-matched currents and complementary absorption characteristics are a prerequisite for high efficiency. Second, identifying the appropriate intermediate layer (IML) to connect the subcells is necessary to minimize the optical and electronic losses. PbS colloidal quantum dots (CQDs) are a notable choice for the subcells due to their low cost, solution processability, and remarkable wide range band gap tunability. Single-layer graphene (Gr) has been proposed to be a promising IML due to its high transparency and conductivity. Here, as a proof of concept, we demonstrate a solution-processed, two-terminal PbS CQDs tandem solar cell employing chemical vapor deposited Gr as the IML. In doing so, we report a PbS CQD cell comprising subcells with bandgaps of 1.4 and 0.95 eV that delivers power conversion efficiency in excess of 7%, substantially higher than that of previously reported CQD tandem cells.

In just 20 years of history, the field of optomechanics has achieved impressive progress, stepping into the quantum regime just 5 years ago. Such remarkable advance relies on the technological revolution of nano-optomechanical systems, whose sensitivity towards thermal decoherence is strongly limited due to their ultra-low mass. Here we report a hybrid approach pushing nano-optomechanics to even lower scales. The concept relies on synthesising an efficient optical scatterer at the tip of singly clamped carbon nanotube resonators. We demonstrate high signal-to-noise motion readout and record force sensitivity, two orders of magnitude below the state of the art. Our work opens the perspective to extend quantum experiments and applications at room temperature.

Developing low-cost photovoltaic absorbers that can harvest the short-wave infrared (SWIR) part of the solar spectrum, which remains unharnessed by current Si-based and perovskite photovoltaic technologies, is a prerequisite for making high-efficiency, low-cost tandem solar cells. Here, infrared PbS colloidal quantum dot (CQD) solar cells employing a hybrid inorganic-organic ligand exchange process that results in an external quantum efficiency of 80% at 1.35 µm are reported, leading to a short-circuit current density of 34 mA cm-2 and a power conversion efficiency (PCE) up to 7.9%, which is a current record for SWIR CQD solar cells. When this cell is placed at the back of an MAPbI3 perovskite film, it delivers an extra 3.3% PCE by harnessing light beyond 750 nm.

Developing low‐cost photovoltaic absorbers that can harvest the short‐wave infrared (SWIR) part of the solar spectrum, which remains unharnessed by current Si‐based and perovskite photovoltaic technologies, is a prerequisite for making high‐efficiency, low‐cost tandem solar cells. Here, infrared PbS colloidal quantum dot (CQD) solar cells employing a hybrid inorganic–organic ligand exchange process that results in an external quantum efficiency of 80% at 1.35 µm are reported, leading to a short‐circuit current density of 34 mA cm−2 and a power conversion efficiency (PCE) up to 7.9%, which is a current record for SWIR CQD solar cells. When this cell is placed at the back of an MAPbI3 perovskite film, it delivers an extra 3.3% PCE by harnessing light beyond 750 nm.

Two-terminal tandem cell architectures are believed to be an effective way to further improve the power conversion efficiency in solution processed photovoltaics. To design an efficient tandem solar cell, two key issues need to be considered. First, subcells with well-matched currents and complementary absorption characteristics are a prerequisite for high efficiency. Second, identifying the appropriate intermediate layer (IML) to connect the subcells is necessary to minimize the optical and electronic losses. PbS colloidal quantum dots (CQDs) are a notable choice for the subcells due to their low cost, solution processability, and remarkable wide range band gap tunability. Single-layer graphene (Gr) has been proposed to be a promising IML due to its high transparency and conductivity. Here, as a proof of concept, we demonstrate a solution-processed, two-terminal PbS CQDs tandem solar cell employing chemical vapor deposited Gr as the IML. In doing so, we report a PbS CQD cell comprising subcells with band...

Perovskite nanocrystal light-emitting diodes (LEDs) employing architecture comprising a ZnO nanoparticles electron-transport layer and a conjugated polymer hole-transport layer have been fabricated. The obtained LEDs demonstrate a maximum external-quantum-efficiency of 6.04%, luminance of 12998 Cd/m2 and stable electroluminescence at 519 nm. Importantly, such high efficiency and bright-ness have been achieved by employing solution processed transport layers, formamidinium lead bromide nanocrystals (CH(NH2)2PbBr3 NCs) synthesized at room-temperature and in air without the use of a Schlenk line, and a procedure based on atomic layer deposition to insolubilize the NC film. The obtained NCs show a photoluminescence quantum yield of 90% that is retained upon film fabrication. The results show that perovskite NC LEDs can achieve high-performance without the use of transport layers deposited through evaporation in ultra-high-vacuum.

In just 20 years of history, the field of optomechanics has achieved impressive progress, stepping into the quantum regime just 5 years ago. Such remarkable advance relies on the technological revolution of nano-optomechanical systems, whose sensitivity towards thermal decoherence is strongly limited due to their ultra-low mass. Here we report a hybrid approach pushing nano-optomechanics to even lower scales. The concept relies on synthesising an efficient optical scatterer at the tip of singly clamped carbon nanotube resonators. We demonstrate high signal-to-noise motion readout and record force sensitivity, two orders of magnitude below the state of the art. Our work opens the perspective to extend quantum experiments and applications at room temperature., Optomechanics has recently moved into the quantum regime. Here, Tavernarakis et al. demonstrate that a hybrid optomechanical device made up of a carbon nanotube with a metal nanoparticle at its tip can push force measurements towards the quantum regime at room temperature.

The power conversion efficiency of colloidal PbS‐quantum‐dot (QD)‐based solar cells is significantly hampered by lower‐than‐expected open circuit voltage (VOC). The VOC deficit is considerably higher in QD‐based solar cells compared to other types of existing solar cells due to in‐gap trap‐induced bulk recombination of photogenerated carriers. Here, this study reports a ligand exchange procedure based on a mixture of zinc iodide and 3‐mercaptopropyonic acid to reduce the VOC deficit without compromising the high current density. This layer‐by‐layer solid state ligand exchange treatment enhances the photovoltaic performance from 6.62 to 9.92% with a significant improvement in VOC from 0.58 to 0.66 V. This study further employs optoelectronic characterization, X‐ray photoelectron spectroscopy, and photoluminescence spectroscopy to understand the origin of VOC improvement. The mixed‐ligand treatment reduces the sub‐bandgap traps and significantly reduces bulk recombination in the devices.

The power conversion efficiency of colloidal PbS-quantum-dot (QD)-based solar cells is significantly hampered by lower-than-expected open circuit voltage (VOC). The VOC deficit is considerably higher in QD-based solar cells compared to other types of existing solar cells due to in-gap trap-induced bulk recombination of photogenerated carriers. Here, this study reports a ligand exchange procedure based on a mixture of zinc iodide and 3-mercaptopropyonic acid to reduce the VOC deficit without compromising the high current density. This layer-by-layer solid state ligand exchange treatment enhances the photovoltaic performance from 6.62 to 9.92% with a significant improvement in VOC from 0.58 to 0.66 V. This study further employs optoelectronic characterization, X-ray photoelectron spectroscopy, and photoluminescence spectroscopy to understand the origin of VOC improvement. The mixed-ligand treatment reduces the sub-bandgap traps and significantly reduces bulk recombination in the devices.

In this paper we report our first experimental results towards the establishment of a novel nanooptomechanical platform consisting of a hybrid, carbon nanotube-based mechanical resonator. We have been able to optically measure and actively control these resonators demonstrating a record force sensitivity at ambient temperature. Finally, we have observed optomechanically-induced dynamical effects and optomechanical enhancement of the force sensitivity in a cavity-free scheme.