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Quantitative detection of various molecules at very low concentrations in complex mixtures has been the main objective in many fields of science and engineering, from the detection of cancer-causing mutagens and early disease markers to environmental pollutants and bioterror agents 1 – 5 . Moreover, technologies that can detect these analytes without external labels or modifications are extremely valuable and often preferred 6 . In this regard, surface-enhanced Raman spectroscopy can detect molecular species in complex mixtures on the basis only of their intrinsic and unique vibrational signatures 7 . However, the development of surface-enhanced Raman spectroscopy for this purpose has been challenging so far because of uncontrollable signal heterogeneity and poor reproducibility at low analyte concentrations 8 . Here, as a proof of concept, we show that, using digital (nano)colloid-enhanced Raman spectroscopy, reproducible quantification of a broad range of target molecules at very low concentrations can be routinely achieved with single-molecule counting, limited only by the Poisson noise of the measurement process. As metallic colloidal nanoparticles that enhance these vibrational signatures, including hydroxylamine–reduced-silver colloids, can be fabricated at large scale under routine conditions, we anticipate that digital (nano)colloid-enhanced Raman spectroscopy will become the technology of choice for the reliable and ultrasensitive detection of various analytes, including those of great importance for human health. Research published in Nature shows that surface-enhanced Raman spectroscopy carried out with colloids can quantify a range of molecules down to concentrations at the femtomolar level.

Tin-based perovskite solar cells (TPSCs) are among the best candidates for lead-free photovoltaic technology owing to their low toxicity and high theoretical efficiency. However, the efficiency and stability of TPSCs lag far behind their lead counterparts because of the poor controllability of perovskite film growth and the intrinsically easy oxidation of Sn 2+ . Here we synthesize two pyridyl-substituted fulleropyrrolidines (PPF) with cis (CPPF) and trans (TPPF) configurations and use them as precursor additives. The spatial configurations of the CPPF and TPPF greatly affect their electron density distributions and interactions with perovskite components. Compared with the CPPF, the TPPF has spatially separated pyridine groups that can catch more perovskite colloids through coordination bonds, thus slowing the perovskite crystallization process. The resultant perovskite film displayed better crystal orientation and compactness. The TPPF also remains located at the grain boundaries, improves the interface energy level alignment and suppresses Sn 2+ oxidation. As a result, the TPPF-based TPSCs exhibit a high power conversion efficiency of 15.38% (certified 15.14%) and excellent stability, maintaining 99% and 93% of their initial efficiencies after 3,000 h of storage and 500 h of continuous illumination, respectively. This work highlights the importance of regulating coordination in the precursor solution in preparing high-quality tin-based perovskite films, paving the way to more efficient and stable TPSCs. Two precursor additives improve the performance of tin-based perovskite solar cells, delivering a power conversion efficiency of 15.38% and maintaining 93% of the initial efficiency after 500 h of continuous illumination.

Graphene-based membranes have great potential to revolutionize nanofiltration technology, but achieving high solute rejections at high water flux remains extremely challenging. Herein, a family of ultrafine metal oxide/reduced graphene oxide (rGO) nanocomposites are synthesized through a heterogenous nucleation and diffusion-controlled growth process for dye nanofiltration. The synthesis is based on the utilization of oxygen functional groups on GO surface as preferential active sites for heterogeneous nucleation, leading to the formation of sub-3 nm size, monodispersing as well as high-density loading of metal oxide nanoparticles. The anchored ultrafine nanoparticles could inhibit the wrinkling of the rGO nanosheet, forming highly stable colloidal solutions for the solution processing fabrication of nanofiltration membranes. By functioning as pillars, the nanoparticles remarkably increase both vertical interlayer spacing and lateral tortuous paths of the rGO membranes, offering a water permeability of 225 L m −2 h −1 bar −1 and selectivity up to 98% in the size-exclusion separation of methyl blue. Graphene oxide nanofiltration membranes with tunable interlayer spacing tend to be either unstable in water or have low water permeation rates. Here the authors report a general synthetic method to achieve ultrafine metal oxide - reduced graphene oxide nanocomposites for dye filtration, achieving high water permeability and selectivity.

Near-infrared light-emitting diodes based on solution-processed semiconductors, such as organics, halide perovskites and colloidal quantum dots, have emerged as a viable technological platform for biomedical applications, night vision, surveillance and optical communications. The recently gained increased understanding of the relationship between materials structure and photophysical properties has enabled the design of efficient emitters leading to devices with external quantum efficiencies exceeding 20%. Despite considerable strides made, challenges remain in achieving high radiance, reducing efficiency roll-off and extending operating lifetime. This Review summarizes recent advances on emissive materials synthetic methods and device key attributes that collectively contribute to improved performance of the fabricated light-emitting devices.A summary of recent advances in the near-infrared light-emitting diodes that are fabricated by solution-processed means, with coverage of devices based on organic semiconductors, halide perovskites and colloidal quantum dots.

Planar perovskite solar cells (PSCs) made entirely via solution processing at low temperatures (<150°C) offer promise for simple manufacturing, compatibility with flexible substrates, and perovskite-based tandem devices. However, these PSCs require an electron-selective layer that performs well with similar processing. We report a contact-passivation strategy using chlorine-capped TiO₂ colloidal nanocrystal film that mitigates interfacial recombination and improves interface binding in low-temperature planar solar cells. We fabricated solar cells with certified efficiencies of 20.1 and 19.5% for active areas of 0.049 and 1.1 square centimeters, respectively, achieved via low-temperature solution processing. Solar cells with efficiency greater than 20% retained 90% (97% after dark recovery) of their initial performance after 500 hours of continuous room-temperature operation at their maximum power point under 1-sun illumination (where 1 sun is defined as the standard illumination at AM1.5, or 1 kilowatt/square meter).

Chemically made colloidal semiconductor quantum dots have long been proposed as scalable and color-tunable single emitters in quantum optics, but they have typically suffered from prohibitively incoherent emission. We now demonstrate that individual colloidal lead halide perovskite quantum dots (PQDs) display highly efficient single-photon emission with optical coherence times as long as 80 picoseconds, an appreciable fraction of their 210-picosecond radiative lifetimes. These measurements suggest that PQDs should be explored as building blocks in sources of indistinguishable single photons and entangled photon pairs. Our results present a starting point for the rational design of lead halide perovskite–based quantum emitters that have fast emission, wide spectral tunability, and scalable production and that benefit from the hybrid integration with nanophotonic components that has been demonstrated for colloidal materials.

It is known that purely repulsive self-propelled colloids can undergo bulk liquid-vapor phase separation. In experiments and large-scale simulations, however, more complex steady states are also seen, comprising a dynamic population of dense clusters in a sea of vapor, or dilute bubbles in a liquid. Here, we show that these microphase-separated states should emerge generically in active matter, without any need to invoke system-specific details. We give a coarse-grained description of them and predict transitions between regimes of bulk phase separation and microphase separation. We achieve these results by extending theϕ4field theory of passive phase separation to allow for all local currents that break detailed balance at leading order in the gradient expansion. These local active currents, whose form we show to emerge from coarse graining of microscopic models, include a mixture of irrotational and rotational contributions and can be viewed as arising from an effective nonlocal chemical potential. Such contributions influence, and in some parameter ranges reverse, the classical Ostwald process that would normally drive bulk phase separation to completion.

Photodetectors that are sensitive in the shortwave-infrared (SWIR) range (1–2 µm) are of great interest for applications such as machine vision, autonomous driving and three-dimensional, night and adverse weather imaging, among others. Currently available technologies in the SWIR range rely on costly epitaxial semiconductors that are not monolithically integrated with complementary metal–oxide–semiconductor electronics. Solution-processed quantum dots can address this challenge by enabling low-cost manufacturing and simple monolithic integration on silicon in a back-end-of-line process. So far, colloidal quantum dot materials to access the SWIR regime are mostly based on lead sulfide and mercury telluride compounds, imposing major regulatory concerns for their deployment in consumer electronics due to the presence of toxic heavy metals. Here we report a new synthesis method for environmentally friendly silver telluride quantum dots and their application in high-performance SWIR photodetectors. The colloidal quantum dot photodetector stack employs materials compliant with the Restriction of Hazardous Substances directives and is sensitive in the spectral range from 350 nm to 1,600 nm. The room-temperature detectivity is of the order of 10 12  Jones, the 3 dB bandwidth is in excess of 0.1 MHz and the linear dynamic range is over 118 dB. We also realize a monolithically integrated SWIR imager based on solution-processed, toxic-heavy-metal-free materials, thus paving the way for this technology to the consumer electronics market. Silver telluride quantum dots are employed in shortwave-infrared photodetectors and in monolithically integrated imagers that are free from toxic heavy metals and fully solution processable.

Infrared multispectral imaging is attracting great interest with the increasing demand for sensitive, low-cost and scalable devices that can distinguish coincident spectral information. However, the widespread use of such detectors is still limited by the high cost of epitaxial semiconductors. In contrast, the solution processability and wide spectral tunability of colloidal quantum dots (CQDs) have inspired various inexpensive, high-performance optoelectronic devices. Here, we demonstrate a two-terminal CQD dual-band detector, which provides a bias-switchable spectral response in two distinct bands. A vertical stack of two rectifying junctions in a back-to-back diode configuration is created by engineering a strong and spatially stable doping process. By controlling the bias polarity and magnitude, the detector can be rapidly switched between short-wave infrared and mid-wave infrared at modulation frequencies up to 100 kHz with D* above 1010 jones at cryogenic temperature. The detector performance is illustrated by dual-band infrared imaging and remote temperature monitoring.Colloidal quantum dot detectors, switchable between short-wave infrared and mid-wave infrared, are demonstrated.

Colloidal quantum dots (QDs) combine the superior light-emission characteristics of quantum-confined semiconductors with the chemical flexibility of molecular systems. These properties could, in principle, enable solution-processable laser diodes with an ultrawide range of accessible colours. However, the realization of such devices has been hampered by fast optical gain decay due to non-radiative Auger recombination and poor stability of QD solids at the high current densities required for the lasing regime. Recently, these problems have been resolved, which resulted in the development of electrically pumped optical gain devices operating at ultrahigh current densities of around 1,000 A cm−2. The next step is the realization of a QD laser diode (QLD). Here we assess the status of the QD lasing field, examine the remaining challenges on the path to a QLD and discuss practical strategies for attaining electrically pumped QD lasing.Colloidal quantum dots may offer solution-processable lasers, with a wide range of colours available. Technical hurdles and progress towards realization of useful quantum dot laser diodes is reviewed.