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To quantitatively evaluate the output performance of triboelectric nanogenerators, figures of merit have been developed. However, the current figures of merit, without considering the breakdown effect that seriously affects the effective maximized energy output, are limited for application. Meanwhile, a method to evaluate output capability of nanogenerators is needed. Here, a standardized method that considers the breakdown effect is proposed for output capability assessment of nanogenerators. Contact separation and contact freestanding-triboelectric-layer modes triboelectric nanogenerators are used to demonstrate this method, and the effective maximized energy output and revised figures of merit are calculated based on the experimental results. These results are consistent with those theoretically calculated based on Paschen’s law. This method is also conducted to evaluate a film-based piezoelectric nanogenerator, demonstrating its universal applicability for nanogenerators. This study proposes a standardized method for evaluating the effective output capability of nanogenerators, which is crucial for standardized evaluation and application of nanogenerator technologies. Figures of merit are used to evaluate output performance of triboelectric nanogenerators, but do not account for the breakdown effect that inhibits maximum output. Here the authors propose a standardized assessment method for output capability of nanogenerators that takes breakdown limits into consideration.

In the quest for environmental sustainability, the rising demand for electric vehicles and renewable energy technologies has substantially increased the need for efficient lithium extraction methods. Traditional lithium production, relying on geographically concentrated hard-rock ores and salar brines, is associated with considerable energy consumption, greenhouse gas emissions, groundwater depletion and land disturbance, thereby posing notable environmental and supply chain challenges. On the other hand, low-quality brines—such as those found in sedimentary waters, geothermal fluids, oilfield-produced waters, seawater and some salar brines and salt lakes—hold large potential owing to their extensive reserves and widespread geographical distribution. However, extracting lithium from these sources presents technical challenges owing to low lithium concentrations and high magnesium-to-lithium ratios. This Review explores the latest advances and continuing challenges in lithium extraction from these demanding yet promising sources, covering a variety of methods, including precipitation, solvent extraction, sorption, membrane-based separation and electrochemical-based separation. Furthermore, we share perspectives on the future development of lithium extraction technologies, framed within the basic principles of separation processes. The aim is to encourage the development of innovative extraction methods capable of making use of the substantial potential of low-quality brines. Precipitation, solvent extraction, sorption, membrane-based separation and electrochemical-based separation are described as promising methods for extracting lithium from low-quality brines, which have extensive reserves and widespread geographical distributions.

Materials with switchable absorption properties have been widely used for smart window applications to reduce energy consumption and enhance occupant comfort in buildings. In this work, we combine the benefits of smart windows with energy conversion by producing a photovoltaic device with a switchable absorber layer that dynamically responds to sunlight. Upon illumination, photothermal heating switches the absorber layer—composed of a metal halide perovskite-methylamine complex—from a transparent state (68% visible transmittance) to an absorbing, photovoltaic colored state (less than 3% visible transmittance) due to dissociation of methylamine. After cooling, the methylamine complex is re-formed, returning the absorber layer to the transparent state in which the device acts as a window to visible light. The thermodynamics of switching and performance of the device are described. This work validates a photovoltaic window technology that circumvents the fundamental tradeoff between efficient solar conversion and high visible light transmittance that limits conventional semitransparent PV window designs. Conventional smart windows with tunable transparency are based on electrochromic systems that consumes energy. Here Wheeler et al. demonstrate a halide perovskite based photo-switchable window that dynamically responds to sunlight and change colors via reversible phase transitions.

Respiration stands as a vital process reflecting physiological and pathological human health status. Exhaled breath analysis offers a facile, non-invasive, swift, and cost-effective approach for diagnosing and monitoring diseases by detecting concentration changes of specific biomarkers. In this study, we employed Polyethylene oxide/copper (I) oxide composite nanofibers (PCNFs), synthesized via the electrospinning method as the sensing material to measure ethanol levels (1–200 ppm) in an exhaled breath simulator environment. The integrated contact-separation triboelectric nanogenerator was utilized to power the self-powered PCNFs exhaled breath sensor. The PCNFs-based gas sensor demonstrates promising results with values of 0.9 and 3.2 for detecting 5 ppm and 200 ppm ethanol, respectively, in the presence of interfering gas at 90% relative humidity (RH). Notably, the sensor displayed remarkable ethanol selectivity, with ratios of 10:1 to methanol and 25:1 to acetone. Response and recovery times for 200 ppm ethanol at 90 RH% were rapid, at 2.7 s and 5.8 s, respectively. The PCNFs-based exhaled breath sensor demonstrated consistent and stable performance in practical conditions, showcasing its potential for integration into wearable devices. This self-powered breath sensor enabling continuous monitoring of lung cancer symptoms and facilitating compliance checks with legal alcohol consumption limits.

In perovskite solar cells, the interfaces between the perovskite and charge-transporting layers contain high concentrations of defects (about 100 times that within the perovskite layer), specifically, deep-level defects, which substantially reduce the power conversion efficiency of the devices 1 – 3 . Recent efforts to reduce these interfacial defects have focused mainly on surface passivation 4 – 6 . However, passivating the perovskite surface that interfaces with the electron-transporting layer is difficult, because the surface-treatment agents on the electron-transporting layer may dissolve while coating the perovskite thin film. Alternatively, interfacial defects may not be a concern if a coherent interface could be formed between the electron-transporting and perovskite layers. Here we report the formation of an interlayer between a SnO 2 electron-transporting layer and a halide perovskite light-absorbing layer, achieved by coupling Cl-bonded SnO 2 with a Cl-containing perovskite precursor. This interlayer has atomically coherent features, which enhance charge extraction and transport from the perovskite layer, and fewer interfacial defects. The existence of such a coherent interlayer allowed us to fabricate perovskite solar cells with a power conversion efficiency of 25.8 per cent (certified 25.5 per cent)under standard illumination. Furthermore, unencapsulated devices maintained about 90 per cent of their initial efficiency even after continuous light exposure for 500 hours. Our findings provide guidelines for designing defect-minimizing interfaces between metal halide perovskites and electron-transporting layers. An atomically coherent interlayer between the electron-transporting and perovskite layers in perovskite solar cells enhances charge extraction and transport from the perovskite, enabling high power conversion efficiency.

Metal halide perovskites of the general formula ABX 3 —where A is a monovalent cation such as caesium, methylammonium or formamidinium; B is divalent lead, tin or germanium; and X is a halide anion—have shown great potential as light harvesters for thin-film photovoltaics 1 – 5 . Among a large number of compositions investigated, the cubic α-phase of formamidinium lead triiodide (FAPbI 3 ) has emerged as the most promising semiconductor for highly efficient and stable perovskite solar cells 6 – 9 , and maximizing the performance of this material in such devices is of vital importance for the perovskite research community. Here we introduce an anion engineering concept that uses the pseudo-halide anion formate (HCOO − ) to suppress anion-vacancy defects that are present at grain boundaries and at the surface of the perovskite films and to augment the crystallinity of the films. The resulting solar cell devices attain a power conversion efficiency of 25.6 per cent (certified 25.2 per cent), have long-term operational stability (450 hours) and show intense electroluminescence with external quantum efficiencies of more than 10 per cent. Our findings provide a direct route to eliminate the most abundant and deleterious lattice defects present in metal halide perovskites, providing a facile access to solution-processable films with improved optoelectronic performance. Incorporation of the pseudo-halide anion formate during the fabrication of α-FAPbI 3 perovskite films eliminates deleterious iodide vacancies, yielding solar cell devices with a certified power conversion efficiency of 25.21 per cent and long-term operational stability.

When translating photovoltaic technology from laboratory to commercial products, low cost, high power conversion efficiency, and high stability (long lifetime) are the three key metrics to consider in addition to other factors, such as low toxicity, low energy payback time, etc. As one of the most promising photovoltaic materials with high efficiency, today organic–inorganic metal halide perovskites draw tremendous attention from fundamental research, but their practical relevance still remains unclear owing to the notorious short device operation time. In this comment, we discuss the stability issue of perovskite photovoltaics and call for standardized protocols for device characterizations that could possibly match the silicon industrial standards.

The nanoscale fibrillar morphology, featuring long-range structural order, provides abundant interfaces for efficient exciton dissociation and high-quality pathways for effective charge transport, is a promising morphology for high performance organic solar cells. Here, we synthesize a thiophene terminated non-fullerene acceptor, L8-ThCl, to induce the fibrillization of both polymer donor and host acceptor, that surpasses the 20% efficiency milestone of organic solar cells. After adding L8-ThCl, the original weak and less continuous nanofibrils of polymer donors, i.e. PM6 or D18, are well enlarged and refined, whilst the host acceptor L8-BO also assembles into nanofibrils with enhanced structural order. By adapting the layer-by-layer deposition method, the enhanced structural order can be retained to significantly boost the power conversion efficiency, with specific values of 19.4% and 20.1% for the PM6:L8-ThCl/L8-BO:L8-ThCl and D18:L8-ThCl/L8-BO:L8-ThCl devices, with the latter being certified 20.0%, which is the highest certified efficiency reported so far for single-junction organic solar cells. The nanoscale fibrillar morphology of the photoactive layer is critical to improve performance of organic solar cells. Here, the authors incorporate thiophene terminal groups in the non-fullerene acceptor, realizing nanofibrils with enhanced structural order and certified device efficiency of 20%.

Triboelectric energy harvesting has been applied to various fields, from large-scale power generation to small electronics. Triboelectric energy is generated when certain materials come into frictional contact, e.g., static electricity from rubbing a shoe on a carpet. In particular, textile-based triboelectric energy-harvesting technologies are one of the most promising approaches because they are not only flexible, light, and comfortable but also wearable. Most previous textile-based triboelectric generators (TEGs) generate energy by vertically pressing and rubbing something. However, we propose a corrugated textile-based triboelectric generator (CT-TEG) that can generate energy by stretching. Moreover, the CT-TEG is sewn into a corrugated structure that contains an effective air gap without additional spacers. The resulting CT-TEG can generate considerable energy from various deformations, not only by pressing and rubbing but also by stretching. The maximum output performances of the CT-TEG can reach up to 28.13 V and 2.71 μA with stretching and releasing motions. Additionally, we demonstrate the generation of sufficient energy from various activities of a human body to power about 54 LEDs. These results demonstrate the potential application of CT-TEGs for self-powered systems.

Controlling the crystallinity and surface morphology of perovskite layers by methods such as solvent engineering 1 , 2 and methylammonium chloride addition 3 – 7 is an effective strategy for achieving high-efficiency perovskite solar cells. In particular, it is essential to deposit α-formamidinium lead iodide (FAPbI 3 ) perovskite thin films with few defects due to their excellent crystallinity and large grain size. Here we report the controlled crystallization of perovskite thin films with the combination of alkylammonium chlorides (RACl) added to FAPbI 3 . The δ-phase to α-phase transition of FAPbI 3 and the crystallization process and surface morphology of the perovskite thin films coated with RACl under various conditions were investigated through in situ grazing-incidence wide-angle X-ray diffraction and scanning electron microscopy. RACl added to the precursor solution was believed to be easily volatilized during coating and annealing owing to dissociation into RA 0 and HCl with deprotonation of RA + induced by RA⋯H + -Cl − binding to PbI 2 in FAPbI 3 . Thus, the type and amount of RACl determined the δ-phase to α-phase transition rate, crystallinity, preferred orientation and surface morphology of the final α-FAPbI 3 . The resulting perovskite thin layers facilitated the fabrication of perovskite solar cells with a power-conversion efficiency of 26.08% (certified 25.73%) under standard illumination. In situ grazing-incidence wide-angle X-ray diffraction and scanning electron microscopy were used to evaluate the crystallization process and surface morphology of perovskite thin films coated with alkylammonium chlorides, which were used to fabricate high-efficiency perovskite solar cells.