Controlled growth of 3R phase niobium diselenide and its properties.

Inversion symmetry broken 3R phase transition metal dichalcogenides (TMDs) show fascinating prospects in spintronics, valleytronics, and nonlinear optics. However, the controlled synthesis of 3R phase TMDs is still a great challenge. In this work, two-dimensional 3R-NbSe2 single crystals up to 0.2 mm were synthesized for the first time through chemical vapor deposition method by designing a space-confined system. The crystal size and morphology can be controlled by the location of the stacked substrates and the amount of the Nb2O5 precursor. Scanning transmission electron microscopy and Raman measurements reveal the NbSe2 exhibits a pure 3R stacking mode with relatively weak interlayer van der Waals interactions. Importantly, 3R-NbSe2 shows obvious second harmonic generation signal which intensity intensified as thickness increases. Density functional theory calculations and optical absorption demonstrate the coexistence of metallic and semiconducting optical properties of 3R-NbSe2. We designed a NbSe2/WS2/NbSe2 photodetector utilizing the metallicity of 3R-NbSe2, which shows good performance especially an ultrafast response (6-7 µs, 0.5 ms - 7.9 s for Au electrodes in literature). The proposed strategy and findings are of great significance for the growth of many other 3R-TMDs and applications of nonlinear optical and ultrafast devices.

Patterned Micro Flexible Supercapacitors based on the Rapid Transfer-Printing Method.

Developing a simple and rapidly preparative method for patterned flexible supercapacitors is essential and indispensable for the swift advancement of portable devices integrated with micro devices. In this study, we employed a cost-effective and rapid fabrication method based on transfer-printing technology to produce patterned micro flexible supercapacitors with various substrates. The resulting flexible micro supercapacitors not only allow for customized patterns with strong flexibility and resistance to bending, while maintaining a certain level of performance, but also facilitate the creation of diverse circuits to tailor voltage and current to specific requirements. Patterned micro flexible supercapacitors with a thickness of 0.02 mm, based on accordion-like Ti3C2Tx MXene materials coated on a substrate, demonstrate a specific capacitance of 142.7 mF cm-2 at 0.5 mA cm-2. The devices exhibit satisfactory capacitance retention (91% after 5000 cycles) and superb mechanical flexibility (71% capacitance retention at 180° bending after 2000 cycles). At a power density of 2.9 mW cm-2, the energy density of the sandwich structure device reaches 126.8 µWh cm-2. This study is expected to contribute new ideas for the design and preparation of patterned flexible supercapacitors.

Interfacial modulation of hollow ZnS-SnS2 microboxs by Ti3C2Tx MXene to construct three-dimensional hybrid anodes for lithium-ion batteries with ultra high stability at low temperature.

Metal sulfides exhibit obvious volume expansion due to the inherent poor conductivity and large temperature fluctuations, leading to reduced storage capacity. Herein, an electrostatic self-assembly strategy was proposed to fabricate a three-dimensional (3D) polyaniline (PANI) encapsulated hollow ZnS-SnS2 (H-ZSS) heterojunction confined on Ti3C2Tx MXene nanosheets (H-ZnS-SnS2@MXene@PANI, denoted as H-ZSSMP), which exhibits remarkable reversible capacity and cyclic stability (520.3 mAh/g at 2 A/g after 1000 cycles) at room temperature. Additionally, specific capacity can stabilized at 362.5 mAh/g for 250 cycles at -20 °C. A full cell with the configuration of H-ZSSMP//lithium iron phosphate (LiFePO4) can retain a satisfactory reversible capacity of 424.7 mAh/g after 100 cycles at 0.1 C. Theory calculations confirm heterogeneous interface can accelerate the transfer of ions through the interfacial regulation effect of MXene on H-ZSS. Our work provides a simple strategy to improve the capacity and stability of lithium-ion batteries (LIBs), as well as the new applications of MXene and bimetallic sulfides as anode materials, which will facilitate the development of MXene based composites for energy storage.

Air-stable self-powered photodetector based on TaSe2/WS2/TaSe2 asymmetric heterojunction with surface self-passivation.

Two-dimensional (2D) transition metal dichalcogenides are highly suitable for constructing junction photodetectors because of their suspended bond-free surface and adjustable bandgap. Additional stable layers are often used to ensure the stability of photodetectors. Unfortunately, they often increase the complexity of preparation and cause performance degradation of devices. Considering the self-passivation behavior of TaSe2, we designed and fabricated a novel self-powered TaSe2/WS2/TaSe2 asymmetric heterojunction photodetector. The heterojunction photodetector shows excellent photoelectric performance and photovoltaic characteristics, achieving a high responsivity of 292 mA/W, an excellent specific detectivity of 2.43 × 1011 Jones, a considerable external quantum efficiency of 57 %, a large optical switching ratio of 2.6 × 105, a fast rise/decay time of 43/54 µs, a high open-circuit voltage of 0.23 V, and a short-circuit current of 2.28 nA under 633 nm laser irradiation at zero bias. Moreover, the device also shows a favorable optical response to 488 and 532 nm lasers. Notably, it exhibits excellent environmental long-term stability with the performance only decreasing âˆ¼ 5.6 % after exposed to air for 3 months. This study provides a strategy for the development of air-stable self-powered photodetectors based on 2D materials.

Self-Driven Gr/WSe2/Gr Photodetector with High Performance Based on Asymmetric Schottky van der Waals Contacts.

Two-dimensional (2D) self-driven photodetectors have a wide range of applications in wearable, imaging, and flexible electronics. However, the preparation of most self-powered photodetectors is still complex and time-consuming. Simultaneously, the constant work function of a metal, numerous defects, and a large Schottky barrier at the 2D/metal interface hinder the transmission and collection of optical carriers, which will suppress the optical responsivity of the device. This paper proposed a self-driven graphene/WSe2/graphene (Gr/WSe2/Gr) photodetector with asymmetric Schottky van der Waals (vdWs) contacts. The vdWs contacts are formed by transferring Gr as electrodes using the dry-transfer method, obviating the limitations of defects and Fermi-level pinning at the interface of electrodes made by conventional metal deposition methods to a great extent and resulting in superior dynamic response, which leads to a more efficient and faster collection of photogenerated carriers. This work also demonstrates that the significant surface potential difference of Gr electrodes is a crucial factor to ensure their superior performance. The self-driven Gr/WSe2/Gr photodetector exhibits an ultrahigh Ilight/Idark ratio of 106 with a responsivity value of 20.31 mA/W and an open-circuit voltage of 0.37 V at zero bias. The photodetector also has ultrafast response speeds of 42.9 and 56.0 µs. This paper provides a feasible way to develop self-driven optoelectronic devices with a simple structure and excellent performance.

Molecularly Imprinted Electrochemical Sensors Based on Ti3C2Tx-MXene and Graphene Composite Modifications for Ultrasensitive Cortisol Detection.

The increasing pressure and unhealthy lifestyle are gradually eroding the physical and mental health of modern people. As a key hormone responsible for maintaining the normal functioning of human systems, cortisol plays a vital role in regulating physiological activities. Moreover, cortisol can serve as a marker for monitoring psychological stress. The development of cortisol detection sensors carries immense potential, as they not only facilitate timely adjustments and treatments by detecting abnormal physiological indicators but also provide comprehensive data for conducting research on the correlation between cortisol and several potential diseases. Here, we report a molecularly imprinted polymer (MIP) electrochemical biosensor that utilizes a porous composite (MXG) modified electrode. MXG composite is prepared by combining Ti3C2Tx-MXene sheets and graphene (Gr). MXG composite material with high conductive properties and large electroactive surface area promotes the charge transfer capability of the electrode surface, expands the effective surface area of the sensor, and increases the content of cortisol-imprinted cavities on the electrode, thereby improving the sensing ability of the sensor. By optimizing the preparation process, the prepared sensor has an ultralow lower limit of detection of 0.4 fM, a wide detection range of 1 fM-10 µM, and good specificity for steroid hormones and interfering substances with similar cortisol structure. The ability of the sensor to detect cortisol in saliva was also confirmed experimentally. This highly sensitive and selective cortisol sensor is expected to be widely used in the fields of physiological and psychological care.

Multicomponent Hybridization Transition Metal Oxide Electrode Enriched with Oxygen Vacancy for Ultralong-Life Supercapacitor.

Transition metal oxide electrode materials for supercapacitors suffer from poor electrical conductivity and stability, which are the research focus of the energy storage field. Herein, multicomponent hybridization Ni-Cu oxide (NCO-Ar/H2 -10) electrode enriched with oxygen vacancy and high electrical conductivity including the Cu0.2 Ni0.8 O, Cu2 O and CuO is prepared by introducing Cu element into Ni metal oxide with hydrothermal, annealing, and plasma treatment. The NCO-Ar/H2 -10 electrode exhibits high specific capacity (1524 F g-1 at 3 A g-1 ), good rate performance (72%) and outstanding cyclic stability (109% after 40,000 cycles). The NCO-Ar/H2 -10//AC asymmetric supercapacitor (ASC) achieves high energy density of 48.6 Wh kg-1 at 799.6 W kg-1 while exhibiting good cycle life (117.5% after 10,000 cycles). The excellent electrochemical performance mainly comes from the round-trip valence change of Cu+ /Cu2+ in the multicomponent hybridization enhance the surface capacitance during the redox process, and the change of electronic microstructure triggered by a large number of oxygen vacancies reduce the adsorption energy of OH- ions of thin nanosheet with crack of surface edge, ensuring electron and ion-transport processes and remitting the structural collapse of material. This work provides a new strategy for improving the cycling stability of transition metal oxide electrode materials.

Self-Powered UV Photodetector of TiO2 with BaTiO3 Surface Modification and Light-Controlled Logic Circuits Application.

One-dimensional (1D) metal oxides with excellent carrier transport and light absorption properties can be applied to photodetectors (PDs), facilitating device miniaturization, portability, and integration. Surface modification of 1D semiconductors can reduce carrier recombination in PDs as a way to increase photocurrent and decrease dark current of PDs. Herein, ultrathin BaTiO3 (BTO) shell layers are grown on the surface of TiO2 nanorod arrays (NRs) by in situ conversion using hydrothermal reaction, and the self-powered TiO2-BTO NRs PDs are constructed. The effect of the thickness of BTO shell layers on the photoresponse characteristics of self-powered TiO2-BTO NRs PDs is investigated by controlling the Ba2+ conversion concentration. The results show that the BTO shell layer reduces the dark current of the PDs because of the decreased interfacial transfer resistance and improved transfer of photogenerated carriers for building a "bridge" of carrier transport between BTO and TiO2 due to the formation of Ti-O-Ti bonds. Moreover, the presence of the spontaneous polarization electric field in BTO enhances the photocurrent and response speed of PDs. The self-powered TiO2-BTO NRs PDs are integrated in series and parallel to realize the functions of "and" and "or" gates of light-controlled logic gates. The ability to convert light signals into electrical signals for the self-powered PDs in real time demonstrates its great potential for optoelectronic interconnection circuits, which has important application prospects in the field of optical communication.

Highly Sensitive Self-Powered Humidity Sensor Based on a TaS2/Cu2S Heterostructure Driven by a Triboelectric Nanogenerator.

Self-powered humidity sensors with high response and good stability have attracted extensive interest in environmental monitoring, medical and health care, and sentiment detection. Because of its high specific surface area and good conductivity, two-dimensional material has wide application in the field of humidity sensing. In this work, we proposed a novel self-powered high-performance TaS2/Cu2S heterostructure-based humidity sensor driven by a triboelectric nanogenerator (TENG) made with the same structure. The TaS2/Cu2S heterostructure was prepared via the chemical vapor deposition method, and then, electrolytic and ultrasound treatments were introduced to further increase the surface area. The fabricated humidity sensor showed ultrahigh sensitivity (S = 3.08 × 104), fast response (2 s), low hysteresis (3.5%), and great stability. First-principles calculation results demonstrated the existence of an electron transport channel with a low energy barrier (-0.156 eV) from the Cu2S to TaS2 layer in the heterostructure, which improves the surface charge transfer of the material. The TaS2/Cu2S heterojunction-based TENG can generate an output voltage of 30 V and an output current of 2.9 µA. Furthermore, the proposed self-powered humidity sensor verified the potential ability of detecting human respiratory frequency, skin humidity, and environmental humidity. This work provides a new and feasible path for research in the field of humidity sensors and promotes the application development of self-powered electronic devices.

Chemically Welding Silver Nanowires toward Transferable and Flexible Transparent Electrodes in Heaters and Double-Sided Perovskite Solar Cells.

Silver nanowires (AgNWs) are important materials for flexible transparent electrodes (FTEs). However, the loose stacking of nanowire junctions greatly affects the electric conductivity across adjacent nanowires. Soldering can effectively reduce the wire-wire contact resistance of AgNWs by epitaxially depositing nanosolders at the junctions, but the process normally needs to be performed with high energy consumption. In this work, we proposed a simple room-temperature method to achieve precise welding of junctions by adjusting the wettability of the soldered precursor solution on the surfaces of AgNWs. The nanoscale welding at nanowire cross junctions forms efficient conductive networks. Furthermore, reduced graphene oxide (rGO) was used to improve the stability of FTEs by wrapping the rGO around the AgNW surface. The obtained FTE shows a figure-of-merit (FoM) of up to 439.3 (6.5 Ω/sq at a transmittance of 88%) and has significant bending stability and environmental and acidic stability. A flexible transparent heater was successfully constructed, which could reach up to 160 °C within a short response time (43 s) and exhibit excellent switching stability. When laminating this FTE onto half perovskite solar cells as the top electrodes, the obtained double-side devices achieved power conversion efficiencies as high as 16.15% and 13.91% from each side, pointing out a convenient method for fabricating double-sided photovoltaic devices.

Strain Relaxation on Perovskite Surface via Light-Enhanced Ionic Homogeneity.

The efficiency and stability of perovskite solar cells (PSCs) can be either deteriorated or enhanced by strain at interfaces, which is sensitive to various external conditions, particularly light illumination. Here we investigated the vertical strain distribution in perovskite films synthesized under light illumination with various wavelengths. The films were formed by reacting formamidinium iodide (FAI)/methylammonium chloride (MACl) vapor with vapor-deposited PbI2 (CsBr) films. Strain in the films was evaluated with incident-angle-dependent grazing-incidence wide-angle X-ray scattering, which showed out-of-plane compressive and in-plane tensile strains, particularly on the surface. Short-wavelength light relaxed the strain on the perovskite surface via promotion of ionic diffusion, including FA, MA, Cs, and I, to reach vertical ionic homogeneity. With the charge trap concentration being reduced, both the efficiency and stability were greatly improved. This finding provides deep insight into the effect of light on strain in PSCs.

Dual-Band, Efficient Self-Powered Organic Photodetectors with Isotype Subphthalocyanine-Based Heterojunctions toward Secure Optical Communications.

High-performance heterojunction organic photodetectors (OPDs) are of great significance in optical detecting technology due to their tailorable optoelectronic properties. Herein, we designed and synthesized three n-type subphthalocyanine (SubPc) derivatives PhO-BSubPcF12, CHO-PhO-BSubPcF12, and NO2-PhO-BSubPcF12 via axial nonhalogen substitution on fluorinated SubPc. These SubPc derivatives exhibit improved intramolecular charge transfer, high electron mobilities, optimized energy levels, and good thermal stability. The novel isotype p-n SubPc heterojunctions are evaluated as photosensitive layers in OPDs, which show a UV-visible dual-band response and self-powered effect. The optimal OPD with Br-BSubPc/NO2-PhO-BSubPcF12 presents stable and superior performances with a high responsivity (R) of 0.14 A W-1, a peak external quantum efficiency (EQE) of 30.6%, and an extremely low dark current of 0.92 nA cm-2 under a 570-595 nm illumination without a bias voltage. It has outperformed most of the reported SubPc-based OPDs. The better interfacial contact of p-n SubPc derivatives leads to a large depletion region with decreased trap densities as well as a low carrier recombination rate, which is conducive to the photoinduced carriers' separation and well-balanced transport, resulting in high device performances. Moreover, a secure communication strategy is successfully demonstrated by dual-band optimal OPD. This work is expected to provide some guidance for molecular engineering and device performance toward multifunctional electronics.

Spatially Graded Millimeter Sized Mo1-xWxS2 Monolayer Alloys: Synthesis and Memory Effect.

The band gap engineering of two-dimensional (2D) transition metal dichacogenides (TMDs) could significantly broaden their applications, especially in electronics and optoelectronics. Alloying is a more effective approach to synthesize 2D ternary TMD materials with tunable bandgaps by regulating the compositions. Whether the alloying could induce memory effects is of interest as a scientific problem and worthy to be studied. A thermal evaporation-assisted chemical vapor deposition (CVD) method was proposed to grow millimeter size gradient alloyed monolayer Mo1-xWxS2. This method reveals a promising and universal methodology for the development of gradient alloyed TMDs because of the precise controlling of each precursor. The synthesized Mo1-xWxS2 monolayer crystal has a gradient composition with x ranging from 0.1 to 1. The W and Mo atoms homogeneously alloyed with random distribution in the Mo1-xWxS2 monolayer. As reported, the deep energy levels induced by sulfur vacancies can be effectively suppressed to shallow energy levels by alloying TMDs. The series distribution of the shallow energy levels in the band of the graded alloy semiconductor can act as multiple charge trapping states, which leads to obvious memory effects in the device. These results present a new opportunity for memory devices and related applications.

Surface-Orientation Elimination of Vapor-Deposited PbI2 Flakes for Efficient Perovskite Synthesis on Curved Solar Cells.

Vapor deposition of perovskite solar cells (PSCs) has attracted considerable interest for its dry processing characteristics. However, a two-step sequential vapor deposition method suffers from ineffective conversion of PbI2 to perovskite with reasons still unclear. In this report, we carefully investigated the crystallization orientation of PbI2 films deposited by physical vapor deposition via synchrotron grazing-incidence wide-angle X-ray scattering (GIWAXS) and observed an asymmetric scattering pattern with respect to the qz-axis. The observed oriented morphology and texture hinder the diffusion of MAI molecules in the PbI2 films synthesized by vapor deposition, resulting in over 15% PbI2 remaining at the buried interface after reaction with MAI vapor. As a result, the MAPbI3 synthesized in this way was also highly oriented, especially in the surface layers. Surface fumigation (SF) step was introduced to decrease the orientational anisotropy of PbI2, which successfully breaks the diffusion barriers of MAI molecules by forming a complex layer on the PbI2 surface with polar solvent vapors, like dimethyl sulfoxide or 1,3-dimethyl-2-imidazolidinone. We infer that the SF treatment changes the vapor-solid reaction mechanism from reaction-crystallization to dissolution-recrystallization, which largely promotes the conversion of PbI2 to perovskite. Defects were reduced in perovskite synthesized in this way, and a p-i-n device with 19.56% efficiency was fabricated, which is among the highest efficiencies reported for sequential-vapor-deposited PSCs. Notably, this method enables the fabrication of conformal perovskite layers on uneven substrates. An exemplary PSC showing efficiency of 8.93% was fabricated on a precurved substrate. We believe that the method is applicable to the fabrication of tandem or curved PSCs that are compatible with wearable or building/autocar-integrated photovoltaics in the future.

Coexistent Integer Charge Transfer and Charge Transfer Complex in F4-TCNQ-Doped PTAA for Efficient Flexible Organic Light-Emitting Diodes.

Understanding the mechanism of interaction between organic polymers and dopants is of great significance to further enhance the performances of flexible electronics. Here, the two doping mechanisms of charge transfer complex (CTC) and integer charge transfer (ICT) are found to coexist in p-π conjugated PTAA doped with the strong acceptor F4-TCNQ, and their correlation is affected by the HJ-aggregate state of the doped polymer. The growth of the J-aggregate caused by the increase of CTC would lead to a corresponding formation of ICT. The doping efficiency was dominated by the CTC/ICT ratio. On the basis of the analysis of the optical, electrical, and morphological properties of PTAA:F4-TCNQ films, we optimized the CTC/ICT ratio to achieve the efficient hole transport layers that are used in solution-processed flexible phosphorescent organic light-emitting diodes with p-i-n structure. The optimal device presents a very high current efficiency (CE) of 31.12 cd/A and a low turn-on voltage of 3.6 V.

Synthesis of large-area monolayer and few-layer MoSe2 continuous films by chemical vapor deposition without hydrogen assistance and formation mechanism.

Two dimensional (2D) MoSe2 with a layered structure has attracted extensive research due to its excellent electronic and optical properties. The controlled synthesis of large-scale and high-quality MoSe2 is highly desirable but still remains challenging. Ambient pressure chemical vapor deposition (APCVD) is an excellent method for the synthesis of 2D materials but the inevitable use of hydrogen during the growth and the easy formation of cracks in the ultrathin films still need to be solved. In the present work, we reported the synthesis of large-area continuous MoSe2 films with different layers by the APCVD method without the assistance of hydrogen on SiO2/Si substrates just by raising the reaction temperature of Se. The synthesized continuous MoSe2 films can reach several centimeters, which can be seen clearly by naked eyes, and, more importantly, the size of the monolayer film can reach up to 3 mm. The morphology, structural characteristics, and optical properties of the synthesized MoSe2 films have been investigated, demonstrating good performance and high crystallinity of the films. Raman spectra give the empirical expression of the frequency difference between E2g1 and A1g dependence of the layer number (N = 1-10 L) for CVD grown MoSe2, which is useful in layer number identification. Further, the formation mechanism of the MoSe2 continuous film is of interest as a fundamental scientific problem and needs to be studied. We proposed the wing model, boundary layer theory, and diffusion theory to account quantitatively for the formation behavior of the MoSe2 film. The presented facile growth method and theoretical model are useful to synthesize other ultrathin transition metal dichalcogenide films and understand the formation behaviors of the systems.

Hybrid Hole Extraction Layer Enabled High Efficiency in Polymer Solar Cells.

Charge extraction layers with excellent charge extraction capability are essential for achieving high photovoltaic performance in cells. In this work, a hole extraction layer (HEL) is developed by doping conductive polymer TFB into CuSCN (CuSCN:TFB(X)), which exhibits good light transparency and high affinity for the light absorber. Compared to the reference cell, the CuSCN:TFB(X) HEL-based cells show impressive enhancement owing to the increased exciton dissociation and charge extraction processes and weak recombination losses. Furthermore, matched work function, better interface contact, and appropriate domain size also contribute to the enhanced power conversion efficiency. As a consequence, the highest conversion efficiency of 15.28% is observed in a cell based on the PM6:Y6 blend film and CuSCN:TFB(1.0%) HEL, which is >16% higher than the efficiency of 13.13% in a cell with CuSCN HEL.

A Low-Temperature Solution-Processed CuSCN/Polymer Hole Transporting Layer Enables High Efficiency for Organic Solar Cells.

The hole transporting layers (HTLs) between the electrode and light absorber play a vital role in charge extraction and transport processes in organic solar cells (OSCs). Herein, a bilayer structure HTL of CuSCN/TFB is formed by soluble copper(I) thiocyanate (CuSCN) and poly[(9,9-dioctylfluorenyl-2,7-diyl)-alt-(4,4'-(N-(4-butylphenyl)))] (TFB). The excellent charge extraction capability is proved in nonfullerene PM6:Y6 and fullerene PTB7-Th:PC71BM blend system-based cells. The introduction of TFB tunes the work function and polishes the interfacial contact between the HTL and light absorber, which favors the hole extraction process in cells. Meanwhile, lower recombination loss, higher exciton dissociation probability, and larger domain size are observed in CuSCN/TFB HTL-based cells compared to those of the reference cell with the pristine CuSCN HTL, which significantly improve the photovoltaic performance. As a result, a champion efficiency of 15.10% is obtained, which is >14% higher than the efficiency of 13.15% obtained in the reference cell. This study suggests that CuSCN/TFB is a promising HTL to achieve high efficiency for OSCs.

Precursor Engineering of Vapor-Exchange Processes for 20%-Efficient 1 cm2 Inverted-Structure Perovskite Solar Cells.

Due to mass diffusion issues, it is challenging to prepare black-phase thick formamidinium-based perovskite (FAPbI3) films via vapor approaches. Precursor engineering is employed here to overcome the dilemma of thorough reaction and black-phase stabilization of FAPbI3 in a sequential vapor approach. For the first time, FAPbBr3 was used as an additive in the precursor to promote the formation of FAPbI3 perovskite. To balance off the increased crystallization degree of precursor films due to the addition of FAPbBr3, CsI dissolved in dimethyl sulfoxide (DMSO) was further added. It is indicated that the simultaneous incorporation of FAPbBr3 and CsI-DMSO successfully accelerated the formation rate of perovskite and inhibited the formation of FAPbI3 yellow phase. The power conversion efficiency of the as-prepared devices of different areas (0.1125 or 1 cm2) reached 20%, the first report of large-area 20%-efficiency PSCs based on a vapor approach, highlighting its applicability to large-area manufacture in the future. Furthermore, when blade coating is used in preparing the precursor film, the efficiency reached 19%. When the precursor film was prepared by dip coating, we could prepare conformal FAPbI3 coatings on carbon fibers, suggesting possible future applications in fabricating wearable PSCs.

Torsional refrigeration by twisted, coiled, and supercoiled fibers.

Higher-efficiency, lower-cost refrigeration is needed for both large- and small-scale cooling. Refrigerators using entropy changes during cycles of stretching or hydrostatic compression of a solid are possible alternatives to the vapor-compression fridges found in homes. We show that high cooling results from twist changes for twisted, coiled, or supercoiled fibers, including those of natural rubber, nickel titanium, and polyethylene fishing line. Using opposite chiralities of twist and coiling produces supercoiled natural rubber fibers and coiled fishing line fibers that cool when stretched. A demonstrated twist-based device for cooling flowing water provides high cooling energy and device efficiency. Mechanical calculations describe the axial and spring-index dependencies of twist-enhanced cooling and its origin in a phase transformation for polyethylene fibers.