Performance Enhancement of Flexible Piezoelectric Nanogenerator via Doping and Rational 3D Structure Design For Self‐Powered Mechanosensational System

With the rapid development of the Internet of things (IoT), flexible piezoelectric nanogenerators (PENG) have attracted extensive attention for harvesting environmental mechanical energy to power electronics and nanosystems. Herein, porous piezoelectric fillers with samarium/titanium‐doped BiFeO₃ (BFO) are prepared by a freeze‐drying method, and then silicone rubber is filled into the microvoids of the piezoelectric ceramics, forming a unique structure based on silicone rubber matrix with uniformly distributed piezoelectric ceramic. When subjected to external force stimulation, compared with conventional piezocomposite films found on undoped BFO without a porous structure, the PENG possesses higher stress transfer ability and thus boosts output performance. The notable enhancement in the stress transfer ability and piezoelectric potential is proven by COMSOL simulations. The PENG can exhibit a maximum open‐circuit voltage (V_oc) of 16 V and short‐circuit current (I_sc) of 2.8 µA, which is 5.3 and 5.6 times higher than those of conventional piezocomposite films, respectively. The PENG can be used as a triggering signal to control the operation of fire extinguishers and household appliances. This work not only expands the application scope of lead‐free piezoelectric ceramic for energy harvesting, but also provides a novel solution for self‐powered mechanosensation and shows great potential application in IoT.     

Elucidating the Origins of Subgap Tail States and Open‐Circuit Voltage in Methylammonium Lead Triiodide Perovskite Solar Cells

Recombination via subgap trap states is considered a limiting factor in the development of organometal halide perovskite solar cells. Here, the impact of active layer crystallinity on the accumulated charge and open‐circuit voltage (V_oc) in solar cells based on methylammonium lead triiodide (CH₃NH₃PbI₃, MAPI) is demonstrated. It is shown that MAPI crystallinity can be systematically tailored by modulating the stoichiometry of the precursor mix, where small quantities of excess methylammonium iodide (MAI) improve crystallinity, increasing device V_oc by ≈200 mV. Using in situ differential charging and transient photovoltage measurements, charge density and charge carrier recombination lifetime are determined under operational conditions. Increased V_oc is correlated to improved active layer crystallinity and a reduction in the density of trap states in MAPI. Photoluminescence spectroscopy shows that an increase in trap state density correlates with faster carrier trapping and more nonradiative recombination pathways. Fundamental insights into the origin of V_oc in perovskite photovoltaics are provided and it is demonstrated why highly crystalline perovskite films are paramount for high‐performance devices.     

Evaluation of a betavoltaic energy converter supporting scalable modular structure

Distinct from conventional energy‐harvesting (EH) technologies, such as the use of photovoltaic, piezoelectric, and thermoelectric effects, betavoltaic energy conversion can consistently generate uniform electric power, independent of environmental variations, and provide a constant output of high DC voltage, even under conditions of ultra‐low‐power EH. It can also dramatically reduce the energy loss incurred in the processes of voltage boosting and regulation. This study realized betavoltaic cells comprised of p‐i‐n junctions based on silicon carbide, fabricated through a customized semiconductor recipe, and a Ni foil plated with a Ni‐63 radioisotope. The betavoltaic energy converter (BEC) includes an array of 16 parallel‐connected betavoltaic cells. Experimental results demonstrate that the series and parallel connections of two BECs result in an open‐circuit voltage V_oc of 3.06 V with a short‐circuit current I_sc of 48.5 nA, and a V_oc of 1.50 V with an I_sc of 92.6 nA, respectively. The capacitor charging efficiency in terms of the current generated from the two series‐connected BECs was measured to be approximately 90.7%.     

Biocompatible Poly(lactic acid)‐Based Hybrid Piezoelectric and Electret Nanogenerator for Electronic Skin Applications

Human machine interface (HMI) devices, which can convert human motions to electrical signals to control/charge electronic devices, have attracted tremendous attention from the engineering and science fields. Herein, the high output voltage from a nonpiezoelectric meso‐poly(lactic acid) (meso‐PLA) electret‐based triboelectric nanogenerator (NG) is combined with the relatively high current from a double‐layered poly(l ‐lactic acid) (PLLA)‐based piezoelectric nanogenerator (PENG) for an E‐skin (electronic skin) (HMI) device application. The hybrid NG with a cantilever structure can generate an output voltage of 70 V and a current of 25 µA at the resonance frequency of 19.7 Hz and a tip load of 4.71 g. Moreover, the output power of the hybrid NG reaches 0.31 mW, which is 11% higher than that from the PLLA‐based PENG. Furthermore, it is demonstrated that the PLA‐based hybrid NG can be used to turn a light‐emitting diode light on and off through an energy management circuit during a bending test. Finally, it is demonstrated that the PLA‐based woven E‐skin device can generate the output signals of 35 V (V_oc) and 1 µA (I_sc) during an elbow bending test. The advantages of biocompatible, ease of fabrication, and relatively high output power in the hybrid NG device show great promise for future E‐skin applications.     

Hybridization of CsPbBr1.5I1.5 perovskite quantum dots with 9,9-dihexylfluorene co-oligomer for white electroluminescence

Quaternary lead halide CsPbBr_1.5I_1.5 perovskite quantum dots (PQDs) with cubic shapes and emission wavelength at 566 nm were synthesized by hot injection and carefully characterized to better compensate with blue co-oligomer for white light emission. With a very simple device structure, the electroluminescent hybrid device exhibits a turn-on voltage of 4.7 V, a maximum luminance ∼1200 cd/m², and steady CIE coordinates of (0.28, 0.33). Compared to the photoluminescence spectrum, the increased electroluminescence from PQDs in the HFSO/PQD composite film of the device strongly suggests that the emission from CsPbBr_1.5I_1.5 PQDs are partially due to the direct charge injection.     

Full coverage all-inorganic cesium lead halide perovskite film for high-efficiency light-emitting diodes assisted by 1,3,5-tri(m-pyrid-3-yl-phenyl)benzene

A full coverage all-inorganic cesium lead halide perovskite CsPbBr₃ film is achieved by introducing a small organic molecule material, 1,3,5-tri(m-pyrid-3-yl-phenyl)benzene (TmPyPB), as a solution additive. The light-emitting diode (LED) using this CsPbBr₃:TmPyPB perovskite film as light emitting layer exhibit improved electroluminescent (EL) performance with the maximum brightness of 22309 cd/m², highest current efficiency of 8.77 cd/A, and external quantum efficiency (EQE) of 2.27%, which are 8.6, 10.2 and 10.3 times to that of neat CsPbBr₃ film based LED, respectively. The enhanced EL performances are ascribed to less current leakage due to full coverage, and improved electron transporting in the CsPbBr₃:TmPyPB perovskite film.     

Over 24% Efficient Poly(vinylidene fluoride) (PVDF)-Coordinated Perovskite Solar Cells with a Photovoltage up to 1.22 V

Recently, organic–inorganic metal halide perovskite solar cells (PSCs) have achieved rapid improvement, however, the efficiencies are still behind the Shockley–Queisser theory mainly due to their high energy loss (E_LOSS) in open-circuit voltage (V_OC). Due to the polycrystalline nature of the solution-prepared perovskite films, defects at the grain boundaries as the non-radiative recombination centers greatly affect the V_OC and limit the device efficiency. Herein, poly(vinylidene fluoride) (PVDF) is introduced as polymer-templates in the perovskite film, where the fluorine atoms in the PVDF network can form strong hydrogen-bonds with organic cations and coordinate bonds with Pb²⁺. The strong interaction between PVDF and perovksite enables slow crystal growth and efficient defect passivation, which effectively reduce non-radiation recombination and minimize E_LOSS of V_OC. PVDF-based PSCs achieve a champion efficiency of 24.21% with a excellent voltage of 1.22 V, which is one of the highest V_OC values reported for FAMAPb(I/Br)₃-based PSCs. Furthermore, the strong hydrophobic fluorine atoms in PVDF endow the device with excellent humidity stability, the unencapsulated solar cell maintain the initial efficiency of >90% for 2500 h under air ambient of ≈50% humid and a consistently high V_OC of 1.20 V.     

High Efficiency and High Open Circuit Voltage in Quasi 2D Perovskite Based Solar Cells

An important property of hybrid layered perovskite is the possibility to reduce its dimensionality to provide wider band gap and better stability. In this work, 2D perovskite of the structure (PEA)₂(MA)_n–1Pb_nBr_3n+1 has been sensitized, where PEA is phenyl ethyl‐ammonium, MA is methyl‐ammonium, and using only bromide as the halide. The number of the perovskite layers has been varied (n) from n = 1 through n = ∞. Optical and physical characterization verify the layered structure and the increase in the band gap. The photovoltaic performance shows higher open circuit voltage (V_oc) for the quasi 2D perovskite (i.e., n = 40, 50, 60) compared to the 3D perovskite. V_oc of 1.3 V without hole transport material (HTM) and V_oc of 1.46 V using HTM have been demonstrated, with corresponding efficiency of 6.3% and 8.5%, among the highest reported. The lower mobility and transport in the quasi 2D perovskites have been proved effective to gain high V_oc with high efficiency, further supported by ab initio calculations and charge extraction measurements. Bromide is the only halide used in these quasi 2D perovskites, as mixing halides have recently revealed instability of the perovskite structure. These quasi 2D materials are promising candidates for use in optoelectronic applications that simultaneously require high voltage and high efficiency.     

Triboelectric and Piezoelectric Effects in a Combined Tribo‐Piezoelectric Nanogenerator Based on an Interfacial ZnO Nanostructure

In this contribution, combined triboelectric and piezoelectric generators (TPEG) with a sandwich structure of aluminum‐polydimethylsiloxane/polyvinylidene fluoride composite‐carbon (Al‐PPCF‐Carbon) are fabricated for the purpose of mechanical energy harvesting. Improved by the surface modification of PPCF with zinc oxide (ZnO) nanorods through a hydrothermal method, the TPEG generates an open‐circuit voltage (V_oc) of ≈40 V, a short‐circuit current (I_sc) of 0.28 μA with maximum power density of ≈70 mWm^?2_, and maximum conversion efficiency of 34.56%. Subsequently, in order to understand the transduction mechanism of the triboelectric and piezoelectric effects, analyses focusing on the potential composition ratio in the final output and the impact of ZnO interfacial nanostructure are carried out. The observed potential ratio between triboelectric and piezoelectric effects is 12.75:1 and the highest potential improvement by ZnO nanorods of 21.8 V is achieved by the TPEG fabricated with spacer. Finally, the relationships between the voltage, power density, conversion efficiency, and the external load resistances are also discussed. Overall, the fabricated TPEG is proved to be a simple and effective nanogenerator in mechanical energy conversion with enhanced output potential and conversion efficiency.     

Functionalization of Graphene Oxide Films with Au and MoOx Nanoparticles as Efficient p‐Contact Electrodes for Inverted Planar Perovskite Solar Cells

A graphene oxide (GO) film is functionalized with metal (Au) and metal‐oxide (MoO_x) nanoparticles (NPs) as a hole‐extraction layer for high‐performance inverted planar‐heterojunction perovskite solar cells (PSCs). These NPs can increase the work function of GO, which is confirmed with X‐ray photoelectron spectra, Kelvin probe force microscopy, and ultraviolet photoelectron spectra measurements. The down‐shifts of work functions lead to a decreased level of potential energy and hence increased V_oc of the PSC devices. Although the GO‐AuNP film shows rapid hole extraction and increased V_oc, a J_sc improvement is not observed because of localization of the extracted holes inside the AuNP that leads to rapid charge recombination, which is confirmed with transient photoelectric measurements. The power conversion efficiency (PCE) of the GO‐AuNP device attains 14.6%, which is comparable with that of the GO‐based device (14.4%). In contrast, the rapid hole extraction from perovskite to the GO‐MoO_x layer does not cause trapping of holes and delocalization of holes in the GO film accelerates rapid charge transfer to the indium tin oxide substrate; charge recombination in the perovskite/GO‐MoO_x interface is hence significantly retarded. The GO‐MoO_x device consequently shows significantly enhanced V_oc and J_sc, for which its device performance attains PCE of 16.7% with great reproducibility and enduring stability.     

Nickel Metal-Organic Framework/PVDF Composite Nanofibers-based Self-Powered Wireless Sensor for Pulse Monitoring of Underwater Divers via Triboelectrically Generated Maxwell's Displacement Current

With the increasing need for underwater exploration to monitor environment, collect data or recreation, underwater diving and its associated technologies have drawn significant attention. So, a single-electrode triboelectric nanogenerator (STENG) as self-powered wireless sensor based on Maxwell displacement current concept for underwater usages to monitor arterial pulse and body movements of diver is demonstrated. The STENG is fabricated with an optimized 7.5 wt.% of hydrothermally synthesized Ni-MOF and PVDF based composite nanofibers (Ni-MOF/PVDF CNF) on copper foil as electronegative tribo-material and electrospun nylon 66 nanofibers as electropositive tribo-material. The PDMS encapsulation of STENG exhibits water-proof properties with V_oc, I_sc, and charge output at 45 V, 0.77 µA, and 0.169 µC/cycle, respectively under single-finger tapping. As pulse sensor, STENG monitors arterial pulse and wirelessly transmits information underwater (without external power), wherein STENG generated current creates polarized field in water to get transmitted within a certain distance. Additionally, STENG is demonstrated as a strain sensor to monitor joint movements like ‘elbow, shoulder, knee, etc. Detailed reliability studies reveal that the device is robust against multiple cycles of bending, retains its performance in saline/muddy water, and in the presence of obstacles in the transmission path, which confirms its potential in real life conditions for pulse monitoring of underwater divers.     

应用于下一代太阳电池的2.05 eV AlGaInP 子电池研究

研制了应用于下一代高效多结太阳电池中的定电池的 Al0.13GaInP子电池,其实验室效率为10.04%,开路电压为1457.3mV,短路电流为11.9mA。使用量子效率来验证MOVPE生长过程中涉及高Al组分引起的O缺陷对电池性能的影响。相比GaInP单结电池,Al0.13GaInP电池的短路电流下降地较为厉害,实验中生长了GaInP/Al0.13GaInP异质结电池来分析其原因,因此也提出了以牺牲部分开路电压来提升短路电流的一种有效提升电池性能的方法。     

Efficient red phosphorescent organic light emitting diodes based on solution processed all-inorganic cesium lead halide perovskite as hole transporting layer

An efficient red phosphorescent organic light emitting diode (PhOLED) has been realized by utilizing a composite hole transporting layer comprised of all-inorganic cesium lead halide perovskite CsPbBr₃ via spin-coating and 1,3-bis(9-carbazolyl) benzene (mCP) by vacuum depositing, in which CsPbBr₃ film is used as a hole transporting layer and mCP plays a dominant role in electron and exciton blocking. And this PhOLED shows a saturated red emission coordinated at CIE (0.65, 0.33) driven at 7.5 V, a maximum brightness of 20,750 cd/m², and a maximum current efficiency of 10.64 cd/A, which is as 1.87 times as that 5.68 cd/A of the reference PhOLEDs based on traditional small organic molecular hole transporting material N,N′-bis(naphthalen-1-yl)-N,N′-bis(phenyl)-benzi (NPB). The electroluminescent (EL) spectra and the energy level alignment of different PhOLEDs are investigated. The enhanced EL performances are ascribed to improved hole injecting and transporting behaviors, and better electron and exciton confinements by introducing the composite hole transporting layer CsPbBr₃/mCP.     

Engineering the Exciton Dissociation in Quantum‐Confined 2D CsPbBr3 Nanosheet Films

Recent years have witnessed a rapid development of all‐inorganic halide perovskite in optoelectronic devices. Ultrathin 2D CsPbBr₃ nanosheets (NSs) with large lateral dimensions have demonstrated exceptional photophysical properties because of their analogous exciton electronic structure to quantum wells. Despite the incredible progress on device performance, the photophysics and carrier transportation parameters of quantum‐confined CsPbBr₃ NSs are lacking, and the fundamental understanding of the exciton dissociation mechanism is far less developed. Here, a ligands rearrangement mechanism is proposed to explain why annealed NS films have an increased charge transfer rate and a decreased exciton binding energy and lifetime, prompting tunneling as a dominant way of exciton dissociation to separate photogenerated excitons between neighboring NSs. This facile but efficient method provides a new insight to manipulate perovskite nanocrystals coupling. Moreover, ultrathin 2D CsPbBr₃ NS film is demonstrated to have a enhanced absorption cross section and high carrier mobility of 77.9 cm² V^?1 s^?1, contributing to its high responsivity of 0.53 A W^?1. The photodetector has a long‐term stability up to three months, which are responsible for reliable perovskite‐based device performance.     

Epitaxial Growth of Large‐Scale Orthorhombic CsPbBr3 Perovskite Thin Films with Anisotropic Photoresponse Property

Inorganic cesium lead halide perovskite (CsPbX₃, X = Cl, Br, I) is a promising material for developing novel electronic and optoelectronic devices. Despite the substantial progress that has been made in the development of large perovskite single crystals, the fabrication of high‐quality 2D perovskite single‐crystal films, especially perovskite with a low symmetry, still remains a challenge. Herein, large‐scale orthorhombic CsPbBr₃ single‐crystal thin films on zinc‐blende ZnSe crystals are synthesized via vapor‐phase epitaxy. Structural characterizations reveal a “CsPbBr₃(110)//ZnSe(100), CsPbBr₃[?110]//ZnSe[001] and CsPbBr₃[001]//ZnSe[010]” heteroepitaxial relationship between the covering CsPbBr₃ layer and the ZnSe growth substrate. It is exciting that the epitaxial film presents an in‐plane anisotropic absorption property from 350 to 535 nm and polarization‐dependent photoluminescence. Photodetectors based on the epitaxial film exhibit a high photoresponsivity of 200 A W^?1, a large on/off current ratio exceeding 10⁴, a fast photoresponse time of about 20 ms, and good repeatability at room temperature. Importantly, a strong polarization‐dependent photoresponse is also found on the device fabricated using the epitaxial CsPbBr₃ film, making the orthorhombic perovskite promising building blocks for optoelectronic devices featured with anisotropy.     

Correction of the temperature effect on the solar cell Isc − Voc characteristic

In this paper we present a simple method to determine the thermal resistance of a solar cell from its experimental I_sc ? V_oc characteristic. The knowledge of this parameter permits one to obtain the cell junction temperature and, consequently, the real I_sc ? V_oc characteristic of the cell. The method, which does not require any additional measurement, has been applied to our devices: reasonable agreement between theory and experiment was obtained.     

Flexible Piezoelectric Nanocomposite Generators Based on Formamidinium Lead Halide Perovskite Nanoparticles

Organic–inorganic lead halide perovskite materials have recently attracted much attention in the field of optoelectronic devices. Here, a hybrid piezoelectric nanogenerator based on a composite of piezoelectric formamidinium lead halide perovskite (FAPbBr₃) nanoparticles and polydimethylsiloxane polymer is fabricated. Piezoresponse force spectroscopy measurements reveal that the FAPbBr₃ nanoparticles contain well‐developed ferroelectric properties with high piezoelectric charge coefficient (d₃₃) of 25 pmV⁻¹. The flexible device exhibits high performance with a maximum recordable piezoelectric output voltage of 8.5 V and current density of 3.8 μA cm⁻² under periodically vertical compression and release operations. The alternating energy generated from nanogenerators can be used to charge a capacitor and light up a red light‐emitting diode through a bridge rectifier. This result innovatively expands the feasibility of organic–inorganic lead halide perovskite materials for application in a wide variety of high‐performance energy harvesting devices.     

Coumarin based sensitizers with ortho-halides substituted phenylene spacer for dye sensitized solar cells

The performance of DSSCs (dye sensitized solar cells) with a new series of dyes having different halide groups (i.e. F, Cl and Br) on o-position substituted phenyl spacers with same coumarin donor moieties have been reported. Optical, electrochemical, molecular orbital and photovoltaic properties were studied by varying the halide groups using these dyes. The replacement of halide atoms in same coumarin based dye had a significant effect on the short circuit current density (J_sc), open circuit voltage (V_oc), and photo conversion efficiency (PCE). The J_sc and PCE of dye CD-1 (fluorine substituted) are 10.3 mA/cm² and 5.2% respectively, which is higher than CD-2 (chlorine substituted) and CD-3 (bromine substituted) dyes (having PCE 4.1% and 3.5% respectively) devices. The optimized geometry calculation of o-halide phenyl π-spacer dyes were ascertained by density functional theory (DFT) using the B3LYP/6-31G(d,p) basis set. Moreover, we have checked the effect of various substituents in the same dye structure by DFT analysis.     

Anti-Dissociation Passivation via Bidentate Anchoring for Efficient Carbon-Based CsPbI2.6Br0.4 Solar Cells

Molecular passivation on perovskite surface is an effective strategy to inhibit surface defect-assisted recombination and reduce nonradiative recombination loss in perovskite solar cells (PSCs). However, the majority of passivating molecules bind to perovskite surface through weak interactions, resulting in weak passivation effects and susceptible to interference from various factors. Especially in carbon-based perovskite solar cells (C-PSCs), the molecular passivation effect is more susceptible to disturbance in subsequent harsh preparation of carbon electrodes via blade-coating route. Herein, bidentate ligand 2,2′-Bipyridine (2Bipy) is explored to passivate surface defects of CsPbI_2.6Br_0.4 perovskite films. The results indicate that compared with monodentate pyridine (Py), bidentate 2Bipy shows a stronger chelation with uncoordinated Pb(II) defects and exhibits a greater passivation effect on perovskite surface. As a result, 2Bipy-modified perovskite films display a significantly boosted photoluminescence lifetime, accompanied by excellent anchoring stability and anti-dissociation of passivating molecules. Meanwhile, the moisture resistance of the 2Bipy-modified perovskite films is also significantly enhanced. Consequently, the efficiency of C-PSCs is improved to 16.57% (J_sc = 17.16 mA cm⁻², V_oc = 1.198 V, FF = 80.63%). As far as it is known, this value represents a new record efficiency for hole transport material-free inorganic C-PSCs.     

Efficient and Stable Perovskite White Light-Emitting Diodes for Backlit Display

High-quality backlit display puts forward urgent demand for color-converting materials. Recently, metal halide perovskites (MHPs) with full spectral tunability, high photoluminescence quantum yields (PLQYs), and high color purity have found potential application in wide-color-gamut display. Regrettably, naked MHPs suffer from long-term instable issue and cannot pass harsh stability tests. Herein, amorphous-glass-protected green/red CsPbX₃ quantum dots (QDs) are prepared by elaborately optimizing glass structure, perovskite concentration, and in situ crystallization. PLQYs of green CsPbBr₃@glass and red CsPbBr_1.5I_1.5@glass reach 94% and 78%, respectively, which are the highest ones of CsPbX₃@glass composites reported so far and comparable to colloidal counterparts. Benefited from complete isolation of QDs from external environment by glass network, CsPbX₃@glass can endure harsh commercial standard aging tests of 85 °C/85%RH and blue-light-irradiation, which are applied to construct white light-emitting diodes (wLEDs) with high external quantum efficiency of 13.8% and ultra-high luminance of 500 000 cd m⁻². Accordingly, the perovskite wLED arrays-based backlit unit and a prototype display device are designed for the first time, showing more vivid and wide-color-gamut feature benefited from narrowband emissions of CsPbX₃ QDs. This work highlights practical application of CsPbX₃@glass composite as an efficient and stable light color converter in backlit display.