Organic Optoelectronic Synapses for Sound Perception

The neuromorphic systems for sound perception is under highly demanding for the future bioinspired electronics and humanoid robots.However,the sound perception based on volume,tone and timbre remains unknown.Herein,organic optoelectronic synapses(OOSs)are constructed for unprecedented sound recognition.The volume,tone and timbre of sound can be regulated appropriately by the input signal of voltages,frequencies and light intensities of OOSs,according to the amplitude,frequency,and waveform of the sound.The quantitative relation between recognition factor(ζ)and postsynaptic current(I=I_(light)−I_(dark))is established to achieve sound perception.Interestingly,the bell sound for University of Chinese Academy of Sciences is recognized with an accuracy of 99.8%.The mechanism studies reveal that the impedance of the interfacial layers play a critical role in the synaptic performances.This contribution presents unprecedented artificial synapses for sound perception at hardware levels.

Tailoring interphase structure to enable high-rate, durable sodium-ion battery cathode

Na-based layered transition metal oxides with O_(3)-type structure have been considered to be promising cathodes for Na-ion batteries. However, the intrinsically limited Na-ion conductivity induced by the Otype Na-coordinate environment compromises their rate and cycle capability, hindering their practical application. Here, we report an interphase-structure tailoring strategy that improves the electrochemical properties of O_(3)-type layered cathodes achieved through surface coating and doping processes.Specifically, a Zr-doped interphase structure is designed in the model compound NaNi_(1/3)Mn_(1/3)Fe_(1/3)O_(2) using the ionic conductor Na_(3)Zr_(2)Si_(2)PO_(12) as the surface coating material and Zr-dopant provider. We discover that the modified NaNi_(1/3)Mn_(1/3)Fe_(1/3)O_(2)cathode shows a stable Na-storage structure as well as an enhanced rate/cycle capability. Combined with theoretical calculations, it is suggested that the superior electrochemical performances originate from the Zr-doped interphase structure, which has an enlarged Na layer spacing that forms favorable Na-ion diffusion channels. This work highlights a general material interface optimization method which opens a new perspective for fabricating high-performance electrodes for Na-ion batteries and beyond.

Tuning anionic redox activity to boost high-performance sodium-storage in low-cost Na_(0.67)Fe_(0.5)Mn_(0.5)O_(2) cathode

Na-based layered iron-manganese oxide Na_(0.67)Fe_(0.5)Mn_(0.5)O_(2) containing only low-cost elements is a promising cathode for Na-ion batteries used in large-scale energy storage systems.However,the poor cycle stability restricts its practical application.The capacity decay of Na_(0.67)Fe_(0.6)Mn_(0.5)O_(2) mainly originates from the irreversible anionic redox reaction charge compensation due to the high-level hybridization between oxygen and iron.Herein,we rationally design a surface Ti doping strategy to tune the anionic redox reaction activity of Na_(0.67)Fe_(0.5)Mn_(0.5)O_(2) and improve its Na-storage properties.The doped Ti ions not only enlarge the Na migration spacing layer but also improve the structure stability thanks to the strong Ti-O bond.More importantly,the d0-shell electronic structure of Ti^(4+) can suppress the charge transfer from the oxidized anions to cations,thus reducing the anionic redox reaction activity and enhancing the reversibility of charge compensation.The modified Na_(0.67)Fe_(0.5)Mn_(0.5)O_(2) cathode shows a reversible capacity of 198 mA h g^(-1) and an increased capacity retention from 15% to 73% after about1 month of cycling.Meanwhile,a superior Na-ion diffusion kinetics and rate capability are also observed.This work advances the commercialization process of Na-based layered iron-manganese oxide cathodes;on the other hand,the proposed modification strategy paves the way for the design of high-performance electrode materials relying on anionic redox reactions.

Experimental observation of interlayer perpendicular standing spin wave mode with low damping in skyrmion-hosting[Pt/Co/Ta]_(10)multilayer

An interlayer perpendicular standing spin wave mode is observed in the skyrmion-hosting[Pt/Co/Ta]_(10) multilayer by measuring the time-resolved magneto-optical Kerr effect.The observed interlayer mode depends on the interlayer spin-pumping and spin transfer torque among the neighboring Co layers.This mode shows monotonically increasing frequency-field dependence which is similar to the ferromagnetic resonance mode,but within higher frequency range.Besides,the damping of the interlayer mode is found to be a relatively low constant value of 0.027 which is independent of the external field.This work expounds the potential application of the[heavy-metal/ferromagnetic-metal]_(n) multilayers to skyrmion-based magnonic devices which can provide multiple magnon modes,relatively low damping,and skyrmion states,simultaneously.

Magnetic dynamics of two-dimensional itinerant ferromagnet Fe_(3)GeTe_(2)

Among the layered two-dimensional ferromagnetic materials(2D FMs),due to a relatively high T_(C),the van der Waals(vdW)Fe_(3)GeTe_(2)(FGT)crystal is of great importance for investigating its distinct magnetic properties.Here,we have carried out static and dynamic magnetization measurements of the FGT crystal with a Curie temperature TC≈204 K.The M-H hysteresis loops with in-plane and out-of-plane orientations show that FGT has a strong perpendicular magnetic anisotropy with the easy axis along its c-axis.Moreover,we have calculated the uniaxial magnetic anisotropy constant(K_(1))from the SQUID measurements.The dynamic magnetic properties of FGT have been probed by utilizing the high sensitivity electron-spin-resonance(ESR)spectrometer at cryogenic temperatures.Based on an approximation of single magnetic domain mode,the K_(1)and the effective damping constant(αeff)have also been determined from the out-of-plane angular dependence of ferromagnetic resonance(FMR)spectra obtained at the temperature range of 185 K to T_(C).We have found large magnetic damping with the effective damping constantαeff~0.58 along with a broad linewidth(ΔH_(pp)>1000 Oe at 9.48 GHz,H||c-axis).Our results provide useful dynamics information for the development of FGT-based spintronic devices.

Mode Structures and Damping of Quantized Spin Waves in Ferromagnetic Nanowires

Magnonic devices based on spin waves are considered as a new generation of energy-efficient and high-speed devices for storage and processing of information.Here we experimentally demonstrate that three distinct dominated magneto-dynamic modes are excited simultaneously and coexist in a transversely magnetized ferromagnetic wire by the ferromagnetic resonance(FMR)technique.Besides the uniform FMR mode,the spin-wave well mode,the backward volume magnetostatic spin-wave mode,and the perpendicular standing spin-wave mode are experimentally observed and further confirmed with more detailed spatial profiles by micromagnetic simulation.Furthermore,our experimental approach can also access and reveal damping coefficients of these spin-wave modes,which provides essential information for development of magnonic devices in the future.

Temperature dependence of spin pumping in YIG/NiO(x)/W multilayer

We report the temperature dependence of the spin pumping effect for Y_(3)Fe_(5)O_(12)(YIG,0.9μm)/NiO(tNiO)/W(6 nm)(tNiO=0 nm,1 nm,2 nm,and 10 nm)heterostructures.All samples exhibit a strong temperature-dependent inverse spin Hall effect(ISHE)signal I_(c)and sensitivity to the NiO layer thickness.We observe a dramatic decrease of I_(c)with inserting thin NiO layer between YIG and W layers indicating that the inserting of NiO layer significantly suppresses the spin transport from YIG to W.In contrast to the noticeable enhancement in YIG/NiO(tNiO≈1-2 nm)/Pt,the suppression of spin transport may be closely related to the specific interface-dependent spin scattering,spin memory loss,and spin conductance at the NiO/W interface.Besides,the I_(c)of YIG/Ni O/W exhibits a maximum near the TNof the AF NiO layer because the spins are transported dominantly by incoherent thermal magnons.

Enhancing Photovoltaic Performance of Nonfused-Ring Electron Acceptors via Asymmetric End-Group Engineering and Noncovalently Conformational Locks

By employing the asymmetric end-group engineering,an asymmetric nonfused-ring electron acceptor(NFREA)was designed and synthesized.Compared with the symmetric analogs(NoCA-17 and NoCA-18),NoCA-19 possesses broader light absorption range,more coplanarπ-conjugated backbone,and appropriate crystallinity according to the experimental and theoretical results.The organic solar cells based on J52:NoCA-19 exhibited a power conversion efficiency as high as 12.26%,which is much higher than those of J52:NoCA-17(9.50%)and J52:NoCA-18(11.77%),mainly due to more efficient exciton dissociation,better and balanced charge mobility,suppressed recombination loss,shorter charge extraction time,longer charge carrier lifetimes,and more favorable blend film morphology.These findings demonstrate the great potential of asymmetric end-group engineering in exploring low-cost and high-performance NFREAs.

Exciton Bose–Einstein Condensation in Transition Metal Dichalcogenide Monolayer under In-Plane Magnetic Fields

Based on the Gross–Pitaevskii equation,we theoretically investigate exciton Bose–Einstein condensation(BEC)in transition metal dichalcogenide monolayers(TMDC-MLs)under in-plane magnetic fields.We observe that the in-plane magnetic fields exert a strong influence on the exciton BEC wave functions in TMDC-MLs because of the mixing of the bright and dark exciton states via Zeeman effect.This leads to the brightening of the dark exciton BEC states.The competition between the dipole–dipole interactions caused by the long-range Coulomb interaction and the Zeeman effect induced by the in-plane magnetic fields can effectively regulate dark exciton BEC states.Our findings emphasize the utility of TMD-MLs as platforms for investigating collective phenomenon involving excited states.

A Simple Building Block with Noncovalently Conformational Locks towards Constructing Low-Cost and High-Performance Nonfused Ring Electron Acceptors

Nonfused ring electron acceptors(NFREAs)have attracted much attention due to their concise synthetic routes and low cost.However,developing high-performance NFREAs with simple structure remains a great challenge.In this work,a simple building block(POBT)with noncovalently conformational locks(No CLs)was designed and synthesized.Single-crystal X-ray study indicated the presence of S…O NOCLs in POBT,thus enabling it to possess a coplanar conformation comparable to that of fused-ring CPT.Two novel NFREAs based on CPT and POBT were developed,namely TT-CPT and TT-POBT,respectively.Besides,TT-POBT possessed a smaller Stokes shift and a reduced reorganization energy compared with TT-CPT,indicating the introduction of S…O No CLs can enhance the molecular rigidity even if simplifying the molecular structure.As a result,the TT-POBT-based PSC device afforded an impressive power conversion efficiency of 11.15%,much higher than that of TT-CPT counterpart(7.03%),mainly resulting from the tighterπ-πstacking,improved and balanced charge transport,and more favorable film morphology.This work demonstrates the potential of the simple building block POBT with No CLs towards constructing low-cost and highperformance NFREAs.

Insight into the efficiency-stability-cost balanced organic solar cell based on a polymerized nonfused-ring electron acceptor

Organic solar cells(OSCs)have attracted extensive attention from both academia and industry in recent years due to their remarkable improvement in power conversion efficiency(PCE).However,the Golden Triangle(the balance of efficiency-stability-cost)required for large-scale industrialization of OSCs still remains a great challenge.Here,a new nonfused-ring electron acceptor(NFREA)BF and its polymerized counterpart PBF were designed and synthesized,and their photovoltaic performance,storage stability and material cost were systematically investigated.When blended with a widely-used polymer donor PBDB-T,the PBFbased all-polymer solar cell(all-PSC)displayed a record high PCE of 12.61%for polymerized NFREAs(PNFREAs)with an excellent stability(95.2%of initial PCE after 800 h storage),superior to the BF counterpart.Impressively,PBF-based allPSC possesses the highest industrial figure-of-merit(i-FOM)value of 0.309 based on an efficiency-stability-cost evaluation,in comparison to several representative OSC systems(such as PM6:Y6 and PBDB-T:PZ1).This work provides an insight into the balance of efficiency,stability,and cost,and also indicates that the PNFREAs are promising materials toward the commercial application of OSCs.

High-Efficiency and Low-Energy-Loss Organic Solar Cells Enabled by Tuning Conformations of Dimeric Electron Acceptors

Dimeric fused-ring electron acceptors(DFREAs)have attracted much attention due to the combined advantages of their monomeric and polymeric acceptors,including a well-defined molecular structure,excellent repeatability,and stable morphology.However,the additionally introduced single-bonds during dimerization may result in a twisted backbone of DFREAs,which is detrimental to intermolecular packing and charge transport.Herein,three DFREAs are designed and synthesized,in which DFREA conformations were systematically tuned via adjusting the intensities of intramolecular noncovalent interactions(INIs)to achieve high-performance organic solar cells(OSCs).Theoretical and experimental results show that the gradual introduction of S…F INIs can continuously improve molecular planarity and rigidity,resulting in reduced reorganization energies,ordered packing mode,and enhanced crystallization of DFREAs.Benefiting from the incorporation of fourfold S…F INIs,DYF-TF-based binary OSCs show a record high efficiency of 18.26%with an extremely low energy loss(0.493 eV)for DFREAbased OSCs.In addition,DYF-TF-based OSCs exhibited good long-term stability with a T_(80%)lifetime of 2681 h,and the power conversion efficiency of the DYF-TF-based ternary device is further enhanced to 18.73%.This contribution demonstrates the great potential of the INIs strategy in achieving excellent DFREAs materials.

A novel synthesis strategy to improve cycle stability of LiNio.8Mno.1Co0.1O2 at high cut-off voltages through core-shell structuring

Nickel-rich cathode materials have attracted considerable interest because of their high specific capacities,voltage ranges,and low cost.However,serious capacity attenuation and poor rate performance limit their application.This study proposes a novel strategy to improve the cycle stability of the nickel-rich LiNi0.sCo0.1Mn0.1O2(NCM811)layer material by designing core-shell LiNio.sCoo.1 Mno.102(CS-NCM811).CS-NCM811 is designed by the characteristic reaction between dimethylglyoxime(C4H8N2O2)and nickel ion to form Ni(C4H7N2O2)2-The CS-NCM811 is characterized with high nickel content in its core and high manganese content on its surface,leading to a high capacity and excellent cycle stability.The capacity retention of CS-NCM811 was 72.8%,much higher than that of NCM811(47.1%)after 500 cycles at a rate of 5 C.Not only is this method a no vel strategy to desig n high capacity cathode materials but also provides some new in sights into the cycle stability of nickel-rich layered cathode materials.

An A-D-A′-D-A type unfused nonfullerene acceptor for organic solar cells with approaching 14%efficiency

In recent years,power conversion efficiency(PCE)of organic solar cells(OSCs)has made significant improvement.A large number of studies were reported to achieve high PCEs through exploring new active layer materials,especially the high efficiency fused ring acceptors(FRAs).Compared with FRAs,another type of so-called unfused-ring acceptors(UFAs),possessing some advantages such as simple synthesis and low cost,have attracted a lot of attention.Herein,a new UFA BTzO-4F,incorporating with a benzotriazole moiety and S···O intramolecular noncovalent interactions,has been successfully synthesized.The photovoltaic device based on PBDB-T:BTzO-4F achieved a record PCE of 13.8%for UFAs,which indicates that introducing the benzotriazole moiety is an effective strategy for high quality acceptors.Thus,these findings of this work demonstrate the great potential of UFAs for high performance OSCs.

Low-cost polymer acceptors with noncovalently fused-ring backbones for efficient all-polymer solar cells

The polymerization of fused-ring acceptors(FRAs) to afford their corresponding polymeric acceptors for high-performance all-polymer solar cells(all-PSCs) has achieved remarkable progress in the past few years.However,due to the high degree of synthetic complexity for the monomer,the high-cost of these polymeric acceptors may limit their commercial applications.Thus,it is urgent to develop inexpensive and high-performance polymeric acceptors for all-PSCs.Herein,two novel polymeric acceptors(PBTzO and PBTzO-2F) have been designed and synthesized by copolymerization of noncovalently fused ring acceptors(NFRAs),which were employed in all-PSCs for the first time.Upon introducing the “noncovalently conformational locks(NoCLs)” in the backbone and selective fluorination of the end-group,photophysical and electrical properties,and solidstate packing properties of the NFRAs have been rationally tuned.As a result,the PBDB-T:PBTzO-2F based devices presented an excellent power conversion efficiency(PCE) of 11.04%,much higher than that of PBTzO based ones due to the increased charge generation and extraction,improved hole transfer and carrier mobilities,and reduced energy loss.More importantly,PBTzO-2F exhibited a much lower synthetic complexity(SC) index and higher figure-of-merit(FOM) values than the high-performance fused-ring acceptor based polymer acceptors(FRA-PAs) due to the simpler structures and more effective synthesis.This contribution provided a novel idea to achieve low-cost and high-performance all-PSCs.

The establishment of reliability model for LED lamps

In order to verify which of the distributions and established methods of reliability model are more suitable for the analysis of the accelerated aging of LED lamp, three established methods （approximate method, analytical method and two-stage method） of reliability model are used to analyze the experimental data under the condition of the Weibull distribution and Lognormal distribution, in this paper. Ten LED lamps are selected for the accelerated aging experiment and the luminous fluxes are measured at an accelerated aging temperature. AIC information criterion is adopted in the evaluation of the models. The results show that the accuracies of the analytical method and the two-stage method are higher than that of the approximation method, with the widths of confidence intervals of unknown parameters of the reliability model being the smallest for the two-stage method. In a comparison between the two types of distributions, the accuracies are nearly identical.

Air Stable Chalcogen-Doped Rubicenes with Diradical Character

Air stable diradicaloid polycyclic aromatic hydrocarbon(PAH)materials possess unique electronic and magnetic properties for various applications.In general,long conjugated distances between two radical centers are required to improve the air stability,thereby complicating the synthetic procedures.Herein,the chalcogen containing rubicenes(O-,S-,and Se-rubicenes)were systematically investigated to understand the chalcogen effects on chalcogen-rubicene physicochemical properties.Impressively,these rubicenes presented unprecedented diradical characterwithin one simple benzene ring and excellent air stabilities.Theirdiradicalcharacterweremanifested by single-crystal X-ray studies,variable-temperature nuclear magnetic resonance,and electron spin resonance.Furthermore,the nucleus independent chemical shifts andthe anisotropy of the induced currentdensity calculations revealed that the formation of diradical was caused by a pro-aromaticity driving force.Importantly,the diradical character of rubicenes are visualizedbyFractionalOccupationNumberWeighted Electron Density(FOD)plots,which present high NFOD values from 1.651 to 1.830.This contribution provided distinctive insights into the structure and property relationship of PAH diradicals.