Composite polymer electrolytes(CPEs)offer a promising solution for all-solid-state lithium-metal batteries(ASSLMBs).However,conventional nanofillers with Lewis-acid-base surfaces make limited contribution to improving...Composite polymer electrolytes(CPEs)offer a promising solution for all-solid-state lithium-metal batteries(ASSLMBs).However,conventional nanofillers with Lewis-acid-base surfaces make limited contribution to improving the overall performance of CPEs due to their difficulty in achieving robust electrochemical and mechanical interfaces simultaneously.Here,by regulating the surface charge characteristics of halloysite nanotube(HNT),we propose a concept of lithium-ion dynamic interface(Li^(+)-DI)engineering in nano-charged CPE(NCCPE).Results show that the surface charge characteristics of HNTs fundamentally change the Li^(+)-DI,and thereof the mechanical and ion-conduction behaviors of the NCCPEs.Particularly,the HNTs with positively charged surface(HNTs+)lead to a higher Li^(+)transference number(0.86)than that of HNTs-(0.73),but a lower toughness(102.13 MJ m^(-3)for HNTs+and 159.69 MJ m^(-3)for HNTs-).Meanwhile,a strong interface compatibilization effect by Li^(+)is observed for especially the HNTs+-involved Li^(+)-DI,which improves the toughness by 2000%compared with the control.Moreover,HNTs+are more effective to weaken the Li^(+)-solvation strength and facilitate the formation of Li F-rich solid-electrolyte interphase of Li metal compared to HNTs-.The resultant Li|NCCPE|LiFePO4cell delivers a capacity of 144.9 m Ah g^(-1)after 400 cycles at 0.5 C and a capacity retention of 78.6%.This study provides deep insights into understanding the roles of surface charges of nanofillers in regulating the mechanical and electrochemical interfaces in ASSLMBs.展开更多
Efficient utilization of electrostatic charges is paramount for numerous applications,from printing to kinetic energy harvesting.However,existing technologies predominantly focus on the static qualities of these charg...Efficient utilization of electrostatic charges is paramount for numerous applications,from printing to kinetic energy harvesting.However,existing technologies predominantly focus on the static qualities of these charges,neglecting their dynamic capabilities as carriers for energy conversion.Herein,we report a paradigm-shifting strategy that orchestrates the swift transit of surface charges,generated through contact electrification,via a freely moving droplet.This technique ingeniously creates a bespoke charged surface which,in tandem with a droplet acting as a transfer medium to the ground,facilitates targeted charge displacement and amplifies electrical energy collection.The spontaneously generated electric field between the charged surface and needle tip,along with the enhanced water ionization under the electric field,proves pivotal in facilitating controlled charge transfer.By coupling the effects of charge self-transfer,contact electrification,and electrostatic induction,a dual-electrode droplet-driven(DD)triboelectric nanogenerator(TENG)is designed to harvest the water-related energy,exhibiting a two-orderof-magnitude improvement in electrical output compared to traditional single-electrode systems.Our strategy establishes a fundamental groundwork for efficient water drop energy acquisition,offering deep insights and substantial utility for future interdisciplinary research and applications in energy science.展开更多
Efficient interfacial charge transfer and robust interfacial interactions are crucial for achieving the superior spatial separation of carriers and developing efficient heterojunction photocatalysts.Herein,BiOBr/AgBr ...Efficient interfacial charge transfer and robust interfacial interactions are crucial for achieving the superior spatial separation of carriers and developing efficient heterojunction photocatalysts.Herein,BiOBr/AgBr S-scheme heterojunctions are synthesized via the co-sharing of Br atoms using an ion-exchange approach,which involves the in-situ growth of AgBr nanoparticles on the surfaces of BiOBr nanosheets.It is revealed that successful construction of a high-quality interface with strong interactions via Br atom bridge between BiOBr and AgBr,which provided a rapid migration channel for charge carriers.In addition,in-situ XPS,Kelvin probe force microscopy,and electron spin resonance evaluations confirmed the establishment of an S-scheme charge-transfer pathway in this tightly contacted heterojunction,which could efficiently prevent the recombination of photogenerated carriers while retaining carriers with a high redox capacity.Finally,the photocatalytic test confirmed that the BiOBr/AgBr heterojunction showed excellent photocatalytic performance and wide applicability thanks to the construction of high quality heterojunction.Overall,this work highlights the importance of rational designing of heterogeneous interfaces at the atomic level in photocatalysis,and contributes to rationally design BiOBr-based S-scheme heterojunctions photocatalytic materials with high quality atomic cosharing interfaces.展开更多
The photocatalytic reduction of CO_(2)presents a promising avenue for carbon fuel conversion.However,the efficiency of charge utilization remains a critical barrier to industrial applications.In this study,we introduc...The photocatalytic reduction of CO_(2)presents a promising avenue for carbon fuel conversion.However,the efficiency of charge utilization remains a critical barrier to industrial applications.In this study,we introduce a tandem design of Bi_(2)WO_(6)-BiOCl with an atomically matched interface,achieving highly efficient photoreduction of CO_(2)to CO.By incorporating WO_(4)^(2-)ions and tuning coordination environment,the(110)facet of BiOCl was in-situ grown on the(200)facet of Bi_(2)WO_(6).Compared to single phases and ball-milling samples,Bi_(2)WO_(6)-BiOCl exhibits a remarkable CO yield of 68.03μmol g^(-1)h^(-1)with a selectivity of 98%.Atomic visualization and coordination analysis confirm the formation of a coherent interface that facilitates charge migration for efficient electron transport.Density functional theory(DFT)calculations and in-situ Fourier transform infrared(FTIR)spectroscopy provide insights into the intrinsic active sites and reaction mechanisms.The proposed lattice engineering strategies offer a new paradigm for the rational design of heterostructures beyond traditional band alignment at the atomic scale.展开更多
It is still a great challenge at present to combine the high rate capability of the electrochemical capacitor with the high electrochemical capacity feature of rechargeable battery in energy storage and transport devi...It is still a great challenge at present to combine the high rate capability of the electrochemical capacitor with the high electrochemical capacity feature of rechargeable battery in energy storage and transport devices. By studying the lithiation mechanism of Li_4Ti_5O_12 （LTO） using in-situ electron holography, we find that double charge layers are formed at the interface of the insulating Li_4Ti_5O_12 （Li_4） phase and the semiconducting Li_7Ti_5O_12 （Li_7） phase, and can greatly boost the lithiation kinetics. The electron wave phase of the LTO particle is found to gradually shrink with the interface movement, leaving a positive electric field from Li_7 to Li_4 phase. Once the capacitive interface charges are formed, the lithiation of the core/shell particle could be established within 10 s. The ultrafast kinetics is attributed to the built-in interface potential and the mixed Ti3＋/Ti4＋ sites at the interface that could be maximally lowering the thermodynamic barrier for Li ion migration.展开更多
Compared with Zn^(2+),the current mainly reported charge carrier for zinc hybrid capacitors,small-hydrated-sized and light-weight NH_(4)^(+)is expected as a better one to mediate cathodic interfacial electrochemical b...Compared with Zn^(2+),the current mainly reported charge carrier for zinc hybrid capacitors,small-hydrated-sized and light-weight NH_(4)^(+)is expected as a better one to mediate cathodic interfacial electrochemical behaviors,yet has not been unraveled.Here we propose an NH_(4)^(+)-modulated cationic solvation strategy to optimize cathodic spatial charge distribution and achieve dynamic Zn^(2+)/NH_(4)^(+)co-storage for boosting Zinc hybrid capacitors.Owing to the hierarchical cationic solvated structure in hybrid Zn(CF_(3)SO_(3))_(2)–NH_4CF_(3)SO_(3)electrolyte,high-reactive Zn^(2+)and small-hydrate-sized NH_4(H_(2)O))(4)^(+)induce cathodic interfacial Helmholtz plane reconfiguration,thus effectively enhancing the spatial charge density to activate 20%capacity enhancement.Furthermore,cathodic interfacial adsorbed hydrated NH_(4)^(+)ions afford high-kinetics and ultrastable C···H(NH_(4)^(+))charge storage process due to a much lower desolvation energy barrier compared with heavy and rigid Zn(H_(2)O)_6^(2+)(5.81 vs.14.90 eV).Consequently,physical uptake and multielectron redox of Zn^(2+)/NH_(4)^(+)in carbon cathode enable the zinc capacitor to deliver high capacity(240 mAh g^(-1)at 0.5 A g^(-1)),large-current tolerance(130 mAh g^(-1)at 50 A g^(-1))and ultralong lifespan(400,000cycles).This study gives new insights into the design of cathode–electrolyte interfaces toward advanced zinc-based energy storage.展开更多
This paper presents a novel high-voltage lateral double diffused metal-oxide semiconductor （LDMOS） with self- adaptive interface charge （SAC） layer and its physical model of the vertical interface electric field. ...This paper presents a novel high-voltage lateral double diffused metal-oxide semiconductor （LDMOS） with self- adaptive interface charge （SAC） layer and its physical model of the vertical interface electric field. The SAC can be self-adaptive to collect high concentration dynamic inversion holes, which effectively enhance the electric field of dielectric buried layer （EI） and increase breakdown voltage （BV）. The BV and EI of SAC LDMOS increase to 612 V and 600 V/tim from 204 V and 90.7 V/ttm of the conventional silicon-on-insulator, respectively. Moreover, enhancement factors of r/which present the enhanced ability of interface charge on EI are defined and analysed.展开更多
A model based on analysis of the self-consistent Poisson-Schrodinger equation is proposed to investigate the tunneling current of electrons in the inversion layer of a p-type metal-oxide-semiconductor （MOS） structur...A model based on analysis of the self-consistent Poisson-Schrodinger equation is proposed to investigate the tunneling current of electrons in the inversion layer of a p-type metal-oxide-semiconductor （MOS） structure. In this model, the influences of interface trap charge （ITC） at the Si-SiO2 interface and fixed oxide charge （FOC） in the oxide region are taken into account, and one-band effective mass approximation is used. The tunneling probability is obtained by employing the transfer matrix method. Further, the effects of in-plane momentum on the quantization in the electron motion perpendicular to the Si-SiO2 interface of a MOS device are investigated. Theoretical simulation results indicate that both ITC and FOC have great influence on the tunneling current through a MOS structure when their densities are larger than l012 cm 2, which results from the great change of bound electrons near the Si-SiO2 interface and the oxide region. Therefore, for real ultrathin MOS structures with ITC and FOC, this model can give a more accurate description for the tunneling current in the inversion layer.展开更多
The modified dipolar Poisson-Boltzmann （MDPB） equation, where the electrostatics of the dipolar interactions of solvent molecules and also the finite size effects of ions and dipolar solvent molecules are explicitly...The modified dipolar Poisson-Boltzmann （MDPB） equation, where the electrostatics of the dipolar interactions of solvent molecules and also the finite size effects of ions and dipolar solvent molecules are explicitly taken into account on a mean-field level, is studied numerically for a two-plate system with oppositely charged surfaces. The MDPB equation is solved numerically, using the nonlinear Multigrid method, for one-dimensional finite volume meshes. For a high enough surface charge density, numerical results of the MDPB equation reveal that the effective dielectric constant decreases with the increase of the surface charge density. Furthermore, increasing the salt concentration leads to the decrease of the effective dielectric constant close to the charged surfaces. This decrease of the effective dielectric constant with the surface charge density is opposite to the trend from the dipolar Poisson Boltzmann （DPB） equation. This seemingly inconsistent result is due to the fact that the mean-field approach breaks down in such highly charged systems where the counterions and dipoles are strongly attracted to the charged surfaces and form a quasi two-dimensional layer. In the weak-coupling regime with the electrostatic coupling parameter （the ratio of Bjerrum length to Gouy-Chapman length） Ξ 〈 1, where the MDPB equation works, the effective dielectric constant is independent of the distance from the charged surfaces and there is no accumulation of dipoles near the charged surfaces. Therefore, there are no physical and computational advantages for the MDPB equation over the modified Poisson-Boltzmann （MPB） equation where the effect of dipolar interactions of solvent dipoles is implicitly taken into account in the renormalised dielectric constant.展开更多
An analytical model of the power metal–oxide–semiconductor field-effect transistor(MOSFET)with high permittivity insulator structure(HKMOS)with interface charge is established based on superposition and developed fo...An analytical model of the power metal–oxide–semiconductor field-effect transistor(MOSFET)with high permittivity insulator structure(HKMOS)with interface charge is established based on superposition and developed for optimization by charge compensation.In light of charge compensation,the disturbance aroused by interface charge is efficiently compromised by introducing extra charge for maximizing breakdown voltage(BV)and minimizing specific ON-resistance(R_(on,sp)).From this optimization method,it is very efficient to obtain the design parameters to overcome the difficulty in implementing the R_(on,sp)–BV trade-off for quick design.The analytical results prove that in the HKMOS with positive or negative interface charge at a given length of drift region,the extraction of the parameters is qualitatively and quantitatively optimized for trading off BV and Ron,sp with JFET effect taken into account.展开更多
A new SOI power device with multi-region high-concentration fixed charge（MHFC） is reported. The MHFC is formed through implanting Cs or I ion into the buried oxide layer（BOX）, by which the high-concentration dynam...A new SOI power device with multi-region high-concentration fixed charge（MHFC） is reported. The MHFC is formed through implanting Cs or I ion into the buried oxide layer（BOX）, by which the high-concentration dynamic electrons and holes are induced at the top and bottom interfaces of BOX. The inversion holes can enhance the vertical electric field and raise the breakdown voltage since the drain bias is mainly generated from the BOX. A model of breakdown voltage is developed, from which the optimal spacing has also been obtained. The numerical results indicate that the breakdown voltage of device proposed is increased by 287% in comparison to that of conventional LDMOS.展开更多
We study the charge trapping phenomenon that restricts the endurance of n-type ferroelectric field-effect transistors(FeFETs)with metal/ferroelectric/interlayer/Si(MFIS)gate stack structure.In order to explore the phy...We study the charge trapping phenomenon that restricts the endurance of n-type ferroelectric field-effect transistors(FeFETs)with metal/ferroelectric/interlayer/Si(MFIS)gate stack structure.In order to explore the physical mechanism of the endurance failure caused by the charge trapping effect,we first establish a model to simulate the electron trapping behavior in n-type Si FeFET.The model is based on the quantum mechanical electron tunneling theory.And then,we use the pulsed I_d-V_g method to measure the threshold voltage shift between the rising edges and falling edges of the FeFET.Our model fits the experimental data well.By fitting the model with the experimental data,we get the following conclusions.(i)During the positive operation pulse,electrons in the Si substrate are mainly trapped at the interface between the ferroelectric(FE)layer and interlayer(IL)of the FeFET gate stack by inelastic trap-assisted tunneling.(ii)Based on our model,we can get the number of electrons trapped into the gate stack during the positive operation pulse.(iii)The model can be used to evaluate trap parameters,which will help us to further understand the fatigue mechanism of FeFET.展开更多
CMOS image sensors produced by the existing CMOS manufacturing process usually have difficulty achieving complete charge transfer owing to the introduction of potential barriers or Si/SiO_(2)interface state traps in t...CMOS image sensors produced by the existing CMOS manufacturing process usually have difficulty achieving complete charge transfer owing to the introduction of potential barriers or Si/SiO_(2)interface state traps in the charge transfer path,which reduces the charge transfer efficiency and image quality.Until now,scholars have only considered mechanisms that limit charge transfer from the perspectives of potential barriers and spill back effect under high illumination condition.However,the existing models have thus far ignored the charge transfer limitation due to Si/SiO_(2)interface state traps in the transfer gate channel,particularly under low illumination.Therefore,this paper proposes,for the first time,an analytical model for quantifying the incomplete charge transfer caused by Si/SiO_(2)interface state traps in the transfer gate channel under low illumination.This model can predict the variation rules of the number of untransferred charges and charge transfer efficiency when the trap energy level follows Gaussian distribution,exponential distribution and measured distribution.The model was verified with technology computer-aided design simulations,and the results showed that the simulation results exhibit the consistency with the proposed model.展开更多
Discovery of materials using“bottom-up”or“top-down”approach is of great interest in materials science.Layered materials consisting of two-dimensional(2D)building blocks provide a good platform to explore new mater...Discovery of materials using“bottom-up”or“top-down”approach is of great interest in materials science.Layered materials consisting of two-dimensional(2D)building blocks provide a good platform to explore new materials in this respect.In van der Waals(vdW)layered materials,these building blocks are charge neutral and can be isolated from their bulk phase(top-down),but usually grow on substrate.In ionic layered materials,they are charged and usually cannot exist independently but can serve as motifs to construct new materials(bottom-up).In this paper,we introduce our recently constructed databases for 2D material-substrate interface(2DMSI),and 2D charged building blocks.For 2DMSI database,we systematically build a workflow to predict appropriate substrates and their geometries at substrates,and construct the 2DMSI database.For the 2D charged building block database,1208 entries from bulk material database are identified.Information of crystal structure,valence state,source,dimension and so on is provided for each entry with a json format.We also show its application in designing and searching for new functional layered materials.The 2DMSI database,building block database,and designed layered materials are available in Science Data Bank at https://doi.org/10.57760/sciencedb.j00113.00188.展开更多
We investigate the influence of interface charge on electrical performance of NbAIO/A1GaN/GaN metal-oxide- semiconductor high electron mobility transistors （MOSHEMTs）. Through C-V measurements and simulations, we fi...We investigate the influence of interface charge on electrical performance of NbAIO/A1GaN/GaN metal-oxide- semiconductor high electron mobility transistors （MOSHEMTs）. Through C-V measurements and simulations, we find that the donor-type interface fixed charge density Qit of 2.2 × 10^13 cm^-2 exists at the NbA10/A1GaN interface, which induces the shift of the threshold voltage much more negative. Furthermore, a trap density of approximately 0.43 × 10^13-1.14 ×10^13 cm^-2 eV^-1 is obtained at the NaA10/AlGaN interface, which is consistent with the frequency-dependent capacitance and conductance measurement results.展开更多
Interface chemical modulation strategies are considered as promising method to prepare electrocatalysts for the urea oxidation reaction(UOR).However,conventional interface catalysts are generally limited by the inhere...Interface chemical modulation strategies are considered as promising method to prepare electrocatalysts for the urea oxidation reaction(UOR).However,conventional interface catalysts are generally limited by the inherent activity and incompatibility of the individual components themselves,and the irregular charge distribution and slow charge transfer ability between interfaces severely limit the activity of UOR.Therefore,we optimized and designed a Ni_(2)P/CoP interface with modulated surface charge distribution and directed charge transfer to promote UOR activity.Density functional theorycalculations first predict a regular charge transfer from CoP to Ni_(2)P,which creates a built-in electric field between Ni_(2)P and CoP interface.Optimization of the adsorption/desorption process of UOR/HER reaction intermediates leads to the improvement of catalytic activity.Electrochemical impedance spectroscopy and ex situ X-ray photoelectron spectroscopy characterization confirm the unique mechanism of facilitated reaction at the Ni_(2)P/CoP interface.Electrochemical tests further validated the prediction with excellent UOR/HER activities of 1.28 V and 19.7 mV vs.RHE,at 10 mA cm^(-2),respectively.Furthermore,Ni_(2)P/CoP achieves industrial-grade current densities(500 mA cm^(−2))at 1.75 V and 1.87 V in the overall urea electrolyzer(UOR||HER)and overall human urine electrolyzer(HUOR||HER),respectively,and demonstrates considerable durability.展开更多
Perovskite-based photovoltaic materials have been attracting attention for their strikingly improved performance at converting sunlight into electricity.The beneficial and unique optoelectronic characteristics of pero...Perovskite-based photovoltaic materials have been attracting attention for their strikingly improved performance at converting sunlight into electricity.The beneficial and unique optoelectronic characteristics of perovskite structures enable researchers to achieve an incredibly remarkable power conversion efficiency.Flexible hybrid perovskite photovoltaics promise emerging applications in a myriad of optoelectronic and wearable/portable device applications owing to their inherent intriguing physicochemical and photophysical properties which enabled researchers to take forward advanced research in this growing field.Flexible perovskite photovoltaics have attracted significant attention owing to their fascinating material properties with combined merits of high efficiency,light-weight,flexibility,semitransparency,compatibility towards roll-to-roll printing,and large-area mass-scale production.Flexible perovskite-based solar cells comprise of 4 key components that include a flexible substrate,semi-transparent bottom contact electrode,perovskite(light absorber layer)and charge transport(electron/hole)layers and top(usually metal)electrode.Among these components,interfacial layers and contact electrodes play a pivotal role in influencing the overall photovoltaic performance.In this comprehensive review article,we focus on the current developments and latest progress achieved in perovskite photovoltaics concerning the charge selective transport layers/electrodes toward the fabrication of highly stable,efficient flexible devices.As a concluding remark,we briefly summarize the highlights of the review article and make recommendations for future outlook and investigation with perspectives on the perovskite-based optoelectronic functional devices that can be potentially utilized in smart wearable and portable devices.展开更多
Progress in the fast charging of high-capacity silicon monoxide(SiO)-based anode is currently hindered by insufficient conductivity and notable volume expansion.The construction of an interface conductive network effe...Progress in the fast charging of high-capacity silicon monoxide(SiO)-based anode is currently hindered by insufficient conductivity and notable volume expansion.The construction of an interface conductive network effectively addresses the aforementioned problems;however,the impact of its quality on lithium-ion transfer and structure durability is yet to be explored.Herein,the influence of an interface conductive network on ionic transport and mechanical stability under fast charging is explored for the first time.2D modeling simulation and Cryo-transmission electron microscopy precisely reveal the mitigation of interface polarization owing to a higher fraction of conductive inorganic species formation in bilayer solid electrolyte interphase is mainly responsible for a linear decrease in ionic diffusion energy barrier.Furthermore,atomic force microscopy and Raman shift exhibit substantial stress dissipation generated by a complete conductive network,which is critical to the linear reduction of electrode residual stress.This study provides insights into the rational design of optimized interface SiO-based anodes with reinforced fast-charging performance.展开更多
The direct conversion of atmospheric CO_(2) into fuel via photocatalysis exhibits significant practical application value in advancing the carbon cycle.In this study,we established an electro-assisted photocatalytic s...The direct conversion of atmospheric CO_(2) into fuel via photocatalysis exhibits significant practical application value in advancing the carbon cycle.In this study,we established an electro-assisted photocatalytic system with dual compartments and interfaces,and coated Ag nanoparticles on the titanium nanotube arrays(TNTAs)by polydopamine modification.In the absence of sacrificial agent and alkali absorption liquid conditions,the stable,efficient and highly selective conversion of CO_(2) to CO at the gas-solid interface in ambient air was realized by photoelectric synergy.Specifically,with the assistance of potential,the CO formation rates reached 194.9μmol h^(−1) m^(−2) and 103.9μmol h^(−1) m^(−2) under ultraviolet and visible light irradiation,respectively;the corresponding CO_(2) conversion rates in ambient air were 30%and 16%,respectively.The excellent catalytic effect is mainly attributed to the formation of P–N heterojunction during the catalytic process and the surface plasmon resonance effect.Additionally,the introduction of solid agar electrolytes effectively inhibits the hydrogen evolution reaction and improves the electron utilization rate.This system promotes the development of photocatalytic technology for practical applications and provides new insights and support for the carbon cycle.展开更多
Low-efficiency charge transfer is a critical factor to limit the photocatalytic H_(2)evolution activity of semiconductor photocatalysts.The interface design is a promising approach to achieve high chargetransfer effic...Low-efficiency charge transfer is a critical factor to limit the photocatalytic H_(2)evolution activity of semiconductor photocatalysts.The interface design is a promising approach to achieve high chargetransfer efficiency for photocatalysts.Herein,a new 2 D/2 D atomic double-layer WS_(2)/Nb_(2)O_(5)shell/core photocatalyst(DLWS/Nb_(2)O_(5))is designed.The atom-resolved HAADF-STEM results unravel the presence of an unusual 2 D/2 D shell/core interface in DLWS/Nb_(2)O_(5).Taking advantage of the advanced femtosecond-resolved ultrafast TAS spectra,the average lifetime of charge carriers for DLWS/Nb_(2)O_(5)(180.97 ps)is considerably shortened as compared to that of Nb_(2)O_(5)(230.50 ps),strongly indicating that the 2 D/2 D shell/core interface enables DLWS/Nb_(2)O_(5)to achieve ultrafast charge transfer from Nb_(2)O_(5)to atomic double-layer WS_(2),thus yielding a high photocatalytic H_(2)evolution rate of 237.6 mmol/h,up to10.8 times higher than that of pure Nb_(2)O_(5)nanosheet.This study will open a new window for the development of high-efficient photocatalytic systems through the interface design.展开更多
基金the financial support from the National Natural Science Foundation of China(52203123 and 52473248)State Key Laboratory of Polymer Materials Engineering(sklpme2024-2-04)+1 种基金the Fundamental Research Funds for the Central Universitiessponsored by the Double First-Class Construction Funds of Sichuan University。
文摘Composite polymer electrolytes(CPEs)offer a promising solution for all-solid-state lithium-metal batteries(ASSLMBs).However,conventional nanofillers with Lewis-acid-base surfaces make limited contribution to improving the overall performance of CPEs due to their difficulty in achieving robust electrochemical and mechanical interfaces simultaneously.Here,by regulating the surface charge characteristics of halloysite nanotube(HNT),we propose a concept of lithium-ion dynamic interface(Li^(+)-DI)engineering in nano-charged CPE(NCCPE).Results show that the surface charge characteristics of HNTs fundamentally change the Li^(+)-DI,and thereof the mechanical and ion-conduction behaviors of the NCCPEs.Particularly,the HNTs with positively charged surface(HNTs+)lead to a higher Li^(+)transference number(0.86)than that of HNTs-(0.73),but a lower toughness(102.13 MJ m^(-3)for HNTs+and 159.69 MJ m^(-3)for HNTs-).Meanwhile,a strong interface compatibilization effect by Li^(+)is observed for especially the HNTs+-involved Li^(+)-DI,which improves the toughness by 2000%compared with the control.Moreover,HNTs+are more effective to weaken the Li^(+)-solvation strength and facilitate the formation of Li F-rich solid-electrolyte interphase of Li metal compared to HNTs-.The resultant Li|NCCPE|LiFePO4cell delivers a capacity of 144.9 m Ah g^(-1)after 400 cycles at 0.5 C and a capacity retention of 78.6%.This study provides deep insights into understanding the roles of surface charges of nanofillers in regulating the mechanical and electrochemical interfaces in ASSLMBs.
基金supported by the Natural Science Foundation of Zhejiang Province(LZ22C130001)the National Natural Science Foundation of China(32171887,and 52002028,and 52192610)+1 种基金the National Key Research and Development Project from Minister of Science&Technology(2021YFA0202704)Beijing Municipal Science&Technology Commission(Z171100002017017).
文摘Efficient utilization of electrostatic charges is paramount for numerous applications,from printing to kinetic energy harvesting.However,existing technologies predominantly focus on the static qualities of these charges,neglecting their dynamic capabilities as carriers for energy conversion.Herein,we report a paradigm-shifting strategy that orchestrates the swift transit of surface charges,generated through contact electrification,via a freely moving droplet.This technique ingeniously creates a bespoke charged surface which,in tandem with a droplet acting as a transfer medium to the ground,facilitates targeted charge displacement and amplifies electrical energy collection.The spontaneously generated electric field between the charged surface and needle tip,along with the enhanced water ionization under the electric field,proves pivotal in facilitating controlled charge transfer.By coupling the effects of charge self-transfer,contact electrification,and electrostatic induction,a dual-electrode droplet-driven(DD)triboelectric nanogenerator(TENG)is designed to harvest the water-related energy,exhibiting a two-orderof-magnitude improvement in electrical output compared to traditional single-electrode systems.Our strategy establishes a fundamental groundwork for efficient water drop energy acquisition,offering deep insights and substantial utility for future interdisciplinary research and applications in energy science.
基金supported by the National Natural Science Foundation of China (No. 12204207)the National Natural Science Foundation of China-Yunnan Joint Fund (No. U2102215)+1 种基金the National Natural Science Foundation of High and Foreign Experts Introduction Plan (No. G2022039008L)Yunnan XingDian Youth Talent Support Program (No. XDYC-QNRC-2022-0591)。
文摘Efficient interfacial charge transfer and robust interfacial interactions are crucial for achieving the superior spatial separation of carriers and developing efficient heterojunction photocatalysts.Herein,BiOBr/AgBr S-scheme heterojunctions are synthesized via the co-sharing of Br atoms using an ion-exchange approach,which involves the in-situ growth of AgBr nanoparticles on the surfaces of BiOBr nanosheets.It is revealed that successful construction of a high-quality interface with strong interactions via Br atom bridge between BiOBr and AgBr,which provided a rapid migration channel for charge carriers.In addition,in-situ XPS,Kelvin probe force microscopy,and electron spin resonance evaluations confirmed the establishment of an S-scheme charge-transfer pathway in this tightly contacted heterojunction,which could efficiently prevent the recombination of photogenerated carriers while retaining carriers with a high redox capacity.Finally,the photocatalytic test confirmed that the BiOBr/AgBr heterojunction showed excellent photocatalytic performance and wide applicability thanks to the construction of high quality heterojunction.Overall,this work highlights the importance of rational designing of heterogeneous interfaces at the atomic level in photocatalysis,and contributes to rationally design BiOBr-based S-scheme heterojunctions photocatalytic materials with high quality atomic cosharing interfaces.
基金supported by the National Key R&D Program of China(No.2021YFA1200201)the Beijing Outstanding Young Scientists Projects(No.BJJWZYJH01201910005018)+1 种基金The Basic Science Center Program for Multiphase Evolution in Hypergravity of the National Natural Science Foundation of China(No.51988101)the National Natural Science Foundation of China(Nos.52071003 and 91860202)。
文摘The photocatalytic reduction of CO_(2)presents a promising avenue for carbon fuel conversion.However,the efficiency of charge utilization remains a critical barrier to industrial applications.In this study,we introduce a tandem design of Bi_(2)WO_(6)-BiOCl with an atomically matched interface,achieving highly efficient photoreduction of CO_(2)to CO.By incorporating WO_(4)^(2-)ions and tuning coordination environment,the(110)facet of BiOCl was in-situ grown on the(200)facet of Bi_(2)WO_(6).Compared to single phases and ball-milling samples,Bi_(2)WO_(6)-BiOCl exhibits a remarkable CO yield of 68.03μmol g^(-1)h^(-1)with a selectivity of 98%.Atomic visualization and coordination analysis confirm the formation of a coherent interface that facilitates charge migration for efficient electron transport.Density functional theory(DFT)calculations and in-situ Fourier transform infrared(FTIR)spectroscopy provide insights into the intrinsic active sites and reaction mechanisms.The proposed lattice engineering strategies offer a new paradigm for the rational design of heterostructures beyond traditional band alignment at the atomic scale.
基金supported by the National Natural Science Foundation of China (Nos. 51501085, 11704019, 51522212 and 51421002)National Program on Key Basic Research Project (2014CB921002)the Strategic Priority Research Program of Chinese Academy of Sciences (No. XDB07030200)
文摘It is still a great challenge at present to combine the high rate capability of the electrochemical capacitor with the high electrochemical capacity feature of rechargeable battery in energy storage and transport devices. By studying the lithiation mechanism of Li_4Ti_5O_12 （LTO） using in-situ electron holography, we find that double charge layers are formed at the interface of the insulating Li_4Ti_5O_12 （Li_4） phase and the semiconducting Li_7Ti_5O_12 （Li_7） phase, and can greatly boost the lithiation kinetics. The electron wave phase of the LTO particle is found to gradually shrink with the interface movement, leaving a positive electric field from Li_7 to Li_4 phase. Once the capacitive interface charges are formed, the lithiation of the core/shell particle could be established within 10 s. The ultrafast kinetics is attributed to the built-in interface potential and the mixed Ti3＋/Ti4＋ sites at the interface that could be maximally lowering the thermodynamic barrier for Li ion migration.
基金financially supported by the National Natural Science Foundation of China(Nos.22272118,22172111 and 22309134)the Science and Technology Commission of Shanghai Municipality,China(Nos.22ZR1464100,20ZR1460300 and 19DZ2271500)+3 种基金China Postdoctoral Science Foundation(2022M712402)Shanghai Rising-Star Program(23YF1449200)Zhejiang Provincial Science and Technology Project(2022C01182)the Fundamental Research Funds for the Central Universities(22120210529 and 2023-3-YB-07)。
文摘Compared with Zn^(2+),the current mainly reported charge carrier for zinc hybrid capacitors,small-hydrated-sized and light-weight NH_(4)^(+)is expected as a better one to mediate cathodic interfacial electrochemical behaviors,yet has not been unraveled.Here we propose an NH_(4)^(+)-modulated cationic solvation strategy to optimize cathodic spatial charge distribution and achieve dynamic Zn^(2+)/NH_(4)^(+)co-storage for boosting Zinc hybrid capacitors.Owing to the hierarchical cationic solvated structure in hybrid Zn(CF_(3)SO_(3))_(2)–NH_4CF_(3)SO_(3)electrolyte,high-reactive Zn^(2+)and small-hydrate-sized NH_4(H_(2)O))(4)^(+)induce cathodic interfacial Helmholtz plane reconfiguration,thus effectively enhancing the spatial charge density to activate 20%capacity enhancement.Furthermore,cathodic interfacial adsorbed hydrated NH_(4)^(+)ions afford high-kinetics and ultrastable C···H(NH_(4)^(+))charge storage process due to a much lower desolvation energy barrier compared with heavy and rigid Zn(H_(2)O)_6^(2+)(5.81 vs.14.90 eV).Consequently,physical uptake and multielectron redox of Zn^(2+)/NH_(4)^(+)in carbon cathode enable the zinc capacitor to deliver high capacity(240 mAh g^(-1)at 0.5 A g^(-1)),large-current tolerance(130 mAh g^(-1)at 50 A g^(-1))and ultralong lifespan(400,000cycles).This study gives new insights into the design of cathode–electrolyte interfaces toward advanced zinc-based energy storage.
基金Projects supported by the National Natural Science Foundation of China （Grant Nos. 60806025 and 60976060）, the National Laboratory of Analog Integrated Circuit （Grant No. 9140C0903070904）, and the Youth Teacher Foundation of the University of Electroniq Science and Technology of China （Grant No. ix0721）.
文摘This paper presents a novel high-voltage lateral double diffused metal-oxide semiconductor （LDMOS） with self- adaptive interface charge （SAC） layer and its physical model of the vertical interface electric field. The SAC can be self-adaptive to collect high concentration dynamic inversion holes, which effectively enhance the electric field of dielectric buried layer （EI） and increase breakdown voltage （BV）. The BV and EI of SAC LDMOS increase to 612 V and 600 V/tim from 204 V and 90.7 V/ttm of the conventional silicon-on-insulator, respectively. Moreover, enhancement factors of r/which present the enhanced ability of interface charge on EI are defined and analysed.
基金Project supported by the National Natural Science Foundation of China (Grant No. 61076055)the Program for Innovative Research Team of Zhejiang Normal University of China (Grant No. 2007XCXTD-5)the Open Program of Surface Physics Laboratory of Fudan University, China (Grant No. FDSKL2011-04)
文摘A model based on analysis of the self-consistent Poisson-Schrodinger equation is proposed to investigate the tunneling current of electrons in the inversion layer of a p-type metal-oxide-semiconductor （MOS） structure. In this model, the influences of interface trap charge （ITC） at the Si-SiO2 interface and fixed oxide charge （FOC） in the oxide region are taken into account, and one-band effective mass approximation is used. The tunneling probability is obtained by employing the transfer matrix method. Further, the effects of in-plane momentum on the quantization in the electron motion perpendicular to the Si-SiO2 interface of a MOS device are investigated. Theoretical simulation results indicate that both ITC and FOC have great influence on the tunneling current through a MOS structure when their densities are larger than l012 cm 2, which results from the great change of bound electrons near the Si-SiO2 interface and the oxide region. Therefore, for real ultrathin MOS structures with ITC and FOC, this model can give a more accurate description for the tunneling current in the inversion layer.
基金Project supported by the National Natural Science Foundation of China (Grant Nos. 20954001 and 10774079)the Natural Science Foundation of Zhejiang Province of China (Grant No. Y7080401)+1 种基金the Natural Science Foundation of Ningbo City (Grant No. 2009A610056)the Startup Fund and K.C. Wong Magna Fund in Ningbo University
文摘The modified dipolar Poisson-Boltzmann （MDPB） equation, where the electrostatics of the dipolar interactions of solvent molecules and also the finite size effects of ions and dipolar solvent molecules are explicitly taken into account on a mean-field level, is studied numerically for a two-plate system with oppositely charged surfaces. The MDPB equation is solved numerically, using the nonlinear Multigrid method, for one-dimensional finite volume meshes. For a high enough surface charge density, numerical results of the MDPB equation reveal that the effective dielectric constant decreases with the increase of the surface charge density. Furthermore, increasing the salt concentration leads to the decrease of the effective dielectric constant close to the charged surfaces. This decrease of the effective dielectric constant with the surface charge density is opposite to the trend from the dipolar Poisson Boltzmann （DPB） equation. This seemingly inconsistent result is due to the fact that the mean-field approach breaks down in such highly charged systems where the counterions and dipoles are strongly attracted to the charged surfaces and form a quasi two-dimensional layer. In the weak-coupling regime with the electrostatic coupling parameter （the ratio of Bjerrum length to Gouy-Chapman length） Ξ 〈 1, where the MDPB equation works, the effective dielectric constant is independent of the distance from the charged surfaces and there is no accumulation of dipoles near the charged surfaces. Therefore, there are no physical and computational advantages for the MDPB equation over the modified Poisson-Boltzmann （MPB） equation where the effect of dipolar interactions of solvent dipoles is implicitly taken into account in the renormalised dielectric constant.
基金supported by the National Natural Science Foundation of China(Grant No.61404110)the National Higher-education Institution General Research and Development Project(Grant No.2682014CX097)。
文摘An analytical model of the power metal–oxide–semiconductor field-effect transistor(MOSFET)with high permittivity insulator structure(HKMOS)with interface charge is established based on superposition and developed for optimization by charge compensation.In light of charge compensation,the disturbance aroused by interface charge is efficiently compromised by introducing extra charge for maximizing breakdown voltage(BV)and minimizing specific ON-resistance(R_(on,sp)).From this optimization method,it is very efficient to obtain the design parameters to overcome the difficulty in implementing the R_(on,sp)–BV trade-off for quick design.The analytical results prove that in the HKMOS with positive or negative interface charge at a given length of drift region,the extraction of the parameters is qualitatively and quantitatively optimized for trading off BV and Ron,sp with JFET effect taken into account.
基金supported by the State Key Laboratory of Electronic Thin Films and Integrated Devices of China(Grant No.KFJJ201205)the Department of Education Project of Guangxi Province,China(Grant No.201202ZD041)+1 种基金the Postdoctoral Science Foundation Project of China(Grant Nos.2012M521127 and2013T60566)the National Natural Science Foundation of China(Grant Nos.61361011,61274077,and 61464003)
文摘A new SOI power device with multi-region high-concentration fixed charge（MHFC） is reported. The MHFC is formed through implanting Cs or I ion into the buried oxide layer（BOX）, by which the high-concentration dynamic electrons and holes are induced at the top and bottom interfaces of BOX. The inversion holes can enhance the vertical electric field and raise the breakdown voltage since the drain bias is mainly generated from the BOX. A model of breakdown voltage is developed, from which the optimal spacing has also been obtained. The numerical results indicate that the breakdown voltage of device proposed is increased by 287% in comparison to that of conventional LDMOS.
基金Project supported by the National Natural Science Foundation of China(Grant No.92264104)。
文摘We study the charge trapping phenomenon that restricts the endurance of n-type ferroelectric field-effect transistors(FeFETs)with metal/ferroelectric/interlayer/Si(MFIS)gate stack structure.In order to explore the physical mechanism of the endurance failure caused by the charge trapping effect,we first establish a model to simulate the electron trapping behavior in n-type Si FeFET.The model is based on the quantum mechanical electron tunneling theory.And then,we use the pulsed I_d-V_g method to measure the threshold voltage shift between the rising edges and falling edges of the FeFET.Our model fits the experimental data well.By fitting the model with the experimental data,we get the following conclusions.(i)During the positive operation pulse,electrons in the Si substrate are mainly trapped at the interface between the ferroelectric(FE)layer and interlayer(IL)of the FeFET gate stack by inelastic trap-assisted tunneling.(ii)Based on our model,we can get the number of electrons trapped into the gate stack during the positive operation pulse.(iii)The model can be used to evaluate trap parameters,which will help us to further understand the fatigue mechanism of FeFET.
基金supported by the National Natural Science Foundation of China(62171172).
文摘CMOS image sensors produced by the existing CMOS manufacturing process usually have difficulty achieving complete charge transfer owing to the introduction of potential barriers or Si/SiO_(2)interface state traps in the charge transfer path,which reduces the charge transfer efficiency and image quality.Until now,scholars have only considered mechanisms that limit charge transfer from the perspectives of potential barriers and spill back effect under high illumination condition.However,the existing models have thus far ignored the charge transfer limitation due to Si/SiO_(2)interface state traps in the transfer gate channel,particularly under low illumination.Therefore,this paper proposes,for the first time,an analytical model for quantifying the incomplete charge transfer caused by Si/SiO_(2)interface state traps in the transfer gate channel under low illumination.This model can predict the variation rules of the number of untransferred charges and charge transfer efficiency when the trap energy level follows Gaussian distribution,exponential distribution and measured distribution.The model was verified with technology computer-aided design simulations,and the results showed that the simulation results exhibit the consistency with the proposed model.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.61888102,52272172,and 52102193)the Major Program of the National Natural Science Foundation of China(Grant No.92163206)+2 种基金the National Key Research and Development Program of China(Grant Nos.2021YFA1201501 and 2022YFA1204100)the Strategic Priority Research Program of the Chinese Academy of Sciences(Grant No.XDB30000000)the Fundamental Research Funds for the Central Universities.
文摘Discovery of materials using“bottom-up”or“top-down”approach is of great interest in materials science.Layered materials consisting of two-dimensional(2D)building blocks provide a good platform to explore new materials in this respect.In van der Waals(vdW)layered materials,these building blocks are charge neutral and can be isolated from their bulk phase(top-down),but usually grow on substrate.In ionic layered materials,they are charged and usually cannot exist independently but can serve as motifs to construct new materials(bottom-up).In this paper,we introduce our recently constructed databases for 2D material-substrate interface(2DMSI),and 2D charged building blocks.For 2DMSI database,we systematically build a workflow to predict appropriate substrates and their geometries at substrates,and construct the 2DMSI database.For the 2D charged building block database,1208 entries from bulk material database are identified.Information of crystal structure,valence state,source,dimension and so on is provided for each entry with a json format.We also show its application in designing and searching for new functional layered materials.The 2DMSI database,building block database,and designed layered materials are available in Science Data Bank at https://doi.org/10.57760/sciencedb.j00113.00188.
基金Supported by the Basic Science Research Fund for the Central Universities of China under Grant No JB141104
文摘We investigate the influence of interface charge on electrical performance of NbAIO/A1GaN/GaN metal-oxide- semiconductor high electron mobility transistors （MOSHEMTs）. Through C-V measurements and simulations, we find that the donor-type interface fixed charge density Qit of 2.2 × 10^13 cm^-2 exists at the NbA10/A1GaN interface, which induces the shift of the threshold voltage much more negative. Furthermore, a trap density of approximately 0.43 × 10^13-1.14 ×10^13 cm^-2 eV^-1 is obtained at the NaA10/AlGaN interface, which is consistent with the frequency-dependent capacitance and conductance measurement results.
文摘Interface chemical modulation strategies are considered as promising method to prepare electrocatalysts for the urea oxidation reaction(UOR).However,conventional interface catalysts are generally limited by the inherent activity and incompatibility of the individual components themselves,and the irregular charge distribution and slow charge transfer ability between interfaces severely limit the activity of UOR.Therefore,we optimized and designed a Ni_(2)P/CoP interface with modulated surface charge distribution and directed charge transfer to promote UOR activity.Density functional theorycalculations first predict a regular charge transfer from CoP to Ni_(2)P,which creates a built-in electric field between Ni_(2)P and CoP interface.Optimization of the adsorption/desorption process of UOR/HER reaction intermediates leads to the improvement of catalytic activity.Electrochemical impedance spectroscopy and ex situ X-ray photoelectron spectroscopy characterization confirm the unique mechanism of facilitated reaction at the Ni_(2)P/CoP interface.Electrochemical tests further validated the prediction with excellent UOR/HER activities of 1.28 V and 19.7 mV vs.RHE,at 10 mA cm^(-2),respectively.Furthermore,Ni_(2)P/CoP achieves industrial-grade current densities(500 mA cm^(−2))at 1.75 V and 1.87 V in the overall urea electrolyzer(UOR||HER)and overall human urine electrolyzer(HUOR||HER),respectively,and demonstrates considerable durability.
基金the CSIRO Low Emissions Technologies Program for the support of this studythe financial support from the Australian Research Council(ARC)for the Future Fellowship(FT130101337)+4 种基金QUT core funding(QUT/322120-0301/07)supported by NSF MRI(1428992)U.S.-Egypt Science and Technology(S&T)Joint FundSDBoR R&D ProgramEDA University Center Program(ED18DEN3030025)。
文摘Perovskite-based photovoltaic materials have been attracting attention for their strikingly improved performance at converting sunlight into electricity.The beneficial and unique optoelectronic characteristics of perovskite structures enable researchers to achieve an incredibly remarkable power conversion efficiency.Flexible hybrid perovskite photovoltaics promise emerging applications in a myriad of optoelectronic and wearable/portable device applications owing to their inherent intriguing physicochemical and photophysical properties which enabled researchers to take forward advanced research in this growing field.Flexible perovskite photovoltaics have attracted significant attention owing to their fascinating material properties with combined merits of high efficiency,light-weight,flexibility,semitransparency,compatibility towards roll-to-roll printing,and large-area mass-scale production.Flexible perovskite-based solar cells comprise of 4 key components that include a flexible substrate,semi-transparent bottom contact electrode,perovskite(light absorber layer)and charge transport(electron/hole)layers and top(usually metal)electrode.Among these components,interfacial layers and contact electrodes play a pivotal role in influencing the overall photovoltaic performance.In this comprehensive review article,we focus on the current developments and latest progress achieved in perovskite photovoltaics concerning the charge selective transport layers/electrodes toward the fabrication of highly stable,efficient flexible devices.As a concluding remark,we briefly summarize the highlights of the review article and make recommendations for future outlook and investigation with perspectives on the perovskite-based optoelectronic functional devices that can be potentially utilized in smart wearable and portable devices.
基金the National Natural Science Foundation of China(Nos.22209095 and 22238004).
文摘Progress in the fast charging of high-capacity silicon monoxide(SiO)-based anode is currently hindered by insufficient conductivity and notable volume expansion.The construction of an interface conductive network effectively addresses the aforementioned problems;however,the impact of its quality on lithium-ion transfer and structure durability is yet to be explored.Herein,the influence of an interface conductive network on ionic transport and mechanical stability under fast charging is explored for the first time.2D modeling simulation and Cryo-transmission electron microscopy precisely reveal the mitigation of interface polarization owing to a higher fraction of conductive inorganic species formation in bilayer solid electrolyte interphase is mainly responsible for a linear decrease in ionic diffusion energy barrier.Furthermore,atomic force microscopy and Raman shift exhibit substantial stress dissipation generated by a complete conductive network,which is critical to the linear reduction of electrode residual stress.This study provides insights into the rational design of optimized interface SiO-based anodes with reinforced fast-charging performance.
文摘The direct conversion of atmospheric CO_(2) into fuel via photocatalysis exhibits significant practical application value in advancing the carbon cycle.In this study,we established an electro-assisted photocatalytic system with dual compartments and interfaces,and coated Ag nanoparticles on the titanium nanotube arrays(TNTAs)by polydopamine modification.In the absence of sacrificial agent and alkali absorption liquid conditions,the stable,efficient and highly selective conversion of CO_(2) to CO at the gas-solid interface in ambient air was realized by photoelectric synergy.Specifically,with the assistance of potential,the CO formation rates reached 194.9μmol h^(−1) m^(−2) and 103.9μmol h^(−1) m^(−2) under ultraviolet and visible light irradiation,respectively;the corresponding CO_(2) conversion rates in ambient air were 30%and 16%,respectively.The excellent catalytic effect is mainly attributed to the formation of P–N heterojunction during the catalytic process and the surface plasmon resonance effect.Additionally,the introduction of solid agar electrolytes effectively inhibits the hydrogen evolution reaction and improves the electron utilization rate.This system promotes the development of photocatalytic technology for practical applications and provides new insights and support for the carbon cycle.
基金funded by the China Postdoctoral Science Foundation(pre-station,No.2019TQ0050)Applied Basic Research Program of Sichuan Province(No.2020YJ0068)+5 种基金the China Postdoctoral Science Foundation(No.2020M673186)National Natural Science Foundation of China(No.22002014)National Natural Science Foundation of China(No.11804248)the financial support from the National Natural Science Foundation of China(No.21971113)Natural Science Foundation of Tianjin(No.18JCQNJC03200)supported by MOE Tier 1 RG4/17 and MOE Tier 2 MOE2019-T2-2-105。
文摘Low-efficiency charge transfer is a critical factor to limit the photocatalytic H_(2)evolution activity of semiconductor photocatalysts.The interface design is a promising approach to achieve high chargetransfer efficiency for photocatalysts.Herein,a new 2 D/2 D atomic double-layer WS_(2)/Nb_(2)O_(5)shell/core photocatalyst(DLWS/Nb_(2)O_(5))is designed.The atom-resolved HAADF-STEM results unravel the presence of an unusual 2 D/2 D shell/core interface in DLWS/Nb_(2)O_(5).Taking advantage of the advanced femtosecond-resolved ultrafast TAS spectra,the average lifetime of charge carriers for DLWS/Nb_(2)O_(5)(180.97 ps)is considerably shortened as compared to that of Nb_(2)O_(5)(230.50 ps),strongly indicating that the 2 D/2 D shell/core interface enables DLWS/Nb_(2)O_(5)to achieve ultrafast charge transfer from Nb_(2)O_(5)to atomic double-layer WS_(2),thus yielding a high photocatalytic H_(2)evolution rate of 237.6 mmol/h,up to10.8 times higher than that of pure Nb_(2)O_(5)nanosheet.This study will open a new window for the development of high-efficient photocatalytic systems through the interface design.
