CuBi_(2)O_(4)(CBO)photocathodes hold significant promise for efficient photoelectrochemical(PEC)water splitting due to their favorable band gap and theoretical onset potential.However,their practical application is hi...CuBi_(2)O_(4)(CBO)photocathodes hold significant promise for efficient photoelectrochemical(PEC)water splitting due to their favorable band gap and theoretical onset potential.However,their practical application is hindered by poor charge separation efficiency.Herein,we introduce a characteristic in-situ solution Fe-doping strategy that markedly improves photoelectrochemical performance of CBO,doubling the photocurrent density and achieving an unprecedented 190 mV anodic shift in the onset potential.By integrating with an electrochemical oxidation post-treatment,a record incident photon-to-current efficiency(IPCE)exceeding 40% at 0.6 V vs.RHE under visible light illumination is achieved.The versatility of the doping strategy is demonstrated across CBO photocathodes synthesized by different methods with various morphologies,grain sizes,and crystallinities.Mechanistic studies reveal that the gradient distribution of Fe^(3+)ions generates an internal electric field that facilitates efficient charge separation and increases acceptor density.The strong Fe-O bonding also enhances structural stability against photoinduced corrosion.Notably,our investigation uncovers the non-temperature-dependent nature of CBO photocurrent,indicating that PEC performance enhancement primarily depends on reducing carrier recombination rather than improving bulk conductivity.This work lays the groundwork for future advancements in water splitting performance of CBO photocathodes,offering a complementary strategy to conventional methods for enhancing charge separation efficiency.展开更多
A novel CMOS image sensor(CIS) pinned photodiode(PPD) pixel, named as O-T pixel, is proposed and investigated by TCAD simulations. Compared with the conventional PPD pixel, the proposed pixel features the overlapping ...A novel CMOS image sensor(CIS) pinned photodiode(PPD) pixel, named as O-T pixel, is proposed and investigated by TCAD simulations. Compared with the conventional PPD pixel, the proposed pixel features the overlapping gate(OG)and the temporary storage diffusing(TSD) region, based on which the several-nanosecond-level charge transfer could be achieved and the complete charge transfer from the PPD to the floating node(FD) could be realized. And systematic analyses of the influence of the doping conditions of the proposed processes, the OG length, and the photodiode length on the transfer performances of the proposed pixel are conducted. Optimized simulation results show that the total charge transfer time could reach about 5.862 ns from the photodiode to the sensed node and the corresponding charge transfer efficiency could reach as high as 99.995% in the proposed pixel with 10 μm long photodiode and 2.22 μm long OG. These results demonstrate a great potential of the proposed pixel in high-speed applications.展开更多
Photocatalytic reduction of CO_(2)into high-value C_(2)H_(4)offers a promising pathway toward carbon neutrality.Due to the continuous 12-electron-proton coupled reactions and the mutual repulsion of reaction intermedi...Photocatalytic reduction of CO_(2)into high-value C_(2)H_(4)offers a promising pathway toward carbon neutrality.Due to the continuous 12-electron-proton coupled reactions and the mutual repulsion of reaction intermediates,achieving highly selective photocatalytic conversion of CO_(2)to C_(2)H_(4)remains challenging.This work synthesized a CuInS_(2)/CuS heterojunction photocatalyst mediated by a sulfur electron bridge via a one-step solvothermal method,achieving a high selectivity for C_(2)H_(4)conversion(98.22%).The sulfur electron bridge minimized the contact energy barrier between CuInS_(2)and CuS to enhance photogenerated carrier separation efficiency,while the asymmetric active sites in CuInS_(2)effectively reduced mutual repulsion of reaction intermediates.This work develops a hybrid catalytic system enabling synergistic regulation of reaction kinetics and thermodynamics,offering an innovative strategy for highly selective photocatalytic CO₂-to-C_(2)H_(4)production.展开更多
Photoelectrochemical(PEC)water splitting is one of the most promising approaches toward achieving the conversion of solar energy to hydrogen.Hematite is a widely applied photoanode material in PEC water splitting beca...Photoelectrochemical(PEC)water splitting is one of the most promising approaches toward achieving the conversion of solar energy to hydrogen.Hematite is a widely applied photoanode material in PEC water splitting because of its appropriate band structure,non-toxicity,high stability,and low cost.Nevertheless,its relatively low photochemical conversion efficiency limits its application,and enhancing its PEC water splitting efficiency remains a challenge.Consequently,increasing efforts have been rendered toward improving the performance of hematite photoanodes.The entire PEC water splitting efficiency typically includes three parts:the photon absorption efficiency,the separation efficiency of the semiconductor bulk,and the surface injection efficiency.This review briefly discusses the recent advances in studies on hematite photoanodes for water splitting,and through the enhancement of the three above-mentioned efficiencies,the corresponding strategies toward improving the PEC performance of hematite are comprehensively discussed and summarized.展开更多
A novel method to calculate fuel-electric conversion factor for full hybrid electric vehicle（HEV）equipped with continuously variable transmission（CVT）is proposed.Based on consideration of the efficiency of pivotal...A novel method to calculate fuel-electric conversion factor for full hybrid electric vehicle（HEV）equipped with continuously variable transmission（CVT）is proposed.Based on consideration of the efficiency of pivotal components,electric motor,system efficiency optimization models are developed.According to the target of instantaneous optimization of system efficiency,operating ranges of each mode of power-train are determined,and the corresponding energy management strategies are established.The simulation results demonstrate that the energy management strategy proposed can substantially improve the vehicle fuel economy,and keep battery state of charge（SOC）change in a reasonable variation range.展开更多
The space charge accumulation in CdZnTe crystals seriously affects the performance of high-flux pulse detectors.The influence of sub-bandgap illumination on the space charge distribution and device performance in CdZn...The space charge accumulation in CdZnTe crystals seriously affects the performance of high-flux pulse detectors.The influence of sub-bandgap illumination on the space charge distribution and device performance in CdZnTe crystals were studied theoretically by Silvaco TCAD software simulation.The sub-bandgap illumination with a wavelength of 890 nm and intensity of 8×10−8 W/cm2 were used in the simulation to explore the space charge distribution and internal electric field distribution in CdZnTe crystals.The simulation results show that the deep level occupation faction is manipulated by the sub-bandgap illumination,thus space charge concentration can be reduced under the bias voltage of 500 V.A flat electric field distribution is obtained,which significantly improves the charge collection efficiency of the CdZnTe detector.Meanwhile,premised on the high resistivity of CdZnTe crystal,the space charge concentration in the crystal can be further reduced with the wavelength of 850 nm and intensity of 1×10−7 W/cm2 illumination.The electric field distribution is flatter and the carrier collection efficiency of the device can be improved more effectively.展开更多
Fabrication of efficient solid luminogens with tunable emission is both fundamentally significant and technically important. Herein, based on our previous strategy for the construction of efficient and multifunctional...Fabrication of efficient solid luminogens with tunable emission is both fundamentally significant and technically important. Herein, based on our previous strategy for the construction of efficient and multifunctional solid luminogens through the combination of diverse aggregation-induced emission （ALE） units with other functional moieties, a group of luminophores with electron donor-acceptor （D-A） structure and typical intramolecular charge transfer （ICT） characteristics, namely CZ-DCDPP, DPA-DCDPP and DBPA-DCDPP were synthesized and investigated. The presence of twisting and AlE-active 2,3- dicyano-S,6-diphenylpyrazine （DCDPP） moiety endows them highly emissive in the solid states, whereas the introduction of arylamines with varied electron-donating capacity and different conjugation render them with tunable solid emissions from green to red. While CZ-DCDPP and DPA-DCDPP solids exhibit distinct mechanochromism, both DPA-DCDPP and DBPA-DCDPP solids can generate efficient red emission. Owing to their high efficiency, remarkable thermal and morphological stabilities and moreover red emission, they are promising for diverse optoelectronic and biological applications.展开更多
The rational design of a heterostructural photocatalysts with efficient charge separation and accelerated interfacial charge transfer holds great promise for boosting photocatalytic activity.Herein,we have developed a...The rational design of a heterostructural photocatalysts with efficient charge separation and accelerated interfacial charge transfer holds great promise for boosting photocatalytic activity.Herein,we have developed a unique hierarchical In_(4/3)P_(2)S_(6)/TiO_(2) heterojunction with P-O interfacial bonding for photocatalytic water reduction.By integrating emerging In_(4/3)P_(2)S_(6) nanosheets through intense interfacial coupling effect,the optimized In_(4/3)P_(2)S_(6)/TiO_(2) heterostructure exhibits a remarkably enhanced photocatalytic H2 evolution activity compared to that of pristine TiO_(2).Combined experimental and theoretical results confirm that multiple interfacial bonded step-scheme(S-scheme)charge transfer pathways are established in the In_(4/3)P_(2)S_(6)/TiO_(2) photocatalyst,which synergistically promote charge separation and transfer through the robust interfacial electric field and rapid charge migration pathways formed by interfacial bonds.This study emphasizes the significance of developing novel interfacial bonded In_(4/3)P_(2)S_(6)-based S-scheme heterostructures,paving a new strategy towards enhancing photocatalytic activity for H_(2) evolution.展开更多
Semiconductor photocatalysts are extensively applied in environmental treatment and energy conversion.However,one of their major disadvantages is their relatively low photocatalytic performance owing to the recombinat...Semiconductor photocatalysts are extensively applied in environmental treatment and energy conversion.However,one of their major disadvantages is their relatively low photocatalytic performance owing to the recombination of generated electron-hole pairs.The presence of the phase junction is an effective way to promote the photocatalytic activity by increasing the separation efficiency of the electron-hole pairs.Accordingly,extensive research has been conducted on the design of phase junctions of photocatalysts to improve their charge transfer properties and efficiencies.Therefore,for the design of an appropriate phase junction and the understanding of the mechanism of electron-hole separation,the development of the photocatalytic phase junction,including the preparation methods of the heterogeneous materials,is tremendously important and helpful.Herein,the commonly used,externally induced phase transformation fabrication techniques and the primary components of the semiconductors are reviewed.Future directions will still focus on the design and optimization of the phase junction of photocatalytic materials according to the phase transition with higher efficiencies for broadband responses and solar energy utilization.Additionally,the most popular phase transformation fabrication techniques of phase junctions are briefly reviewed from the application viewpoint.展开更多
BiVO_(4) has been attracting a lot of interest in photoelectrochemical (PEC) water oxidation due to its efficient solar absorption and appropriate band positions.So far,sluggish water oxidation kinetics and fast photo...BiVO_(4) has been attracting a lot of interest in photoelectrochemical (PEC) water oxidation due to its efficient solar absorption and appropriate band positions.So far,sluggish water oxidation kinetics and fast photogenerated charge recombination still hinder the PEC performance ofBiVO_(4) .In this study,a novel PEC photoanode was designed by depositing ultrathin FeOOH nanolayers on the surface of nanoporousBiVO_(4) electrode,followed by modification with a cobaloxime (Co(dmgH)_(2)(4-COOH-py)Cl) molecular cocatalyst.Under irradiation of a 100 mW cm^(-2)(AM 1.5G) Xe lamp,the photocurrent density of the cobaloxime/FeOOH/BiVO_(4) composite photoanode reached 5.1 mA cm^(-2)at 1.23 V vs.RHE in 1.0 M potassium borate buffer solution (pH=9.0).The onset potential of the optimal cobaloxime/FeOOH/BiVO_(4) photoanode exhibited a 460 m V cathodic shift relative to bareBiVO_(4) .In addition,the surface charge injection efficiency of the composite photoanode reached~80%at 1.23 V vs.RHE and the incident photon-to-current efficiency (IPCE) reached~88%at 420 nm.展开更多
The charge transfer efficiency improvement method is introduced by optimizing the electrical potential distribution under the transfer gate along the charge transfer path. A non-uniform doped transfer transistor chan-...The charge transfer efficiency improvement method is introduced by optimizing the electrical potential distribution under the transfer gate along the charge transfer path. A non-uniform doped transfer transistor chan- nel is introduced to provide an ascending electrical potential gradient in the transfer transistor channel. With the adjustments to the overlap length between the R1 region and the transfer gate, the doping dose of the R1 region, and the overlap length between the anti-punch-through （APT） implantations and transfer gate, the potential barrier and potential pocket in the connecting region of transfer transistor channel and the pinned photodiode （PPD） are reduced to improve the electrical potential connection. The simulation results show that the percentage of residual charges to total charges drops from 1/10^4 to 1/10^7, and the transfer time is reduced from 500 to 110 ns. This means the charge transfer efficiency is improved.展开更多
Photocatalytic H2 evolution reactions on pristine graphitic carbon nitrides(g-C3N4),as a promising approach for converting solar energy to fuel,are attractive for tackling global energy concerns but still suffer from ...Photocatalytic H2 evolution reactions on pristine graphitic carbon nitrides(g-C3N4),as a promising approach for converting solar energy to fuel,are attractive for tackling global energy concerns but still suffer from low efficiencies.In this article,we report a tractable approach to modifying g-C3N4 with vanadyl phthalocyanine(VOPc/CN)for efficient visible-light-driven hydrogen production.A non-covalent VOPc/CN hybrid photocatalyst formed viaπ-πstacking interactions between the two components,as confirmed by analysis of UV-vis absorption spectra.The VOPc/CN hybrid photocatalyst shows excellent visible-light-driven photocatalytic performance and good stability.Under optimal conditions,the corresponding H2 evolution rate is nearly 6 times higher than that of pure g-C3N4.The role of VOPc in promoting hydrogen evolution activity was to extend the visible light absorption range and prevent the recombination of photoexcited electron-hole pairs effectively.It is expected that this facile modification method could be a new inspiration for the rational design and exploration of g-C3N4-based hybrid systems with strong light absorption and high-efficiency carrier separation.展开更多
We report a photoelectrochemical investigation of BiVO4 photoanodes prepared by successive ionic layer adsorption and reaction(SILAR),a facile method that yields uniform nanoporous films.After characterization of the ...We report a photoelectrochemical investigation of BiVO4 photoanodes prepared by successive ionic layer adsorption and reaction(SILAR),a facile method that yields uniform nanoporous films.After characterization of the phase,morphology,composition,and optical properties of the prepared films,the efficiencies of charge separation(ηsep)and water oxidation(ηox)in solar water splitting cells employing these photoanodes were estimated following a previously reported procedure.Unexpected wavelength and illumination direction dependencies were discovered in the derived efficiencies,casting doubt on the validity of the analysis.An alternative approach using a diffusion–reaction model that explicitly considers the efficiency of electron collection resolved the discrepancies and explained the illumination direction dependence of the photocurrent.Electron diffusion lengths(Ln)of 0.45μm and 0.55μm were derived for pristine and cobalt phosphate(Co-Pi)modified BiVO4,respectively,which are much shorter than the film thickness of^2.1μm.The Co-Pi treatment also increasedηoxfrom 0.86 to^1,which is the main reason for the overall performance enhancement caused by adding Co-Pi.These findings suggest that there is little scope for improving the performance of SILAR-deposited BiVO4 photoanodes by further catalyzing water oxidation,but enhanced performance is achievable if electron transport can be improved.展开更多
Deeply photocatalytic oxidation of NO-to-NO_(3)holds great promise for alleviating NO_(x) pollution.The major challenge of NO photo-oxidation is the highly in-situ generated NO_(2) concentration,and the formation of u...Deeply photocatalytic oxidation of NO-to-NO_(3)holds great promise for alleviating NO_(x) pollution.The major challenge of NO photo-oxidation is the highly in-situ generated NO_(2) concentration,and the formation of unstable nitrate species causes desorption to release NO_(2).In this study,SnO_(2) quantum dots and oxygen vacancies co-modified Zn_(2)SnO_(4)(ZSO-SnO_(2)-OVs)were prepared by a one-step hydrothermal procedure,the NO photo-oxidation was investigated by a combination of solid experimental and theoretical support.Impressively,spectroscopic measurements indicate that fast carrier dynamics can be achieved due to the electron transfer efficiency of ZSO-SnO_(2)-OVs reaching 99.99%,far outperforming the counterpart and previously reported photocatalysts.During NO oxidation,molecular NO/O_(2) and H2O are efficiently adsorbed/activated around OVs and SnO_(2) QDs,respectively.In-situ infrared measurements and calculated electron localized function disclose two main findings:(1)richly electrons enable NO promptly form NOinstead of toxic NO_(2) or NO^(+);(2)the generation of stable and undecomposed bidentate NO_(3)rather than bridging or monodentate one benefits the deep oxidation of NO via shifting reaction sites from O terminals for original ZSO to Sn ones for ZSO-SnO_(2)-OVs.The synergistic action of SnO_(2) QDs and OVs positively contributes to the NO oxidation performance enhancement(60.6%,0.1 g of sample)and high selectivity of NO to NO_(3)(99.2%).Results from this study advance the mechanistic understanding of NO photooxidation and its selectivity to NO_(3)over photocatalysts.展开更多
In recent years the photovoltaic community has witnessed the unprecedented development of perovskite solar cells（PSCs） as they have taken the lead in emergent photovoltaic technologies. The power conversion efficien...In recent years the photovoltaic community has witnessed the unprecedented development of perovskite solar cells（PSCs） as they have taken the lead in emergent photovoltaic technologies. The power conversion efficiency of this new class of solar cells has been increased to a point where they are beginning to compete with more established technologies. Although PSCs have evolved a variety of structures, the use of hole-transporting materials（HTMs） remains indispensable. Here, an overview of the various types of available HTMs is presented. This includes organic and inorganic HTMs and is presented alongside recent progress in associated aspects of PSCs, including device architectures and fabrication techniques to produce high-quality perovskite films. The structure, electrochemistry, and physical properties of a variety of HTMs are discussed, highlighting considerations for those designing new HTMs. Finally, an outlook is presented to provide more concrete direction for the development and optimization of HTMs for highefficiency PSCs.展开更多
Nanostructured TiO2 with differentiate morphologies has attracted tremendous attention due to its wide band-gap nature as well as outstanding optical and electric properties for solar-driven light-toelectricity conver...Nanostructured TiO2 with differentiate morphologies has attracted tremendous attention due to its wide band-gap nature as well as outstanding optical and electric properties for solar-driven light-toelectricity conversion application. Layered-stacking TiO2 film such as double-layer, tri-layer, quadrupleor quintuplicate-layer, is highly desirable to the design of high-performance semiconductor material photoanodes and the development of advanced photovoltaic devices. In this minireview, we will summarize the recent progress and achievements on proof-of-concept of layered-stacking TiO2 films（LTFs） for solar cells with emphasis on the tailored properties and synergistic functionalization of LTFs, such as optimized sensitizer adsorption, broadened light confinement as well as facilitated electron transport characteristics.Various demonstrations of LTFs photovoltaic systems provide lots of possibilities and flexibilities for more efficient solar energy utilization that a wide variety of TiO2 with distinguished morphologies can be integrated into differently structured photoanodes with synergistic and complementary advantages. This key structure engineering technology will also pave the way for the development of next generation state-ofthe-art electronics and optoelectronics. Finally, from our point of view, we conclude the future research interest and efforts for constructing more efficient LTFs as photoelectrode, which will be highly warranted to advance the solar energy conversion process.展开更多
TiO2 nanocrystals/graphene （TiO2/GR） composite are prepared by combining flocculation and hydrothermal reduction technology using graphite oxide and TiO2 colloid as precursors. The obtained materials are examined by...TiO2 nanocrystals/graphene （TiO2/GR） composite are prepared by combining flocculation and hydrothermal reduction technology using graphite oxide and TiO2 colloid as precursors. The obtained materials are examined by scanning electron microscopy, transition electron microscopy, X-ray diffraction, N2 adsorption desorption, and ultraviolet-visible diffuse spectroscopy. The results suggest that the presence of TiO2 nanocrystals with diameter of about 15 nm prevents GR nanosheets from agglomeration. Owing to the uniform distribution of TiO2 nanocrystals on the GR nanosheets, TiO2/GR composite exhibits stronger light absorption in the visible region, higher adsorption capacity to methylene blue and higher efficiency of charge separation and transportation compared with pure TiO2. Moreover, the TiO2/GR composite with a GR content of 30% shows higher photocatalytic removal efficiency of MB from water than that of pure TiO2 and commercial P25 under both UV and sunlight irradiation.展开更多
Photocatalytic H_(2) production has been regarded as a charming strategy for harvesting solar energy to chemical energy yet remains a great challenge due to the weak light absorption in visible range,low charge transf...Photocatalytic H_(2) production has been regarded as a charming strategy for harvesting solar energy to chemical energy yet remains a great challenge due to the weak light absorption in visible range,low charge transfer,and fast recombination of photogenerated carriers.Here,we integrate solar-driven water splitting with benzyl alcohol(BA)oxidation,a typical platform chemical from biomass,for producing H_(2) and benzaldehyde(BAD)over ZnIn_(2)S_(4) nanosheets doped with Ni and N(Ni-N/ZIS).Mechanism studies show that Ni-N/ZIS provides a fast charge channel(i.e.,Ni-N)for separating photogenerated electrons and holes,as a result of significantly enhanced photocatalytic performance.Impressively,Ni-N/ZIS displays a H_(2) productivity of 18.7 mmol g^(-1) h^(-1) with an apparent quantum yield(AQE)of 29.1% at 420 nm,which is 37.4,10.6 and 2.8 times higher than that of pristine ZIS,N/ZIS and Ni/ZIS,surpassing all the reported noble metal-free catalysts.Besides,the productivity of BAD reaches 17.5 mmol g^(-1) h^(-1) under the irradiation of visible light(λ≥420 nm).This work integrates two significant processes(i.e.,solar-driven water splitting with benzyl alcohol oxidation)for producing H_(2) and BAD,respectively,which will contribute to alleviating the current energy and environmental crisis.展开更多
Solid-state batteries(SSBs)are considered as the next-generation battery technology,poised to deliver both high energy and enhanced safety.Nonetheless,their transition from laboratory to market is impeded by several c...Solid-state batteries(SSBs)are considered as the next-generation battery technology,poised to deliver both high energy and enhanced safety.Nonetheless,their transition from laboratory to market is impeded by several critical challenges.Among these,the solid–solid interfaces within SSBs represent a bottleneck,characterized by issues such as poor physical contact,side reactions,temporal separation,and sluggish charge carrier transfer.Developing key materials to construct the efficient solid–solid interface is critical for building high-performance SSBs.Organic mixed ionic–electronic conductors(OMIECs)have emerged as a promising alternative to conventional conductors in addressing the abovementioned issues owing to their intrinsic properties,including the capability of conducting both ions and electrons,mechanical flexibility,and structural designability.This review will first elucidate the necessity of the integration of OMIECs in SSBs.Next,a comprehensive exploration of the composition,preparation methods,key advantages,and basic characterizations of OMIECs is presented.This review then delves into recent research progress on OMIECs in SSBs,with a special focus on their application in cathode coating layers,the creation of a 3D mixed conductive framework for Li hosting,and their integration as inner layers in Li anodes.Conclusively,potential future applications and innovative designs of OMIECs are discussed.展开更多
Understanding the effectiveness of cabin air filters is important for assessing human exposure to ultra- fine particles （UFPs） of vehicular origin. The filtration efficiency of vehicular UFPs with electric charges w...Understanding the effectiveness of cabin air filters is important for assessing human exposure to ultra- fine particles （UFPs） of vehicular origin. The filtration efficiency of vehicular UFPs with electric charges was investigated for different electric charge characteristics （charge state, charge polarity）. The average filtration efficiency increased ~10% as the electric charge state on the particles changed in distribution from lightly charged to highly charged. The enhancement of filtration efficiency due to electric charge was different at various filter-face air velocities. As electric charges increased, the filtration efficiency increased 12% and 9% at low air velocity （0.1 m/s） and high air velocity （0.S m/s）, respectively. The filter fiber material poses somewhat effect on the filtration efficiency change due to the electric charge. The effects of filter usage and charge polarity on filtration efficiency due to the electric charge were negligi- ble. A coefficient was empirically derived and successfully accounts for the electric charge effect on UFP filtratinn efficiency.展开更多
基金financial support by the National Natural Science Foundation of China(NSFC,Grant No.22379153 and 22109128)the Ningbo Key Research and Development Project(2023Z147)the Ningbo 3315 Program。
文摘CuBi_(2)O_(4)(CBO)photocathodes hold significant promise for efficient photoelectrochemical(PEC)water splitting due to their favorable band gap and theoretical onset potential.However,their practical application is hindered by poor charge separation efficiency.Herein,we introduce a characteristic in-situ solution Fe-doping strategy that markedly improves photoelectrochemical performance of CBO,doubling the photocurrent density and achieving an unprecedented 190 mV anodic shift in the onset potential.By integrating with an electrochemical oxidation post-treatment,a record incident photon-to-current efficiency(IPCE)exceeding 40% at 0.6 V vs.RHE under visible light illumination is achieved.The versatility of the doping strategy is demonstrated across CBO photocathodes synthesized by different methods with various morphologies,grain sizes,and crystallinities.Mechanistic studies reveal that the gradient distribution of Fe^(3+)ions generates an internal electric field that facilitates efficient charge separation and increases acceptor density.The strong Fe-O bonding also enhances structural stability against photoinduced corrosion.Notably,our investigation uncovers the non-temperature-dependent nature of CBO photocurrent,indicating that PEC performance enhancement primarily depends on reducing carrier recombination rather than improving bulk conductivity.This work lays the groundwork for future advancements in water splitting performance of CBO photocathodes,offering a complementary strategy to conventional methods for enhancing charge separation efficiency.
基金Project supported by the National Natural Science Foundation of China(Grant No.61574112)。
文摘A novel CMOS image sensor(CIS) pinned photodiode(PPD) pixel, named as O-T pixel, is proposed and investigated by TCAD simulations. Compared with the conventional PPD pixel, the proposed pixel features the overlapping gate(OG)and the temporary storage diffusing(TSD) region, based on which the several-nanosecond-level charge transfer could be achieved and the complete charge transfer from the PPD to the floating node(FD) could be realized. And systematic analyses of the influence of the doping conditions of the proposed processes, the OG length, and the photodiode length on the transfer performances of the proposed pixel are conducted. Optimized simulation results show that the total charge transfer time could reach about 5.862 ns from the photodiode to the sensed node and the corresponding charge transfer efficiency could reach as high as 99.995% in the proposed pixel with 10 μm long photodiode and 2.22 μm long OG. These results demonstrate a great potential of the proposed pixel in high-speed applications.
文摘Photocatalytic reduction of CO_(2)into high-value C_(2)H_(4)offers a promising pathway toward carbon neutrality.Due to the continuous 12-electron-proton coupled reactions and the mutual repulsion of reaction intermediates,achieving highly selective photocatalytic conversion of CO_(2)to C_(2)H_(4)remains challenging.This work synthesized a CuInS_(2)/CuS heterojunction photocatalyst mediated by a sulfur electron bridge via a one-step solvothermal method,achieving a high selectivity for C_(2)H_(4)conversion(98.22%).The sulfur electron bridge minimized the contact energy barrier between CuInS_(2)and CuS to enhance photogenerated carrier separation efficiency,while the asymmetric active sites in CuInS_(2)effectively reduced mutual repulsion of reaction intermediates.This work develops a hybrid catalytic system enabling synergistic regulation of reaction kinetics and thermodynamics,offering an innovative strategy for highly selective photocatalytic CO₂-to-C_(2)H_(4)production.
文摘Photoelectrochemical(PEC)water splitting is one of the most promising approaches toward achieving the conversion of solar energy to hydrogen.Hematite is a widely applied photoanode material in PEC water splitting because of its appropriate band structure,non-toxicity,high stability,and low cost.Nevertheless,its relatively low photochemical conversion efficiency limits its application,and enhancing its PEC water splitting efficiency remains a challenge.Consequently,increasing efforts have been rendered toward improving the performance of hematite photoanodes.The entire PEC water splitting efficiency typically includes three parts:the photon absorption efficiency,the separation efficiency of the semiconductor bulk,and the surface injection efficiency.This review briefly discusses the recent advances in studies on hematite photoanodes for water splitting,and through the enhancement of the three above-mentioned efficiencies,the corresponding strategies toward improving the PEC performance of hematite are comprehensively discussed and summarized.
基金Supported by the National Science and Technology Support Program(2013BAG12B01)Foundational and Advanced Research Program General Project of Chongqing City(cstc2013jcyjjq60002)
文摘A novel method to calculate fuel-electric conversion factor for full hybrid electric vehicle（HEV）equipped with continuously variable transmission（CVT）is proposed.Based on consideration of the efficiency of pivotal components,electric motor,system efficiency optimization models are developed.According to the target of instantaneous optimization of system efficiency,operating ranges of each mode of power-train are determined,and the corresponding energy management strategies are established.The simulation results demonstrate that the energy management strategy proposed can substantially improve the vehicle fuel economy,and keep battery state of charge（SOC）change in a reasonable variation range.
基金Project supported by the Young Scientists Fund of the National Natural Science Foundation of China(Grant Nos.51702271 and 61904155)the Natural Science Foundation of Fujian Province,China(Grant No.2020J05239).
文摘The space charge accumulation in CdZnTe crystals seriously affects the performance of high-flux pulse detectors.The influence of sub-bandgap illumination on the space charge distribution and device performance in CdZnTe crystals were studied theoretically by Silvaco TCAD software simulation.The sub-bandgap illumination with a wavelength of 890 nm and intensity of 8×10−8 W/cm2 were used in the simulation to explore the space charge distribution and internal electric field distribution in CdZnTe crystals.The simulation results show that the deep level occupation faction is manipulated by the sub-bandgap illumination,thus space charge concentration can be reduced under the bias voltage of 500 V.A flat electric field distribution is obtained,which significantly improves the charge collection efficiency of the CdZnTe detector.Meanwhile,premised on the high resistivity of CdZnTe crystal,the space charge concentration in the crystal can be further reduced with the wavelength of 850 nm and intensity of 1×10−7 W/cm2 illumination.The electric field distribution is flatter and the carrier collection efficiency of the device can be improved more effectively.
基金supported by the National Natural Science Foundation of China (No. 51473092)the Shanghai Rising-Star Program (No. 15QA1402500)
文摘Fabrication of efficient solid luminogens with tunable emission is both fundamentally significant and technically important. Herein, based on our previous strategy for the construction of efficient and multifunctional solid luminogens through the combination of diverse aggregation-induced emission （ALE） units with other functional moieties, a group of luminophores with electron donor-acceptor （D-A） structure and typical intramolecular charge transfer （ICT） characteristics, namely CZ-DCDPP, DPA-DCDPP and DBPA-DCDPP were synthesized and investigated. The presence of twisting and AlE-active 2,3- dicyano-S,6-diphenylpyrazine （DCDPP） moiety endows them highly emissive in the solid states, whereas the introduction of arylamines with varied electron-donating capacity and different conjugation render them with tunable solid emissions from green to red. While CZ-DCDPP and DPA-DCDPP solids exhibit distinct mechanochromism, both DPA-DCDPP and DBPA-DCDPP solids can generate efficient red emission. Owing to their high efficiency, remarkable thermal and morphological stabilities and moreover red emission, they are promising for diverse optoelectronic and biological applications.
基金supported by the National Natural Science Foundation of China(No.22405248)the Joint Fund of Science and Technology R&D Plan of Henan Province(No.232301420003).
文摘The rational design of a heterostructural photocatalysts with efficient charge separation and accelerated interfacial charge transfer holds great promise for boosting photocatalytic activity.Herein,we have developed a unique hierarchical In_(4/3)P_(2)S_(6)/TiO_(2) heterojunction with P-O interfacial bonding for photocatalytic water reduction.By integrating emerging In_(4/3)P_(2)S_(6) nanosheets through intense interfacial coupling effect,the optimized In_(4/3)P_(2)S_(6)/TiO_(2) heterostructure exhibits a remarkably enhanced photocatalytic H2 evolution activity compared to that of pristine TiO_(2).Combined experimental and theoretical results confirm that multiple interfacial bonded step-scheme(S-scheme)charge transfer pathways are established in the In_(4/3)P_(2)S_(6)/TiO_(2) photocatalyst,which synergistically promote charge separation and transfer through the robust interfacial electric field and rapid charge migration pathways formed by interfacial bonds.This study emphasizes the significance of developing novel interfacial bonded In_(4/3)P_(2)S_(6)-based S-scheme heterostructures,paving a new strategy towards enhancing photocatalytic activity for H_(2) evolution.
基金supported by the National Natural Science Foundation of China(21707055,21567008,21607064)Program of Qingjiang Excellent Young Talents,Jiangxi University of Science and Technology,Program of 5511 Talents in Scientific and Technological Innovation of Jiangxi Province(20165BCB18014)+3 种基金Academic and Technical Leaders of the Main Disciplines in Jiangxi Province(20172BCB22018)Jiangxi Province Natural Science Foundation(20161BAB203090,20181BAB213010,20181BAB203018)Young Science Foundation of Jiangxi Province Education Office(GJJ160671)Open Project Program of the State Key Laboratory of Photocatalysis on Energy and Environment(SKLPEE-KF201712)in Fuzhou University基金来源:国家自然科学基金(21707055,21567008,21607064)~~
文摘Semiconductor photocatalysts are extensively applied in environmental treatment and energy conversion.However,one of their major disadvantages is their relatively low photocatalytic performance owing to the recombination of generated electron-hole pairs.The presence of the phase junction is an effective way to promote the photocatalytic activity by increasing the separation efficiency of the electron-hole pairs.Accordingly,extensive research has been conducted on the design of phase junctions of photocatalysts to improve their charge transfer properties and efficiencies.Therefore,for the design of an appropriate phase junction and the understanding of the mechanism of electron-hole separation,the development of the photocatalytic phase junction,including the preparation methods of the heterogeneous materials,is tremendously important and helpful.Herein,the commonly used,externally induced phase transformation fabrication techniques and the primary components of the semiconductors are reviewed.Future directions will still focus on the design and optimization of the phase junction of photocatalytic materials according to the phase transition with higher efficiencies for broadband responses and solar energy utilization.Additionally,the most popular phase transformation fabrication techniques of phase junctions are briefly reviewed from the application viewpoint.
基金financially supported by the National Key Research and Development Program of China (2017YFA0402800)the National Natural Science Foundation of China (U1932214, 51772285)the National Synchrotron Radiation Laboratory at USTC。
文摘BiVO_(4) has been attracting a lot of interest in photoelectrochemical (PEC) water oxidation due to its efficient solar absorption and appropriate band positions.So far,sluggish water oxidation kinetics and fast photogenerated charge recombination still hinder the PEC performance ofBiVO_(4) .In this study,a novel PEC photoanode was designed by depositing ultrathin FeOOH nanolayers on the surface of nanoporousBiVO_(4) electrode,followed by modification with a cobaloxime (Co(dmgH)_(2)(4-COOH-py)Cl) molecular cocatalyst.Under irradiation of a 100 mW cm^(-2)(AM 1.5G) Xe lamp,the photocurrent density of the cobaloxime/FeOOH/BiVO_(4) composite photoanode reached 5.1 mA cm^(-2)at 1.23 V vs.RHE in 1.0 M potassium borate buffer solution (pH=9.0).The onset potential of the optimal cobaloxime/FeOOH/BiVO_(4) photoanode exhibited a 460 m V cathodic shift relative to bareBiVO_(4) .In addition,the surface charge injection efficiency of the composite photoanode reached~80%at 1.23 V vs.RHE and the incident photon-to-current efficiency (IPCE) reached~88%at 420 nm.
基金Project supported by National Natural Science Foundation of China(Nos.61036004,61076024)
文摘The charge transfer efficiency improvement method is introduced by optimizing the electrical potential distribution under the transfer gate along the charge transfer path. A non-uniform doped transfer transistor chan- nel is introduced to provide an ascending electrical potential gradient in the transfer transistor channel. With the adjustments to the overlap length between the R1 region and the transfer gate, the doping dose of the R1 region, and the overlap length between the anti-punch-through （APT） implantations and transfer gate, the potential barrier and potential pocket in the connecting region of transfer transistor channel and the pinned photodiode （PPD） are reduced to improve the electrical potential connection. The simulation results show that the percentage of residual charges to total charges drops from 1/10^4 to 1/10^7, and the transfer time is reduced from 500 to 110 ns. This means the charge transfer efficiency is improved.
基金supported by the National Natural Science Foundation of China(51572253,21771171)Scientific Research Grant of Hefei National Synchrotron Radiation Laboratory(UN2017LHJJ)+1 种基金the Fundamental Research Funds for the Central Universitiescooperation between NSFC and Netherlands Organization for Scientific Research(51561135011)~~
文摘Photocatalytic H2 evolution reactions on pristine graphitic carbon nitrides(g-C3N4),as a promising approach for converting solar energy to fuel,are attractive for tackling global energy concerns but still suffer from low efficiencies.In this article,we report a tractable approach to modifying g-C3N4 with vanadyl phthalocyanine(VOPc/CN)for efficient visible-light-driven hydrogen production.A non-covalent VOPc/CN hybrid photocatalyst formed viaπ-πstacking interactions between the two components,as confirmed by analysis of UV-vis absorption spectra.The VOPc/CN hybrid photocatalyst shows excellent visible-light-driven photocatalytic performance and good stability.Under optimal conditions,the corresponding H2 evolution rate is nearly 6 times higher than that of pure g-C3N4.The role of VOPc in promoting hydrogen evolution activity was to extend the visible light absorption range and prevent the recombination of photoexcited electron-hole pairs effectively.It is expected that this facile modification method could be a new inspiration for the rational design and exploration of g-C3N4-based hybrid systems with strong light absorption and high-efficiency carrier separation.
基金Universiti Brunei Darussalam through grant numbers UBD/RSCH/1.4/FICBF(b)/2018/009 and UBD/PNC2/2/RG/1(313).
文摘We report a photoelectrochemical investigation of BiVO4 photoanodes prepared by successive ionic layer adsorption and reaction(SILAR),a facile method that yields uniform nanoporous films.After characterization of the phase,morphology,composition,and optical properties of the prepared films,the efficiencies of charge separation(ηsep)and water oxidation(ηox)in solar water splitting cells employing these photoanodes were estimated following a previously reported procedure.Unexpected wavelength and illumination direction dependencies were discovered in the derived efficiencies,casting doubt on the validity of the analysis.An alternative approach using a diffusion–reaction model that explicitly considers the efficiency of electron collection resolved the discrepancies and explained the illumination direction dependence of the photocurrent.Electron diffusion lengths(Ln)of 0.45μm and 0.55μm were derived for pristine and cobalt phosphate(Co-Pi)modified BiVO4,respectively,which are much shorter than the film thickness of^2.1μm.The Co-Pi treatment also increasedηoxfrom 0.86 to^1,which is the main reason for the overall performance enhancement caused by adding Co-Pi.These findings suggest that there is little scope for improving the performance of SILAR-deposited BiVO4 photoanodes by further catalyzing water oxidation,but enhanced performance is achievable if electron transport can be improved.
基金the National Natural Science Foundation of China(Grant No.51808080)China Postdoctoral Science Foundation(No.2022M710830)+4 种基金Venture and Innovation Support Program for Chongqing Overseas Returnees(No.cx2022005)the Natural Science Foundation Project of CQ CSTC(No.CSTB2022NSCQ-MSX1267)Research Project of Chongqing Education Commission Foundation(No.KJQN201800826)Science and Technology Research Program of Chongqing Municipal Education Commission of China(No.KJZD-K202100801)Post-doctoral Program Funded by Chongqing,and Chongqing University Innovation Research Group project(No.CXQT21023).
文摘Deeply photocatalytic oxidation of NO-to-NO_(3)holds great promise for alleviating NO_(x) pollution.The major challenge of NO photo-oxidation is the highly in-situ generated NO_(2) concentration,and the formation of unstable nitrate species causes desorption to release NO_(2).In this study,SnO_(2) quantum dots and oxygen vacancies co-modified Zn_(2)SnO_(4)(ZSO-SnO_(2)-OVs)were prepared by a one-step hydrothermal procedure,the NO photo-oxidation was investigated by a combination of solid experimental and theoretical support.Impressively,spectroscopic measurements indicate that fast carrier dynamics can be achieved due to the electron transfer efficiency of ZSO-SnO_(2)-OVs reaching 99.99%,far outperforming the counterpart and previously reported photocatalysts.During NO oxidation,molecular NO/O_(2) and H2O are efficiently adsorbed/activated around OVs and SnO_(2) QDs,respectively.In-situ infrared measurements and calculated electron localized function disclose two main findings:(1)richly electrons enable NO promptly form NOinstead of toxic NO_(2) or NO^(+);(2)the generation of stable and undecomposed bidentate NO_(3)rather than bridging or monodentate one benefits the deep oxidation of NO via shifting reaction sites from O terminals for original ZSO to Sn ones for ZSO-SnO_(2)-OVs.The synergistic action of SnO_(2) QDs and OVs positively contributes to the NO oxidation performance enhancement(60.6%,0.1 g of sample)and high selectivity of NO to NO_(3)(99.2%).Results from this study advance the mechanistic understanding of NO photooxidation and its selectivity to NO_(3)over photocatalysts.
基金financial support from the Natural Science Foundation of China (grant numbers: 51661135021, 21606039, 91233201, and 21276044)
文摘In recent years the photovoltaic community has witnessed the unprecedented development of perovskite solar cells（PSCs） as they have taken the lead in emergent photovoltaic technologies. The power conversion efficiency of this new class of solar cells has been increased to a point where they are beginning to compete with more established technologies. Although PSCs have evolved a variety of structures, the use of hole-transporting materials（HTMs） remains indispensable. Here, an overview of the various types of available HTMs is presented. This includes organic and inorganic HTMs and is presented alongside recent progress in associated aspects of PSCs, including device architectures and fabrication techniques to produce high-quality perovskite films. The structure, electrochemistry, and physical properties of a variety of HTMs are discussed, highlighting considerations for those designing new HTMs. Finally, an outlook is presented to provide more concrete direction for the development and optimization of HTMs for highefficiency PSCs.
基金the financial supports from the NSFC(51472274)the GDUPS(2016)+2 种基金the program of Guangzhou Science and Technology Project(201504010031)the NSF of Guangdong Province(S2013030013474)the Fundamental Research Funds for the Central Universities
文摘Nanostructured TiO2 with differentiate morphologies has attracted tremendous attention due to its wide band-gap nature as well as outstanding optical and electric properties for solar-driven light-toelectricity conversion application. Layered-stacking TiO2 film such as double-layer, tri-layer, quadrupleor quintuplicate-layer, is highly desirable to the design of high-performance semiconductor material photoanodes and the development of advanced photovoltaic devices. In this minireview, we will summarize the recent progress and achievements on proof-of-concept of layered-stacking TiO2 films（LTFs） for solar cells with emphasis on the tailored properties and synergistic functionalization of LTFs, such as optimized sensitizer adsorption, broadened light confinement as well as facilitated electron transport characteristics.Various demonstrations of LTFs photovoltaic systems provide lots of possibilities and flexibilities for more efficient solar energy utilization that a wide variety of TiO2 with distinguished morphologies can be integrated into differently structured photoanodes with synergistic and complementary advantages. This key structure engineering technology will also pave the way for the development of next generation state-ofthe-art electronics and optoelectronics. Finally, from our point of view, we conclude the future research interest and efforts for constructing more efficient LTFs as photoelectrode, which will be highly warranted to advance the solar energy conversion process.
文摘TiO2 nanocrystals/graphene （TiO2/GR） composite are prepared by combining flocculation and hydrothermal reduction technology using graphite oxide and TiO2 colloid as precursors. The obtained materials are examined by scanning electron microscopy, transition electron microscopy, X-ray diffraction, N2 adsorption desorption, and ultraviolet-visible diffuse spectroscopy. The results suggest that the presence of TiO2 nanocrystals with diameter of about 15 nm prevents GR nanosheets from agglomeration. Owing to the uniform distribution of TiO2 nanocrystals on the GR nanosheets, TiO2/GR composite exhibits stronger light absorption in the visible region, higher adsorption capacity to methylene blue and higher efficiency of charge separation and transportation compared with pure TiO2. Moreover, the TiO2/GR composite with a GR content of 30% shows higher photocatalytic removal efficiency of MB from water than that of pure TiO2 and commercial P25 under both UV and sunlight irradiation.
基金supported by the National Key R&D Program of China(2022YFA1504500)National Natural Science Foundation of China(52472310,22025108,U21A20327,and 22121001)+4 种基金Gusu Leading Talent Program(ZXL2024347)Guangdong Provincial Natural Science Fund for Distinguished Young Scholars(2021B1515020081)Pioneer Hundred Talents Program of Chinese Academy of SciencesNatural Science Foundation of the Jiangsu Higher Education Institutions(22KJA430009)Science and Technology Development Plan of Suzhou(ZXL2022176).
文摘Photocatalytic H_(2) production has been regarded as a charming strategy for harvesting solar energy to chemical energy yet remains a great challenge due to the weak light absorption in visible range,low charge transfer,and fast recombination of photogenerated carriers.Here,we integrate solar-driven water splitting with benzyl alcohol(BA)oxidation,a typical platform chemical from biomass,for producing H_(2) and benzaldehyde(BAD)over ZnIn_(2)S_(4) nanosheets doped with Ni and N(Ni-N/ZIS).Mechanism studies show that Ni-N/ZIS provides a fast charge channel(i.e.,Ni-N)for separating photogenerated electrons and holes,as a result of significantly enhanced photocatalytic performance.Impressively,Ni-N/ZIS displays a H_(2) productivity of 18.7 mmol g^(-1) h^(-1) with an apparent quantum yield(AQE)of 29.1% at 420 nm,which is 37.4,10.6 and 2.8 times higher than that of pristine ZIS,N/ZIS and Ni/ZIS,surpassing all the reported noble metal-free catalysts.Besides,the productivity of BAD reaches 17.5 mmol g^(-1) h^(-1) under the irradiation of visible light(λ≥420 nm).This work integrates two significant processes(i.e.,solar-driven water splitting with benzyl alcohol oxidation)for producing H_(2) and BAD,respectively,which will contribute to alleviating the current energy and environmental crisis.
基金supported by the National Key R&D Program of China(grant no.2021YFB3800300)the National Natural Science Foundation of China(grant nos.22179143,22309201,and 22309202)the Jiangsu Funding Program for Excellent Postdoctoral Talent,and the Gusu Leading Talents Program(grant no.ZXL2023190).
文摘Solid-state batteries(SSBs)are considered as the next-generation battery technology,poised to deliver both high energy and enhanced safety.Nonetheless,their transition from laboratory to market is impeded by several critical challenges.Among these,the solid–solid interfaces within SSBs represent a bottleneck,characterized by issues such as poor physical contact,side reactions,temporal separation,and sluggish charge carrier transfer.Developing key materials to construct the efficient solid–solid interface is critical for building high-performance SSBs.Organic mixed ionic–electronic conductors(OMIECs)have emerged as a promising alternative to conventional conductors in addressing the abovementioned issues owing to their intrinsic properties,including the capability of conducting both ions and electrons,mechanical flexibility,and structural designability.This review will first elucidate the necessity of the integration of OMIECs in SSBs.Next,a comprehensive exploration of the composition,preparation methods,key advantages,and basic characterizations of OMIECs is presented.This review then delves into recent research progress on OMIECs in SSBs,with a special focus on their application in cathode coating layers,the creation of a 3D mixed conductive framework for Li hosting,and their integration as inner layers in Li anodes.Conclusively,potential future applications and innovative designs of OMIECs are discussed.
基金This study is based on work partially supported by the National Natural Science Foundation of China （grant no. 51208372） and the Fundamental Research Funds for the Central Universities （grant no. 2013KJ020）.
文摘Understanding the effectiveness of cabin air filters is important for assessing human exposure to ultra- fine particles （UFPs） of vehicular origin. The filtration efficiency of vehicular UFPs with electric charges was investigated for different electric charge characteristics （charge state, charge polarity）. The average filtration efficiency increased ~10% as the electric charge state on the particles changed in distribution from lightly charged to highly charged. The enhancement of filtration efficiency due to electric charge was different at various filter-face air velocities. As electric charges increased, the filtration efficiency increased 12% and 9% at low air velocity （0.1 m/s） and high air velocity （0.S m/s）, respectively. The filter fiber material poses somewhat effect on the filtration efficiency change due to the electric charge. The effects of filter usage and charge polarity on filtration efficiency due to the electric charge were negligi- ble. A coefficient was empirically derived and successfully accounts for the electric charge effect on UFP filtratinn efficiency.
