Two-dimensional(2D)materials have come to light due to their unique thickness that owns abundant exposed edges with enhanced electrocatalytic properties.2D molybdenum disulfide(MoS_(2))nanosheet has aroused considerab...Two-dimensional(2D)materials have come to light due to their unique thickness that owns abundant exposed edges with enhanced electrocatalytic properties.2D molybdenum disulfide(MoS_(2))nanosheet has aroused considerable attention due to its tunable surface chemistry and high electrochemical sur-face area.Nonetheless,several shortcomings associated with MoS_(2),such as its naturally existing semi-conducting 2H phase,which has limited active sites due to the inert basal plane,restrict its application in water electrocatalysis.Taking into account the benefits of the 1T/2H phase of MoS_(2),as well as the importance of engineering 2D/2D heterojunction interface for boosted electrocatalysis,metallic Ti_(3)C_(2)Tx was integrated with 1T/2H MoS_(2) to develop 2D/2D 1T/2H MoS_(2)/Ti_(3)C_(2)Tx heterostructured nanocompos-ites.Herein,with only 25%of the intercalating agent,1T/2H MoS_(2) with the highest 1T phase content of~82%was successfully synthesized.It was further incorporated with 1 wt%of Ti_(3)C_(2)Tx through a com-bination of ultrasonication and mechanical stirring process.The 1T/2H MoS_(2)(25D)/Ti_(3)C_(2)Tx-1(MTC-1)manifested outstanding electrocatalytic performance with an overpotential and Tafel slope of 280 mV(83.80 mV dec^(-1))and 300 mV(117.2 mV dec^(-1)),for catalyzing acidic and alkaline medium HER,respec-tively.Pivotally,the as-prepared catalysts also illustrated long-term stability for more than 40 h.The coupling method for the 2D nanosheets is crucial to suppress the oxidation of Ti_(3)C_(2)Tx and the restack-ing issue of 2D nanosheets.The superior HER activity is ascribed to the synergistic effect between the heterostructure,enhancing the electronic structure and charge separation capability.The intrinsic prop-erty of the catalyst further confirms by turnover frequency(TOF)calculation.As such,this research paves the way for designing high-efficiency 2D electrocatalysts and sheds light on the further advancement of tunable 2D electrocatalysts for robust water splitting and beyond.展开更多
Herein,a new type of two-dimensional(2D)/2D Ti_(3)C_(2)/TiO_(2) heterojunction was developed for efficient photocatalytic nitrogen reduction reaction(NRR),in which TiO_(2) nanosheets(TiO_(2) Ns)were designed as the ma...Herein,a new type of two-dimensional(2D)/2D Ti_(3)C_(2)/TiO_(2) heterojunction was developed for efficient photocatalytic nitrogen reduction reaction(NRR),in which TiO_(2) nanosheets(TiO_(2) Ns)were designed as the main catalyst,while Ti_(3)C_(2) MXene served as the co-catalyst.Experimental and theoretical results revealed that Ti_(3)C_(2) MXene introduced electron-rich unsaturated Ti sites,serving as highly active sites for both the adsorption and activation of N_(2) on the Ti_(3)C_(2)/TiO_(2) heterojunction.Furthermore,the 2D/2D Ti_(3)C_(2)/TiO_(2) heterostructure greatly promoted the directional separation and transfer of charge carriers,facilitated by the internal electric field.This structural feature enabled the spatial separation of the N_(2) reduction and H2 O oxidation half-reactions on the distinct surfaces of Ti_(3)C_(2)(001)and TiO_(2)(001),con-sequently reducing the reaction energy barrier for each respective process.The synergistic effects arising from the interface and surface interactions within the heterojunction conspicuously improved the photo-catalytic NRR activity.As a result,the optimized Ti_(3)C_(2)/TiO_(2) heterojunction exhibited a high NH_(3) produc-tion rate of 24.4μmol g−1 h−1 in the absence of sacrificial agents,representing a remarkable 12.8-fold increase compared to individual TiO_(2) Ns.This work provides new insights into rational design of high-performance heterogeneous photocatalysts and offers a deeper understanding of the mechanism under-lying surface active sites in the photocatalytic NRR process.展开更多
The 2D/3D heterojunction perovskites have garnered increasing attention due to their exceptional moisture and thermal stability.However,few works have paid attention to the influence of the subsequent change process o...The 2D/3D heterojunction perovskites have garnered increasing attention due to their exceptional moisture and thermal stability.However,few works have paid attention to the influence of the subsequent change process of 2D/3D heterojunction PSC on the stability of PSCs.Moreover,the evolution of the interface and carrier dynamic behavior of the 2D/3D perovskite films with long-term operation has not been systematically developed befo re.In this work,the effects of 2D/3 D heterojunction evolution on the interface of perovskite films and different carrier dynamics during 2D/3D evolution are systematically analyzed for the first time.The decomposition of 2D/3D heterojunction in the perovskite film will have a certain impact on the surface and carrier dynamics behavior of perovskite.During the evolution of 2D/3D heterojunction,PbI_(2)crystals will appear,which will improve the interfacial energy level matching between the electron transport layer and perovskite film.With a long evolution time,some holes will appear on the surface of perovskite film.The open circuit voltage(V_(OC))of PSCs increased from 1.14 to1.18 V and the PCE increased to 23.21%after 300 h storage in the nitrogen atmosphere,and maintained 89%initial performance for with 3000 h stability test in N_(2)box.This discovery has a significant role in promoting the development of inverted heterojunction PSCs and constructing the revolution mechanism of charge carrier dynamic.展开更多
The introduction of two-dimensional(2D)perovskite layers on top of three-dimensional(3D)perovskite films enhances the performance and stability of perovskite solar cells(PSCs).However,the electronic effect of the spac...The introduction of two-dimensional(2D)perovskite layers on top of three-dimensional(3D)perovskite films enhances the performance and stability of perovskite solar cells(PSCs).However,the electronic effect of the spacer cation and the quality of the 2D capping layer are critical factors in achieving the required results.In this study,we compared two fluorinated salts:4-(trifluoromethyl)benzamidine hydrochloride(4TF-BA·HCl)and 4-fluorobenzamidine hydrochloride(4F-BA·HCl)to engineer the 3D/2D perovskite films.Surprisingly,4F-BA formed a high-performance 3D/2D heterojunction,while4TF-BA produced an amorphous layer on the perovskite films.Our findings indicate that the balanced intramolecular charge polarization,which leads to effective hydrogen bonding,is more favorable in 4F-BA than in 4TF-BA,promoting the formation of a crystalline 2D perovskite.Nevertheless,4TF-BA managed to improve efficiency to 24%,surpassing the control device,primarily due to the natural passivation capabilities of benzamidine.Interestingly,the devices based on 4F-BA demonstrated an efficiency exceeding 25%with greater longevity under various storage conditions compared to 4TF-BA-based and the control devices.展开更多
The growing global energy demand and worsening climate change highlight the urgent need for clean,efficient and sustainable energy solutions.Among emerging technologies,atomically thin two-dimensional(2D)materials off...The growing global energy demand and worsening climate change highlight the urgent need for clean,efficient and sustainable energy solutions.Among emerging technologies,atomically thin two-dimensional(2D)materials offer unique advantages in photovoltaics due to their tunable optoelectronic properties,high surface area and efficient charge transport capabilities.This review explores recent progress in photovoltaics incorporating 2D materials,focusing on their application as hole and electron transport layers to optimize bandgap alignment,enhance carrier mobility and improve chemical stability.A comprehensive analysis is presented on perovskite solar cells utilizing 2D materials,with a particular focus on strategies to enhance crystallization,passivate defects and improve overall cell efficiency.Additionally,the application of 2D materials in organic solar cells is examined,particularly for reducing recombination losses and enhancing charge extraction through work function modification.Their impact on dye-sensitized solar cells,including catalytic activity and counter electrode performance,is also explored.Finally,the review outlines key challenges,material limitations and performance metrics,offering insight into the future development of nextgeneration photovoltaic devices encouraged by 2D materials.展开更多
A two-dimensional(2D)/2D hybrid heterojunction with face-to-face interfacial assembly is a desirable dimensionality design with significant potential for various photocatalytic applications due to the large interfacia...A two-dimensional(2D)/2D hybrid heterojunction with face-to-face interfacial assembly is a desirable dimensionality design with significant potential for various photocatalytic applications due to the large interfacial contact area,which facilitates charge migration and separation.Herein,we developed an ef-ficient 2D/2D hybrid heterojunction consisting of BiOIO 3 nanoplates(BIO)and g-C_(3)N_(4) nanosheets(CN)using a simple but effective in situ growth method for photocatalytic aqueous antibiotic degradation and H_(2) generation.The face-to-face interfacial assembly of the BIO and CN components in the BIO/CN hy-brid heterojunction was verified using electron microscopy.Remarkably,the BIO/CN hybrid heterojunc-tion outperformed both the BIO and CN counterparts in terms of norfloxacin degradation and H_(2) gen-eration under simulated solar light irradiation.Moreover,the photocatalytic performance of the hybrid catalyst remained nearly unchanged throughout five consecutive test runs.The exceptional performance and stability of the hybrid catalyst are attributable to its extended optical absorption range,large interfa-cial contact area provided by the face-to-face assembly in the 2D/2D hybrid configuration,and enhanced photoexcited charge separation efficiency and redox power of the separated charges,which are supported by an efficient S-scheme charge transfer mechanism.This study illuminates the rational construction of novel 2D/2D S-scheme hybrid heterojunction photocatalysts with practical applications in environmental remediation and sustainable energy generation.展开更多
Fabrication of 2D/2D heterojunction photocatalysts have attracted more attentions due to their inherent merits involving the large contact interface,short charge migration distance and plentiful active sites,which are...Fabrication of 2D/2D heterojunction photocatalysts have attracted more attentions due to their inherent merits involving the large contact interface,short charge migration distance and plentiful active sites,which are beneficial for the enhancement of photocatalytic activity.Herein,a series of 2D/2D MoS_(2)/Cd S type-I heterojunctions were prepared by incorporation the exfoliating of bulk CdS and MoS_(2) with postsintering procedure.Multiple characteristic techniques were employed to corroborate the formation of heterojunctions.By optimizing the 2D MoS_(2) amounts in the heterojunction,the 7 wt.%2D/2D MoS_(2)/CdS heterojunction displayed the maximal photocatalytic H2 evolution rate of 18.43 mmol h^(-1) g^(-1) under visible light irradiation in the presence of lactic acid as the sacrificial reagent,which was 6 times higher than that of pristine 2D CdS.Based on the photoelectrochemical and photoluminescence spectra tests,it could be deduced that the charge separation and transfer of 2D/2D MoS_(2)/CdS heterojunction was tremendously improved,and the recombination of photoinduced electron-hole pairs was effectively impeded.Moreover,the 2D MoS_(2) was used as a cocatalyst to provide the abundant active sites and lower the overpotential for H_(2) generation reaction.The current work would offer an insight to fabricate the 2D/2D heterojunction photocatalysts for splitting H_(2)O into H_(2).展开更多
Heterojunction design in a two-dimensional(2D)fashion has been deemed beneficial for improving the photocatalytic activity of g-C_(3)N_(4)because of the promoted interfacial charge transfer,yet still facing challenges...Heterojunction design in a two-dimensional(2D)fashion has been deemed beneficial for improving the photocatalytic activity of g-C_(3)N_(4)because of the promoted interfacial charge transfer,yet still facing challenges.Herein,we construct a novel 2D/2D Cu_(3)P nanosheet/P-doped g-C_(3)N_(4)(PCN)nanosheet heterojunction photocatalyst(PCN/Cu_(3)P)through a simple in-situ phosphorization treatment of 2D/2D CuS/g-C_(3)N_(4)composite for photocatalytic H2 evolution.We demonstrate that the 2D lamellar structure of both CuS and g-C_(3)N_(4)could be well reserved in the phosphorization process,while CuS and g-C_(3)N_(4)in-situ transformed into Cu_(3)P and PCN,respectively,leading to the formation of PCN/Cu_(3)P tight 2D/2D heterojunction.Owing to the large contact area provided by intimate face-to-face 2D/2D structure,the PCN/Cu_(3)P photocatalyst exhibits significantly enhanced charge separation efficiency,thus achieving a boosted visible-light-driven photocatalytic behavior.The highest rate for H2 evolution reaches 5.12 umol·h^(-1),nearly 24 times and 368 times higher than that of pristine PCN and g-C_(3)N_(4),respectively.This work represents an excellent example in elaborately con-structing g-C_(3)N_(4)-based 2D/2D heterostructure and could be extended to other photocatalyst/co-catalyst system.展开更多
为研发同时预防和控制猪圆环病毒2d基因型(PCV2d)和猪伪狂犬病病毒(PRV)的疫苗,将PCV2dORF2基因克隆到含有绿色荧光蛋白(EGFP)基因的PRV转移质粒pG中BamHⅠ位点,获得重组质粒pG-PCV2d-EGFP。运用转染试剂ZLip2000将其与PRV变异株3基因...为研发同时预防和控制猪圆环病毒2d基因型(PCV2d)和猪伪狂犬病病毒(PRV)的疫苗,将PCV2dORF2基因克隆到含有绿色荧光蛋白(EGFP)基因的PRV转移质粒pG中BamHⅠ位点,获得重组质粒pG-PCV2d-EGFP。运用转染试剂ZLip2000将其与PRV变异株3基因缺失毒株gE^(-)/g^(-)/TK^(-)PRV NY DNA转入ST细胞中,经绿色荧光蚀斑纯化,得到表达EGFP的重组病毒rPRV-PCV2d-EGFP。采用CRISPR/Cas9基因双敲除质粒敲除重组病毒中EGFP基因,经蚀斑纯化,拯救出不表达EGFP的重组病毒rPRV-PCV2d。重组病毒rPRV-PCV2d与亲本株gE^(-)/g^(-)/TK^(-)PRV NY具有相近的遗传稳定性,且能够表达PCV2d衣壳(Cap)蛋白。在6周龄小鼠免疫试验中,与商品化PCV2灭活疫苗相比,rPRV-PCV2d刺激小鼠机体诱导了更高的PCV2特异性抗体,且用PCV2d强毒株攻毒后,rPRV-PCV2d显著降低了小鼠心脏、肝脏、脾脏等组织中PCV2d载量。此外,rPRV-PCV2d在小鼠体内激发PRV特异性免疫应答,并能阻止PRV强毒对小鼠的侵袭。表明rPRV-PCV2d具有良好的免疫原性。展开更多
基金Ministry of Higher Education(MOHE)Malaysia under the Fundamental Research Grant Scheme(FRGS)(Ref No:FRGS/1/2020/TK0/XMU/02/1)We would also like to thank the Ministry of Science,Technology and Innovation(MOSTI)Malaysia under the Strategic Research Fund(SRF-APP)(S.22015)+5 种基金The authors would also like to acknowledge the financial support provided by the National Natural Science Foundation of China(Ref No.22202168)Guangdong Basic and Applied Basic Re-search Foundation(Ref No.2021A1515111019)We would also like to acknowledge the financial support from the State Key Labo-ratory of Physical Chemistry of Solid Surfaces,Xiamen University(No.2023X11)This work is also funded by Xiamen University Malaysia Investigatorship Grant(Grant No.IENG/0038)Xiamen University Malaysia Research Fund(ICOE/0001,XMUMRF/2021-C8/IENG/0041 and XMUMRF/2019-C3/IENG/0013)Hengyuan International Sdn.Bhd.(Grant No.EENG/0003).
文摘Two-dimensional(2D)materials have come to light due to their unique thickness that owns abundant exposed edges with enhanced electrocatalytic properties.2D molybdenum disulfide(MoS_(2))nanosheet has aroused considerable attention due to its tunable surface chemistry and high electrochemical sur-face area.Nonetheless,several shortcomings associated with MoS_(2),such as its naturally existing semi-conducting 2H phase,which has limited active sites due to the inert basal plane,restrict its application in water electrocatalysis.Taking into account the benefits of the 1T/2H phase of MoS_(2),as well as the importance of engineering 2D/2D heterojunction interface for boosted electrocatalysis,metallic Ti_(3)C_(2)Tx was integrated with 1T/2H MoS_(2) to develop 2D/2D 1T/2H MoS_(2)/Ti_(3)C_(2)Tx heterostructured nanocompos-ites.Herein,with only 25%of the intercalating agent,1T/2H MoS_(2) with the highest 1T phase content of~82%was successfully synthesized.It was further incorporated with 1 wt%of Ti_(3)C_(2)Tx through a com-bination of ultrasonication and mechanical stirring process.The 1T/2H MoS_(2)(25D)/Ti_(3)C_(2)Tx-1(MTC-1)manifested outstanding electrocatalytic performance with an overpotential and Tafel slope of 280 mV(83.80 mV dec^(-1))and 300 mV(117.2 mV dec^(-1)),for catalyzing acidic and alkaline medium HER,respec-tively.Pivotally,the as-prepared catalysts also illustrated long-term stability for more than 40 h.The coupling method for the 2D nanosheets is crucial to suppress the oxidation of Ti_(3)C_(2)Tx and the restack-ing issue of 2D nanosheets.The superior HER activity is ascribed to the synergistic effect between the heterostructure,enhancing the electronic structure and charge separation capability.The intrinsic prop-erty of the catalyst further confirms by turnover frequency(TOF)calculation.As such,this research paves the way for designing high-efficiency 2D electrocatalysts and sheds light on the further advancement of tunable 2D electrocatalysts for robust water splitting and beyond.
基金supported by the National Natural Science Foundation of China(No.21773089)the Henan Center for Outstanding Overseas Scientist(No.GZS2024004).
文摘Herein,a new type of two-dimensional(2D)/2D Ti_(3)C_(2)/TiO_(2) heterojunction was developed for efficient photocatalytic nitrogen reduction reaction(NRR),in which TiO_(2) nanosheets(TiO_(2) Ns)were designed as the main catalyst,while Ti_(3)C_(2) MXene served as the co-catalyst.Experimental and theoretical results revealed that Ti_(3)C_(2) MXene introduced electron-rich unsaturated Ti sites,serving as highly active sites for both the adsorption and activation of N_(2) on the Ti_(3)C_(2)/TiO_(2) heterojunction.Furthermore,the 2D/2D Ti_(3)C_(2)/TiO_(2) heterostructure greatly promoted the directional separation and transfer of charge carriers,facilitated by the internal electric field.This structural feature enabled the spatial separation of the N_(2) reduction and H2 O oxidation half-reactions on the distinct surfaces of Ti_(3)C_(2)(001)and TiO_(2)(001),con-sequently reducing the reaction energy barrier for each respective process.The synergistic effects arising from the interface and surface interactions within the heterojunction conspicuously improved the photo-catalytic NRR activity.As a result,the optimized Ti_(3)C_(2)/TiO_(2) heterojunction exhibited a high NH_(3) produc-tion rate of 24.4μmol g−1 h−1 in the absence of sacrificial agents,representing a remarkable 12.8-fold increase compared to individual TiO_(2) Ns.This work provides new insights into rational design of high-performance heterogeneous photocatalysts and offers a deeper understanding of the mechanism under-lying surface active sites in the photocatalytic NRR process.
基金financial support provided by the Sichuan Science and Technology Program(No.2022NSFSC0226)Sichuan Science and Technology Program(No.2023ZYD0163)+6 种基金the Production-Education Integration Demonstration Project of Sichuan Provincethe Photovoltaic Industry Production-Education Integration Comprehensive Demonstration Base of Sichuan Province(Sichuan Financial Education[2022]No.106)China Tianfu Yongxing Laboratory Science and Technology Key Project(2023KJGG15)National Key Research and Development Program of China(2022YFB3803300)Beijing Natural Science Foundation(IS23037)the Department for Energy Security and Net Zero(project ID:NEXTCCUS)the ACT program(Accelerating CCS Technologies,Horizon2020 project NO.691712)。
文摘The 2D/3D heterojunction perovskites have garnered increasing attention due to their exceptional moisture and thermal stability.However,few works have paid attention to the influence of the subsequent change process of 2D/3D heterojunction PSC on the stability of PSCs.Moreover,the evolution of the interface and carrier dynamic behavior of the 2D/3D perovskite films with long-term operation has not been systematically developed befo re.In this work,the effects of 2D/3 D heterojunction evolution on the interface of perovskite films and different carrier dynamics during 2D/3D evolution are systematically analyzed for the first time.The decomposition of 2D/3D heterojunction in the perovskite film will have a certain impact on the surface and carrier dynamics behavior of perovskite.During the evolution of 2D/3D heterojunction,PbI_(2)crystals will appear,which will improve the interfacial energy level matching between the electron transport layer and perovskite film.With a long evolution time,some holes will appear on the surface of perovskite film.The open circuit voltage(V_(OC))of PSCs increased from 1.14 to1.18 V and the PCE increased to 23.21%after 300 h storage in the nitrogen atmosphere,and maintained 89%initial performance for with 3000 h stability test in N_(2)box.This discovery has a significant role in promoting the development of inverted heterojunction PSCs and constructing the revolution mechanism of charge carrier dynamic.
基金supported by the National Key Research and Development Programs-Intergovernmental International Cooperation in Science and Technology Innovation Project(Grant No.2022YFE0118400)the Natural Science Foundation of Hunan Province(2023JJ50132)+1 种基金Shenzhen Science and Technology Innovation Committee(Grants Nos.JCYJ20220818100211025,and KCXST20221021111616039)Shenzhen Science and Technology Program(No.20231128110928003)。
文摘The introduction of two-dimensional(2D)perovskite layers on top of three-dimensional(3D)perovskite films enhances the performance and stability of perovskite solar cells(PSCs).However,the electronic effect of the spacer cation and the quality of the 2D capping layer are critical factors in achieving the required results.In this study,we compared two fluorinated salts:4-(trifluoromethyl)benzamidine hydrochloride(4TF-BA·HCl)and 4-fluorobenzamidine hydrochloride(4F-BA·HCl)to engineer the 3D/2D perovskite films.Surprisingly,4F-BA formed a high-performance 3D/2D heterojunction,while4TF-BA produced an amorphous layer on the perovskite films.Our findings indicate that the balanced intramolecular charge polarization,which leads to effective hydrogen bonding,is more favorable in 4F-BA than in 4TF-BA,promoting the formation of a crystalline 2D perovskite.Nevertheless,4TF-BA managed to improve efficiency to 24%,surpassing the control device,primarily due to the natural passivation capabilities of benzamidine.Interestingly,the devices based on 4F-BA demonstrated an efficiency exceeding 25%with greater longevity under various storage conditions compared to 4TF-BA-based and the control devices.
基金supported by the IITP(Institute of Information & Communications Technology Planning & Evaluation)-ITRC(Information Technology Research Center) grant funded by the Korea government(Ministry of Science and ICT) (IITP-2025-RS-2024-00437191, and RS-2025-02303505)partly supported by the Korea Basic Science Institute (National Research Facilities and Equipment Center) grant funded by the Ministry of Education. (No. 2022R1A6C101A774)the Deanship of Research and Graduate Studies at King Khalid University, Saudi Arabia, through Large Research Project under grant number RGP-2/527/46
文摘The growing global energy demand and worsening climate change highlight the urgent need for clean,efficient and sustainable energy solutions.Among emerging technologies,atomically thin two-dimensional(2D)materials offer unique advantages in photovoltaics due to their tunable optoelectronic properties,high surface area and efficient charge transport capabilities.This review explores recent progress in photovoltaics incorporating 2D materials,focusing on their application as hole and electron transport layers to optimize bandgap alignment,enhance carrier mobility and improve chemical stability.A comprehensive analysis is presented on perovskite solar cells utilizing 2D materials,with a particular focus on strategies to enhance crystallization,passivate defects and improve overall cell efficiency.Additionally,the application of 2D materials in organic solar cells is examined,particularly for reducing recombination losses and enhancing charge extraction through work function modification.Their impact on dye-sensitized solar cells,including catalytic activity and counter electrode performance,is also explored.Finally,the review outlines key challenges,material limitations and performance metrics,offering insight into the future development of nextgeneration photovoltaic devices encouraged by 2D materials.
基金supported by the National Research Foundation of Korea(NRF)grant funded by the Korea government(MSIT)(No.NRF-2018R1A5A1025137).
文摘A two-dimensional(2D)/2D hybrid heterojunction with face-to-face interfacial assembly is a desirable dimensionality design with significant potential for various photocatalytic applications due to the large interfacial contact area,which facilitates charge migration and separation.Herein,we developed an ef-ficient 2D/2D hybrid heterojunction consisting of BiOIO 3 nanoplates(BIO)and g-C_(3)N_(4) nanosheets(CN)using a simple but effective in situ growth method for photocatalytic aqueous antibiotic degradation and H_(2) generation.The face-to-face interfacial assembly of the BIO and CN components in the BIO/CN hy-brid heterojunction was verified using electron microscopy.Remarkably,the BIO/CN hybrid heterojunc-tion outperformed both the BIO and CN counterparts in terms of norfloxacin degradation and H_(2) gen-eration under simulated solar light irradiation.Moreover,the photocatalytic performance of the hybrid catalyst remained nearly unchanged throughout five consecutive test runs.The exceptional performance and stability of the hybrid catalyst are attributable to its extended optical absorption range,large interfa-cial contact area provided by the face-to-face assembly in the 2D/2D hybrid configuration,and enhanced photoexcited charge separation efficiency and redox power of the separated charges,which are supported by an efficient S-scheme charge transfer mechanism.This study illuminates the rational construction of novel 2D/2D S-scheme hybrid heterojunction photocatalysts with practical applications in environmental remediation and sustainable energy generation.
基金financially supported by the Science and Technology Investigation Project of Hubei Provincial Department of Education,China(No.D20181805)。
文摘Fabrication of 2D/2D heterojunction photocatalysts have attracted more attentions due to their inherent merits involving the large contact interface,short charge migration distance and plentiful active sites,which are beneficial for the enhancement of photocatalytic activity.Herein,a series of 2D/2D MoS_(2)/Cd S type-I heterojunctions were prepared by incorporation the exfoliating of bulk CdS and MoS_(2) with postsintering procedure.Multiple characteristic techniques were employed to corroborate the formation of heterojunctions.By optimizing the 2D MoS_(2) amounts in the heterojunction,the 7 wt.%2D/2D MoS_(2)/CdS heterojunction displayed the maximal photocatalytic H2 evolution rate of 18.43 mmol h^(-1) g^(-1) under visible light irradiation in the presence of lactic acid as the sacrificial reagent,which was 6 times higher than that of pristine 2D CdS.Based on the photoelectrochemical and photoluminescence spectra tests,it could be deduced that the charge separation and transfer of 2D/2D MoS_(2)/CdS heterojunction was tremendously improved,and the recombination of photoinduced electron-hole pairs was effectively impeded.Moreover,the 2D MoS_(2) was used as a cocatalyst to provide the abundant active sites and lower the overpotential for H_(2) generation reaction.The current work would offer an insight to fabricate the 2D/2D heterojunction photocatalysts for splitting H_(2)O into H_(2).
基金We acknowledge the support from the National Natural Science Foundation of China(Nos.51876173 and 52142604)the Natural Science Foundation of Jiangsu Province(No.BK20190054)+2 种基金the Suzhou Science and Technology Program(SYG202101)Fok Ying-Tung Education Foundation(No.171048)the China Fundamental Research Funds for the Central Universities.
文摘Heterojunction design in a two-dimensional(2D)fashion has been deemed beneficial for improving the photocatalytic activity of g-C_(3)N_(4)because of the promoted interfacial charge transfer,yet still facing challenges.Herein,we construct a novel 2D/2D Cu_(3)P nanosheet/P-doped g-C_(3)N_(4)(PCN)nanosheet heterojunction photocatalyst(PCN/Cu_(3)P)through a simple in-situ phosphorization treatment of 2D/2D CuS/g-C_(3)N_(4)composite for photocatalytic H2 evolution.We demonstrate that the 2D lamellar structure of both CuS and g-C_(3)N_(4)could be well reserved in the phosphorization process,while CuS and g-C_(3)N_(4)in-situ transformed into Cu_(3)P and PCN,respectively,leading to the formation of PCN/Cu_(3)P tight 2D/2D heterojunction.Owing to the large contact area provided by intimate face-to-face 2D/2D structure,the PCN/Cu_(3)P photocatalyst exhibits significantly enhanced charge separation efficiency,thus achieving a boosted visible-light-driven photocatalytic behavior.The highest rate for H2 evolution reaches 5.12 umol·h^(-1),nearly 24 times and 368 times higher than that of pristine PCN and g-C_(3)N_(4),respectively.This work represents an excellent example in elaborately con-structing g-C_(3)N_(4)-based 2D/2D heterostructure and could be extended to other photocatalyst/co-catalyst system.
文摘为研发同时预防和控制猪圆环病毒2d基因型(PCV2d)和猪伪狂犬病病毒(PRV)的疫苗,将PCV2dORF2基因克隆到含有绿色荧光蛋白(EGFP)基因的PRV转移质粒pG中BamHⅠ位点,获得重组质粒pG-PCV2d-EGFP。运用转染试剂ZLip2000将其与PRV变异株3基因缺失毒株gE^(-)/g^(-)/TK^(-)PRV NY DNA转入ST细胞中,经绿色荧光蚀斑纯化,得到表达EGFP的重组病毒rPRV-PCV2d-EGFP。采用CRISPR/Cas9基因双敲除质粒敲除重组病毒中EGFP基因,经蚀斑纯化,拯救出不表达EGFP的重组病毒rPRV-PCV2d。重组病毒rPRV-PCV2d与亲本株gE^(-)/g^(-)/TK^(-)PRV NY具有相近的遗传稳定性,且能够表达PCV2d衣壳(Cap)蛋白。在6周龄小鼠免疫试验中,与商品化PCV2灭活疫苗相比,rPRV-PCV2d刺激小鼠机体诱导了更高的PCV2特异性抗体,且用PCV2d强毒株攻毒后,rPRV-PCV2d显著降低了小鼠心脏、肝脏、脾脏等组织中PCV2d载量。此外,rPRV-PCV2d在小鼠体内激发PRV特异性免疫应答,并能阻止PRV强毒对小鼠的侵袭。表明rPRV-PCV2d具有良好的免疫原性。
