In this work,a novel Bi_(2)S_(3)/Bi_(5)O_(7)I p-n heterojunction with three-dimensional rod-like nanostructure was successfully constructed through an in-situ topotactic ion exchange approach.A possible evolution mech...In this work,a novel Bi_(2)S_(3)/Bi_(5)O_(7)I p-n heterojunction with three-dimensional rod-like nanostructure was successfully constructed through an in-situ topotactic ion exchange approach.A possible evolution mech-anism from Bi_(5)O_(7)I nanobelts(NBs)into Bi_(2)S_(3)/Bi_(5)O_(7)I rod-like heterostructures(BSI RHs)was proposed,depicting the self-assembly process of internal Bi_(5)O_(7)I NBs and outside networks interwoven by Bi_(2)S_(3)nanorods(NRs),which abided by the Ostwald ripening and epitaxial growth.Owing to the formation of p-n heterojunction and rich oxygen vacancies(OVs),the visible-light absorption ability and separation of photogenerated charge carriers of BSI RHs were highly promoted,leading to a greatly improved photocatalytic ability than that of Bi_(2)S_(3)and Bi_(5)O_(7)I.BSI-1 exhibited the strongest photocatalytic performance,and almost all rhodamine B(RhB)and Pseudomonas aeruginosa(P.aeruginosa)can be thoroughly removed within 90 min.Moreover,a possible photocatalytic mechanism of BSI RHs was proposed based on the tests of active species trapping,electron spin resonance(ESR),photoelectrochemistry(PEC),and photoluminescence(PL)combined with the density functional theory(DFT)simulated computation,vali-dating the dominating roles of·O_(2)^(−)and h+during the photocatalytic process.This work is expected to motivate further efforts for developing novel heterostructures with highly efficient photocatalytic performances,which presents a promising application prospect in the fields of energy and environment.展开更多
In this study,a novel Bi_(2)S_(3)/BiOI Z-scheme photocatalyst with 3D porous hierarchical network-like heterostructure(BSBI NHs)and rich oxygen vacancies(OVs)was fabricated by a facile ion exchange method followed by ...In this study,a novel Bi_(2)S_(3)/BiOI Z-scheme photocatalyst with 3D porous hierarchical network-like heterostructure(BSBI NHs)and rich oxygen vacancies(OVs)was fabricated by a facile ion exchange method followed by the in-situ growth process.A possible formation mechanism of BSBI NHs was studied,showing the self-assembled process of in-situ interwoven growth of 1D Bi_(2)S_(3) nanorods(NRs)on the surface of 2D BiOI disk-like nanoplates(NPs),which followed the Ostwald ripening and epitaxial growth.The modification of BiOI NPs by Bi_(2)S_(3) NRs brought about the formation of Z-scheme heterojunction and massive OVs,which improved the visible-light response property and promoted the separation of photoexcited charge carriers of BSBI NHs.BSBI NHs exhibited a significantly enhanced photocatalytic activity compared with Bi_(2)S_(3) and BiOI,and BSBI-1 can remove almost all bacteria and Rhodamine B(RhB)after 60 min visible light illumination.In addition,the photocatalytic mechanism was studied and speculated based on the tests of active species capture,electron spin resonance(ESR),and density functional theory(DFT)simulation calculation,proving the primary roles of·OH,·O_(2)^(-)and h^(+)during the photocatalytic reaction.This work provides new insights into the design and exploitation of novel heterojunctions with highly efficient photocatalytic performances for environmental remediation applications.展开更多
This study addresses the challenges posed by dispersive soil in various engineering fields,including hydraulic and agricultural engineering,by exploring the effects of physical adsorption on soil modification.The prim...This study addresses the challenges posed by dispersive soil in various engineering fields,including hydraulic and agricultural engineering,by exploring the effects of physical adsorption on soil modification.The primary objective is to identify an environmentally friendly stabilizer that can alleviate cracking and erosion resulting from soil dispersivity.Activated carbon(AC),known for its porous nature,was examined for its potential to enhance soil strength and erosion resistance.The charge neutralization process was evaluated by monitoring pH and conductivity,in addition to a comprehensive analysis of microscopic and mineral properties.The results show that high sodium levels or low clay contents result in the dispersive nature of soil in water.However,the incorporation of AC can transform such soil into a non-dispersive state.Moreover,both soil strength and erosion resistance exhibited enhancements with increasing AC content and curing duration.The incorporation of AC resulted in a maximum 5.6-fold increase in unconfined compressive strength and a 1.8-fold increase in tensile strength for dispersive soil.Notably,a significant correlation was observed during the curing phase among soil dispersivity,mechanical properties,and pH values.Microscopic analyses revealed that the porous structure of AC facilitated a filling effect and enhanced adsorption capacity,which contributed to improved soil characteristics and reduced dispersivity.The release of hydrogen ions and the formation of aggregates promote water stability.Validation tests conducted on dispersive soil from northern Shaanxi demonstrated the efficacy of physical adsorption using AC as a viable method for modifying dispersive soil in the water conservancy hub.展开更多
Cobalt-based catalysts were regarded as highly effective for pollutant degradation through peroxymono-sulfate activation.Nevertheless,conventional synthesis methods for cobalt-based catalysts were associ-ated with iss...Cobalt-based catalysts were regarded as highly effective for pollutant degradation through peroxymono-sulfate activation.Nevertheless,conventional synthesis methods for cobalt-based catalysts were associ-ated with issues of cobalt ion leakage,which posed a risk of secondary environmental contamination.Addressing this issue,a novel cobalt-based catalyst,CoS nanoparticles,was biosynthesized by Shewanella algae and designated as SA@CoS.SA@CoS,a nanoflower coated with proteins/peptides,contained a sig-nificant number of sulfur vacancies.Compared to chemically synthesized CoS,SA@CoS exhibited lower cobalt ion release(0.13 mg/L)and higher catalytic activity.Based on this,SA@CoS was employed to de-grade Rhodamine B(RhB)and tetracycline(TC)by activating peroxymonosulfate.The results indicated that the degradation efficiencies of RhB and TC could reach 99.9%and 90.5%within 10 min,respec-tively.Further analyses revealed that both radical(·O_(2)^(-),·OH and SO_(4)^(·-))and non-radical(_(1)O_(2))pathways were involved in the degradation of RhB and TC,with the non-radical pathway dominating the degra-dation process.This work not only offered a facile approach for the biosynthesis of stable cobalt-based catalysts,but also underscored the immense potential of biogenic nano-catalysts in the realm of environ-mental remediation.展开更多
基金This work was financially supported by the Basic Scientific Fund for National Public Research Institutes of China(Nos.2020S02 and 2019Y03)the Key Research and Development Program of Shandong Province(Major Scientific and Technological Innovation Project)(No.2019JZZY020711)+1 种基金the Young Elite Scientists Sponsor-ship Program by CAST(No.YESS20210201)National Natural Science Foundation of China(No.51702328).
文摘In this work,a novel Bi_(2)S_(3)/Bi_(5)O_(7)I p-n heterojunction with three-dimensional rod-like nanostructure was successfully constructed through an in-situ topotactic ion exchange approach.A possible evolution mech-anism from Bi_(5)O_(7)I nanobelts(NBs)into Bi_(2)S_(3)/Bi_(5)O_(7)I rod-like heterostructures(BSI RHs)was proposed,depicting the self-assembly process of internal Bi_(5)O_(7)I NBs and outside networks interwoven by Bi_(2)S_(3)nanorods(NRs),which abided by the Ostwald ripening and epitaxial growth.Owing to the formation of p-n heterojunction and rich oxygen vacancies(OVs),the visible-light absorption ability and separation of photogenerated charge carriers of BSI RHs were highly promoted,leading to a greatly improved photocatalytic ability than that of Bi_(2)S_(3)and Bi_(5)O_(7)I.BSI-1 exhibited the strongest photocatalytic performance,and almost all rhodamine B(RhB)and Pseudomonas aeruginosa(P.aeruginosa)can be thoroughly removed within 90 min.Moreover,a possible photocatalytic mechanism of BSI RHs was proposed based on the tests of active species trapping,electron spin resonance(ESR),photoelectrochemistry(PEC),and photoluminescence(PL)combined with the density functional theory(DFT)simulated computation,vali-dating the dominating roles of·O_(2)^(−)and h+during the photocatalytic process.This work is expected to motivate further efforts for developing novel heterostructures with highly efficient photocatalytic performances,which presents a promising application prospect in the fields of energy and environment.
基金financially supported by the Basic Scientific Fund for National Public Research Institutes of China(Nos.2020S02 and 2019Y03)the National Natural Science Foundation of China(No.51702328)+1 种基金the Key Research and Development Program of Shandong Province(Major Scientific and Technological Innovation Project)(No.2019JZZY020711)the Young Elite Scientists Sponsorship Program by CAST(No.YESS20210201).
文摘In this study,a novel Bi_(2)S_(3)/BiOI Z-scheme photocatalyst with 3D porous hierarchical network-like heterostructure(BSBI NHs)and rich oxygen vacancies(OVs)was fabricated by a facile ion exchange method followed by the in-situ growth process.A possible formation mechanism of BSBI NHs was studied,showing the self-assembled process of in-situ interwoven growth of 1D Bi_(2)S_(3) nanorods(NRs)on the surface of 2D BiOI disk-like nanoplates(NPs),which followed the Ostwald ripening and epitaxial growth.The modification of BiOI NPs by Bi_(2)S_(3) NRs brought about the formation of Z-scheme heterojunction and massive OVs,which improved the visible-light response property and promoted the separation of photoexcited charge carriers of BSBI NHs.BSBI NHs exhibited a significantly enhanced photocatalytic activity compared with Bi_(2)S_(3) and BiOI,and BSBI-1 can remove almost all bacteria and Rhodamine B(RhB)after 60 min visible light illumination.In addition,the photocatalytic mechanism was studied and speculated based on the tests of active species capture,electron spin resonance(ESR),and density functional theory(DFT)simulation calculation,proving the primary roles of·OH,·O_(2)^(-)and h^(+)during the photocatalytic reaction.This work provides new insights into the design and exploitation of novel heterojunctions with highly efficient photocatalytic performances for environmental remediation applications.
基金financially supported by the National Postdoctoral Program for Innovative Talents(Grant No.BX20200287)the National Natural Science Foundation of China(Grant Nos.52079116 and 52378322).
文摘This study addresses the challenges posed by dispersive soil in various engineering fields,including hydraulic and agricultural engineering,by exploring the effects of physical adsorption on soil modification.The primary objective is to identify an environmentally friendly stabilizer that can alleviate cracking and erosion resulting from soil dispersivity.Activated carbon(AC),known for its porous nature,was examined for its potential to enhance soil strength and erosion resistance.The charge neutralization process was evaluated by monitoring pH and conductivity,in addition to a comprehensive analysis of microscopic and mineral properties.The results show that high sodium levels or low clay contents result in the dispersive nature of soil in water.However,the incorporation of AC can transform such soil into a non-dispersive state.Moreover,both soil strength and erosion resistance exhibited enhancements with increasing AC content and curing duration.The incorporation of AC resulted in a maximum 5.6-fold increase in unconfined compressive strength and a 1.8-fold increase in tensile strength for dispersive soil.Notably,a significant correlation was observed during the curing phase among soil dispersivity,mechanical properties,and pH values.Microscopic analyses revealed that the porous structure of AC facilitated a filling effect and enhanced adsorption capacity,which contributed to improved soil characteristics and reduced dispersivity.The release of hydrogen ions and the formation of aggregates promote water stability.Validation tests conducted on dispersive soil from northern Shaanxi demonstrated the efficacy of physical adsorption using AC as a viable method for modifying dispersive soil in the water conservancy hub.
基金supported by the National Natural Science Foundation of China(No.42376204)the Shandong Provin-cial Natural Science Foundation(No.ZR2022MD023)+3 种基金the Interna-tional Partnership Program by Chinese Academy of Sciences(No.058GJHZ2023058FN)the Young Elite Scientists Sponsorship Pro-gram by CAST(No.YESS20210201)the Key R&D Program of Shan-dong Province,China(Nos.2022CXPT027 and 2023CXPT008)Guangxi Science and Technology Program(Guike AA23026007).
文摘Cobalt-based catalysts were regarded as highly effective for pollutant degradation through peroxymono-sulfate activation.Nevertheless,conventional synthesis methods for cobalt-based catalysts were associ-ated with issues of cobalt ion leakage,which posed a risk of secondary environmental contamination.Addressing this issue,a novel cobalt-based catalyst,CoS nanoparticles,was biosynthesized by Shewanella algae and designated as SA@CoS.SA@CoS,a nanoflower coated with proteins/peptides,contained a sig-nificant number of sulfur vacancies.Compared to chemically synthesized CoS,SA@CoS exhibited lower cobalt ion release(0.13 mg/L)and higher catalytic activity.Based on this,SA@CoS was employed to de-grade Rhodamine B(RhB)and tetracycline(TC)by activating peroxymonosulfate.The results indicated that the degradation efficiencies of RhB and TC could reach 99.9%and 90.5%within 10 min,respec-tively.Further analyses revealed that both radical(·O_(2)^(-),·OH and SO_(4)^(·-))and non-radical(_(1)O_(2))pathways were involved in the degradation of RhB and TC,with the non-radical pathway dominating the degra-dation process.This work not only offered a facile approach for the biosynthesis of stable cobalt-based catalysts,but also underscored the immense potential of biogenic nano-catalysts in the realm of environ-mental remediation.
