Superwetting materials have drawn unprecedented attention in the treatment of oily wastewater due to their preferable anti-fouling property and selective oil/water separation.However,it is still a challenge to fabrica...Superwetting materials have drawn unprecedented attention in the treatment of oily wastewater due to their preferable anti-fouling property and selective oil/water separation.However,it is still a challenge to fabricate multifunctional and environmentally friendly materials,which can be stably applied to purify the actual complicated wastewater.Here,a Ag/Ag/α-Fe_(2)O_(3) heterostructure anchored copper mesh was intentionally synthesized using a facile two-step hydrothermal method.The resultant mesh with superhydrophilicity and underwater superoleophobicity was capable of separating various oil/water mixtures with superior separation efficiency and high permeationflux driven by gravity.Benefiting from the joint effects of the smaller band gap of Ag/α-Fe_(2)O_(3) heterojunction,inherent antibacterial capacity of Ag/α-Fe_(2)O_(3) and Ag nanoparticles,favorable conductive substrate,as well as the hierarchical structure with superwettability,such mesh presented remarkably enhanced degradation capability toward organic dyes under visible light irradiation and antibacterial activity against both Escherichia coli(E.coli)and Staphylococcus aureus(S.aureus)compared with the pure Ag/α-Fe_(2)O_(3) coated mesh.Impressively,the mesh exhibited bifunctional water purification performance,in which organic dyes were eliminated simultaneously from water during oil/water separation in onefiltration process.More importantly,this mesh behaved exceptional chemical resistance,mechanical stability and long-term reusability.Therefore,this material with multifunctional integration may hold promising potential for steady water purification in practice.展开更多
It is of great necessity yet still a challenge to develop superwetting functional interfacial materials for simultaneously separating insoluble oil and degrading soluble dye pollutants in practical wastewater.In this ...It is of great necessity yet still a challenge to develop superwetting functional interfacial materials for simultaneously separating insoluble oil and degrading soluble dye pollutants in practical wastewater.In this work,a Ag-CuO heterostructure-decorated mesh was fabricated via facile alkali etchingcalcination and photoreduction approaches.The as-synthesized mesh with superhydrophilicity and underwater superoleophobicity displayed high separation efficiency(>99.998%)for diverse oil/water mixtures.Besides,it demonstrated more superior photocatalytic performance in dye degradation than those of bare CuO nanostructure-coated materials,which is primarily attributed to the intensive visible light harvesting and efficient electron-holes separation occurred on noble metal-semiconductor heterostructures.Furthermore,on account of the tenacity of Cu substrate as well as enhanced structural stability,this binary composite-decorated mesh exhibited highly reliable durability and robustness after 10 cycles of photocatalytic degradation tests,and even being ultrasonic worn for 30 min.More importantly,our developed mesh was capable of in situ catalytic degrading water-soluble organic dyes during oil/water separation under visible light irradiation.Therefore,such a dexterous and feasible strategy may afford a new route to construct bifunctional and predurable materials for actual sewage purification.展开更多
Rare-earth metal dialkyl complexes[1-Bn-3-(DippN=CH)C_(8)H_(4)N]RE(CH_(2)SiMe_(3))2(thf)2(Dipp=2,6-iPr_(2)C_(6)H_(3),RE=Y(1)and Er(2))were prepared through the cyclometalation reactions of the N-Bn-3-imino-functionali...Rare-earth metal dialkyl complexes[1-Bn-3-(DippN=CH)C_(8)H_(4)N]RE(CH_(2)SiMe_(3))2(thf)2(Dipp=2,6-iPr_(2)C_(6)H_(3),RE=Y(1)and Er(2))were prepared through the cyclometalation reactions of the N-Bn-3-imino-functionalized indolyl ligand 1-Bn-3-(DippN=CH)C8H5N with one equivalent of rare-earth metal trialkyl precursors.The structures of compounds 1 and 2 were confirmed by X-ray crystal analyses and characterized by elemental analysis,IR,NMR spectroscopy wherein applicable.In the presence of cocatalysts,these rare-earth metal dialkyl complexes initiated isoprene polymerization with a high activity(95% conversion of 2000 equivalent of isoprene in 360 min),producing polymers with high regioselectivity(1,4-polymers up to 91%).展开更多
Present-day Liþstorage materials generally suffer from sluggish low-temperature electrochemical kinetics and poor high-temperature cycling stability.Herein,based on a Ca2þsubstituted Mg_(2)Nb_(34)O_(87) anod...Present-day Liþstorage materials generally suffer from sluggish low-temperature electrochemical kinetics and poor high-temperature cycling stability.Herein,based on a Ca2þsubstituted Mg_(2)Nb_(34)O_(87) anode material,we demonstrate that decreasing the ionic packing factor is a two-fold strategy to enhance the low-temperature electrochemical kinetics and high-temperature cyclic stability.The resulting Mg_(1.5)Ca_(0.5)Nb_(34)O_(87) shows the smallest ionic packing factor among Wadsley–Roth niobate materials.Compared with Mg_(2)Nb_(34)O_(87),Mg1.5Ca0.5Nb_(34)O_(87) delivers a 1.6 times faster Liþdiffusivity at-20℃,leading to 56%larger reversible capacity and 1.5 times higher rate capability.Furthermore,Mg_(1.5)Ca_(0.5)Nb_(34)O_(87) exhibits an 11%smaller maximum unit-cell volume expansion upon lithiation at 60℃,resulting in better cyclic stability;at 10C after 500 cycles,it has a 7.1%higher capacity retention,and its reversible capacity at 10C is 57%larger.Therefore,Mg_(1.5)Ca_(0.5)Nb_(34)O_(87) is an allclimate anode material capable of working at harsh temperatures,even when its particle sizes are in the order of micrometers.展开更多
基金This work was financially supported by the Shandong Provincial Natural Science Foundation(ZR2020QB116)the Excellent Young Talents Foundation in Universities of Anhui Province(gxyq2021223)the Key Research Project of Natural Science in Universities of Anhui Province.(KJ2020A0749).
文摘Superwetting materials have drawn unprecedented attention in the treatment of oily wastewater due to their preferable anti-fouling property and selective oil/water separation.However,it is still a challenge to fabricate multifunctional and environmentally friendly materials,which can be stably applied to purify the actual complicated wastewater.Here,a Ag/Ag/α-Fe_(2)O_(3) heterostructure anchored copper mesh was intentionally synthesized using a facile two-step hydrothermal method.The resultant mesh with superhydrophilicity and underwater superoleophobicity was capable of separating various oil/water mixtures with superior separation efficiency and high permeationflux driven by gravity.Benefiting from the joint effects of the smaller band gap of Ag/α-Fe_(2)O_(3) heterojunction,inherent antibacterial capacity of Ag/α-Fe_(2)O_(3) and Ag nanoparticles,favorable conductive substrate,as well as the hierarchical structure with superwettability,such mesh presented remarkably enhanced degradation capability toward organic dyes under visible light irradiation and antibacterial activity against both Escherichia coli(E.coli)and Staphylococcus aureus(S.aureus)compared with the pure Ag/α-Fe_(2)O_(3) coated mesh.Impressively,the mesh exhibited bifunctional water purification performance,in which organic dyes were eliminated simultaneously from water during oil/water separation in onefiltration process.More importantly,this mesh behaved exceptional chemical resistance,mechanical stability and long-term reusability.Therefore,this material with multifunctional integration may hold promising potential for steady water purification in practice.
基金supported by the National Natural Science Foundation of China(21303232)the China Postdoctoral Science Foundation(2018M632610)
文摘It is of great necessity yet still a challenge to develop superwetting functional interfacial materials for simultaneously separating insoluble oil and degrading soluble dye pollutants in practical wastewater.In this work,a Ag-CuO heterostructure-decorated mesh was fabricated via facile alkali etchingcalcination and photoreduction approaches.The as-synthesized mesh with superhydrophilicity and underwater superoleophobicity displayed high separation efficiency(>99.998%)for diverse oil/water mixtures.Besides,it demonstrated more superior photocatalytic performance in dye degradation than those of bare CuO nanostructure-coated materials,which is primarily attributed to the intensive visible light harvesting and efficient electron-holes separation occurred on noble metal-semiconductor heterostructures.Furthermore,on account of the tenacity of Cu substrate as well as enhanced structural stability,this binary composite-decorated mesh exhibited highly reliable durability and robustness after 10 cycles of photocatalytic degradation tests,and even being ultrasonic worn for 30 min.More importantly,our developed mesh was capable of in situ catalytic degrading water-soluble organic dyes during oil/water separation under visible light irradiation.Therefore,such a dexterous and feasible strategy may afford a new route to construct bifunctional and predurable materials for actual sewage purification.
基金supported by the Natural Science Foundation of Anhui Province(No.2008085ME174)financial support from Anhui Normal University(FMS201915)。
文摘Rare-earth metal dialkyl complexes[1-Bn-3-(DippN=CH)C_(8)H_(4)N]RE(CH_(2)SiMe_(3))2(thf)2(Dipp=2,6-iPr_(2)C_(6)H_(3),RE=Y(1)and Er(2))were prepared through the cyclometalation reactions of the N-Bn-3-imino-functionalized indolyl ligand 1-Bn-3-(DippN=CH)C8H5N with one equivalent of rare-earth metal trialkyl precursors.The structures of compounds 1 and 2 were confirmed by X-ray crystal analyses and characterized by elemental analysis,IR,NMR spectroscopy wherein applicable.In the presence of cocatalysts,these rare-earth metal dialkyl complexes initiated isoprene polymerization with a high activity(95% conversion of 2000 equivalent of isoprene in 360 min),producing polymers with high regioselectivity(1,4-polymers up to 91%).
基金supported by the National Natural Science Foundation of China (51762014)Key Research Project of Natural Science in Universities of Anhui Province (KJ2020A0749)Excellent Young Talents Foundation in Universities of Anhui Province (gxyq2021223).
文摘Present-day Liþstorage materials generally suffer from sluggish low-temperature electrochemical kinetics and poor high-temperature cycling stability.Herein,based on a Ca2þsubstituted Mg_(2)Nb_(34)O_(87) anode material,we demonstrate that decreasing the ionic packing factor is a two-fold strategy to enhance the low-temperature electrochemical kinetics and high-temperature cyclic stability.The resulting Mg_(1.5)Ca_(0.5)Nb_(34)O_(87) shows the smallest ionic packing factor among Wadsley–Roth niobate materials.Compared with Mg_(2)Nb_(34)O_(87),Mg1.5Ca0.5Nb_(34)O_(87) delivers a 1.6 times faster Liþdiffusivity at-20℃,leading to 56%larger reversible capacity and 1.5 times higher rate capability.Furthermore,Mg_(1.5)Ca_(0.5)Nb_(34)O_(87) exhibits an 11%smaller maximum unit-cell volume expansion upon lithiation at 60℃,resulting in better cyclic stability;at 10C after 500 cycles,it has a 7.1%higher capacity retention,and its reversible capacity at 10C is 57%larger.Therefore,Mg_(1.5)Ca_(0.5)Nb_(34)O_(87) is an allclimate anode material capable of working at harsh temperatures,even when its particle sizes are in the order of micrometers.
