Ethylene glycol oxidation reaction(EGOR)is important to address the environmental issues caused by the increased production of polyethylene terephthalate(PET).Metal organic frameworks(MOFs)with superior stability,high...Ethylene glycol oxidation reaction(EGOR)is important to address the environmental issues caused by the increased production of polyethylene terephthalate(PET).Metal organic frameworks(MOFs)with superior stability,high specific surface area and excellent catalytic performance can convert PET into valuable products through EGOR and hydrogen evolution reaction(HER).Herein,a microbial template strategy was adopted to prepare carbon sphere-supported orthogonal nanosheet bimetallic MOF catalysts.The prepared catalyst needs only 1.42 V,307 mV,and 1.83 V at a current density of 100 mA cm^(-2) for EGOR,HER,and EGOR//HER,respectively.More importantly,it can stably perform for at least 160 h at a current density of 500 mA cm^(-2).The high specific surface area of bimetallic MOF and the synergistic effect of yeast carbon shell increase the contact area between the intrinsic active sites and*OH and EG,thus improving the EGOR and HER catalytic activity and stability.This work provides a novel strategy to construct bimetallic orthogonal electrocatalysts with efficient HER//EGOR performance,which is of great significance for achieving sustainable energy conversion and environmental purification.展开更多
Traditional photo-electcatalyst structures of small noble metal nanoparticles assembling into large-scale photoactive semiconductors still suffer from agglomeration of noble metal nanoparticles,insufficient charge tra...Traditional photo-electcatalyst structures of small noble metal nanoparticles assembling into large-scale photoactive semiconductors still suffer from agglomeration of noble metal nanoparticles,insufficient charge transfer,undesirable photoresponse ability that restricted the photo-electrocatalytic performance.To this end,a novel design strategy is proposed in this work,namely integrating small-scale photoactive materials(doped graphene quantum dots,S,N-GQDs)with large-sized noble metal(Pd P)nanoflowers to form novel photo-electrocatalysts for high-efficient alcohol oxidation reaction.As expected,superior electrocatalytic performance of Pd P/S,N-GQDs for ethylene glycol oxidation is acquired,thanks to the nanoflower structure with larger specific surface area and abundant active sites.Furthermore,nonmetal P are demonstrated,especially optimizing the adsorption strength,enhancing the interfacial contact,reducing metal agglomeration,ensuring uniform and efficient doping of S,N-GQDs,and ultimately significantly boost the catalytic activity of photo-electrocatalysts.展开更多
Ethylene glycol(EG)is a biomass derivative of polyethylene terephthalate(PET),and its electrocatalytic conversion into high-value chemicals has sparked widespread interest.This study reviews the most recent research d...Ethylene glycol(EG)is a biomass derivative of polyethylene terephthalate(PET),and its electrocatalytic conversion into high-value chemicals has sparked widespread interest.This study reviews the most recent research development in electrocatalysis-based EG to glycolic acid(GA)conversion.Firstly,the strategies and research results of modulating the electronic structure of catalysts for efficient selective GA production from EG are reviewed.Second,by reviewing the data of in-situ Fourier transform infrared spectroscopy and in-situ electrochemically attenuated total reflection surface enhanced infrared absorption spectroscopy,the reaction pathway and catalytic mechanism of EG partial oxidation to GA were clarified.Finally,the design and regulation of catalysts for selective oxidation of EG by electrocatalysis in the future are prospected.展开更多
For future clean energy demand,it is essential to develop highly efficient and durable materials for use in renewable energy conversion devices.Herein,we report an electrocatalyst loaded with Pd-Pb-Bi nanoalloys on re...For future clean energy demand,it is essential to develop highly efficient and durable materials for use in renewable energy conversion devices.Herein,we report an electrocatalyst loaded with Pd-Pb-Bi nanoalloys on reduced graphene(rGO)-wrapped In_(2)O_(3)(PdPbBi@rGO/In_(2)O_(3))prepared by a hydrothermal method.PdPbBi@rGO/In_(2)O_(3)exhibits higher forward current density(229.12 mA·cm^(-2)),larger electrochemical active surface area(ECSA)(85.87 m^(2)·g^(-1)Pd),smaller impedance(12.68Ω)and lower E_(onset)(-0.56 V)than commercial Pd/C.Specifically,the current density and ECS A are 8.46 and3.38 times higher than those of commercial Pd/C(27.07 mA·cm^(-2),25.41 m^(2)·g^(-1)Pd),respectively.Furthermore,the oxidation mechanism of ethylene glycol and the removal of carbon monoxide[CO]_(ads)from the surface of Pd are also discussed in detail.The columnar support structure wrapped by rGO provides a huge active surface area for catalysis.Moreover,the electronic effect of Pd-PbBi nanoalloys can accelerate the removal of CO intermediate species,obtain more Pd active sites and improve the electrocatalytic performance.Our first synthesis of this highly electrocatalyst offers promising value for commercial application in direct fuel cells.展开更多
Hydrogen peroxide(H_(2)O_(2))electrosynthesis via two-electron oxygen reduction reaction(2e-ORR)is a promising alternative for the energy-intensive anthraquinone process.However,the instability of the catalytic metal ...Hydrogen peroxide(H_(2)O_(2))electrosynthesis via two-electron oxygen reduction reaction(2e-ORR)is a promising alternative for the energy-intensive anthraquinone process.However,the instability of the catalytic metal sites in the state-of-the-art metal single-atom catalysts(M-SACs)hinders their further industrial applications,and the high potential and valueless oxygen product of the conventional anodic oxygen evolution reaction(OER)further limit the economic efficiency of this technology.To address this,a dynamically local structure reconstruction strategy is proposed to in situ transfer the active sites from unstable metal sites to the stable surrounding carbon sites for efficient and durable 2e^(-)ORR electrocatalysis.For the as-designed Mn-N_(3)O-C catalyst,by reconstructing Mn sites into Mn(^(*)OH),the Mn sites were passivated and carbon sites adjacent to the O atom were verified to be the actual active sites by in situ characterization and theoretical calculation.Consequently,Mn-N_(3)O-C exhibited>80%Faradaic efficiency and superior long-term durability over 100 h for H_(2)O_(2)electrosynthesis at~120 mA cm^(-2).In addition,coupling anodic ethylene glycol oxidation reaction(EGOR)further improves the efficiency and economic viability of the H_(2)O_(2)electrosynthesis system.This two-pronged strategy thus opens up a new opportunity for the development of stable H_(2)O_(2)electrosynthesis with low energy consumption and superior economic performance.展开更多
Pt-WO3 nanoparticles uniformly dispersed on Vulcan XC-72R carbon black were prepared by an ethylene glycol method.The morphology,composition,nanostructure,electrochemical characteristics and electrocatalytic activity ...Pt-WO3 nanoparticles uniformly dispersed on Vulcan XC-72R carbon black were prepared by an ethylene glycol method.The morphology,composition,nanostructure,electrochemical characteristics and electrocatalytic activity were characterized,and the formation mechanism was investigated.The average particle size was 2.3 nm,the same as that of Pt/C catalyst.The W/Pt atomic ratio was 1/20,much lower than the design of 1/3.The deposition of WO3·xH2O nanoparticles on Vulcan XC-72R carbon black was found to be very difficult by TEM.From XPS and XRD,the Pt nanoparticles were formed in the colloidal solution of Na2WO4,the EG insoluble Na2WO4 resulted in the decreased relative crystallinity and increased crystalline lattice constant compared with those of Pt/C catalyst and,subsequently,the higher specific electrocatalytic activity as determined by CV.The Pt-mass and Pt-electrochemically-active-specific-surface-area based anodic peak current densities for ethanol oxidation were 422.2 mA·mg-1Pt and 0.43 mA·cm-2Pt,1.2 and 1.1 times higher than those of Pt/C catalyst,respectively.展开更多
The electrochemical upcycling of polyethylene terephthalate(PET)into high-value products,alongside hydrogen production under ambient conditions,represents a promising approach to sustainable waste management.However,t...The electrochemical upcycling of polyethylene terephthalate(PET)into high-value products,alongside hydrogen production under ambient conditions,represents a promising approach to sustainable waste management.However,the mechanism underlying efficient PET-derived ethylene glycol oxidation reactions(EGOR),driven by the enhanced adsorption of key intermediates,remains unclear.In this work,built-in electric fields(BIEF)were deliberately engineered within the heterojunction Ni(OH)_(2)-Ni_(3)S_(2)/NF catalyst,effectively elevating the d-band center and thereby enhancing the adsorption of EG and hydroxyl(*OH)species.This modification significantly accelerates reaction kinetics compared to Ni3S2/NF.Remarkably,the Ni(OH)_(2)-Ni_(3)S_(2)/NF catalyst achieves an industrial current density of 616.0 mA·cm^(-2) at 1.50 V vs.reversible hydrogen electrode(RHE),exhibiting a Faradaic efficiency(FE)of 89%for formate(FA)at 1.45 V vs.RHE.In situ electrochemical infrared absorption spectroscopy(IRAS)and theoretical calculations reveal that FA was primarily generated through C-C bond cleavage in glycolic acid.This study also elucidates the critical relationship between BIEF and d-band center,offering a viable strategy to enhance intermediate adsorption during the EGOR process.展开更多
Co-electrolysis of waste plastics and carbon dioxide(CO_(2)) into value-added chemicals or fuels is a promising pathway for a sustainable society, but efficient and selective conversion remains a challenge. Herein, a ...Co-electrolysis of waste plastics and carbon dioxide(CO_(2)) into value-added chemicals or fuels is a promising pathway for a sustainable society, but efficient and selective conversion remains a challenge. Herein, a gold-mediated nickel hydroxide(Au/Ni(OH)_(2)) is developed to oxidize waste plastic-derived ethylene glycol(EG) into formate. In-situ electrochemical experiments and theoretical results reveal that the introduction of Au favors the redox properties and EG adsorption behavior of Ni(OH)_(2). The Au/Ni(OH)_(2) catalyst shows an excellent formate selectivity of >90% at high current densities of above 100 m A cm^(-2). When coupled with sputtered bismuth(Bi) cathode for CO_(2) reduction, a high formate Faradic efficiency(FE) of 188.2% at 200 m A cm^(-2)and a good formate productivity of 7.33 mmol m^(-2)s^(-1)at 10 A are obtained in a flow cell and a zero-gap membrane electrode assembly(MEA) cell, respectively. This work demonstrates a promising strategy to convert waste plastics and CO_(2) into valuable products.展开更多
The synthesis of atomically ordered Pt-based intermetallic electrocatalysts for the direct alcohol fuel cells generally requires the addition of surfactants or the high-temperature annealing.However,some residual surf...The synthesis of atomically ordered Pt-based intermetallic electrocatalysts for the direct alcohol fuel cells generally requires the addition of surfactants or the high-temperature annealing.However,some residual surfactants on the surface of the assynthesized catalysts would prevent the exposure of catalytic active sites,the high-temperature annealing process is easy to accelerate the sintering of the metal,which both lead to the decline of electrocatalytic performance.Herein,we construct the atomically ordered bimetallic PtBi intermetallics with clean surfaces and unique three-dimensional hollow acorn-shell-like structure(3D PtBi HASL)by a simple,low-temperature,surfactant-free one-pot synthetic approach.Benefiting from the special hollow structures,the obtained 3D PtBi HASL intermetallics expose abundant accessible active sites.Moreover,the introduction of oxophilic metal Bi can enhance adsorption of OHads,thereby significantly facilitating removal of poisoned intermediates.Density functional theory(DFT)simulations further indicate that formation of the PtBi intermetallic phase with the downshift of the Pt d-band center endows 3D Pt49.4Bi50.6 HASL intermetallics with significantly attenuated COads and enhanced OHads adsorption,bringing about the boosting electrocatalytic property.The mass activity of the 3D Pt49.4Bi50.6 HASL intermetallics for ethylene glycol oxidation reaction is as high as 24.67 A·mgPt^(−1),which is 12.98 times higher than that of commercial Pt/C(1.90 A·mgPt^(−1)).This work may inspire the design of Pt-based intermetallics as high-efficiency anode electrocatalysts for fuel cell applications.展开更多
Delicately designed metal–organic framework(MOF)-derived nanostructured electrocatalysts are essential for improving the reaction kinetics of the oxygen evolution reaction and tuning the selectivity of small organic ...Delicately designed metal–organic framework(MOF)-derived nanostructured electrocatalysts are essential for improving the reaction kinetics of the oxygen evolution reaction and tuning the selectivity of small organic molecule oxidation reactions.Herein,novel oxalate-modified hollow CoFe-based layered double hydroxide nanocages(h-CoFe-LDH NCs)and yolk–shell ZIF@CoFe-LDH nanocages(ys-ZIF@CoFe-LDH NCs)are developed through an etching–doping reconstruction strategy from a Co-based MOF precursor(ZIF-67).The distinctive nanostructures,along with the incorporation of the secondary metal element and intercalated oxalate groups,enable h-CoFe-LDH NCs and ys-ZIF@CoFe-LDH NCs to expose more active sites with high intrinsic activity.The resultant h-CoFe-LDH NCs exhibit outstanding OER activity with an overpotential of only 278 mV to deliver a current density of 50 mA cm^(-2).Additionally,controlling the reconstruction degree enables the formation of ys-ZIF@CoFe-LDH NCs with a yolk–shell nanocage nanostructure,which show outstanding electrocatalytic performance for the selective ethylene glycol oxidation reaction(EGOR)toward formate,with a Faradaic efficiency of up to 91%.Consequently,a hybrid water electrolysis system integrating the EGOR and the hydrogen evolution reaction using Pt/C||ys-ZIF@CoFe-LDH NCs is explored for energy-saving hydrogen production,requiring a cell voltage 127 mV lower than water electrolysis to achieve a current density of 50 mA cm^(-2).This work demonstrates a feasible way to design advanced MOF-derived electrocatalysts toward enhanced electrocatalytic reactions.展开更多
The global annual production of poly(ethylene terephthalate)(PET)has reached 82 million tons,yet only a small fraction(less than 20%)is recycled.The ultra-slow degradation rate of PET results in the accumulation of PE...The global annual production of poly(ethylene terephthalate)(PET)has reached 82 million tons,yet only a small fraction(less than 20%)is recycled.The ultra-slow degradation rate of PET results in the accumulation of PET waste in the environment,causing serious plastic pollution and posing severe challenges to ecosystems.In response,great efforts have been directed toward developing a cascade degradation and electrocatalytic upcycling strategy,which serves as a“waste-towealth”pathway.This strategy involves electro-reforming PEThydrolyzed intermediates or using PET pyrolyzed products as electrocatalysts to generate high-value products.This review provides an overview of the state-of-the-art strategies for the“degradation-electrocatalytic upcycling(De-eUp)”of PET waste.Initially,an introduction to the strategy is provided,categorizing it into two main frameworks:“pyrolysis-electrocatalytic upcycling”and“hydrolysis-electrocatalytic upcycling”.The section on“pyrolysis-electrocatalytic upcycling”delves into the degradation methods for designing derived carbon nanomaterials and their utilization as high-performance electrocatalysts.The“hydrolysis-electrocatalytic upcycling”section discusses recent advancements in electro-reforming of PET hydrolyzed intermediates for the production of C_(1) and C_(2) products.The review concludes by examining the challenges and future prospects in developing an efficient and economical PET upcycling strategy.It is anticipated that this review will stimulate further progress in plastic waste valorization.展开更多
Electrocatalytic water splitting provides a potentially sustainable approach for hydrogen production,but is typically restrained by kinetically slow anodic oxygen evolution reaction(OER)which is of lesser value.Here,f...Electrocatalytic water splitting provides a potentially sustainable approach for hydrogen production,but is typically restrained by kinetically slow anodic oxygen evolution reaction(OER)which is of lesser value.Here,free-standing,hetero-structured Ni_(3)N-Ni_(0.2)Mo_(0.8)N nanowire arrays are prepared on carbon cloth(CC)electrodes for hydrogen evolution reaction(HER)and glycerol oxidation reaction(GOR)to formate with a remarkably high Faradaic efficiency of 96%.A two-electrode electrolyzer for GOR-assisted hydrogen production operates with a current density of 10 mA cm^(-2)at an applied cell voltage of 1.40 V,220 mV lower than for alkaline water splitting.In-situ Raman measurements identify Ni(Ⅲ)as the active form of the catalyst for GOR rather than Ni(IV)and in-situ Fourier transform infrared(FTIR)spectroscopy measurements reveal pathways for GOR to formate.From density functional theory(DFT)calculations,the Ni_(3)N-Ni_(0.2)Mo_(0.8)N heterostructure is beneficial for optimizing adsorption energies of reagents and intermediates and for promoting HER and GOR activities by charge redistribution across the heterointerface.The same electrode also catalyzes conversion of ethylene glycol from polyethylene terephthalate(PET)plastic hydrolysate into formate.The combined results show that electrolytic H_(2) and formate production from alkaline glycerol and ethylene glycol solutions provide a promising strategy as a cost-effective energy supply.展开更多
We describe here an electro-reforming strategy to upcycle polyethylene terephthalate(PET)waste with simultaneous hydrogen production by a bifunctional nickel-cobalt nitride nanosheets electrocatalyst.PET plastics are ...We describe here an electro-reforming strategy to upcycle polyethylene terephthalate(PET)waste with simultaneous hydrogen production by a bifunctional nickel-cobalt nitride nanosheets electrocatalyst.PET plastics are digested in alkaline solution giving an electrochemically active monomer ethylene glycol(EG).The introduction of Co in Co-Ni3N/carbon cloth(CC)promotes the redox behavior of Ni2+/Ni3+,which is beneficial for EG oxidation at an ultra-low potential(1.15 V vs.reversible hydrogen electrode(RHE))and breaks through the limitation of high catalytic potentials of simple Ni-based electrocatalysts(1.30 V).In PET hydrolysate with Co-Ni3N/CC couples,an integrated EG oxidation-hydrogen production system achieves a current density of 50 mA·cm^(−2)at a cell voltage of 1.46 V,which is 370 mV lower than the conventional water splitting.The in-situ Raman and Fourier transform infrared(FTIR)spectroscopies and density functional theory(DFT)calculations identify the catalytic mechanism and point to advantages of heterostructure engineering in optimizing adsorption energies and promoting catalytic activities for EG oxidation.展开更多
基金the financial support of the Hubei Key Laboratory for Processing and Application of Catalytic Materials(202440704)the National Natural Science Foundation of China(22102125)The financial support of the Open Research Fund(2024JYBKF06)of Key Laboratory of Material Chemistry for Energy Conversion and Storage,Ministry of Education is also acknowledged.
文摘Ethylene glycol oxidation reaction(EGOR)is important to address the environmental issues caused by the increased production of polyethylene terephthalate(PET).Metal organic frameworks(MOFs)with superior stability,high specific surface area and excellent catalytic performance can convert PET into valuable products through EGOR and hydrogen evolution reaction(HER).Herein,a microbial template strategy was adopted to prepare carbon sphere-supported orthogonal nanosheet bimetallic MOF catalysts.The prepared catalyst needs only 1.42 V,307 mV,and 1.83 V at a current density of 100 mA cm^(-2) for EGOR,HER,and EGOR//HER,respectively.More importantly,it can stably perform for at least 160 h at a current density of 500 mA cm^(-2).The high specific surface area of bimetallic MOF and the synergistic effect of yeast carbon shell increase the contact area between the intrinsic active sites and*OH and EG,thus improving the EGOR and HER catalytic activity and stability.This work provides a novel strategy to construct bimetallic orthogonal electrocatalysts with efficient HER//EGOR performance,which is of great significance for achieving sustainable energy conversion and environmental purification.
基金supported by Zhejiang Provincial Natural Science Foundation of China(No.LTGS23B030002)the National Natural Science Foundation of China(Nos.21978111 and 22278175)。
文摘Traditional photo-electcatalyst structures of small noble metal nanoparticles assembling into large-scale photoactive semiconductors still suffer from agglomeration of noble metal nanoparticles,insufficient charge transfer,undesirable photoresponse ability that restricted the photo-electrocatalytic performance.To this end,a novel design strategy is proposed in this work,namely integrating small-scale photoactive materials(doped graphene quantum dots,S,N-GQDs)with large-sized noble metal(Pd P)nanoflowers to form novel photo-electrocatalysts for high-efficient alcohol oxidation reaction.As expected,superior electrocatalytic performance of Pd P/S,N-GQDs for ethylene glycol oxidation is acquired,thanks to the nanoflower structure with larger specific surface area and abundant active sites.Furthermore,nonmetal P are demonstrated,especially optimizing the adsorption strength,enhancing the interfacial contact,reducing metal agglomeration,ensuring uniform and efficient doping of S,N-GQDs,and ultimately significantly boost the catalytic activity of photo-electrocatalysts.
文摘Ethylene glycol(EG)is a biomass derivative of polyethylene terephthalate(PET),and its electrocatalytic conversion into high-value chemicals has sparked widespread interest.This study reviews the most recent research development in electrocatalysis-based EG to glycolic acid(GA)conversion.Firstly,the strategies and research results of modulating the electronic structure of catalysts for efficient selective GA production from EG are reviewed.Second,by reviewing the data of in-situ Fourier transform infrared spectroscopy and in-situ electrochemically attenuated total reflection surface enhanced infrared absorption spectroscopy,the reaction pathway and catalytic mechanism of EG partial oxidation to GA were clarified.Finally,the design and regulation of catalysts for selective oxidation of EG by electrocatalysis in the future are prospected.
基金financially supported by the Key Laboratory of Organic Functional Molecule Synthesis and Applications,Ministry of Education(No.KLSAOFM1913)。
文摘For future clean energy demand,it is essential to develop highly efficient and durable materials for use in renewable energy conversion devices.Herein,we report an electrocatalyst loaded with Pd-Pb-Bi nanoalloys on reduced graphene(rGO)-wrapped In_(2)O_(3)(PdPbBi@rGO/In_(2)O_(3))prepared by a hydrothermal method.PdPbBi@rGO/In_(2)O_(3)exhibits higher forward current density(229.12 mA·cm^(-2)),larger electrochemical active surface area(ECSA)(85.87 m^(2)·g^(-1)Pd),smaller impedance(12.68Ω)and lower E_(onset)(-0.56 V)than commercial Pd/C.Specifically,the current density and ECS A are 8.46 and3.38 times higher than those of commercial Pd/C(27.07 mA·cm^(-2),25.41 m^(2)·g^(-1)Pd),respectively.Furthermore,the oxidation mechanism of ethylene glycol and the removal of carbon monoxide[CO]_(ads)from the surface of Pd are also discussed in detail.The columnar support structure wrapped by rGO provides a huge active surface area for catalysis.Moreover,the electronic effect of Pd-PbBi nanoalloys can accelerate the removal of CO intermediate species,obtain more Pd active sites and improve the electrocatalytic performance.Our first synthesis of this highly electrocatalyst offers promising value for commercial application in direct fuel cells.
基金supported by the National Natural Science Foundation of China(22379111 and 22179093)。
文摘Hydrogen peroxide(H_(2)O_(2))electrosynthesis via two-electron oxygen reduction reaction(2e-ORR)is a promising alternative for the energy-intensive anthraquinone process.However,the instability of the catalytic metal sites in the state-of-the-art metal single-atom catalysts(M-SACs)hinders their further industrial applications,and the high potential and valueless oxygen product of the conventional anodic oxygen evolution reaction(OER)further limit the economic efficiency of this technology.To address this,a dynamically local structure reconstruction strategy is proposed to in situ transfer the active sites from unstable metal sites to the stable surrounding carbon sites for efficient and durable 2e^(-)ORR electrocatalysis.For the as-designed Mn-N_(3)O-C catalyst,by reconstructing Mn sites into Mn(^(*)OH),the Mn sites were passivated and carbon sites adjacent to the O atom were verified to be the actual active sites by in situ characterization and theoretical calculation.Consequently,Mn-N_(3)O-C exhibited>80%Faradaic efficiency and superior long-term durability over 100 h for H_(2)O_(2)electrosynthesis at~120 mA cm^(-2).In addition,coupling anodic ethylene glycol oxidation reaction(EGOR)further improves the efficiency and economic viability of the H_(2)O_(2)electrosynthesis system.This two-pronged strategy thus opens up a new opportunity for the development of stable H_(2)O_(2)electrosynthesis with low energy consumption and superior economic performance.
基金Funded by the National Basic Research Program of China (No. 2009CB220100)the Beijing Excellent Talent Support Program (No. 20071D1600300396)
文摘Pt-WO3 nanoparticles uniformly dispersed on Vulcan XC-72R carbon black were prepared by an ethylene glycol method.The morphology,composition,nanostructure,electrochemical characteristics and electrocatalytic activity were characterized,and the formation mechanism was investigated.The average particle size was 2.3 nm,the same as that of Pt/C catalyst.The W/Pt atomic ratio was 1/20,much lower than the design of 1/3.The deposition of WO3·xH2O nanoparticles on Vulcan XC-72R carbon black was found to be very difficult by TEM.From XPS and XRD,the Pt nanoparticles were formed in the colloidal solution of Na2WO4,the EG insoluble Na2WO4 resulted in the decreased relative crystallinity and increased crystalline lattice constant compared with those of Pt/C catalyst and,subsequently,the higher specific electrocatalytic activity as determined by CV.The Pt-mass and Pt-electrochemically-active-specific-surface-area based anodic peak current densities for ethanol oxidation were 422.2 mA·mg-1Pt and 0.43 mA·cm-2Pt,1.2 and 1.1 times higher than those of Pt/C catalyst,respectively.
基金financially supported by the National Natural Science Foundation of China(Nos.22279124 and 52261145700)the Natural Science Foundation of Shandong Province(No.ZR2020ZD10)the Fundamental Research Funds for the Central Universities(No.202262010).
文摘The electrochemical upcycling of polyethylene terephthalate(PET)into high-value products,alongside hydrogen production under ambient conditions,represents a promising approach to sustainable waste management.However,the mechanism underlying efficient PET-derived ethylene glycol oxidation reactions(EGOR),driven by the enhanced adsorption of key intermediates,remains unclear.In this work,built-in electric fields(BIEF)were deliberately engineered within the heterojunction Ni(OH)_(2)-Ni_(3)S_(2)/NF catalyst,effectively elevating the d-band center and thereby enhancing the adsorption of EG and hydroxyl(*OH)species.This modification significantly accelerates reaction kinetics compared to Ni3S2/NF.Remarkably,the Ni(OH)_(2)-Ni_(3)S_(2)/NF catalyst achieves an industrial current density of 616.0 mA·cm^(-2) at 1.50 V vs.reversible hydrogen electrode(RHE),exhibiting a Faradaic efficiency(FE)of 89%for formate(FA)at 1.45 V vs.RHE.In situ electrochemical infrared absorption spectroscopy(IRAS)and theoretical calculations reveal that FA was primarily generated through C-C bond cleavage in glycolic acid.This study also elucidates the critical relationship between BIEF and d-band center,offering a viable strategy to enhance intermediate adsorption during the EGOR process.
基金the financial support from the National Key Research and Development Program of China(2019YFE0123400 and 2022YFE0114800)the Excellent Young Scholar Fund from the National Natural Science Foundation of China (22122903)+4 种基金the Tianjin Distinguished Young Scholar Fund (20JCJQJC00260)the Major Science and Technology Project of Anhui Province(202203f07020007)Anhui Conch Group Co.,Ltd.the financial support from the National Natural Science Foundation of China (22309089)the project funded by China Postdoctoral Science Foundation (2023M731800)。
文摘Co-electrolysis of waste plastics and carbon dioxide(CO_(2)) into value-added chemicals or fuels is a promising pathway for a sustainable society, but efficient and selective conversion remains a challenge. Herein, a gold-mediated nickel hydroxide(Au/Ni(OH)_(2)) is developed to oxidize waste plastic-derived ethylene glycol(EG) into formate. In-situ electrochemical experiments and theoretical results reveal that the introduction of Au favors the redox properties and EG adsorption behavior of Ni(OH)_(2). The Au/Ni(OH)_(2) catalyst shows an excellent formate selectivity of >90% at high current densities of above 100 m A cm^(-2). When coupled with sputtered bismuth(Bi) cathode for CO_(2) reduction, a high formate Faradic efficiency(FE) of 188.2% at 200 m A cm^(-2)and a good formate productivity of 7.33 mmol m^(-2)s^(-1)at 10 A are obtained in a flow cell and a zero-gap membrane electrode assembly(MEA) cell, respectively. This work demonstrates a promising strategy to convert waste plastics and CO_(2) into valuable products.
基金the Natural Science Foundation of Anhui Province(Nos.2108085MB55 and 2208085MB24)the National Natural Science Foundation of China(Nos.21571001,21706048,and 21701001)the Natural Science Research Project of Anhui Province(Nos.KJ2021A0004 and KJ2020ZD04).
文摘The synthesis of atomically ordered Pt-based intermetallic electrocatalysts for the direct alcohol fuel cells generally requires the addition of surfactants or the high-temperature annealing.However,some residual surfactants on the surface of the assynthesized catalysts would prevent the exposure of catalytic active sites,the high-temperature annealing process is easy to accelerate the sintering of the metal,which both lead to the decline of electrocatalytic performance.Herein,we construct the atomically ordered bimetallic PtBi intermetallics with clean surfaces and unique three-dimensional hollow acorn-shell-like structure(3D PtBi HASL)by a simple,low-temperature,surfactant-free one-pot synthetic approach.Benefiting from the special hollow structures,the obtained 3D PtBi HASL intermetallics expose abundant accessible active sites.Moreover,the introduction of oxophilic metal Bi can enhance adsorption of OHads,thereby significantly facilitating removal of poisoned intermediates.Density functional theory(DFT)simulations further indicate that formation of the PtBi intermetallic phase with the downshift of the Pt d-band center endows 3D Pt49.4Bi50.6 HASL intermetallics with significantly attenuated COads and enhanced OHads adsorption,bringing about the boosting electrocatalytic property.The mass activity of the 3D Pt49.4Bi50.6 HASL intermetallics for ethylene glycol oxidation reaction is as high as 24.67 A·mgPt^(−1),which is 12.98 times higher than that of commercial Pt/C(1.90 A·mgPt^(−1)).This work may inspire the design of Pt-based intermetallics as high-efficiency anode electrocatalysts for fuel cell applications.
基金financial support of the National Natural Science Foundation of China(21901246,22105203 and 22205235)the Natural Science Foundation of Fujian Province(2020J01116 and 2021J06033)+1 种基金support under the Australian Research Council's Discovery Projects funding scheme(DP220103458)Future Fellowship(FT190100658).
文摘Delicately designed metal–organic framework(MOF)-derived nanostructured electrocatalysts are essential for improving the reaction kinetics of the oxygen evolution reaction and tuning the selectivity of small organic molecule oxidation reactions.Herein,novel oxalate-modified hollow CoFe-based layered double hydroxide nanocages(h-CoFe-LDH NCs)and yolk–shell ZIF@CoFe-LDH nanocages(ys-ZIF@CoFe-LDH NCs)are developed through an etching–doping reconstruction strategy from a Co-based MOF precursor(ZIF-67).The distinctive nanostructures,along with the incorporation of the secondary metal element and intercalated oxalate groups,enable h-CoFe-LDH NCs and ys-ZIF@CoFe-LDH NCs to expose more active sites with high intrinsic activity.The resultant h-CoFe-LDH NCs exhibit outstanding OER activity with an overpotential of only 278 mV to deliver a current density of 50 mA cm^(-2).Additionally,controlling the reconstruction degree enables the formation of ys-ZIF@CoFe-LDH NCs with a yolk–shell nanocage nanostructure,which show outstanding electrocatalytic performance for the selective ethylene glycol oxidation reaction(EGOR)toward formate,with a Faradaic efficiency of up to 91%.Consequently,a hybrid water electrolysis system integrating the EGOR and the hydrogen evolution reaction using Pt/C||ys-ZIF@CoFe-LDH NCs is explored for energy-saving hydrogen production,requiring a cell voltage 127 mV lower than water electrolysis to achieve a current density of 50 mA cm^(-2).This work demonstrates a feasible way to design advanced MOF-derived electrocatalysts toward enhanced electrocatalytic reactions.
基金support of the National key research and development program(No.2023YFB250400)the National Natural Science Foundation of China(No.52271222)+2 种基金the Science and Technology Commission of Shanghai Municipal(Nos.23DZ1202500 and 21010503100)the Shanghai Young Outstanding Academic Leaders Plan(Overseas)the Shanghai Pujiang Program(No.23PJ1409300).
文摘The global annual production of poly(ethylene terephthalate)(PET)has reached 82 million tons,yet only a small fraction(less than 20%)is recycled.The ultra-slow degradation rate of PET results in the accumulation of PET waste in the environment,causing serious plastic pollution and posing severe challenges to ecosystems.In response,great efforts have been directed toward developing a cascade degradation and electrocatalytic upcycling strategy,which serves as a“waste-towealth”pathway.This strategy involves electro-reforming PEThydrolyzed intermediates or using PET pyrolyzed products as electrocatalysts to generate high-value products.This review provides an overview of the state-of-the-art strategies for the“degradation-electrocatalytic upcycling(De-eUp)”of PET waste.Initially,an introduction to the strategy is provided,categorizing it into two main frameworks:“pyrolysis-electrocatalytic upcycling”and“hydrolysis-electrocatalytic upcycling”.The section on“pyrolysis-electrocatalytic upcycling”delves into the degradation methods for designing derived carbon nanomaterials and their utilization as high-performance electrocatalysts.The“hydrolysis-electrocatalytic upcycling”section discusses recent advancements in electro-reforming of PET hydrolyzed intermediates for the production of C_(1) and C_(2) products.The review concludes by examining the challenges and future prospects in developing an efficient and economical PET upcycling strategy.It is anticipated that this review will stimulate further progress in plastic waste valorization.
基金supported by the National Natural Science Foundation of China(22072107,21872105)the Science&Technology Commission of Shanghai Municipality(19DZ2271500)the Fundamental Research Funds for the Central Universities。
文摘Electrocatalytic water splitting provides a potentially sustainable approach for hydrogen production,but is typically restrained by kinetically slow anodic oxygen evolution reaction(OER)which is of lesser value.Here,free-standing,hetero-structured Ni_(3)N-Ni_(0.2)Mo_(0.8)N nanowire arrays are prepared on carbon cloth(CC)electrodes for hydrogen evolution reaction(HER)and glycerol oxidation reaction(GOR)to formate with a remarkably high Faradaic efficiency of 96%.A two-electrode electrolyzer for GOR-assisted hydrogen production operates with a current density of 10 mA cm^(-2)at an applied cell voltage of 1.40 V,220 mV lower than for alkaline water splitting.In-situ Raman measurements identify Ni(Ⅲ)as the active form of the catalyst for GOR rather than Ni(IV)and in-situ Fourier transform infrared(FTIR)spectroscopy measurements reveal pathways for GOR to formate.From density functional theory(DFT)calculations,the Ni_(3)N-Ni_(0.2)Mo_(0.8)N heterostructure is beneficial for optimizing adsorption energies of reagents and intermediates and for promoting HER and GOR activities by charge redistribution across the heterointerface.The same electrode also catalyzes conversion of ethylene glycol from polyethylene terephthalate(PET)plastic hydrolysate into formate.The combined results show that electrolytic H_(2) and formate production from alkaline glycerol and ethylene glycol solutions provide a promising strategy as a cost-effective energy supply.
基金supported by the National Natural Science Foundation of China(Nos.22072107 and 21872105)the Science&Technology Commission of Shanghai Municipality(No.19DZ2271500)the Fundamental Research Funds for the Central Universities.
文摘We describe here an electro-reforming strategy to upcycle polyethylene terephthalate(PET)waste with simultaneous hydrogen production by a bifunctional nickel-cobalt nitride nanosheets electrocatalyst.PET plastics are digested in alkaline solution giving an electrochemically active monomer ethylene glycol(EG).The introduction of Co in Co-Ni3N/carbon cloth(CC)promotes the redox behavior of Ni2+/Ni3+,which is beneficial for EG oxidation at an ultra-low potential(1.15 V vs.reversible hydrogen electrode(RHE))and breaks through the limitation of high catalytic potentials of simple Ni-based electrocatalysts(1.30 V).In PET hydrolysate with Co-Ni3N/CC couples,an integrated EG oxidation-hydrogen production system achieves a current density of 50 mA·cm^(−2)at a cell voltage of 1.46 V,which is 370 mV lower than the conventional water splitting.The in-situ Raman and Fourier transform infrared(FTIR)spectroscopies and density functional theory(DFT)calculations identify the catalytic mechanism and point to advantages of heterostructure engineering in optimizing adsorption energies and promoting catalytic activities for EG oxidation.
