Electrocatalysts with high activity and long-term durability are vital toward large-scale hydrogen pro-duction from electrocatalytic water splitting.Here,the self-supported electrode(FeO_(χ)H_(y)@Ni_(3)B/NF)with hier...Electrocatalysts with high activity and long-term durability are vital toward large-scale hydrogen pro-duction from electrocatalytic water splitting.Here,the self-supported electrode(FeO_(χ)H_(y)@Ni_(3)B/NF)with hierarchical heterostructure was simply prepared by using Ni_(3)B chunks grown on nickel foam as sub-strate to in situ form vertical FeO_(χ)H_(y)nanosheets.Such hybrid shows efficient oxygen evolution reaction activity with overpotentials as low as 267 and 249 mV at 100 mA cm^(-2)in 1 M KOH solution and 30 wt%KOH solution,respectively.Meanwhile,it also exhibits excellent catalytic stability,sustaining catalysis at 500 mA cm^(-2)in 1 M KOH solution for 200 h,and even for 200 h at 1000 mA cm^(-2)in 30 wt%KOH solution.Further experimental results reveal that the FeO_(χ)H_(y)@Ni_(3)B/NF is endowed with superhydrophilic and superaerophobic surface properties,which not only provide more mass transport channels,as well as facilitated the diffusion of reaction intermediates and gas bubbles.Also,it holds faster reaction kinetics,more accessible active sites and accelerated electron transfer rates due to strong synergistic interactions attheheterogeneous interface.展开更多
Atom-level modulation of the coordination environment for single-atom catalysts(SACs)is considered as an effective strategy for elevating the catalytic performance.For the MNxsite,breaking the symmetrical geometry and...Atom-level modulation of the coordination environment for single-atom catalysts(SACs)is considered as an effective strategy for elevating the catalytic performance.For the MNxsite,breaking the symmetrical geometry and charge distribution by introducing relatively weak electronegative atoms into the first/second shell is an efficient way,but it remains challenging for elucidating the underlying mechanism of interaction.Herein,a practical strategy was reported to rationally design single cobalt atoms coordinated with both phosphorus and nitrogen atoms in a hierarchically porous carbon derived from metal-organic frameworks.X-ray absorption spectrum reveals that atomically dispersed Co sites are coordinated with four N atoms in the first shell and varying numbers of P atoms in the second shell(denoted as Co-N/P-C).The prepared catalyst exhibits excellent oxygen reduction reaction(ORR)activity as well as zinc-air battery performance.The introduction of P atoms in the Co-SACs weakens the interaction between Co and N,significantly promoting the adsorption process of ^(*)OOH,resulting in the acceleration of reaction kinetics and reduction of thermodynamic barrier,responsible for the increased intrinsic activity.Our discovery provides insights into an ultimate design of single-atom catalysts with adjustable electrocatalytic activities for efficient electrochemical energy conversion.展开更多
The poor stability of non-noble metal catalysts in oxygen reduction reaction(ORR) is a main bottleneck that limits their big-scale application in metal-air batteries. Herein, we construct a chainmail catalyst(Co-NC-AD...The poor stability of non-noble metal catalysts in oxygen reduction reaction(ORR) is a main bottleneck that limits their big-scale application in metal-air batteries. Herein, we construct a chainmail catalyst(Co-NC-AD) with outstanding stability, via the competitive complexation and post absorption strategy,consisting of highly graphitic layers wrapped uniform-size Co nanoparticles(Co-NPs). Experiments combined with density functional theory(DFT) calculations jointly confirmed that the electron transfer occurred from the inner Co-NPs to the external graphitic layers. It facilitated the adsorption process of oxygen molecules and the hybridization of the O-2 p and C-1 p orbitals, which accelerated the ORR reaction kinetics. Consequently, our prepared Co-NC-AD shows excellent ORR activity, offered with a more positive initial potential(E_(onset)= 0.95 V) and half-wave potential(E_(1/2)= 0.86 V). The remarkable stability and resistance of methanol poisoning are merited from the protection effect of stable graphitic layers. In addition, the high electrochemical performance of Co-NC-AD-based zinc-air battery demonstrates their potential for practical applications. Therefore, our work provides new ideas for the design of nanoconfined catalysts with high stability and activity.展开更多
Oxygen evolution reaction(OER)is a bottleneck half-reaction in many important energy conversion processes(e.g.,water splitting),and one of the key issues lies to develop high-efficiency,cost-effective OER electrocatal...Oxygen evolution reaction(OER)is a bottleneck half-reaction in many important energy conversion processes(e.g.,water splitting),and one of the key issues lies to develop high-efficiency,cost-effective OER electrocatalysts.Rather than those popular extrinsic modulations of any catalysts with gradually degraded performance,we aim at the utilization of the intermediates offered from the undergoing OER as long-standing electrocatalysts.Herein,by inverted design,we extracted the bimetallic borides(FeCoB_(2))-derived intermediates metal borates in the OER,unlocking their potential as a selffunctionalized highly active catalytic phase in-situ formed on the metal boride surface for continuing OER operation.Mechanistically,the surface metal atoms are oxidized to oxyhydroxides,and the surface metalloids(B)are further transformed to the corresponding oxoanions to form metal borates.Such OER self-produced electrocatalyst exhibits a small overpotential of 295 mV at 10 mA/cm2 and its high catalytic activity lasts even after 200 h.Compared with FeCoB_(2),the catalytic activity of this electrochemically activated FeCoB_(2) is~7 times higher.The in-situ formed metal borate is dominatingly responsible for the obtained high catalytic activity.Such unique OER-produced self-functionalization surfaces of metal borates afford to greatly reduce the energy barrier of the continuing OER,thereby accelerating the reaction process.展开更多
基金supported by the National Natural Science Foundation of China (12234018,52101256,51872115)
文摘Electrocatalysts with high activity and long-term durability are vital toward large-scale hydrogen pro-duction from electrocatalytic water splitting.Here,the self-supported electrode(FeO_(χ)H_(y)@Ni_(3)B/NF)with hierarchical heterostructure was simply prepared by using Ni_(3)B chunks grown on nickel foam as sub-strate to in situ form vertical FeO_(χ)H_(y)nanosheets.Such hybrid shows efficient oxygen evolution reaction activity with overpotentials as low as 267 and 249 mV at 100 mA cm^(-2)in 1 M KOH solution and 30 wt%KOH solution,respectively.Meanwhile,it also exhibits excellent catalytic stability,sustaining catalysis at 500 mA cm^(-2)in 1 M KOH solution for 200 h,and even for 200 h at 1000 mA cm^(-2)in 30 wt%KOH solution.Further experimental results reveal that the FeO_(χ)H_(y)@Ni_(3)B/NF is endowed with superhydrophilic and superaerophobic surface properties,which not only provide more mass transport channels,as well as facilitated the diffusion of reaction intermediates and gas bubbles.Also,it holds faster reaction kinetics,more accessible active sites and accelerated electron transfer rates due to strong synergistic interactions attheheterogeneous interface.
基金supported by the National Natural Science Foundation of China(51872115,12234018 and 52101256)Beijing Synchrotron Radiation Facility(BSRF,4B9A)。
文摘Atom-level modulation of the coordination environment for single-atom catalysts(SACs)is considered as an effective strategy for elevating the catalytic performance.For the MNxsite,breaking the symmetrical geometry and charge distribution by introducing relatively weak electronegative atoms into the first/second shell is an efficient way,but it remains challenging for elucidating the underlying mechanism of interaction.Herein,a practical strategy was reported to rationally design single cobalt atoms coordinated with both phosphorus and nitrogen atoms in a hierarchically porous carbon derived from metal-organic frameworks.X-ray absorption spectrum reveals that atomically dispersed Co sites are coordinated with four N atoms in the first shell and varying numbers of P atoms in the second shell(denoted as Co-N/P-C).The prepared catalyst exhibits excellent oxygen reduction reaction(ORR)activity as well as zinc-air battery performance.The introduction of P atoms in the Co-SACs weakens the interaction between Co and N,significantly promoting the adsorption process of ^(*)OOH,resulting in the acceleration of reaction kinetics and reduction of thermodynamic barrier,responsible for the increased intrinsic activity.Our discovery provides insights into an ultimate design of single-atom catalysts with adjustable electrocatalytic activities for efficient electrochemical energy conversion.
基金supported by the National Natural Science Foundation of China(51872115,51932003)the 2020 International Cooperation Project of the Department of Science and Technology of Jilin Province(20200801001GH)+1 种基金the Project supported by State Key Laboratory of Luminescence and Applications(KLA-2020-05)the Project for Self-innovation Capability Construction of Jilin Province Development and Reform Commission(2021C026)。
文摘The poor stability of non-noble metal catalysts in oxygen reduction reaction(ORR) is a main bottleneck that limits their big-scale application in metal-air batteries. Herein, we construct a chainmail catalyst(Co-NC-AD) with outstanding stability, via the competitive complexation and post absorption strategy,consisting of highly graphitic layers wrapped uniform-size Co nanoparticles(Co-NPs). Experiments combined with density functional theory(DFT) calculations jointly confirmed that the electron transfer occurred from the inner Co-NPs to the external graphitic layers. It facilitated the adsorption process of oxygen molecules and the hybridization of the O-2 p and C-1 p orbitals, which accelerated the ORR reaction kinetics. Consequently, our prepared Co-NC-AD shows excellent ORR activity, offered with a more positive initial potential(E_(onset)= 0.95 V) and half-wave potential(E_(1/2)= 0.86 V). The remarkable stability and resistance of methanol poisoning are merited from the protection effect of stable graphitic layers. In addition, the high electrochemical performance of Co-NC-AD-based zinc-air battery demonstrates their potential for practical applications. Therefore, our work provides new ideas for the design of nanoconfined catalysts with high stability and activity.
基金Financially supported by the National Natural Science Foundation of China(51872115,52101256,51932003)China Postdoctoral Science Foundation Project(2020M680043)+1 种基金Science and Technology Research Project of the Department of Education of Jilin Province(JJKH20211083KJ)2020 International Cooperation Project of the Department of Science and Technology of Jilin Province(20200801001GH)。
文摘Oxygen evolution reaction(OER)is a bottleneck half-reaction in many important energy conversion processes(e.g.,water splitting),and one of the key issues lies to develop high-efficiency,cost-effective OER electrocatalysts.Rather than those popular extrinsic modulations of any catalysts with gradually degraded performance,we aim at the utilization of the intermediates offered from the undergoing OER as long-standing electrocatalysts.Herein,by inverted design,we extracted the bimetallic borides(FeCoB_(2))-derived intermediates metal borates in the OER,unlocking their potential as a selffunctionalized highly active catalytic phase in-situ formed on the metal boride surface for continuing OER operation.Mechanistically,the surface metal atoms are oxidized to oxyhydroxides,and the surface metalloids(B)are further transformed to the corresponding oxoanions to form metal borates.Such OER self-produced electrocatalyst exhibits a small overpotential of 295 mV at 10 mA/cm2 and its high catalytic activity lasts even after 200 h.Compared with FeCoB_(2),the catalytic activity of this electrochemically activated FeCoB_(2) is~7 times higher.The in-situ formed metal borate is dominatingly responsible for the obtained high catalytic activity.Such unique OER-produced self-functionalization surfaces of metal borates afford to greatly reduce the energy barrier of the continuing OER,thereby accelerating the reaction process.
