Design of electrochemical active boron(B)site at solid materials to understand the relationships between the localized structure,charge state at the B site and electrocatalytic activity plays a crucial role in boostin...Design of electrochemical active boron(B)site at solid materials to understand the relationships between the localized structure,charge state at the B site and electrocatalytic activity plays a crucial role in boosting the green electrochemical synthesis of hydrogen peroxide(H_(2)O_(2))via two-electron oxygen reduction(2eORR)pathway.Herein,we demonstrate a carbon(C)and nitrogen(N)localized bonding microenvironment to modulate the charge state of B site at the boron-carbon nitride solid(BCNs)to realize the efficient selective electrocatalytic H_(2)O_(2)production.The localized chemical structure of N-B-N,N-B-C and C-B-C bonds at B site can be regulated through solid-state reaction between boron nitride(BN)and porous carbon(C)at variable temperatures.The optimized BCN-1100 achieves an outstanding H_(2)O_(2)selectivity of 89%and electron transfer number of 2.2(at 0.55 V vs.RHE),with the production of 10.55mmol/L during 2.5 h and the catalytic stability duration for 15000 cycles.Further first-principles calculations identified the dependency of localized bonding microenvironment on the OOH~*adsorption energies and relevant charge states at the boron site.The localized structure of B site with BNC_(2)-Gr configuration is predicted to be the highest 2eORR activity.展开更多
In this work,Eu^(3+)doped SrTiO_(3)powders were synthesized by sol-gel method and the influences of Eu^(3+)dopants on the crystalline structure,micro structure mo rphology,electronic band-gap and photocatalytic perfor...In this work,Eu^(3+)doped SrTiO_(3)powders were synthesized by sol-gel method and the influences of Eu^(3+)dopants on the crystalline structure,micro structure mo rphology,electronic band-gap and photocatalytic performance for degradation of o rganic pollutant were investigated in detail.Research results reveal that the incorporated Eu^(3+)ions in SrTiO_(3)lattice are preferable to substitute the Sr^(2+)-Ti^(4+)ions pair by two Eu^(3+)ions.The presence of Eu^(3+)ions plays a significant role for the microstructure morphology of the S rTiO_(3)powders,leading to the formation of smaller size nanoparticles with a higher specific surface area.The light absorption capability of the resulting materials is improved owing to the narrowing of the band-gap induced by Eu^(3+)dopants.As a result,the enhanced photocatalytic activity application for photodegradation of Rhodamine B solution is demonstrated for the SrTiO_(3)powders doped with Eu^(3+)ions.展开更多
基金financially supported by the National Natural Science Foundation of China(Nos.22161036,11904187,21961024 and 21961025)Natural Science Foundation of Inner Mongolia(Nos.2018JQ05 and 2019BS02007)+2 种基金Incentive Funding from Nano Innovation Institute(NII)of Inner Mongolia Minzu Universitythe Inner Mongolia Autonomous Region Funding Project for Science&Technology Achievement Transformation(Nos.CGZH2018156 and 2019GG261)Doctoral Scientific Research Foundation of Inner Mongolia Minzu University(Nos.BS437 and BS480)。
文摘Design of electrochemical active boron(B)site at solid materials to understand the relationships between the localized structure,charge state at the B site and electrocatalytic activity plays a crucial role in boosting the green electrochemical synthesis of hydrogen peroxide(H_(2)O_(2))via two-electron oxygen reduction(2eORR)pathway.Herein,we demonstrate a carbon(C)and nitrogen(N)localized bonding microenvironment to modulate the charge state of B site at the boron-carbon nitride solid(BCNs)to realize the efficient selective electrocatalytic H_(2)O_(2)production.The localized chemical structure of N-B-N,N-B-C and C-B-C bonds at B site can be regulated through solid-state reaction between boron nitride(BN)and porous carbon(C)at variable temperatures.The optimized BCN-1100 achieves an outstanding H_(2)O_(2)selectivity of 89%and electron transfer number of 2.2(at 0.55 V vs.RHE),with the production of 10.55mmol/L during 2.5 h and the catalytic stability duration for 15000 cycles.Further first-principles calculations identified the dependency of localized bonding microenvironment on the OOH~*adsorption energies and relevant charge states at the boron site.The localized structure of B site with BNC_(2)-Gr configuration is predicted to be the highest 2eORR activity.
基金Project supported by the National Natural Science Foundation of China(51777138)Natural Science Foundation of Tianjin City(18JCZDJC99700,18JCYBJC87400,18JCQNJC73900)Scientific Developing Foundation of Tianjin Education Commission(2018KJ130)。
文摘In this work,Eu^(3+)doped SrTiO_(3)powders were synthesized by sol-gel method and the influences of Eu^(3+)dopants on the crystalline structure,micro structure mo rphology,electronic band-gap and photocatalytic performance for degradation of o rganic pollutant were investigated in detail.Research results reveal that the incorporated Eu^(3+)ions in SrTiO_(3)lattice are preferable to substitute the Sr^(2+)-Ti^(4+)ions pair by two Eu^(3+)ions.The presence of Eu^(3+)ions plays a significant role for the microstructure morphology of the S rTiO_(3)powders,leading to the formation of smaller size nanoparticles with a higher specific surface area.The light absorption capability of the resulting materials is improved owing to the narrowing of the band-gap induced by Eu^(3+)dopants.As a result,the enhanced photocatalytic activity application for photodegradation of Rhodamine B solution is demonstrated for the SrTiO_(3)powders doped with Eu^(3+)ions.