Carbon materials with adjustable porosity,controllable het-eroatom doping and low-cost have been received considerable attention as supercapacitor electrodes.However,using carbon materials with abundant micropores,a h...Carbon materials with adjustable porosity,controllable het-eroatom doping and low-cost have been received considerable attention as supercapacitor electrodes.However,using carbon materials with abundant micropores,a high surface area and a high-dopant content for an aqueous su-percapacitor with a high energy output still remains a challenge.We report the easy synthesis of interconnected carbon spheres by a polymerization re-action between p-benzaldehyde and 2,6-diaminopyridine.The synthesis in-volves adjusting the mass ratio of the copolymer and KOH activator to achieve increased charge storage ability and high energy output,which are attributed to the high ion-accessible area provided by the large number of micropores,high N/O contents and rapid ion diffusion channels in the porous structure.At a PMEC∶KOH mass ratio of 1∶1,the high electrolyte ion-adsorption area(2599.76 m^(2) g^(−1))and the N/O dopant atoms of the conductive framework of a typical carbon electrode produce a superior specific capacity(303.2 F g^(−1)@0.5 A g^(−1))giving an assembled symmetric capacitor a high energy delivery of 11.3 Wh kg^(−1)@250 W kg^(−1).This study presents a simple strategy for synthesizing microporous carbon and highlights its potential use in KOH-based supercapacitors.展开更多
Materials with low thermal conductivity are applied extensively in energy management,and breaking the amorphous limits of thermal conductivity to solids has attracted widespread attention from scientists.Doping is a c...Materials with low thermal conductivity are applied extensively in energy management,and breaking the amorphous limits of thermal conductivity to solids has attracted widespread attention from scientists.Doping is a common strategy for achieving low thermal conductivity that can offer abundant scattering centers in which heavier dopants always result in lower phonon group velocities and lower thermal conductivities.However,the amount of equivalent heavyatom single dopant available is limited.Unfortunately,nonequivalent heavy dopants have finite solubility because of charge imbalance.Here,we propose a charge balance strategy for SnS by substituting Sn2+with Ag^(+)and heavy Bi^(3+),improving the doping limit of Ag from 2%to 3%.Ag and Bi codoping increases the point defect concentration and introduces abundant boundaries simultaneously,scattering the phonons at both the atomic scale and nanoscale.The thermal conductivity of Ag0.03Bi0.03Sn0.94S decreased to 0.535 W·m^(−1)·K^(−1)at room temperature and 0.388 W·m^(−1)·K^(−1)at 275°C,which is below the amorphous limit of 0.450 W·m^(−1)·K^(−1)for SnS.This strategy offers a simple way to enhance the doping limit and achieve ultralow thermal conductivity in solids below the amorphous limit without precise structural modification.展开更多
The 3μm laser emission of Er 3+ ( 4 I 11/2 → 4 I 13/2 )in the YAG crystal is,in principle,selfsaturation transition,the lifetime of the upper laser level( 4 I 11/2 )being smaller than that of the olwer one( 4 I 13/2...The 3μm laser emission of Er 3+ ( 4 I 11/2 → 4 I 13/2 )in the YAG crystal is,in principle,selfsaturation transition,the lifetime of the upper laser level( 4 I 11/2 )being smaller than that of the olwer one( 4 I 13/2 ).The effect of the selfsaturation limit the laser output. In present work,for the first time,we report on the investigation of the utility of Pr 3+ as a sensitizer of Er 3+ ion,using Pr 3+ 4 f 2-4 f5d transition.The radiation emission from 4f5d configuration of Pr 3+ ion have been observed in the YAG∶Pr 3+ crystal.This shows that under suitable conditions this radiant process can compete successfully by non radiative decay to the 4 f configuration.Using Er 3+ Pr 3 codoped YAG it is possible to predict the position of the lowest 4 f 2-4 f5d absorption bands of Pr 3+ ion in the ultraviolet range and to present the occurrence of the energy transfer from Pr 3+ to Er 3+ ion.By xenon flash lamp pumped 2.93μm laser action in the YAG∶(Er 3+ ,Pr 3+ ) crystals was demonstrated at room temperature.展开更多
基金financially supported by University-level key projects of Anhui University of Science and Technology(QNZD2021-04,QNZD2021-07)Scientific Research Foundation for High-level Talents of Anhui University of Science and Technology(2021yjrc22,13210572)+2 种基金Huainan Science and Technology Bureau Plan Project(2023A3111)Open Research Fund Program of Engineering Technology Research Center of Coal Resources Comprehensive Utilization(MTYJZX202204)Natural Science Research Project of Anhui Educational Committee(2023AH051184,2023AH051210)。
文摘Carbon materials with adjustable porosity,controllable het-eroatom doping and low-cost have been received considerable attention as supercapacitor electrodes.However,using carbon materials with abundant micropores,a high surface area and a high-dopant content for an aqueous su-percapacitor with a high energy output still remains a challenge.We report the easy synthesis of interconnected carbon spheres by a polymerization re-action between p-benzaldehyde and 2,6-diaminopyridine.The synthesis in-volves adjusting the mass ratio of the copolymer and KOH activator to achieve increased charge storage ability and high energy output,which are attributed to the high ion-accessible area provided by the large number of micropores,high N/O contents and rapid ion diffusion channels in the porous structure.At a PMEC∶KOH mass ratio of 1∶1,the high electrolyte ion-adsorption area(2599.76 m^(2) g^(−1))and the N/O dopant atoms of the conductive framework of a typical carbon electrode produce a superior specific capacity(303.2 F g^(−1)@0.5 A g^(−1))giving an assembled symmetric capacitor a high energy delivery of 11.3 Wh kg^(−1)@250 W kg^(−1).This study presents a simple strategy for synthesizing microporous carbon and highlights its potential use in KOH-based supercapacitors.
基金supported by the CAS Project for Young Scientists in Basic Research(YSBR-070)the National Natural Science Foundation of China(21925110,21890750,U2032161,12147105)+8 种基金the USTC Research Funds of the Double First-Class Initiative(YD2060002004)the National Key Research and Development Program of China(2022YFA1203600,2022YFA1203601,2022YFA1203602)the Natural Science Foundation of China-Anhui Joint Fund(U23A20121)the Outstanding Youth Foundation of Anhui Province(2208085J14)the Anhui Provincial Key Research and Development Project(202004a050200760)the Key R&D Program of Shandong Province(2021CXGC010302)the Users with Excellence Project of Hefei Science Center CAS(2021HSC-UE004)the Fellowship of the China Postdoctoral Science Foundation(2022M710141)the open foundation of the Key Laboratory of the Engineering Research Center of Building Energy Efficiency Control and Evaluation,Ministry of Education(AHJZNX-2023-04).
文摘Materials with low thermal conductivity are applied extensively in energy management,and breaking the amorphous limits of thermal conductivity to solids has attracted widespread attention from scientists.Doping is a common strategy for achieving low thermal conductivity that can offer abundant scattering centers in which heavier dopants always result in lower phonon group velocities and lower thermal conductivities.However,the amount of equivalent heavyatom single dopant available is limited.Unfortunately,nonequivalent heavy dopants have finite solubility because of charge imbalance.Here,we propose a charge balance strategy for SnS by substituting Sn2+with Ag^(+)and heavy Bi^(3+),improving the doping limit of Ag from 2%to 3%.Ag and Bi codoping increases the point defect concentration and introduces abundant boundaries simultaneously,scattering the phonons at both the atomic scale and nanoscale.The thermal conductivity of Ag0.03Bi0.03Sn0.94S decreased to 0.535 W·m^(−1)·K^(−1)at room temperature and 0.388 W·m^(−1)·K^(−1)at 275°C,which is below the amorphous limit of 0.450 W·m^(−1)·K^(−1)for SnS.This strategy offers a simple way to enhance the doping limit and achieve ultralow thermal conductivity in solids below the amorphous limit without precise structural modification.
文摘The 3μm laser emission of Er 3+ ( 4 I 11/2 → 4 I 13/2 )in the YAG crystal is,in principle,selfsaturation transition,the lifetime of the upper laser level( 4 I 11/2 )being smaller than that of the olwer one( 4 I 13/2 ).The effect of the selfsaturation limit the laser output. In present work,for the first time,we report on the investigation of the utility of Pr 3+ as a sensitizer of Er 3+ ion,using Pr 3+ 4 f 2-4 f5d transition.The radiation emission from 4f5d configuration of Pr 3+ ion have been observed in the YAG∶Pr 3+ crystal.This shows that under suitable conditions this radiant process can compete successfully by non radiative decay to the 4 f configuration.Using Er 3+ Pr 3 codoped YAG it is possible to predict the position of the lowest 4 f 2-4 f5d absorption bands of Pr 3+ ion in the ultraviolet range and to present the occurrence of the energy transfer from Pr 3+ to Er 3+ ion.By xenon flash lamp pumped 2.93μm laser action in the YAG∶(Er 3+ ,Pr 3+ ) crystals was demonstrated at room temperature.
