We report a compact experimental setup for producing a quantum degenerate mixture of Bose23Na and Fermi40K gases. The atoms are collected in dual dark magneto–optical traps(MOT) with species timesharing loading to re...We report a compact experimental setup for producing a quantum degenerate mixture of Bose23Na and Fermi40K gases. The atoms are collected in dual dark magneto–optical traps(MOT) with species timesharing loading to reduce the light-induced loss, and then further cooled using the gray molasses technique on the D2line for23Na and D1line for40K. The microwave evaporation cooling is used to cool23Na in |F = 2, mF= 2〉 in an optically plugged magnetic trap, meanwhile,40K in |F = 9/2, mF= 9/2〉 is sympathetically cooled. Then the mixture is loaded into a large volume optical dipole trap where23Na atoms are immediately transferred to |1, 1〉 for further effective cooling to avoid the strong three-body loss between23Na atoms in |2, 2〉 and40K atoms in |9/2, 9/2〉. At the end of the evaporation in optical trap, a degenerate Fermi gas of40K with 1.9 × 10^(5) atoms at T/TF= 0.5 in the |9/2, 9/2〉 hyperfine state coexists with a Bose–Einstein condensate(BEC) of23Na with 8 × 10^(4) atoms in the |1, 1〉 hyperfine state at 300 n K. We also can produce the two species mixture with the tunable population imbalance by adjusting the 23Na magneto–optical trap loading time.展开更多
The development of low-cost,high-performance catalysts at the atomic scale has become a challenging issue for the large-scale applications of renewable clean energy technologies.Herein,on the basis of density function...The development of low-cost,high-performance catalysts at the atomic scale has become a challenging issue for the large-scale applications of renewable clean energy technologies.Herein,on the basis of density functional theory calculation,we systematically investigate the effect of the local environment on the activity and selectivity of electrochemical carbon dioxide reduction reaction over single/multi-atom alloy clusters formed by the transition metal(Fe,Co,and Ni)-doped Cu13/55 clusters.Our findings reveal that the catalytic performance of multi-atom alloy clusters far exceeds that of Cu(211)surface.Notably,the Co666 configuration exhibits exceptional performance with a remarkably low free energy barrier of just 0.33 eV.Furthermore,our investigations demonstrate that catalytic performance is predominantly determined by the relative proportion of modifying metallic dopant species that generate a coordination number of 6.This ratio principally influences the adsorption strength of key intermediates(HCOO*and H2COO*).Bader charge analyses and free energy calculations elucidate a new mechanistic pathway,wherein the hydrogenation of CO_(2)at C-sites catalyzes the reduction of CO_(2)to CH_(4).This theoretical research provides valuable insights into the fundamental processes and energy landscapes involved in converting CO_(2)to CH_(4)on the studied catalytic structure,potentially paving the way for more efficient and sustainable carbon dioxide utilization strategies.展开更多
基金supported by the Innovation Program for Quantum Science and Technology (Grant No. 2021ZD0302003)the National Key Research and Development Program of China (Grant Nos. 2022YFA1404101, 2018YFA0307601,and 2021YFA1401700)+1 种基金the National Natural Science Foundation of China (Grant Nos. 12034011, 92065108, 11974224, 12022406, and 12004229)the Fund for Shanxi 1331 Project Key Subjects Construction。
文摘We report a compact experimental setup for producing a quantum degenerate mixture of Bose23Na and Fermi40K gases. The atoms are collected in dual dark magneto–optical traps(MOT) with species timesharing loading to reduce the light-induced loss, and then further cooled using the gray molasses technique on the D2line for23Na and D1line for40K. The microwave evaporation cooling is used to cool23Na in |F = 2, mF= 2〉 in an optically plugged magnetic trap, meanwhile,40K in |F = 9/2, mF= 9/2〉 is sympathetically cooled. Then the mixture is loaded into a large volume optical dipole trap where23Na atoms are immediately transferred to |1, 1〉 for further effective cooling to avoid the strong three-body loss between23Na atoms in |2, 2〉 and40K atoms in |9/2, 9/2〉. At the end of the evaporation in optical trap, a degenerate Fermi gas of40K with 1.9 × 10^(5) atoms at T/TF= 0.5 in the |9/2, 9/2〉 hyperfine state coexists with a Bose–Einstein condensate(BEC) of23Na with 8 × 10^(4) atoms in the |1, 1〉 hyperfine state at 300 n K. We also can produce the two species mixture with the tunable population imbalance by adjusting the 23Na magneto–optical trap loading time.
基金the National Natural Science Foundation of China(22203046 and 52102265)Jiangsu Provincial Natural Science Foundation(BK20230368 and BK20210604)+2 种基金the Project of State Key Laboratory of Organic Electronics and Information Displays,Nanjing University of Posts and Telecommunications(GZR2023010003,GZR2022010017 and GDX2022010010)the Natural Science Research Start-up Foundation of Recruiting Talents of Nanjing University of Posts and Telecommunications(NY221128,NY223099 and NY223054)the Natural Science Research Start-up Foundation of Recruiting Talents of Suzhou Vocational Institute of Industrial Technology(SYG202354)。
文摘The development of low-cost,high-performance catalysts at the atomic scale has become a challenging issue for the large-scale applications of renewable clean energy technologies.Herein,on the basis of density functional theory calculation,we systematically investigate the effect of the local environment on the activity and selectivity of electrochemical carbon dioxide reduction reaction over single/multi-atom alloy clusters formed by the transition metal(Fe,Co,and Ni)-doped Cu13/55 clusters.Our findings reveal that the catalytic performance of multi-atom alloy clusters far exceeds that of Cu(211)surface.Notably,the Co666 configuration exhibits exceptional performance with a remarkably low free energy barrier of just 0.33 eV.Furthermore,our investigations demonstrate that catalytic performance is predominantly determined by the relative proportion of modifying metallic dopant species that generate a coordination number of 6.This ratio principally influences the adsorption strength of key intermediates(HCOO*and H2COO*).Bader charge analyses and free energy calculations elucidate a new mechanistic pathway,wherein the hydrogenation of CO_(2)at C-sites catalyzes the reduction of CO_(2)to CH_(4).This theoretical research provides valuable insights into the fundamental processes and energy landscapes involved in converting CO_(2)to CH_(4)on the studied catalytic structure,potentially paving the way for more efficient and sustainable carbon dioxide utilization strategies.