【摘 要】
：
Many non-precious metal-based catalysts with high intrinsic activity for catalytic reactions are prone to structural degradation in practical application,which leads to poor stability.In this work,we propose c-CoSe2/o-CoSe2 as the oxygen electrode of lith
【机 构】
：
College of Materials and Chemistry&Chemical Engineering,Chengdu University of Technology,Chengdu 610
论文部分内容阅读
Many non-precious metal-based catalysts with high intrinsic activity for catalytic reactions are prone to structural degradation in practical application,which leads to poor stability.In this work,we propose c-CoSe2/o-CoSe2 as the oxygen electrode of lithium-oxygen batteries(LOBs)to improve its cycle stability.The heterogeneous interface inside c-CoSe2/o-CoSe2 leads to an increase in the covalence bonds between Co and Se ions,which greatly enhances the robustness of the crystal lattice,thereby improving the sta-bility of the catalyst.In addition,the strong interaction between the mixed phases is favorable for ad-justing the electron density around the active sites and boosting oxygen electrode kinetics.Moreover,the epitaxial growth of o-CoSe2 on c-CoSe2 will cause abundant heterogeneous interfaces and slight lattice distortion along the interfaces,thereby providing sufficient catalytic reaction sites.The DFT calculation results show that the optimized adsorption of intermediates at the heterogeneous interface plays an im-portant role in boosting oxygen electrode reactions and improving the electrochemical performance of LOBs.The experimental results show that LOBs with the c-CoSe2/o-CoSe2 electrodes exhibit outstanding performance,including large specific capacity of about 23,878 mA h g-1,high coulombic efficiency of up to 93.66％,and excellent stability of over 176 cycles(1410 h).
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