No abstract

Cathodic polysulfide electrocatalysts are introduced to confidently accelerate the polysulfide conversion to propel the increased practical density of lithium−sulfur (Li−S) batteries. Defect engineering as an advanced functional strategy has been confirmed to have the competent capability of optimizing the electrocatalytic kinetics. In this work, the conventional phosphorization process is used to process Co 3 O 4 anchored on nitrogen-doped carbon nanotubes. Unexpectedly, there is no phase change, only phosphorus doping with rich lattice dislocation on Co 3 O 4 . With the combined characterization of X-ray diffraction, highresolution transmission electron microscopy and X-ray photoelectron spectroscopy, it is found that phosphorus doping transfers part of the oxygen vacancies to the lattice oxygen of Co 3 O 4 , which can induce the catalytic active species Co−O−P. The concomitant lattice dislocations can strengthen the chemical adsorption of phosphorus-doped Co 3 O 4 for polysulfides and even elevate more catalytically active sites. With the use of defect-rich phosphorus-doped Co 3 O 4 embedded in a nitrogen-doped carbon nanotube (P-Co 3 O 4 /NCNT) as an electrocatalyst, Li−S batteries showcase enhanced oxidation and reduction kinetics and an improved rate performance. This work provides new insight into the rational design of the electrocatalyst of heteroatom-doped metal compounds for high-performance Li−S batteries.