RESUMO
Polysulfide shuttle and sluggish sulfur redox kinetics remain key challenges in lithium-sulfur batteries. Previous researches have shown that introducing oxygen into transition metal sulfides helps to capture polysulfides and enhance their conversion kinetics. Based on this, further investigations are conducted to explore the impact of oxygen doping levels on the physical-chemical properties and electrocatalytic performance of MoS2. The findings reveal that MoS2 doped with high-content oxygen exhibits enhanced conductivity and polysulfides conversion kinetics compared to MoS2 with low-content oxygen doping, which can be attributed to the alteration of crystal structure from 2H-phase to the 1T-phase, the introduction of increased Li-O interactions, and the effect of defects resulting from high-oxygen doping. Consequently, the lithium-sulfur batteries using high-oxygen doped MoS2 as a catalyst deliver a high discharge capacity of 1015 mAh g-1 at 0.25C and maintain 78.5% capacity after 300 more cycles. Specifically, lithium-sulfur batteries employing paper-based electrodedemonstrate an areal capacity of 3.91 mAh cm-2 at 0.15C, even with sulfur loading of 4.1 mg cm-2 and electrolyte of 6.7 µL mg-1. These results indicate that oxygen doping levels can modify the properties of MoS2, and high-oxygen doped MoS2 shows promise as an efficient catalyst for lithium-sulfur batteries.
RESUMO
At present, the self-supporting paper-based electrode has some problems, such as low mechanical strength and insufficient flexibility, which restrict its application in flexible electronics. In this paper, FWF is used as the skeleton fiber, and the contact area and the number of hydrogen bonds of the fiber are increased by grinding the fiber and adding nanofibers to bridge it, and a level three gradient enhanced skeleton support network structure is constructed, which effectively improves the mechanical strength and foldability of the paper-based electrodes. The tensile strength of FWF15-BNF5 paper-based electrode is 7.4 MPa, the elongation at break is increased to 3.7%, the electrode thickness is as low as 66 µm, the electrical conductivities is 5.6 S cm-1, and the contact angle to electrolyte as low as 45°, which has excellent electrolyte wettability, flexibility, and foldability. After three-layer superimposed rolling, the discharge areal capacity reached 3.3 mAh cm-2 and 2.9 mAh cm-2 at the rate of 0.1 C and 1.5 C, respectively, which was superior to the commercial LFP electrode, it had good cycle stability, and the areal capacity was 3.0 mAh cm-2 and 2.8 mAh cm-2 after 100 cycles at the rate of 0.3 C and 1.5 C.
RESUMO
Exploring new materials and methods to achieve high utilization of sulfur with lean electrolyte is still a common concern in lithium-sulfur batteries. Here, high-density oxygen doping chemistry is introduced for making highly conducting, chemically stable sulfides with a much higher affinity to lithium polysulfides. It is found that doping large amounts of oxygen into NiCo2 S4 is feasible and can make it outperform the pristine oxides and natively oxidized sulfides. Taking the advantages of high conductivity, chemical stability, the introduced large Li-O interactions, and activated Co (Ni) facets for catalyzing Sn 2- , the NiCo2 (O-S)4 is able to accelerate the Li2 S-S8 redox kinetics. Specifically, lithium-sulfur batteries using free-standing NiCo2 (O-S)4 paper and interlayer exhibit the highest capacity of 8.68 mAh cm-2 at 1.0 mA cm-2 even with a sulfur loading of 8.75 mg cm-2 and lean electrolyte of 3.8 µL g-1 . The high-density oxygen doping chemistry can be also applied to other metal compounds, suggesting a potential way for developing more powerful catalysts towards high performance of Li-S batteries.
