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Operando soft X-ray absorption spectroscopic study on microporous carbon-supported sulfur cathodes

机译:微孔碳支撑硫阴极的Operando软X射线吸收光谱研究

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摘要

Sulfur is a promising material for next-generation cathodes, owing to its high energy and low cost. However, sulfur cathodes have the disadvantage of serious cyclability issues due to the dissolution of polysulfides that form as intermediate products during discharge/charge cycling. Filling sulfur into the micropores of porous carbon is an effective method to suppress its dissolution. Although microporous carbon-supported sulfur cathodes show an electrochemical behavior different from that of the conventional sulfur ones, the corresponding reaction mechanism is not clearly understood. In this study, we focused on clarifying the reaction mechanism of microporous carbon-supported sulfur cathodes by operando soft X-ray absorption spectroscopy. In the microporous carbon support, sulfur was present as smaller fragments compared to conventional sulfur. During the first discharge process, the sulfur species in the microporous carbon were initially reduced to S _(6) ~(2?) and S _(2) ~(2?) and then to Li _(2) S. The S _(6) ~(2?) and S _(2) ~(2?) species were observed first, with S _(2) ~(2?) being the main polysulfide species during the discharge process, while Li _(2) S was produced in the final discharge process. The narrow pores of microporous carbon prevent the dissolution of polysulfides and influence the reaction mechanism of sulfur cathodes.
机译:硫是下一代阴极的有希望的材料,由于其高能量和低成本。然而,由于在放电/电荷循环期间形成中间产物的多硫化物溶解,硫阴极具有严重的可靠性问题的缺点。将硫填充到多孔碳的微孔中是抑制其溶解的有效方法。虽然微孔碳负载的硫阴极显示出与常规硫的电化学行为不同,但不清楚地清楚地理解相应的反应机制。在这项研究中,我们专注于通过Operando软X射线吸收光谱阐明微孔碳负载硫阴极的反应机理。在微孔碳载体中,与常规硫相比,硫作为较小的片段存在。在第一次放电过程中,微孔碳中的硫物质最初将其还原为S _(6)〜(2?)和S _(2)〜(2?),然后到Li _(2)S. S _(6)〜(2?)和S _(2)〜(2?)首先观察到物种,S_(2)〜(2?)是在放电过程中主要多硫化物物种,而LI _( 2)S是在最终放电过程中产生的。微孔碳的狭窄孔可防止多硫化物的溶解并影响硫阴极的反应机理。

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