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原位 X 射线散射研究氮掺杂有序介孔碳中的硫扩散

Sulfur Diffusion within Nitrogen-Doped Ordered Mesoporous Carbons Determined by in Situ X-ray Scattering.

机构信息

Department of Polymer Science, Goodyear Polymer Center , The University of Akron , 170 University Circle , Akron , Ohio 44325 , United States.

Department of Polymer Engineering , The University of Akron , 250 S Forge Street , Akron , Ohio 44325 , United States.

出版信息

Langmuir. 2018 Jul 31;34(30):8767-8776. doi: 10.1021/acs.langmuir.8b01375. Epub 2018 Jul 18.

Abstract

The low intrinsic conductivity of sulfur necessitates conductive additives, such as mesoporous carbons, to the cathode to enable high-performance metal-sulfur batteries. Simultaneous efforts to address polysulfide shuttling have introduced nitrogen-doped carbons to provide both conductivity and suppressed shuttling because of their strong interaction with sulfur. The strength of this interaction will impact the ability to fill the mesopores with sulfur via melt infusion. Here, we systematically investigate how nitrogen doping influences the rate that molten sulfur can infiltrate the mesopores and the overall extent of pore filling of highly ordered mesoporous doped carbons using in situ small angle X-ray scattering (SAXS). The similarity in electron density between molten sulfur and the soft carbon framework of the mesoporous material leads to a precipitous decrease in the scattered intensity associated with the ordered structure as voids are filled with sulfur. As the nitrogen doping increases from 1 to 20 at. %, the effective diffusivity of sulfur in the mesopores decreases by an order of magnitude (2.7 × 10 to 2.3 × 10 cm/s). The scattering becomes nearly invariant within 20 min of melt infiltration at 155 °C for all but the most doped carbon, which indicates that submicron-sized mesoporous carbon particles can be filled rapidly. Additionally, the nitrogen doping decreases the sulfur content that can be accommodated within the mesopores from 95% of the mesopores filled without doping to only 64% filled with 20 at. % N as determined by the residual scattering intensity. Sulfur does not crystallize within the mesopores of the nitrogen-doped carbons, which is further indicative of the strong interactions between the nitrogen species and sulfur that can inhibit polysulfide shuttling. In situ SAXS provides insights into the diffusion of sulfur in mesopores and how the surface chemistry of nitrogen-doped carbon appears to significantly hinder the infiltration by sulfur.

摘要

硫的本征电导率较低,需要在阴极中添加介孔碳等导电添加剂,以实现高性能的金属-硫电池。同时,为了解决多硫化物穿梭问题,引入了氮掺杂碳,由于其与硫的强相互作用,既能提供导电性,又能抑制穿梭。这种相互作用的强度将影响通过熔融注入将硫填充到介孔中的能力。在这里,我们系统地研究了氮掺杂如何影响熔融硫渗透介孔的速率以及高度有序介孔掺杂碳的整体孔填充程度,使用原位小角 X 射线散射(SAXS)。熔融硫与介孔材料的软碳骨架之间的电子密度相似,导致有序结构的散射强度急剧下降,因为空隙被硫填充。随着氮掺杂从 1 增加到 20 原子%,介孔中硫的有效扩散系数降低了一个数量级(2.7×10-10 到 2.3×10-10 cm/s)。在 155°C 下,除了最掺杂的碳之外,所有碳在熔融渗透 20 分钟内的散射几乎不变,这表明亚微米介孔碳颗粒可以快速填充。此外,氮掺杂降低了介孔中可以容纳的硫含量,从无掺杂时填充 95%的介孔降低到 20 原子%氮掺杂时仅填充 64%,这是通过残留散射强度确定的。氮掺杂碳的介孔中硫不会结晶,这进一步表明氮物种与硫之间的强相互作用可以抑制多硫化物穿梭。原位 SAXS 提供了对硫在介孔中扩散的深入了解,以及氮掺杂碳的表面化学似乎如何显著阻碍硫的渗透。

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