{"title":"多孔富氮碳纳米管中的原位碳化钼电催化剂促进钠-金属-硫电池的快速动力学","authors":"Hongchang Hao, Yixian Wang, Naman Katyal, Guang Yang, Hui Dong, Pengcheng Liu, Sooyeon Hwang, Jagannath Mantha, Graeme Henkelman, Yixin Xu, Jorge Anibal Boscoboinik, Jagjit Nanda, David Mitlin","doi":"10.1002/adma.202106572","DOIUrl":null,"url":null,"abstract":"<p>This is the first report of molybdenum carbide-based electrocatalyst for sulfur-based sodium-metal batteries. MoC/Mo<sub>2</sub>C is in situ grown on nitrogen-doped carbon nanotubes in parallel with formation of extensive nanoporosity. Sulfur impregnation (50 wt% S) results in unique triphasic architecture termed molybdenum carbide–porous carbon nanotubes host (MoC/Mo<sub>2</sub>C@PCNT–S). Quasi-solid-state phase transformation to Na<sub>2</sub>S is promoted in carbonate electrolyte, with in situ time-resolved Raman, X-ray photoelectron spectroscopy, and optical analyses demonstrating minimal soluble polysulfides. MoC/Mo<sub>2</sub>C@PCNT–S cathodes deliver among the most promising rate performance characteristics in the literature, achieving 987 mAh g<sup>−1</sup> at 1 A g<sup>−1</sup>, 818 mAh g<sup>−1</sup> at 3 A g<sup>−1</sup>, and 621 mAh g<sup>−1</sup> at 5 A g<sup>−1</sup>. The cells deliver superior cycling stability, retaining 650 mAh g<sup>−1</sup> after 1000 cycles at 1.5 A g<sup>−1</sup>, corresponding to 0.028% capacity decay per cycle. High mass loading cathodes (64 wt% S, 12.7 mg cm<sup>−2</sup>) also show cycling stability. Density functional theory demonstrates that formation energy of Na<sub>2</sub>S<i><sub>x</sub></i> (1 ≤ <i>x</i> ≤ 4) on surface of MoC/Mo<sub>2</sub>C is significantly lowered compared to analogous redox in liquid. Strong binding of Na<sub>2</sub>S<i><sub>x</sub></i> (1 ≤ <i>x</i> ≤ 4) on MoC/Mo<sub>2</sub>C surfaces results from charge transfer between the sulfur and Mo sites on carbides’ surface.</p>","PeriodicalId":114,"journal":{"name":"Advanced Materials","volume":"34 26","pages":""},"PeriodicalIF":27.4000,"publicationDate":"2022-04-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"26","resultStr":"{\"title\":\"Molybdenum Carbide Electrocatalyst In Situ Embedded in Porous Nitrogen-Rich Carbon Nanotubes Promotes Rapid Kinetics in Sodium-Metal–Sulfur Batteries\",\"authors\":\"Hongchang Hao, Yixian Wang, Naman Katyal, Guang Yang, Hui Dong, Pengcheng Liu, Sooyeon Hwang, Jagannath Mantha, Graeme Henkelman, Yixin Xu, Jorge Anibal Boscoboinik, Jagjit Nanda, David Mitlin\",\"doi\":\"10.1002/adma.202106572\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>This is the first report of molybdenum carbide-based electrocatalyst for sulfur-based sodium-metal batteries. 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High mass loading cathodes (64 wt% S, 12.7 mg cm<sup>−2</sup>) also show cycling stability. Density functional theory demonstrates that formation energy of Na<sub>2</sub>S<i><sub>x</sub></i> (1 ≤ <i>x</i> ≤ 4) on surface of MoC/Mo<sub>2</sub>C is significantly lowered compared to analogous redox in liquid. 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引用次数: 26
摘要
本文首次报道了基于碳化钼的硫基钠金属电池电催化剂。MoC/Mo2C在氮掺杂碳纳米管上原位生长,并形成广泛的纳米孔。硫浸渍(50 wt% S)产生独特的三相结构,称为碳化钼-多孔碳纳米管宿主(MoC/Mo2C@PCNT -S)。碳酸盐电解质促进了向Na2S的准固态相变,现场时间分辨拉曼光谱、x射线光电子能谱和光学分析表明,可溶多硫化物极少。MoC/Mo2C@PCNT -S阴极在文献中提供最有希望的速率性能特征,在1 A g - 1时达到987 mAh g - 1,在3 A g - 1时达到818 mAh g - 1,在5 A g - 1时达到621 mAh g - 1。电池具有优异的循环稳定性,在1.5 A g−1下循环1000次后仍保持650 mAh g−1,相当于每循环0.028%的容量衰减。高质量负载阴极(64 wt% S, 12.7 mg cm−2)也表现出循环稳定性。密度泛函理论表明,Na2Sx在MoC/Mo2C表面的形成能(1≤x≤4)与在液体中类似氧化还原相比显著降低。Na2Sx(1≤x≤4)在MoC/Mo2C表面的强结合是由碳化物表面的硫位和Mo位之间的电荷转移引起的。
Molybdenum Carbide Electrocatalyst In Situ Embedded in Porous Nitrogen-Rich Carbon Nanotubes Promotes Rapid Kinetics in Sodium-Metal–Sulfur Batteries
This is the first report of molybdenum carbide-based electrocatalyst for sulfur-based sodium-metal batteries. MoC/Mo2C is in situ grown on nitrogen-doped carbon nanotubes in parallel with formation of extensive nanoporosity. Sulfur impregnation (50 wt% S) results in unique triphasic architecture termed molybdenum carbide–porous carbon nanotubes host (MoC/Mo2C@PCNT–S). Quasi-solid-state phase transformation to Na2S is promoted in carbonate electrolyte, with in situ time-resolved Raman, X-ray photoelectron spectroscopy, and optical analyses demonstrating minimal soluble polysulfides. MoC/Mo2C@PCNT–S cathodes deliver among the most promising rate performance characteristics in the literature, achieving 987 mAh g−1 at 1 A g−1, 818 mAh g−1 at 3 A g−1, and 621 mAh g−1 at 5 A g−1. The cells deliver superior cycling stability, retaining 650 mAh g−1 after 1000 cycles at 1.5 A g−1, corresponding to 0.028% capacity decay per cycle. High mass loading cathodes (64 wt% S, 12.7 mg cm−2) also show cycling stability. Density functional theory demonstrates that formation energy of Na2Sx (1 ≤ x ≤ 4) on surface of MoC/Mo2C is significantly lowered compared to analogous redox in liquid. Strong binding of Na2Sx (1 ≤ x ≤ 4) on MoC/Mo2C surfaces results from charge transfer between the sulfur and Mo sites on carbides’ surface.
期刊介绍:
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