材料科学
多硫化物
X射线光电子能谱
化学工程
电池(电)
电催化剂
异质结
上部结构
氧化还原
纳米技术
电极
电解质
电化学
光电子学
物理化学
化学
冶金
工程类
功率(物理)
地质学
物理
海洋学
量子力学
作者
Shipeng Zhang,Yu Yao,Xiaojuan Jiao,Mingze Ma,Huijuan Huang,Xuefeng Zhou,Lifeng Wang,Jintao Bai,Yan Yu
标识
DOI:10.1002/adma.202103846
摘要
Room-temperature sodium-sulfur (RT Na-S) batteries are highly desirable for a sustainable large-scale energy-storage system due to their high energy density and low cost. Nevertheless, practical applications of RT Na-S batteries are still prevented by the shuttle effect of sodium polysulfides (NaPS), slow reaction kinetics of S, and incomplete conversion process of NaPS. Here, Mo2 N-W2 N heterostructures embedded in a spherical carbon superstructure (Mo2 N-W2 N@PC) are designed to efficiently suppress the "polysulfide shuttle" and promote NaPS redox reactions. The designed Mo2 N-W2 N@PC heterostructure with abundant heterointerfaces, high conductivity, and porosity can facilitate electron/ion diffusion and provide high catalytic activity for efficient NaPS conversion. The obtained Na-S battery delivers high reversible capacity with superior long-term cyclability (517 mAh g-1 at 1 A g-1 after 400 cycles) and unprecedented rate capability (417 mAh g-1 at 2 A g-1 ). Furthermore, the electrocatalysis mechanism is revealed by combining in situ X-ray diffraction (XRD), ex situ X-ray photoelectron spectroscopy (XPS), UV-vis spectra, and precipitation experiments. This work demonstrates a novel heterostructure design strategy that enables high-performance Na-S batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI