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A porous Co–Ru@C shell as a bifunctional catalyst for lithium–oxygen batteries

We use SiO(2) as a template and dopamine as a carbon source to synthesize a hollow C shell, and we load Co and Ru nanoparticles onto it to obtain a Co–Ru@C shell composite. The diameter and thickness of the C shell are 100 nm and 5–10 nm, respectively, and numerous holes of different sizes exist on...

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Detalles Bibliográficos
Autores principales: Chen, Xiang, Zhang, Xiuhui, Chen, Chunguang, Huang, Tao, Yu, Aishui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081741/
https://www.ncbi.nlm.nih.gov/pubmed/35540248
http://dx.doi.org/10.1039/c8ra04144j
Descripción
Sumario:We use SiO(2) as a template and dopamine as a carbon source to synthesize a hollow C shell, and we load Co and Ru nanoparticles onto it to obtain a Co–Ru@C shell composite. The diameter and thickness of the C shell are 100 nm and 5–10 nm, respectively, and numerous holes of different sizes exist on the C shell. Meanwhile, numerous C shells stack together to form macropores, thereby forming a hierarchical porous structure in the material. Brunauer–Emmett–Teller surface area analysis reveals that the specific surface area and pore volume of the Co–Ru@C shell are 631.57 m(2) g(−1) and 2.20 cc g(−1), respectively, which can result in many three-phase interfaces and provide more space for the deposition of discharge products. Compared with Co@C shell and C shell electrodes, the obtained Co–Ru@C shell-based electrodes exhibit the highest discharge capacity, the lowest oxygen reduction reaction/oxygen evolution reaction overpotential and the best cycle stability, indicating the excellent catalytic ability of the Co–Ru@C shell.