Affiliation:
1. Departamento de Ingeniería Química, Universidad Autónoma de Madrid, C/Tomás y Valiente 7, 28049 Madrid, Spain
2. Instituto de Cerámica y Vidrio, Consejo Superior de Investigaciones Científicas, C/Kelsen 5, 28049 Madrid, Spain
Abstract
The design of a material porous microstructure with interconnected micro-meso-macropores is a key issue for the successful development of carbon-derived materials for supercapacitor applications. Another important issue is the nature of these carbon materials. For those reasons, in this study, novel hierarchical micro-meso-macroporous silicon oxycarbide-derived carbon (SiOC-DC) was obtained via chlorine etching of carbon-enriched SiOC prepared via pyrolysis (1100–1400 °C) of sol-gel triethoxysilane/dimethyldiphenysiloxane hybrids. In addition, and for the first time, non-conventional Raman parameters combined with the analysis of their microstructural characteristics were considered to establish their relationships with their electrochemical response. The sample pyrolyzed at 1100 °C showed planar and less-defective carbon domains together with the largest specific surface area (SSA) and the highest volume of micro-meso-macropores, which upgraded their electrochemical response. This sample has the highest specific capacitance (Cs = 101 Fg−1 (0.2 Ag−1)), energy (Ed = 12–7 Wh−1 kg−1), and power densities (Pd = 0.32–35 kw kg−1), showing a good capacitance retention ratio up to 98% after 10,000 charge–discharge cycles at 0.5 Ag−1. At a pyrolysis temperature ≥ 1200 °C, the carbon domains were highly ordered and tortuous with a high degree of interconnection. However, SSA and pore volumes (micro-meso-macropores) were significantly reduced and downgraded the Cs, Ed, and Pd values.
Funder
Ministerio de Industria, Comercio y Turismo and European Union
Spanish Ministerio de Economía y Competitividad
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis
Cited by
3 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献