4.6 Article

105 Cyclable Pseudocapacitive Na-Ion Storage of Hierarchically Structured Phosphorus-Incorporating Nanoporous Carbons in Organic Electrolytes

Journal

ACS ENERGY LETTERS
Volume 3, Issue 3, Pages 724-732

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsenergylett.8b00068

Keywords

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Funding

  1. National Research Foundation (NRF) - Ministry of Science, ICT, and Future Planning [2017M2A2A6A01021187]
  2. Energy Technology Development Project (ETDP) - Ministry of Trade, Industry, and Energy, Republic of Korea [20172410100150]
  3. Korea Evaluation Institute of Industrial Technology (KEIT) [20172410100150] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  4. Ministry of Science & ICT (MSIT), Republic of Korea [2E28340] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Despite the significant impact of sodium (Na) storage systems in terms of natural abundance and environmental friendliness, high-performance pseudocapacitive mterials in organic electrolytes remain challenging. Here, we demonstrate the pseudocapacitive Na-ion storage of hierarchically structured, phosphorus-incorporating steam-activated nanoporous carbons (P-aCNs) with improved rate and cyclic capabilities in organic electrolytes. The P-aCNs with a hierarchical honeycomb structure are derived from lignocellulosic biomass via a proposed synthetic process. The prominent pseudocapacitive behaviors of the P-containing groups in organic Na-ion electrolytes are confirmed by the surface area-independent and surface-confined capacitances, distinctive redox waves, and strong binding with Na-ions. In particular, the P-aCN demonstrates the cyclic stability of 96.0% over 100 000 cycles in the full cell, achieving a high capacitance of 265.43 F g(-1) and rate capability of 75%. These Na-ion pseudocapacitive features of P-aCNs arising from the hierarchical interconnected porosity and the redox-active P=O bonds are comprehensively investigated by experimental and computational analyses.

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