105 Cyclable Pseudocapacitive Na-Ion Storage of Hierarchically Structured Phosphorus-Incorporating Nanoporous Carbons in Organic Electrolytes AITranslate
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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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DOI:https://doi.org/10.1021/acsenergylett.8b00068
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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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| GB/T 7714-2015 | [1] Sul Ki Park, Sung Hyun Kwon, Seung Geol Lee, et al. ACS Energy Letters, 2018(3). DOI:10.1021/acsenergylett.8b00068. |
| MLA | [1] Sul Ki Park, et al., ACS Energy Letters, no. 3, 2018, https://doi.org/10.1021/acsenergylett.8b00068. |
| APA | [1] Sul Ki Park, Sung Hyun Kwon, Seung Geol Lee, Min Sung Choi, Dong Hoon Suh, Puritut Nakhanivej, Hyunjoo Lee, & Ho Seok Park. (2018). ACS Energy Letters(3). https://doi.org/10.1021/acsenergylett.8b00068 |
| IEEE | [1] Sul Ki Park, Sung Hyun Kwon, Seung Geol Lee, Min Sung Choi, Dong Hoon Suh, Puritut Nakhanivej, Hyunjoo Lee, and Ho Seok Park, ACS Energy Letters, no. 3, 2018, doi: 10.1021/acsenergylett.8b00068. |
