Base de dados : MEDLINE
Pesquisa : G01.358.500.249.270 [Categoria DeCS]
Referências encontradas : 1766 [refinar]
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  1 / 1766 MEDLINE  
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[PMID]:28741864
[Au] Autor:Lee J; Srimuk P; Aristizabal K; Kim C; Choudhury S; Nah YC; Mücklich F; Presser V
[Ad] Endereço:Leibniz Institute for New Materials (INM), Campus D2 2, 66123, Saarbrücken, Germany.
[Ti] Título:Pseudocapacitive Desalination of Brackish Water and Seawater with Vanadium-Pentoxide-Decorated Multiwalled Carbon Nanotubes.
[So] Source:ChemSusChem;10(18):3611-3623, 2017 09 22.
[Is] ISSN:1864-564X
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:A hybrid membrane pseudocapacitive deionization (MPDI) system consisting of a hydrated vanadium pentoxide (hV O )-decorated multi-walled carbon nanotube (MWCNT) electrode and one activated carbon electrode enables sodium ions to be removed by pseudocapacitive intercalation with the MWCNT-hV O electrode and chloride ion to be removed by non-faradaic electrosorption of the porous carbon electrode. The MWCNT-hV O electrode was synthesized by electrochemical deposition of hydrated vanadium pentoxide on the MWCNT paper. The stable electrochemical operating window for the MWCNT-hV O electrode was between -0.5 V and +0.4 V versus Ag/AgCl, which provided a specific capacity of 44 mAh g (corresponding with 244 F g ) in aqueous 1 m NaCl. The desalination performance of the MPDI system was investigated in aqueous 200 mm NaCl (brackish water) and 600 mm NaCl (seawater) solutions. With the aid of an anion and a cation exchange membrane, the MPDI hybrid cell was operated from -0.4 to +0.8 V cell voltage without crossing the reduction and oxidation potential limit of both electrodes. For the 600 mm NaCl solution, the NaCl salt adsorption capacity of the cell was 23.6±2.2 mg g , which is equivalent to 35.7±3.3 mg g normalized to the mass of the MWCNT-hV O electrode. Additionally, we propose a normalization method for the electrode material with faradaic reactions based on sodium uptake capacities.
[Mh] Termos MeSH primário: Capacitância Elétrica
Nanotubos de Carbono/química
Águas Salinas/química
Salinidade
Água do Mar/química
Compostos de Vanádio/química
Purificação da Água/métodos
[Mh] Termos MeSH secundário: Adsorção
Eletroquímica
Eletrodos
Sódio/química
Sódio/isolamento & purificação
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Nanotubes, Carbon); 0 (Vanadium Compounds); 9NEZ333N27 (Sodium); BVG363OH7A (vanadium pentoxide)
[Em] Mês de entrada:1710
[Cu] Atualização por classe:180118
[Lr] Data última revisão:
180118
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170726
[St] Status:MEDLINE
[do] DOI:10.1002/cssc.201701215


  2 / 1766 MEDLINE  
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[PMID]:28453182
[Au] Autor:Thangavel R; Kaliyappan K; Ramasamy HV; Sun X; Lee YS
[Ad] Endereço:Faculty of Applied Chemical Engineering, Chonnam National University, Gwang-ju, 500-757, Korea.
[Ti] Título:Engineering the Pores of Biomass-Derived Carbon: Insights for Achieving Ultrahigh Stability at High Power in High-Energy Supercapacitors.
[So] Source:ChemSusChem;10(13):2805-2815, 2017 07 10.
[Is] ISSN:1864-564X
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:Electrochemical supercapacitors with high energy density are promising devices due to their simple construction and long-term cycling performance. The development of a supercapacitor based on electrical double-layer charge storage with high energy density that can preserve its cyclability at higher power presents an ongoing challenge. Herein, we provide insights to achieve a high energy density at high power with an ultrahigh stability in an electrical double-layer capacitor (EDLC) system by using carbon from a biomass precursor (cinnamon sticks) in a sodium ion-based organic electrolyte. Herein, we investigated the dependence of EDLC performance on structural, textural, and functional properties of porous carbon engineered by using various activation agents. The results demonstrate that the performance of EDLCs is not only dependent on their textural properties but also on their structural features and surface functionalities, as is evident from the electrochemical studies. The electrochemical results are highly promising and revealed that the porous carbon with poor textural properties has great potential to deliver high capacitance and outstanding stability over 300 000 cycles compared with porous carbon with good textural properties. A very low capacitance degradation of around 0.066 % per 1000 cycles, along with high energy density (≈71 Wh kg ) and high power density, have been achieved. These results offer a new platform for the application of low-surface-area biomass-derived carbons in the design of highly stable high-energy supercapacitors.
[Mh] Termos MeSH primário: Biomassa
Carbono/química
Capacitância Elétrica
Engenharia
[Mh] Termos MeSH secundário: Adsorção
Animais
Condutividade Elétrica
Eletroquímica
Química Verde
Porosidade
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
7440-44-0 (Carbon)
[Em] Mês de entrada:1708
[Cu] Atualização por classe:180118
[Lr] Data última revisão:
180118
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170429
[St] Status:MEDLINE
[do] DOI:10.1002/cssc.201700492


  3 / 1766 MEDLINE  
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[PMID]:28857459
[Au] Autor:Xu S; Wang T; Ma Y; Jiang W; Wang S; Hong M; Hu N; Su Y; Zhang Y; Yang Z
[Ad] Endereço:Key Laboratory for Thin Film and Microfabrication of Ministry of Education, Department of Micro/Nano Electronics, School of Electronic Information and Electrical Engineering, Shanghai Jiao Tong University, Shanghai, 200240, P.R. China.
[Ti] Título:Cobalt Doping To Boost the Electrochemical Properties of Ni@Ni S Nanowire Films for High-Performance Supercapacitors.
[So] Source:ChemSusChem;10(20):4056-4065, 2017 Oct 23.
[Is] ISSN:1864-564X
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:Metal sulfides have aroused great interest for energy storage. However, their low specific capacities and inferior rate capabilities hinder their practical applications. In this work, a facile cobalt-doping process is used to boost the electrochemical performance of Ni@Ni S core-sheath nanowire film electrodes for high-performance electrochemical energy storage. Co ions are doped successfully and uniformly into Ni S nanosheets through a facile ion-exchange process. The electrochemical properties of film electrodes are improved greatly, and an ultrahigh volumetric capacity (increased from 105 to 730 C cm at 0.25 A cm ) and excellent rate capability are obtained after Co is doped into Ni@Ni S core-sheath nanowires. A hybrid asymmetric supercapacitor with Co-doped Ni@Ni S as the positive electrode and graphene-carbon nanotubes as the negative electrode is assembled and exhibits an ultrahigh volumetric capacitance of 142 F cm (based on the total volume of both electrodes) at 0.5 A cm and excellent cycling stability (only 3 % capacitance decrease after 5000 cycles). Moreover, the volumetric energy density can reach 44.5 mWh cm , which is much larger than those of thin-film lithium batteries (1-10 mWh cm ). These results may provide useful insights for the fabrication of high-performance film electrodes for energy-storage applications.
[Mh] Termos MeSH primário: Cobalto/química
Capacitância Elétrica
Níquel/química
[Mh] Termos MeSH secundário: Eletroquímica
Modelos Moleculares
Conformação Molecular
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
3G0H8C9362 (Cobalt); 7OV03QG267 (Nickel); I6929D52YQ (nickel sulfide)
[Em] Mês de entrada:1711
[Cu] Atualização por classe:171106
[Lr] Data última revisão:
171106
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170901
[St] Status:MEDLINE
[do] DOI:10.1002/cssc.201701305


  4 / 1766 MEDLINE  
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[PMID]:28834366
[Au] Autor:Chen TH; Yang CH; Su CY; Lee TC; Dong QF; Chang JK
[Ad] Endereço:Institute of Materials Science and Engineering, National Central University, 300, Zhongda Rd., Zhongli District, Taoyuan City, 32001, Taiwan.
[Ti] Título:Electrolyte Engineering: Optimizing High-Rate Double-Layer Capacitances of Micropore- and Mesopore-Rich Activated Carbon.
[So] Source:ChemSusChem;10(18):3534-3539, 2017 Sep 22.
[Is] ISSN:1864-564X
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:Various types of electrolyte cations as well as binary cations are used to optimize the capacitive performance of activated carbon (AC) with different pore structures. The high-rate capability of micropore-rich AC, governed by the mobility of desolvated cations, can outperform that of mesopore-rich AC, which essentially depends on the electrolyte conductivity.
[Mh] Termos MeSH primário: Carvão Vegetal/química
Capacitância Elétrica
Eletrólitos/química
Engenharia
[Mh] Termos MeSH secundário: Porosidade
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Electrolytes); 16291-96-6 (Charcoal)
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171017
[Lr] Data última revisão:
171017
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170824
[St] Status:MEDLINE
[do] DOI:10.1002/cssc.201701476


  5 / 1766 MEDLINE  
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[PMID]:28669852
[Au] Autor:Lasic E; Stenovec M; Kreft M; Robinson PJ; Zorec R
[Ad] Endereço:Laboratory of Neuroendocrinology-Molecular Cell Physiology, Institute of Pathophysiology, Faculty of Medicine, University of Ljubljana, Zaloska 4, 1000 Ljubljana, Slovenia.
[Ti] Título:Dynamin regulates the fusion pore of endo- and exocytotic vesicles as revealed by membrane capacitance measurements.
[So] Source:Biochim Biophys Acta;1861(9):2293-2303, 2017 09.
[Is] ISSN:0006-3002
[Cp] País de publicação:Netherlands
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Dynamin is a multidomain GTPase exhibiting mechanochemical and catalytic properties involved in vesicle scission from the plasmalemma during endocytosis. New evidence indicates that dynamin is also involved in exocytotic release of catecholamines, suggesting the existence of a dynamin-regulated structure that couples endo- to exocytosis. METHODS: Thus we here employed high-resolution cell-attached capacitance measurements and super-resolution structured illumination microscopy to directly examine single vesicle interactions with the plasmalemma in cultured rat astrocytes treated with distinct pharmacological modulators of dynamin activity. Fluorescent dextrans and the lipophilic plasmalemmal marker DiD were utilized to monitor uptake and distribution of vesicles in the peri-plasmalemmal space and in the cell cytosol. RESULTS: Dynamin inhibition with Dynole™-34-2 and Dyngo™-4a prevented vesicle internalization into the cytosol and decreased fusion pore conductance of vesicles that remained attached to the plasmalemma via a narrow fusion pore that lapsed into a state of repetitive opening and closing - flickering. In contrast, the dynamin activator Ryngo™-1-23 promoted vesicle internalization and favored fusion pore closure by prolonging closed and shortening open fusion pore dwell times. Immunocytochemical staining revealed dextran uptake into dynamin-positive vesicles and increased dextran uptake into Syt4- and VAMP2-positive vesicles after dynamin inhibition, indicating prolonged retention of these vesicles at the plasmalemma. CONCLUSIONS: Our results have provided direct evidence for a role of dynamin in regulation of fusion pore geometry and kinetics of endo- and exocytotic vesicles, indicating that both share a common dynamin-regulated structural intermediate, the fusion pore.
[Mh] Termos MeSH primário: Dinaminas/fisiologia
Endocitose
Exocitose
Fusão de Membrana
Vesículas Secretórias/fisiologia
[Mh] Termos MeSH secundário: Animais
Células Cultivadas
Dextranos/farmacocinética
Dinaminas/antagonistas & inibidores
Capacitância Elétrica
Feminino
Ratos
Ratos Wistar
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Dextrans); EC 3.6.5.5 (Dynamins)
[Em] Mês de entrada:1711
[Cu] Atualização por classe:171108
[Lr] Data última revisão:
171108
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170704
[St] Status:MEDLINE


  6 / 1766 MEDLINE  
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[PMID]:28586123
[Au] Autor:Biemolt J; Denekamp IM; Slot TK; Rothenberg G; Eisenberg D
[Ad] Endereço:Van't Hoff Institute for Molecular Sciences, University of Amsterdam, Science Park 904, Amsterdam, 1098, XH, The Netherlands.
[Ti] Título:Boosting the Supercapacitance of Nitrogen-Doped Carbon by Tuning Surface Functionalities.
[So] Source:ChemSusChem;10(20):4018-4024, 2017 Oct 23.
[Is] ISSN:1864-564X
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:The specific capacitance of a highly porous, nitrogen-doped carbon is nearly tripled by orthogonal optimization of the microstructure and surface chemistry. First, the carbons' hierarchical pore structure and specific surface area were tweaked by controlling the temperature and sequence of the thermal treatments. The best process (pyrolysis at 900 °C, washing, and subsequent annealing at 1000 °C) yielded a carbon with a specific capacitance of 117 F g -nearly double that of a carbon made by a typical single-step synthesis at 700 °C. Following the structural optimization, the surface chemistry of the carbons was enriched by applying an oxidation routine based on a mixture of nitric and sulfuric acid in a 1:4 ratio at two different treatment temperatures (0 and 20 °C) and different treatment times. The optimal treatment times were 4 h at 0 °C and only 1 h at 20 °C. Overall, the specific capacitance nearly tripled relative to the original carbon, reaching 168 F g . The inherent nitrogen doping of the carbon comes into interplay with the acid-induced surface functionalization, creating a mixture of oxygen- and nitrogen-oxygen functionalities. The evolution of the surface chemistry was carefully followed by X-ray photoelectron spectroscopy and by N sorption porosimetry, revealing stepwise surface functionalization and simultaneous carbon etching. Overall, these processes are responsible for the peak-shaped capacitance trends in the carbons.
[Mh] Termos MeSH primário: Carbono/química
Capacitância Elétrica
Nitrogênio/química
[Mh] Termos MeSH secundário: Propriedades de Superfície
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
7440-44-0 (Carbon); N762921K75 (Nitrogen)
[Em] Mês de entrada:1711
[Cu] Atualização por classe:171106
[Lr] Data última revisão:
171106
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170607
[St] Status:MEDLINE
[do] DOI:10.1002/cssc.201700902


  7 / 1766 MEDLINE  
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[PMID]:28523755
[Au] Autor:Dubal DP; Chodankar NR; Vinu A; Kim DH; Gomez-Romero P
[Ad] Endereço:School of Chemical Engineering, The University of Adelaide, Adelaide, South Australia, 5005, Australia.
[Ti] Título:Asymmetric Supercapacitors Based on Reduced Graphene Oxide with Different Polyoxometalates as Positive and Negative Electrodes.
[So] Source:ChemSusChem;10(13):2742-2750, 2017 Jul 10.
[Is] ISSN:1864-564X
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:Nanofabrication using a "bottom-up" approach of hybrid electrode materials into a well-defined architecture is essential for next-generation miniaturized energy storage devices. This paper describes the design and fabrication of reduced graphene oxide (rGO)/polyoxometalate (POM)-based hybrid electrode materials and their successful exploitation for asymmetric supercapacitors. First, redox active nanoclusters of POMs [phosphomolybdic acid (PMo ) and phosphotungstic acid (PW )] were uniformly decorated on the surface of rGO nanosheets to take full advantage of both charge-storing mechanisms (faradaic from POMs and electric double layer from rGO). The as-synthesized rGO-PMo and rGO-PW hybrid electrodes exhibited impressive electrochemical performances with specific capacitances of 299 (269 mF cm ) and 370 F g (369 mF cm ) in 1 m H SO as electrolyte at 5 mA cm . An asymmetric supercapacitor was then fabricated using rGO-PMo as the positive and rGO-PW as the negative electrode. This rGO-PMo ∥rGO-PW asymmetric cell could be successfully cycled in a wide voltage window up to 1.6 V and hence exhibited an excellent energy density of 39 Wh kg (1.3 mWh cm ) at a power density of 658 W kg (23 mW cm ).
[Mh] Termos MeSH primário: Capacitância Elétrica
Grafite/química
Óxidos/química
Compostos de Tungstênio/química
[Mh] Termos MeSH secundário: Eletroquímica
Eletrodos
Modelos Moleculares
Conformação Molecular
Oxirredução
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Oxides); 0 (Tungsten Compounds); 0 (polyoxometalate I); 7782-42-5 (Graphite)
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170808
[Lr] Data última revisão:
170808
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170520
[St] Status:MEDLINE
[do] DOI:10.1002/cssc.201700792


  8 / 1766 MEDLINE  
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[PMID]:28474863
[Au] Autor:Morag A; Becker JY; Jelinek R
[Ad] Endereço:Department of Chemistry, Ben-Gurion University of the Negev, Beer-Sheva, 8410501, Israel.
[Ti] Título:Freestanding Gold/Graphene-Oxide/Manganese Oxide Microsupercapacitor Displaying High Areal Energy Density.
[So] Source:ChemSusChem;10(13):2736-2741, 2017 Jul 10.
[Is] ISSN:1864-564X
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:Microsupercapacitors are touted as one of the promising "next frontiers" in energy-storage research and applications. Despite their potential, significant challenges still exist in terms of physical properties and electrochemical performance, particularly attaining high energy density, stability, ease of synthesis, and feasibility of large-scale production. We present new freestanding microporous electrodes comprising self-assembled scaffold of gold and reduced graphene oxide (rGO) nanowires coated with MnO . The electrodes exhibited excellent electrochemical characteristics, particularly superior high areal capacitance. Moreover, the freestanding Au/rGO scaffold also served as the current collector, obviating the need for an additional electrode support required in most reported supercapacitors, thus enabling low volume and weight devices with a high overall device specific energy. Stacked symmetrical solid-state supercapacitors were fabricated using the Au/rGO/MnO electrodes in parallel configurations showing the advantage of using freestanding electrodes in the fabrication of low-volume devices.
[Mh] Termos MeSH primário: Capacitância Elétrica
Ouro/química
Grafite/química
Compostos de Manganês/química
Microtecnologia/métodos
Óxidos/química
[Mh] Termos MeSH secundário: Eletroquímica
Eletrodos
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Manganese Compounds); 0 (Oxides); 64J2OA7MH3 (manganese oxide); 7440-57-5 (Gold); 7782-42-5 (Graphite)
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170808
[Lr] Data última revisão:
170808
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170506
[St] Status:MEDLINE
[do] DOI:10.1002/cssc.201700500


  9 / 1766 MEDLINE  
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[PMID]:28440020
[Au] Autor:Zhao X; Li M; Dong H; Liu Y; Hu H; Cai Y; Liang Y; Xiao Y; Zheng M
[Ad] Endereço:Department of Materials Science and Engineering, College of Materials and Energy, South China Agricultural University, Guangzhou, 510642, P. R. China.
[Ti] Título:Interconnected 3 D Network of Graphene-Oxide Nanosheets Decorated with Carbon Dots for High-Performance Supercapacitors.
[So] Source:ChemSusChem;10(12):2626-2634, 2017 Jun 22.
[Is] ISSN:1864-564X
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:Interconnected 3 D nanosheet networks of reduced graphene oxide decorated with carbon dots (rGO/CDs) are successfully fabricated through a simple one-pot hydrothermal process. The as-prepared rGO/CDs present appropriate 3 D interconnectivity and abundant stable oxygen-containing functional groups, to which we can attribute the excellent electrochemical performance such as high specific capacitance, good rate capability, and great cycling stability. Employed as binder-free electrodes for supercapacitors, the resulting rGO/CDs exhibit excellent long-term cycling stability (ca. 92 % capacitance retention after 20 000 charge/discharge cycles at current density of 10 A g ) as well as a maximum specific capacitance of about 308 F g at current density of 0.5 A g , which is much higher than that of rGO (200 F g ) and CDs (2.2 F g ). This work provides a promising strategy to fabricate graphene-based nanomaterials with greatly boosted electrochemical performances by decoration of with CDs.
[Mh] Termos MeSH primário: Capacitância Elétrica
Grafite/química
Nanoestruturas/química
Nanotecnologia
Óxidos/química
[Mh] Termos MeSH secundário: Eletroquímica
Eletrodos
Modelos Moleculares
Conformação Molecular
Porosidade
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Oxides); 7782-42-5 (Graphite)
[Em] Mês de entrada:1707
[Cu] Atualização por classe:170726
[Lr] Data última revisão:
170726
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170426
[St] Status:MEDLINE
[do] DOI:10.1002/cssc.201700474


  10 / 1766 MEDLINE  
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[PMID]:28436604
[Au] Autor:Schneidermann C; Jäckel N; Oswald S; Giebeler L; Presser V; Borchardt L
[Ad] Endereço:Department of Inorganic Chemistry, Technische Universität Dresden, Bergstraße 66, 01069, Dresden, Germany.
[Ti] Título:Solvent-Free Mechanochemical Synthesis of Nitrogen-Doped Nanoporous Carbon for Electrochemical Energy Storage.
[So] Source:ChemSusChem;10(11):2416-2424, 2017 Jun 09.
[Is] ISSN:1864-564X
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:Nitrogen-doped nanoporous carbons were synthesized by a solvent-free mechanochemically induced one-pot synthesis. This facile approach involves the mechanochemical treatment and carbonization of three solid materials: potassium carbonate, urea, and lignin, which is a waste product from pulp industry. The resulting nitrogen-doped porous carbons offer a very high specific surface area up to 3000 m g and large pore volume up to 2 cm g . The mechanochemical reaction and the impact of activation and functionalization are investigated by nitrogen and water physisorption and high-resolution X-ray photoelectron spectroscopy (XPS). Our N-doped carbons are highly suitable for electrochemical energy storage as supercapacitor electrodes, showing high specific capacitances in aqueous 1 m Li SO electrolyte (177 F g ), organic 1 m tetraethylammonium tetrafluoroborate in acetonitrile (147 F g ), and an ionic liquid (1-ethyl-3-methylimidazolium tetrafluoroborate; 192 F g ). This new mechanochemical pathway synergistically combines attractive energy-storage ratings with a scalable, time-efficient, cost-effective, and environmentally favorable synthesis.
[Mh] Termos MeSH primário: Carbono/química
Capacitância Elétrica
[Mh] Termos MeSH secundário: Carbonatos/química
Eletrodos
Eletrólitos/química
Lignanas/química
Nanoporos
Nitrogênio/química
Potássio/química
Ureia/química
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Carbonates); 0 (Electrolytes); 0 (Lignans); 7440-44-0 (Carbon); 8W8T17847W (Urea); BQN1B9B9HA (potassium carbonate); N762921K75 (Nitrogen); RWP5GA015D (Potassium)
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170816
[Lr] Data última revisão:
170816
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170425
[St] Status:MEDLINE
[do] DOI:10.1002/cssc.201700459



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