The effect of finite pore length on ion structure and charging

被引:34
作者
Breitsprecher, Konrad [1 ]
Abele, Manuel [1 ]
Kondrat, Svyatoslav [1 ,2 ]
Holm, Christian [1 ]
机构
[1] Univ Stuttgart, Inst Computat Phys, Allmandring 3, D-70569 Stuttgart, Germany
[2] Polish Acad Sci, Inst Phys Chem, Kasprzaka 44-52, PL-01224 Warsaw, Poland
关键词
ENERGY-STORAGE; ELECTROCHEMICAL CAPACITORS; CARBON; LIQUID; SIZE; SUPERCAPACITORS; ELECTROLYTES; SIMULATION; ELECTRODES; DYNAMICS;
D O I
10.1063/1.4986346
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nanoporous supercapacitors play an important role in modern energy storage systems, and their modeling is essential to predict and optimize the charging behaviour. Two classes of models have been developed that consist of finite and infinitely long pores. Here, we show that although both types of models predict qualitatively consistent results, there are important differences emerging due to the finite pore length. In particular, we find that the ion density inside a finite pore is not constant, but increases linearly from the pore entrance to the pore end, where the ions form a strongly layered structure. This hinders a direct quantitative comparison between the two models. In addition, we show that although the ion density between the electrodes changes appreciably with the applied potential, this change has a minor effect on charging. Our simulations also reveal a complex charging behaviour, which is adsorption-driven at high voltages, but it is dominated either by co-ion desorption or by adsorption of both types of ions at low voltages, depending on the ion concentration. Published by AIP Publishing.
引用
收藏
页数:10
相关论文
共 56 条
[1]  
Arnold A., 2013, Meshfree Methods for Partial Differential Equations, V6, P1, DOI [10.1007/978-3-642-32979-1_1, DOI 10.1007/978-3-642-32979-11, DOI 10.1007/978-3-642-32979-1_1]
[2]   Comparison of scalable fast methods for long-range interactions [J].
Arnold, Axel ;
Fahrenberger, Florian ;
Holm, Christian ;
Lenz, Olaf ;
Bolten, Matthias ;
Dachsel, Holger ;
Halver, Rene ;
Kabadshow, Ivo ;
Gaehler, Franz ;
Heber, Frederik ;
Iseringhausen, Julian ;
Hofmann, Michael ;
Pippig, Michael ;
Potts, Daniel ;
Sutmann, Godehard .
PHYSICAL REVIEW E, 2013, 88 (06)
[3]   Efficient Algorithms for Electrostatic Interactions Including Dielectric Contrasts [J].
Arnold, Axel ;
Breitsprecher, Konrad ;
Fahrenberger, Florian ;
Kesselheim, Stefan ;
Lenz, Olaf ;
Holm, Christian .
ENTROPY, 2013, 15 (11) :4569-4588
[4]   Electrode Models for Ionic Liquid-Based Capacitors [J].
Breitsprecher, Konrad ;
Szuttor, Kai ;
Holm, Christian .
JOURNAL OF PHYSICAL CHEMISTRY C, 2015, 119 (39) :22445-22451
[5]   Coarse-grained simulations of an ionic liquid-based capacitor: II. Asymmetry in ion shape and charge localization [J].
Breitsprecher, Konrad ;
Kosovan, Peter ;
Holm, Christian .
JOURNAL OF PHYSICS-CONDENSED MATTER, 2014, 26 (28)
[6]   Coarse-grained simulations of an ionic liquid-based capacitor: I. Density, ion size, and valency effects [J].
Breitsprecher, Konrad ;
Kosovan, Peter ;
Holm, Christian .
JOURNAL OF PHYSICS-CONDENSED MATTER, 2014, 26 (28)
[7]   Capacitance of Nanoporous Carbon-Based Supercapacitors Is a Trade-Off between the Concentration and the Separability of the Ions [J].
Burt, Ryan ;
Breitsprecher, Konrad ;
Daffos, Barbara ;
Taberna, Pierre-Louis ;
Simon, Patrice ;
Birkett, Greg ;
Zhao, X. S. ;
Holm, Christian ;
Salanne, Mathieu .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2016, 7 (19) :4015-4021
[8]  
Chmiola J, 2006, SCIENCE, V313, P1760, DOI 10.1126/science/1132195
[9]   Phase behaviour and structure of a superionic liquid in nonpolarized nanoconfinement [J].
Dudka, Maxym ;
Kondrat, Svyatoslav ;
Kornyshev, Alexei ;
Oshanin, Gleb .
JOURNAL OF PHYSICS-CONDENSED MATTER, 2016, 28 (46)
[10]   High capacitance of coarse-grained carbide derived carbon electrodes [J].
Dyatkin, Boris ;
Gogotsi, Oleksiy ;
Malinovskiy, Bohdan ;
Zozulya, Yuliya ;
Simon, Patrice ;
Gogotsi, Yury .
JOURNAL OF POWER SOURCES, 2016, 306 :32-41