Water, Not Salt, Causes Most of the Seebeck Effect of Nonisothermal Aqueous Electrolytes

被引:4
|
作者
Nickel, Ole [1 ]
Ahrens-Iwers, Ludwig J. V. [2 ]
Meissner, Robert H. [1 ,3 ]
Janssen, Mathijs [4 ]
机构
[1] Hamburg Univ Technol, Inst Polymers & Composites, Hamburg, Germany
[2] Hamburg Univ Technol, Inst Adv Ceram, Hamburg, Germany
[3] Helmholtz Zentrum Hereon, Inst Surface Sci, Geesthacht, Germany
[4] Norwegian Univ Life Sci, Fac Sci & Technol, As, Norway
关键词
LIQUID-VAPOR INTERFACE; MOLECULAR-DYNAMICS; THERMOELECTRIC-MATERIALS; THERMODYNAMIC PROPERTIES; HEAT; TRANSPORT; SIMULATION; HYDRATION; SURFACE; POLARIZATION;
D O I
10.1103/PhysRevLett.132.186201
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
A temperature difference between two electrolyte-immersed electrodes often yields a voltage Delta yr between them. This electrolyte Seebeck effect is usually explained by cations and anions flowing differently in thermal gradients. However, using molecular simulations, we found almost the same Delta yr for cells filled with pure water as with aqueous alkali halides. Water layering and orientation near polarizable electrodes cause a large temperature-dependent potential drop X there. The difference in X of hot and cold electrodes captures most of the thermovoltage, Delta yr approximate to Xhot - Xcold.
引用
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页数:6
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