{"title":"高精度计算电荷转移后同质二聚或歧化反应的时序电位图","authors":"L.K. Bieniasz","doi":"10.1016/j.electacta.2024.145332","DOIUrl":null,"url":null,"abstract":"A theoretical model of constant current chronopotentiometry is considered, for a reversible charge transfer followed by an irreversible homogeneous dimerization or disproportionation reactions at a planar electrode. The model is expressed by a system of two partial differential reaction–diffusion equations, one or both being nonlinear. This system decomposes into two independent initial boundary value problems, which allows one to obtain semi-analytical series solutions of the model. Detailed derivations and analysis of the series are presented. Highly accurate numerical reference solutions are also obtained. Hybrid algorithms are devised for computing electrode potential-time responses. The algorithms combine the series solution for small time, with asymptotic approximants for large time, and fitted polynomials for intermediate time. The algorithms are efficient and highly accurate: the relative error modulus does not exceed ca. <span><span><math><mrow is=\"true\"><mn is=\"true\">1</mn><msup is=\"true\"><mrow is=\"true\"><mn is=\"true\">0</mn></mrow><mrow is=\"true\"><mo is=\"true\">−</mo><mn is=\"true\">19</mn></mrow></msup><mo is=\"true\" linebreak=\"goodbreak\" linebreakstyle=\"after\">−</mo><mn is=\"true\">1</mn><msup is=\"true\"><mrow is=\"true\"><mn is=\"true\">0</mn></mrow><mrow is=\"true\"><mo is=\"true\">−</mo><mn is=\"true\">18</mn></mrow></msup></mrow></math></span><script type=\"math/mml\"><math><mrow is=\"true\"><mn is=\"true\">1</mn><msup is=\"true\"><mrow is=\"true\"><mn is=\"true\">0</mn></mrow><mrow is=\"true\"><mo is=\"true\">−</mo><mn is=\"true\">19</mn></mrow></msup><mo linebreak=\"goodbreak\" linebreakstyle=\"after\" is=\"true\">−</mo><mn is=\"true\">1</mn><msup is=\"true\"><mrow is=\"true\"><mn is=\"true\">0</mn></mrow><mrow is=\"true\"><mo is=\"true\">−</mo><mn is=\"true\">18</mn></mrow></msup></mrow></math></script></span>, except for the small neighbourhoods of the transition time, and of the time where the potential response passes through zero. 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引用次数: 0
摘要
针对平面电极上可逆的电荷转移和不可逆的同质二聚或歧化反应,研究了恒定电流计时电位计的理论模型。该模型由两个偏微分反应-扩散方程系统表示,其中一个或两个都是非线性的。该系统分解为两个独立的初始边界值问题,因此可以得到模型的半解析序列解。本文详细推导和分析了这些序列。同时还获得了高精度的数值参考解。为计算电极电位-时间响应设计了混合算法。这些算法结合了小时间的序列解、大时间的渐近近似值以及中间时间的拟合多项式。这些算法效率高、精度高:相对误差模数不超过约 10-19-10-1810-19-10-18,过渡时间的小邻域和电位响应通过零点的时间除外。为这些计算提供了一套 C++ 例程。
Highly accurate computation of chronopotentiograms for a charge transfer followed by homogeneous dimerization or disproportionation reactions
A theoretical model of constant current chronopotentiometry is considered, for a reversible charge transfer followed by an irreversible homogeneous dimerization or disproportionation reactions at a planar electrode. The model is expressed by a system of two partial differential reaction–diffusion equations, one or both being nonlinear. This system decomposes into two independent initial boundary value problems, which allows one to obtain semi-analytical series solutions of the model. Detailed derivations and analysis of the series are presented. Highly accurate numerical reference solutions are also obtained. Hybrid algorithms are devised for computing electrode potential-time responses. The algorithms combine the series solution for small time, with asymptotic approximants for large time, and fitted polynomials for intermediate time. The algorithms are efficient and highly accurate: the relative error modulus does not exceed ca. , except for the small neighbourhoods of the transition time, and of the time where the potential response passes through zero. A set of C++ routines for these calculations is made available.
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.