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通过初始充电的电位阶跃分析来确定钒氧化还原流电池的电解质失衡。

Electrolyte Imbalance Determination of a Vanadium Redox Flow Battery by Potential-Step Analysis of the Initial Charging.

机构信息

Urban and Residential Technologies, DLR Institute of Networked Energy Systems, Carl-von-Ossietzky-Str. 15, 26129, Oldenburg, Germany.

VANEVO GmbH, Johann-Hinrich-Engelbart-Weg 2, 26131, Oldenburg, Germany.

出版信息

ChemSusChem. 2020 Apr 21;13(8):2066-2071. doi: 10.1002/cssc.201903485. Epub 2020 Feb 28.

Abstract

Vanadium redox flow batteries (VRFB) suffer from capacity fades owing to side reactions and crossover effects through the membrane. These processes lead to a deviation of the optimal initial average oxidation state (AOS=+3.5) of vanadium species in both half-cell electrolytes. To rebalance the electrolyte solutions, it is first necessary to determine the current AOS. In this study, a new method was developed that enables an accurate determination of the AOS. A potential-step analysis was performed with mixed electrolyte solutions of both half-cells during the initial charging. The potential was recorded with a simple open-circuit voltage (OCV) cell, and the potential-steps were analyzed. A correlation between the duration of the potential plateaus in the OCV and the amount of vanadium ions of a certain oxidation state in the half-cell electrolytes was found and used to precisely determine the AOS with a maximum error of 3.6 %.

摘要

钒氧化还原流电池 (VRFB) 由于通过膜的副反应和交叉效应而遭受容量衰减。这些过程导致两个半电池电解液中钒物种的最佳初始平均氧化态 (AOS=+3.5) 发生偏离。为了重新平衡电解液,首先需要确定当前 AOS。在这项研究中,开发了一种新方法,能够准确确定 AOS。在初始充电过程中,对半电池的混合电解液进行了电位阶跃分析。使用简单的开路电压 (OCV) 电池记录电位,并对电位阶跃进行分析。在 OCV 中电位平台的持续时间与半电池电解液中特定氧化态的钒离子量之间存在相关性,并用于精确确定 AOS,最大误差为 3.6%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a75/7216990/4eb694288bde/CSSC-13-2066-g001.jpg

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