中文摘要
有機氧化還原液流電池(Organic redox flow batteries, ORFBs)，因其低成本和可長時間提供高能量密度能量，被視為一種很有潛力的能源裝置。本論文將一種具有活性的氧化還原的新型有機電解質(CDA和CDO)搭配不同的鹼性隔膜（E28-GT、G60、GRT、FA、GT和RT等隔膜）應用於有機氧化還原液流電池（ORFBs）。結果顯示在K4Fe(CN)6半電池中CDA與CDO電解質在使用G60、GRT、FA、與RT的隔離膜，分別在2.5mA cm‒2並與第50圈後釋放出 10.0/0.72，12.7/0.32，22.0/0.34和11.0/0.32 Wh L‒1的能量密度。CDA在相較CDO的情況下，與第50圈後擁有更加優越的能量密度。於此判斷由於CDA擁有有效互動的胺族（N‒H）在與G60, GRT, FA和RT可以提高吸水能力與OH‒之導性。儘管如此，首圈的CDA/ K4Fe(CN)6與CDO/K4Fe(CN)6之半電池在使用 E28 GT依然可以提供12.2/37.55 Wh L‒1的能量密度，再於50圈後都降至9.78/4.0 Wh L‒1 。CDA在使用GT時，由於其較差的吸水能力導致OH-導性被降低的情況下， 首圈可以提供17.46 Wh L‒1，但與此同時也於50圈後掉至12.6 Wh L‒1 .首圈的CDA/K4Fe(CN)6 與 CDO/K4Fe(CN)6 半電池在使用E28-GT, G60, GRT, FA GT 與 RT時，能量密度分別為20.46/88.73, 23.72/1.68, 26.31/0.75, 45.83/0.77, 55.74/1.4 與 80/0.76% 都於50圈後分別達24.77/38.68, 68/30.58, 72.9/18.76, 78.69/24.6, 66.15/35.94, 與 70.48/18.76%。在此可以清楚觀察到隔離膜相對電池性能的影響。G60, GRT, FA, 與 RT相較E28-GT 與 GT對於 CDA與CDO擁有更好的動力學可逆性，更低的容量損失，更高的效率。因G60, GRT, FA, 與 RT相對E28-GT 與 GT擁有的低電阻，高離子傳導與吸水能力，優化CDA/K4Fe(CN)6 相較 CDO/K4Fe(CN)6 半電池的兼容性與效率。FA隔離膜是於CDA 與 CDO在50圈後，擁有最佳的性能表現之隔離膜。為了可以更佳的了解FA對於CDA 與 CDO這兩種電解質與K4Fe(CN)6 成半電池的有效性, 實驗在2.5 mA cm‒2持續進行至100圈, 並取得27.08/20.78 Wh L‒1 的能量密度與80.5 與 53.35%的效率。這兩種有機電解質在使用FA的隔離膜，都擁有穩定的圈數表現（100% 庫倫效率） 。然而CDA相較CDO依然擁有更高的能量密度，因其擁有更佳的潤濕效應。CDA因擁有N-H基的存在有效的幫助FA的潤濕並且提升電化學反應。CDA 與 CDO在還原液流電池中，不只是影響著隔離膜，同時也為兩顆原子之間存在的結構差異。此被觀察的效應是與CDA/K4Fe(CN)6 與 CDO/K4Fe(CN)6 全電池在提供2.0/1.07 Wh L‒1（首圈） 改變至 to 5.56/1.18 Wh L‒1 (第100圈), 能量效率也從 37.55/45.1% (首圈) 改變至 66.59/51.53% (第100圈) .這暗示著2.0與0.32離子在100圈後的可逆性。因此，此兩種電解質的性能顯示著其高電阻與低導電性的CDO中的OH‒ ，造成其最終的低能量密度與效率。在此，CDA的仲胺表現出更佳優越的能量密度。此外，CDA（FA）的EIS結果顯示相較CDA來的低，可以被理解為更多的潤濕性，更好的吸水性，還有由於CDA中的 N‒H族的相應，相較CDO也有著更優的OH‒導性。有趣的發現是CDA/K4Fe(CN)6在使用FA的情況下，除了更好的性能表現，也同時在超過100圈有著更低的容量損耗。

關鍵字：有機氧化還原液流電池(ORFBs)、白屈氨酸(CDA)、白屈菜酸(CDO)、鹼性膜、儲能

Abstract
Organic redox flow batteries are a promising energy device due to their low-cost and ability of delivering high energy density for long time. In this thesis, a redox active organic electrolyte CDA and CDO are used for redox flow battery (RFB) using alkaline membranes (like E28 GT, G60, GRT, FA, GT and RT). The assembled CDA and CDO anolytes with K4Fe(CN)6 half cells, using G60, GRT, FA and RT separators deliver energy densities of 10.0/0.72, 12.7/0.32, 22.0/0.34, and 11.0/0.32 Wh L‒1, respectively in 1st cycle and improved to 21.88/16.1, 23.37/13.58, 26.9/16.1, and 36.78/13.6 Wh L‒1, respectively after 50th cycles at 2.5 mA cm‒2. The CDA provided great energy densities storage compared to CDO after 50th cycles. This is due to the fact that, the effective interaction of amine (N‒H) group containing CDA with G60, GRT, FA and RT, rise water uptake ability and OH‒ conductivity. However, in the first cycle the CDA/K4Fe(CN)6 and CDO/K4Fe(CN)6 half-cell could supplied energy densities of 12.2/37.55 Wh L‒1 by E28 GT, respectively and dropped to 9.78/4.0 Wh L‒1 after 50th cycles. Similarly, CDA delivered 17.46 by GT in the first cycle and decrease to 12.6 Wh L‒1, respectively after 50th cycles, because of less water uptake ability HO‒ conductivity reduced in this case. In first cycle, the CDA/ K4Fe(CN)6 and CDO/K4Fe(CN)6 half-cell energy efficiencies (EE) were 20.46/88.73, 23.72/1.68, 26.31/0.75, 45.83/0.77, 55.74/1.4 and 80/0.76% by E28-GT, G60, GRT, FA GT and RT and changed 24.77/38.68, 68/30.58, 72.9/18.76, 78.69/24.6, 66.15/35.94, and 70.48/18.76% after 50th cycles, respectively. Herein, the effect of membranes on battery performance can be observed clearly. In CDA and CDO the G60, GRT, FA, and RT were shown better kinetic reversibility, with less capacity loss and high efficacies compared to E28-GT and GT. The obtained low resistance, high ion conductivity and water uptake ability of G60, GRT, FA, and RT relative to E28-GT and GT confirmed their more compatibility and efficiency with CDA/K4Fe(CN)6 than CDO/K4Fe(CN)6 cells. From all performed membrane the FA exhibited best performance in CDA and CDO cells after 50th cycles. To better understand the effectiveness of FA the CDA and CDO anolytes and K4Fe(CN)6 half cells, conducted for 100 cycles and obtained 27.08/20.78 Wh L‒1 energy density, with 80.5 and 53.35% efficiencies, respectively at 2.5 mA cm‒2. The two organic anolytes using FA also shown stable cycling performances with 100% coulombic efficiency. However, CDA shown a high energy density than CDO, because of wettability effect. The presence of (N‒H) in CDA help to increase FA wettability and improve its electrochemical performance.
The CDA and CDO redox flow battery not only affected by membranes but also by structural difference existed between the two atoms. The effect was observed in CDA/K4Fe(CN)6 and CDO/K4Fe(CN)6 full cell by providing 2.0/1.07 Wh L‒1 (first cycle) and changed to 5.56/ 1.18 Wh L‒1 (after 100 cycles), with 37.55/45.1% (first cycle) and 66.59/51.53% (after 100 cycles) energy efficiency, respectively. This implies 2.0 and 0.51 electrons were reversibly after 100 cycles. Hence, the performance of two anolytes cell show that the high resistance and less conductivity of OH‒ in CDO possess by FA, causes to lower its final energy density and efficiency. Here what can be understood is the secondary amine in CDA exhibited superior energy density. Furthermore, the EIS result of CDA (FA) determined to be lower than that of CDO, indicating the more wettability, higher water uptake ability, and OH‒ conductivity of CDA than CDO, because of the effect of N‒H group in CDA. Interestingly, CDA/K4Fe(CN)6 by FA exhibited an excellent performance with less capacity loss over 100 cycles.

Keywords: ORFBs, CDA, CDO, alkaline membranes, energy storage.

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