研究生: |
沈曉萱 Shen, Hsiao Hsuan |
---|---|
論文名稱: |
碳材的表面電化學修飾對有機系超高電容表現之研究 Improving capacitive performance of activated carbon by electrochemical modification in organic-based supercapacitors |
指導教授: |
胡啟章
Hu, Chi Chang |
口試委員: |
溫添進
Wen, Ten Chin 鄧熙聖 Teng, Hsi Sheng 杜正恭 Duh, Jenq Gong 曾堯宣 Tseng, Yao Hsuan 蔡德豪 Tsai, De Hao 蔡林仁 Tsai, Lin Jen |
學位類別: |
博士 Doctor |
系所名稱: |
工學院 - 化學工程學系 Department of Chemical Engineering |
論文出版年: | 2016 |
畢業學年度: | 104 |
語文別: | 中文 |
論文頁數: | 126 |
中文關鍵詞: | 超級電容器 、有機電解液 、活性碳 、電化學修飾 、非對稱組裝 |
外文關鍵詞: | Supercapacitor, Organic electrolyte, Activated carbon, Electrochemical modification, Asymmetric design |
相關次數: | 點閱:1 下載:0 |
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本研究致力於碳材之有機系超高電容器之開發,目的為利用碳材之表面修飾及非對稱組裝系統,將操作電位提高,進而達到超級電容器之比能量提升。
本研究利用電化學進行單一商用活性碳材之開發,並藉由分析其材料之特性界定其電化學行為之表現。本文第四章節中,旨於探討未修飾之商用活性碳之操作電位窗,實驗利用學術與工業界皆普遍利用之循環充放電測試法及定電位極化法進行電化學測試,並搭配電化學阻抗頻譜圖以界定其操作電位窗,進而定義兩法於超級電容器壽命測試上之相對關係。於材料分析上,利用X光能譜儀標定電解質中之特定元素之增長作為操作電位之界限指標。第五章則利用與前章節使用之同一碳材,開發一電化學表面修飾法進行電極材料改值,此法利用多次循環充放電而能增加其於有機系電解液之電容,並同時展延其電位窗以提升其比能量。並藉由X光能譜儀和掃描式電子顯微鏡分析電極表面之修飾狀態,再進一步利用電化學阻抗頻譜圖確立修飾效果於超級電容器之影響性。
於後一章節中,主要延續前章之電化學修飾法之探討。實驗利用循環充放電測試法及定電位極化法之相對關係,將循環充放電之關係量化使定電位極化等效運用,以達修飾材料並縮短製程時間之效果。並藉由掃描式電子顯微鏡和臨場拉曼進行材料分析,以了解材料於製程中之變化。第七章則根據碳材之不同特性歸納其電化學行為差異,選用一商業奈米碳材作為正極材料,排除商用活性碳於有機電解液之正極電位窗限制,進行非對稱組裝測試。實驗說明此設計得一寬廣電位窗之非對稱電容器,而能大幅提高操作電位,因此,利用穿透式與掃描式電子顯微鏡、非臨場拉曼分析、X光能譜儀和比表面積測試,歸納奈米碳材與活性碳之性質差異。
This study aims at enlargement of operating voltage of carbon-based electrochemical capacitors (ECs) in organic-based electrolyte (1M TEABF4/PC), it relatively leads to improving specific energy, and especially demonstrates the unique electrochemical modification (EM) of ECs.
There are three parts in this work; criteria of activated carbons (ACs), capacitance enhancement of ACs and asymmetric cell consist of ACs and carbon black (CB). The operating cell voltage is developed from 2.1 V, 2.6 V to 3 V by electrochemical technique in these three parts. In first part, the combination of potential-stressed floating test and EIS analyses precisely determines the working potential window between -1.9 and 0.2 V (against Ag/AgNO3), which is a reliable method to efficiently define the working potential window. In this potential range, ECs exhibits about 6% capacitance loss during the charge-discharge test for 10,000 cycles at 0.5 A g-1 between 1.9 and 2.1 V. Then, a novel EM to enhance the specific capacitance (CS) and operating voltage of ACs was demonstrated in second part. This EM has been optimized by repeating 5 times of 100 charge-discharge cycles between -1.9 and 0.5 V (against Ag/AgNO3) in the fresh electrolyte. Moreover, the EM was evaluated by a series of consecutive floating tests from 0 V to 0.5 V (against Ag/AgNO3) each for 3050 seconds (s) with 100 mV as interval.
The surface morphology of ACs was thereafter examined by scanning electron microscope, reveals a film-like material which was formed onto the surface of ACs electrode during EM. Moreover, a film-like material has been identified to contain N, B, and F by X-ray photoelectron spectroscopic measurements. Besides, the characteristics of vibrational modes of ACs were investigated by in situ Raman spectroscopy, which shows the D band peak position of activated carbon present a blue-shift due to the surface structure change. After EM process, an asymmetric supercapacitor (ASC) consisting of the above modified-AC positive electrode and an as-received AC negative electrode, which shows excellent charge-discharge stability from the 1.9 % decay in the cell capacitance after 10,000-cycle stability test at 5 A g-1 between 0 and 2.6 V. In third part, the upper limit of the double-layer potential window for the interface between propylene carbonate and CB with low defects but relatively high specific surface area is effectively extended from 0.1 to 1 V (against Ag/AgNO3), compared with AC. Accordingly, commercial CB and AC are respectively employed as positive and negative electrode materials to construct an advanced ASC with cell voltage reaching 3 V, which is very stable in 10000-cycle charge-discharge tests at 1 A g-1 between 2.7 and 3 V.
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