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研究生: 黃凱琳
Huang, Kai-Lin
論文名稱: 碳支撐銅錫奈米觸媒於電化學二氧化碳還原反應效能之研究
The Electrochemical CO2 Reduction Reaction on Carbon-Supported Cu-Sn Nanocatalysts
指導教授: 王禎翰
Wang, Jeng-Han
口試委員: 王冠文 洪偉修 王禎翰
口試日期: 2021/06/18
學位類別: 碩士
Master
系所名稱: 化學系
Department of Chemistry
論文出版年: 2021
畢業學年度: 109
語文別: 中文
論文頁數: 93
中文關鍵詞: 銅錫奈米觸媒二氧化碳還原反應法拉第效率雙金屬效應
英文關鍵詞: CuSn nanocatalysts (CuSn NCs), CO2 reduction reaction (CO2RR), faradiac efficiency (FE), bimetallic effect
DOI URL: http://doi.org/10.6345/NTNU202100778
論文種類: 學術論文
相關次數: 點閱:115下載:4
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  • 電化學二氧化碳還原反應(CO2RR)為將二氧化碳轉化為有價值的化學燃料和解決全球暖化提供了有效的方法。本研究針對優化銅錫奈米觸媒以獲得最佳的CO2RR效能。以油胺法製備銅錫奈米觸媒並利用能量散射光譜儀(EDS)、感應耦合電漿質譜分析儀(ICP-MS)、X光繞射分析儀(XRD)、X光光電子光譜(XPS)做觸媒特性鑑定。電催化性能藉由電流密度和主要產物一氧化碳法拉第效率來檢驗。透過調整適當銅錫比例來優化銅錫奈米觸媒的化學性質;Cu98Sn2/C在-0.7 V (vs. RHE)下表現出54.0%一氧化碳法拉第效率的最佳活性。觸媒結構的物理性質受合成溫度控制;於493 K下合成出均勻分散在表面的銅和錫,在-0.8 V (vs. RHE)下有最高的一氧化碳法拉第效率88.6%。此外,對兩種錫前驅物做比較發現在油胺法中使用二水氯化亞錫於合成上是更好的選擇。

    Electrochemical carbon dioxide reduction reaction (CO2RR) provides an effective way to convert carbon dioxide into valuable chemical fuels and resolve the detrimental problem of global warming. Our present work aims to optimize CuSn nanocatalysts for achieveing the best CO2RR performance. CuSn nanocatalysts were synthesized by oleylamine method and characterized by various technqies, including EDS, ICP-MS, XRD and XPS. The electrocatalytic performance was examined by current density and Faradiac efficiency (FE) of CO, the main reduction product. The chemical character of CuSn nanocatalysts was optimized by adjusting the proper Cu/Sn ratio; Cu98Sn2/C showed the best activity of 54.0% CO FE at -0.7 V (vs.RHE). The physical character of catalyst structure was controlled by the synthetic temperature; evenly dispersed surface Cu and Sn, synthesized at 493 K, had the highest CO FE of 88.6% at -0.8 V (vs. RHE). Addtionally, couple tin precursors were examined and found that dehydrated tin(II) chloride is a better option for the synthesis in oleylamine method.

    謝誌 i 摘要 ii Abstract iii 目錄 iv 圖目錄 vii 表目錄 x 第一章 緒論 1 1-1 前言 1 1-2 二氧化碳還原反應介紹 2 1-3 金屬觸媒介紹 4 1-4 雙金屬觸媒介紹 6 1-5 核殼結構雙金屬奈米粒子觸媒介紹 7 1-6 研究動機 8 第二章 實驗方法 9 2-1 實驗藥品、氣體及儀器 10 2-1-1 實驗藥品 10 2-1-2 實驗氣體 11 2-1-3 實驗儀器 12 2-2 油胺法製備觸媒 13 2-2-1 觸媒Cu/C的製備 13 2-2-2 觸媒CuxSny/C的製備 14 2-2-3 觸媒CuxSny-T/C (T=453, 473, 493, 523 K) 的製備 15 2-2-4 不同Sn前驅物之觸媒CuxSny-precursor-T/C的製備 16 2-3 觸媒鑑定 18 2-3-1 能量散射光譜儀(Energy Dispersive X-Ray Spectroscopy, EDS) 18 2-3-2 感應耦合電漿質譜分析儀(Inductively Coupled Plasma-Mass Spectrometer, ICP-MS) 19 2-3-3 X光繞射分析儀(X-Ray Diffraction analysis, XRD) 19 2-3-4 X光光電子光譜(X-ray Photoelectron Spectroscopy, XPS) 21 2-4 觸媒電化學分析 22 2-4-1 工作電極製備 22 2-4-2 電化學活性反應面積(Electrochemically active surface area, ECSA) 23 2-4-3 電化學二氧化碳還原反應(Carbon dioxide reduction reaction, CO2RR) 24 2-4-4 氣相層析儀(Gas chromatography, GC) 27 第三章 結果與討論 29 3-1 組成對於觸媒CuxSny/C鑑定與效能之影響 29 3-1-1 能量散射光譜儀(EDS)及感應耦合電漿質譜分析儀(ICP-MS) 29 3-1-2 X光光電子光譜(XPS) 31 3-1-3 X光繞射分析儀(X-Ray Diffraction analysis, XRD) 36 3-1-4 電化學活性反應面積(Electrochemically active surface area, ECSA) 39 3-1-5 電化學二氧化碳還原反應(CO2RR) 40 3-1-6 總結 45 3-2 結構對於觸媒CuxSny-T/C (T=453, 473, 493, 523 K)鑑定與效能之影響 46 3-2-1 能量散射光譜儀(EDS)及感應耦合電漿質譜分析儀(ICP-MS) 46 3-2-2 X光光電子光譜(XPS) 47 3-2-3 X光繞射分析儀(X-Ray Diffraction analysis, XRD) 53 3-2-4 電化學活性反應面積(Electrochemically active surface area, ECSA) 56 3-2-5 電化學二氧化碳還原反應(CO2RR) 58 3-2-6 總結 65 3-3 Sn前驅物對於觸媒CuxSny-precursor-T/C鑑定與效能之影響 66 3-3-1 能量散射光譜儀(EDS)及感應耦合電漿質譜分析儀(ICP-MS) 66 3-3-2 X光光電子光譜(XPS) 68 3-3-3 X光繞射分析儀(X-Ray Diffraction analysis, XRD) 74 3-3-4 電化學活性反應面積(Electrochemically active surface area, ECSA) 77 3-3-5 電化學二氧化碳還原反應(CO2RR) 78 3-3-6 總結 83 第四章 結論 84 參考資料 86 附錄 90

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