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研究生: 陳惠榆
Chen, Hui-Yu
論文名稱: 異相催化反應之理論計算研究: 甲醇-d4分解反應與Fischer-Tropsch合成反應
Computational Study of Heterogeneous Catalysis Reactions: Methanol-d4 Decomposition and Fischer-Tropsch Synthesis
指導教授: 王禎翰
Wang, Jeng-Han
學位類別: 碩士
Master
系所名稱: 化學系
Department of Chemistry
論文出版年: 2015
畢業學年度: 103
語文別: 中文
論文頁數: 72
中文關鍵詞: 密度泛函理論異相催化反應甲醇分解反應Fischer-Tropsch合成反應
英文關鍵詞: density function theory, heterogeneous catalysis, methanol decomposition, Fischer-Tropsch synthesis, Rhodium, Ruthenium, Cobalt, Sodium, Potassium
論文種類: 學術論文
相關次數: 點閱:139下載:8
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  • 本論文包含兩個異相催化反應之理論計算研究:甲醇-d4在Rh催化劑分解反應及Fischer-Tropsch(F-T)合成反應。在第一個主題中,我們計算甲醇-d4在Rh(100)、放大的Rh(100)e及球狀Rh38表面,脫氫產生CO及D2分子的反應路徑,與表面大小的相關性,且與真空實驗系統做比對。由計算結果得知,在小的表面Rh38,甲醇-d4斷O-D鍵的活化能降低,使甲醇-d4容易分解,其結果與實驗觀察一致。此外,我們計算Rh表面及團簇上CO數目對吸附能的影響。CO吸附行為在平坦Rh(100)及球狀Rh38兩種表面差異甚大,在平坦的Rh(100)及Rh(100)e表面,CO分子垂直吸附於表面,然而,在球狀Rh38表面,CO分子吸附為輻射狀,此吸附結構會造成CO在球狀Rh38表面分子間作用力較小;因此,隨著CO覆蓋率上升,在Rh38表面吸附能下降幅度較Rh(100)表面為平緩。
    在第二個部分中,我們探討Fischer-Tropsch (F-T) 合成反應在Ru(0001)和Co(0001)表面的反應機構。根據計算結果可知,不論在Ru(0001)還是Co(0001)表面,CO傾向生成中間物CHO;在Co(0001)表面,CHO會繼續氫化生成CH2O及CH3O,但在Ru(0001)表面則是傾向斷C-O鍵。此兩表面路徑差異,對應在Co催化劑上有高的CH4選擇率,而在Ru催化劑則是生成含碳長鏈產物。因此,我們利用物理方法:改變表面粗糙度,及化學方法:表面加入promoter,增加Co催化劑活性作為改善。在物理方法中,我們計算波浪狀(11-20)及(1-100)表面,發現CO斷鍵在此兩表面更為容易,減少CH4選擇率。在化學方法中,探討加入Na及K金屬的Co(0001)表面,由計算結果得知,Na及K提升CHO的C-O斷鍵能力,大於氫化能力,增加F-T合成反應活性。

    This thesis computationally studied two related topics in heterogeneous catalysis, methanol-d4 decomposition on Rh catalysts and Fischer-Tropsch synthesis (FTS). In the first topic we thoroughly examined the decomposition pathway from methanol-d4 to CO and D2 on the prefect and expanded Rh(100) surfaces as well as spherical-shaped Rh38, which correspond to different-sized Rh nanoclusters in the experiment. Our computational result found that smaller Rh cluster, Rh38, can better decompose methanol because of the the decreased activation energy for O-D bond scission of methanol-d4, in consistent with the experimental observation. Additionally, we examined the adsorption behavior of surface CO on those Rh surface and cluster. CO adsorption behaves differently on flat Rh(100) and spherical Rh38. Surface CO perpendicularly adsorbed on the planes of Rh(100) and Rh(100)e, whereas the adspecies radically adsorbed the sphere of Rh38 that can ease the interaction among them and Eads reduction. Thus, the Eads of surface CO decreases rather slower on smaller sized Rh38 than the Rh(100) surfaces at higher surface coverage.
    In the second part, we computational examined the reaction mechanism of FTS on Ru(0001) and Co(0001) surfaces. According to the calculations, CO prefers the hydrogenation reaction forming CHO intermediate on both Ru(0001) and Co(0001) surfaces initially. Surface CHO prefers further hydrogenation forming CH2O or CH3O on Co(0001) while favors C-O bond cleavage on Ru(0001). The different reaction pathways for CHO are responsible for the higher CH4 selectivity on Co-based materials while products with longer carbon chian prefers on Ru-based catalysts. Furthermore, we used physical, such as surface roughness, and chemical, surface with promotors, methods to improve Co catalysted reactivity. In the physical method, we computed CO dissociation on step (11-20) and (1-100) surfaces and found CO can better dissociate on the surfaces to lower the CH4 selectivity. In the chemical method, FTS reactions were investigated on Co surface with with Na and K adatoms. The computed result found that adatoms can effectively promote C-O dissocation than hydrogenation of CHO to enhance FTS activity.

    致謝 I 中文摘要 II Abstract III 目錄 V 圖目錄 VII 表目錄 X 第一章 序論 1 1-1 催化反應介紹 1 1-2 異相催化反應在能源問題上的應用 3 1-3 研究方向 4 第二章 理論原理與計算 5 2-1 計算方法:密度泛函理論(Density functional theory ,DFT) 5 2-1-1 The Kohn-Sham equations 5 2-1-2交換相關函數(Exchange-Correlation Functions) 8 2-2 基底(Basis set) 9 2-2-1布洛赫定理與平面波基組 (Bloch theorem and plane wave basis sets) 9 2-2-2有效核勢(Pseudopotential or Effective core potential,ECP ) 10 2-3 系統與軟體 12 2-3-1國家高速網路與計算中心 12 2-3-2操作軟體VASP(Vienna Ab-initio simulation Package) 12 2-4 計算流程 20 第三章 探討奈米團簇、表面大小對Rh(銠)金屬上甲醇-d4 (CD3OD)分解之影響及表面CO覆蓋率對吸附能之影響 21 3-1 甲醇催化分解對能源上的應用及介紹 21 3-2 計算參數設定 22 3-3 結果與討論 24 3-3-1吸附物在Rh表面上的結構與吸附能 24 3-3-2反應機構 26 3-3-3 Rh表面大小及表面COm*覆蓋率的不同對吸附能的影響 34 3-3-4結果討論 38 第4章 Fischer-Tropsch合成反應在Ru及Co (0001)表面CO活化反應及利用物理及化學方法改善Ru及Co催化反應之理論計算研究 39 4-1 Fischer-Tropsch合成反應介紹 39 4-2 計算參數設定 40 4-2-1表面一:平坦的(0001)表面 40 4-2-2表面二:波浪狀的(11-20)表面 41 4-2-3表面二:鋸齒狀的(1-100)表面 41 4-2-4表面四:加入金屬M當promoter的Co(0001)表面(M = Na、K) 42 4-3 結果與討論 43 4-3-1 Ru(0001)和Co(0001)表面CO活化反應機構研究 43 4-3-2利用物理方法改變表面粗糙度:波浪狀表面(11-20)、鋸齒狀表面(1-100)與平坦表面(0001)吸附能、反應能量及活化能的比較 53 4-3-3利用化學方法改善催化劑:Co(0001)表面加入Na、K當promoter 58 4-4 結論 66 4-5 未來展望 68 參考文獻 69

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