化學系

Permanent URI for this communityhttp://rportal.lib.ntnu.edu.tw/handle/20.500.12235/57

國立臺灣師範大學化學系座落於公館校區理學院大樓。本系成立於民國五十一年,最初僅設大學部。之後於民國六十三年、七十八年陸續成立化學研究所碩士班和博士班。本系教育目標旨在培養化學專業人才與中等學校自然及化學專業師資,授課著重理論及應用性。本系所現有師資為專任教授25人,另外尚有與中央研究院合聘教授3位,在分析、有機、無機及物理化學四個學門的基礎上發展跨領域之教學研究合作計畫。此外,本系另有助教13位,職技員工1位,協助處理一般學生實驗及行政事務。學生方面,大學部現實際共322人,碩士班現實際就學研究生共174人,博士班現實際就學共55人。

本系一向秉持著教學與研究並重,近年來為配合許多研究計畫的需求,研究設備亦不斷的更新。本系所的研究計畫大部分來自國科會的經費補助。此外,本系提供研究生獎助學金,研究生可支領助教獎學金(TA)、研究獎學金(RA)和部分的個別教授所提供的博士班學生獎學金(fellowships)。成績優良的大學部學生也可以申請獎學金。

本校圖書館藏書豐富,除了本部圖書館外,分部理學院圖書館西文藏書現有13萬餘冊,西文期刊合訂本有911餘種期刊,將近約3萬冊。此外,西文現期期刊約450種,涵蓋化學、生化、生物科技、材料及其他科學類等領域。目前本系各研究室連接校園網路,將館藏查詢、圖書流通、期刊目錄轉載等功能,納入圖書館資訊系統中,並提供多種光碟資料庫之檢索及線上資料庫如Science Citation Index,Chemical Citation Index,Chemical Abstracts,Beilstein,MDL資料庫與STICNET全國科技資訊網路之查詢。

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    FeS2 Nanocrystal Ink as a Catalytic Electrode for Dye-Sensitized Solar Cells
    (Wiley-VCH Verlag, 2013-06-24) Y.-C. Wang; D.-Y. Wang; Y.-T. Jiang; H.-A. Chen; Chia-Chun Chen; K.-C. Ho; - H.-L. Chou; Chun-Wei Chen
    Calligraphic counter electrodes: An important photovoltaic application using FeS2 nanocrystal (NC) pyrite ink to fabricate a counter electrode as an alternative to Pt in dye-sensitized solar cells is demonstrated. FeS2 NC ink exhibits excellent electrochemical catalytic activity and remarkable electrochemical stability. ITO=indium-doped tin oxide.
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    Platinum-Decorated Ruthenium Nanoparticles for Enhanced Methanol Electrooxidation
    (Wiley-VCH Verlag, 2010-02-08) C.-H. Chen; L. S. Sarma; D. -Y. Wang; F.-J. Lai; C.-C. AI Andra; S.-H. Chang; D.-G. Liu; Chia-Chun Chen; J.-F. Lee; B.-J. Hwang
    A promising electrocatalyst based on the reduction of Pt2+ ions on the surface of hexagonally close-packed (hcp) Ru core nanoparticles has been prepared by a redox–transmetalation process. This simple synthetic process generates a Pt-on-Ru catalyst with a lower Pt content than commercially available Pt[BOND]Ru electrocatalysts and with a long-range ordered hcp structure, which can significantly reduce the Pt loading. X-Ray absorption spectroscopy of the Pt-on-Ru catalyst reveals pronounced electronic modifications when compared to the commercial Pt[BOND]Ru black catalyst. The Pt-on-Ru catalyst exhibits a higher mass-specific current than the Pt[BOND]Ru black catalyst in solution in 0.5 m H2SO4 with 10 vol. % CH3OH under the conditions of rotating disk experiments. Further optimization of this synthetic procedure may yield even more active electrocatalysts with a significant reduction in noble metal loadings.