English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 64178/96951 (66%)
造訪人次 : 10198403      線上人數 : 18515
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library & TKU Library IR team.
搜尋範圍 查詢小技巧:
  • 您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
  • 進階搜尋
    請使用永久網址來引用或連結此文件: https://tkuir.lib.tku.edu.tw/dspace/handle/987654321/118697


    題名: Enhancing solar-driven water splitting with surface-engineered nanostructures
    作者: Shen, S.;Lindley, S. A.;Dong, C. L.;Chen, E.;Lu, Y. R.;Zhou, J.;Hu, Y.;Wheeler, D. A.;Guo, P.;Zhang, J.;Kliger, D. S.;Mao, S. S.
    日期: 2018-12-13
    上傳時間: 2020-06-01 12:14:11 (UTC+8)
    摘要: Functional nanoscale interfaces that promote the transport of photoexcited charge carriers are fundamental to efficient hydrogen production during photoelectrochemical (PEC) splitting of water. Here, the realization of a functional one‐dimensional nanostructure achieved through surface engineering of hematite (α‐Fe2O3) nanorods with a TiO2 overlayer is reported. The surface‐engineered hematite nanostructure exhibits significantly improved PEC performance as compared to untreated α‐Fe2O3, with an increase in the maximum incident photon‐to‐current efficiency (IPCE) of nearly 400% at 350 nm. While addition of the TiO2 overlayer did not alter the lifetime of photoexcited charge carriers, as evidenced from transient absorption spectroscopy, it is found that the presence of TiO2 could enhance oxygen electrocatalysis by interfacial electron enrichment, largely attributed to enhanced O(2p )−Fe(3d ) hybridization. Moreover, the interfacial electronic structure revealed from XANES measurements of the α‐Fe2O3/TiO2 nanorods suggests that photoexcited holes in α‐Fe2O3 may efficiently transfer through the TiO2 overlayer to the electrolyte while electrons migrate to the external circuit along the one‐dimensional nanorods, thereby promoting charge separation and enhancing PEC splitting of water.
    關聯: Solar RRL 3(3), 1800285
    DOI: 10.1002/solr.201800285
    顯示於類別:[物理學系暨研究所] 期刊論文

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    index.html0KbHTML109檢視/開啟

    在機構典藏中所有的資料項目都受到原著作權保護.

    TAIR相關文章

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library & TKU Library IR teams. Copyright ©   - 回饋