論文

査読有り 本文へのリンクあり
2019年

Origin of the overall water splitting activity of Ta<inf>3</inf>N<inf>5</inf> revealed by ultrafast transient absorption spectroscopy

Chemical Science
  • Dharmapura H.K. Murthy
  • ,
  • Hiroyuki Matsuzaki
  • ,
  • Zheng Wang
  • ,
  • Yohichi Suzuki
  • ,
  • Takashi Hisatomi
  • ,
  • Kazuhiko Seki
  • ,
  • Yasunobu Inoue
  • ,
  • Kazunari Domen
  • ,
  • Akihiro Furube

10
20
開始ページ
5353
終了ページ
5362
記述言語
掲載種別
研究論文(学術雑誌)
DOI
10.1039/c9sc00217k

© The Royal Society of Chemistry. Tantalum nitride (Ta3N5) is one of the few visible light absorbing photocatalysts capable of overall water splitting (OWS), by which the evolution of both H2 and O2 is possible. Despite favourable energetics, realizing the OWS or efficient H2 evolution in Ta3N5 prepared by the nitridation of tantalum oxide (Ta2O5) or Ta foil remains a challenge even after 15 years of intensive research. Recently our group demonstrated OWS in Ta3N5 when prepared by the short time nitridation of potassium tantalate (KTaO3). To obtain a mechanistic insight on the role of Ta precursor and nitridation time in realizing OWS, ultrafast dynamics of electrons (3435 nm probe) and holes (545 nm probe) is investigated using transient absorption spectroscopy. Electrons decay majorly by trapping in Ta3N5 prepared by the nitridation of Ta2O5, which do not show OWS. However, OWS activity in Ta3N5 prepared by 0.25 hour nitridation of KTaO3 is particularly favoured by the virtually absent electron and hole trapping. On further increasing the nitridation time of KTaO3 from 0.25 to 10 hour, trapping of both electron and hole is enhanced which concurrently results in a reduction of the OWS activity. Insights from correlating the synthesis conditions - structural defects - carrier dynamics - photocatalytic activity is of importance in designing novel photocatalysts to enhance solar fuel production.

リンク情報
DOI
https://doi.org/10.1039/c9sc00217k
Scopus
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85066063712&origin=inward 本文へのリンクあり
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https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85066063712&origin=inward
ID情報
  • DOI : 10.1039/c9sc00217k
  • ISSN : 2041-6520
  • eISSN : 2041-6539
  • SCOPUS ID : 85066063712

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