Ta3N5/Co(OH)x composites as photocatalysts for photoelectrochemical water splitting. Issue 4 (9th November 2018)

• Record Type: Journal Article
• Authors: Xu, Kaiqi; Chatzitakis, Athanasios; Jensen, Ingvild Julie Thue; Grandcolas, Mathieu; Norby, Truls
• Is Part Of: Photochemical & photobiological sciences. Volume 18:Issue 4(2019)
• Page Start: 837
• Page End: 844
• Publication Date: 2018-11-09
• Subjects: Photochemistry -- Periodicals; Photobiology -- Periodicals; 541.35
• DOI: 10.1039/c8pp00312b
• Languages: English
• ISSNs: 1474-905X

Abstract

Abstract : Elaboration of the stability issue related to the morphology of nanotubes, and enhancement of the PEC stability by loading double co-catalysts. Abstract : Ta3 N5 nanotubes (NTs) were obtained from nitridation of Ta2 O5 NTs, which were grown directly on Ta foil through a 2-step anodization procedure. With Co(OH) x decoration, a photocurrent density as high as 2.3 mA cm −2 (1.23 V vs. NHE) was reached under AM1.5G simulated solar light; however, the electrode suffered from photocorrosion. More stable photoelectrochemical (PEC) performance was achieved by first loading Co(OH) x, followed by loading cobalt phosphate (Co–Pi) as double co-catalysts. The Co(OH) x /Co–Pi double co-catalysts may act as a hole storage layer that slows down the photocorrosion caused by the accumulated holes on the surface of the electrode. A "waggling" appearance close to the "mouth" of Ta2 O5 NTs was observed, and may indicate structural instability of the "mouth" region, which breaks into segments after nitridation and forms a top layer of broken Ta3 N5 NTs. A unique mesoporous structure of the walls of the Ta3 N5 NTs, which is reported here the first time, is also a result of the nitridation process. We believe that the mesoporous structure makes it difficult for the nanotubes to be fully covered by the co-catalyst layer, hence rationalizing the remaining degradation by photocorrosion.