Stability improvement of a Pt/TiO2 photocatalyst during photocatalytic pure water splitting. Issue 45 (11th November 2022)

• Record Type: Journal Article
• Authors: Zhang, Xinyi; Bo, Chunling; Cao, Shuang; Cheng, Zhijie; Xiao, Zhaozhong; Liu, Xiaolong; Tan, Ting; Piao, Lingyu
• Is Part Of: Journal of materials chemistry. Volume 10:Issue 45(2022)
• Page Start: 24381
• Page End: 24387
• Publication Date: 2022-11-11
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/d2ta06961j
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : The Pt/b-TiO2 NF photocatalyst is deactivated due to the accumulation of product H2 inhibits forward reaction and gradual substitution of H2 O2 for H2 O in the absorption site on the photocatalyst surface, its stability can be improved in a simple way. Abstract : The stability of a photocatalyst is a crucial indicator for its widespread use, which is significantly connected with deactivation and regeneration processes. Nevertheless, in the field of photocatalytic water splitting for hydrogen production, the deactivation and regeneration of photocatalysts have not been paid enough attention. In this work, the deactivation mechanism of a brookite TiO2 nanoflutes decorated with Pt (Pt/b-TiO2 NFs) photocatalyst used in photocatalytic pure water splitting was investigated, and simple and effective methods to improve stability were proposed as well. There are two reasons for the decrease of photocatalyst stability: the accumulation of H2 and the adsorption of the product H2 O2 . The physical structure of the Pt/b-TiO2 NF photocatalysts is stable during the reaction. As the reaction progresses, the products H2 and H2 O2 accumulate gradually, and H2 O2 attaches more tightly to the photocatalyst surface, steadily replacing the adsorption site of the reactant H2 O. Hence, the forward reaction is suppressed and a sharp decrease in the adsorption of the reactant H2 O is observed. Timely transfer of large amounts of H2 can avoid the inhibition of the forward reaction and thus stabilize the photocatalysts for more than 500 h at a time, which is 15–20 times more than that has been reported. To solve the adsorption problem of H2 O2, the Pt/b-TiO2 NF photocatalysts can be completely regenerated by mechanical disturbance. The same batch of the Pt/b-TiO2 NF photocatalysts can operate continuously for at least 400 h. This work is of great significance for promoting the large-scale application of photocatalytic water splitting to produce H2 .