Pt Deposites on TiO<sub>2</sub> for Photocatalytic H<sub>2</sub> Evolution: Pt Is Not Only the Cocatalyst, but Also the Defect Repair Agent

Pt, as a common cocatalyst, has been widely used in photocatalytic H<sub>2</sub> evolution. However, the specific role of Pt in photocatalytic H<sub>2</sub> evolution has not been thoroughly studied. In this paper, by employing three Pt sources with different charges (positiv...

Full description

Bibliographic Details
Main Authors: Zhan Shu, Yandi Cai, Jiawei Ji, Changjin Tang, Shuohan Yu, Weixin Zou, Lin Dong
Format: Article
Language:English
Published: MDPI AG 2020-09-01
Series:Catalysts
Subjects:
Online Access:https://www.mdpi.com/2073-4344/10/9/1047
id doaj-26b10f243f824fb9b8e49b0db2918aa8
record_format Article
spelling doaj-26b10f243f824fb9b8e49b0db2918aa82020-11-25T03:06:07ZengMDPI AGCatalysts2073-43442020-09-01101047104710.3390/catal10091047Pt Deposites on TiO<sub>2</sub> for Photocatalytic H<sub>2</sub> Evolution: Pt Is Not Only the Cocatalyst, but Also the Defect Repair AgentZhan Shu0Yandi Cai1Jiawei Ji2Changjin Tang3Shuohan Yu4Weixin Zou5Lin Dong6Key Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Key Laboratory of Vehicle Emissions Control, School of Environment, Center of Modern Analysis, Nanjing University, Nanjing 210093, ChinaKey Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Key Laboratory of Vehicle Emissions Control, School of Environment, Center of Modern Analysis, Nanjing University, Nanjing 210093, ChinaKey Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Key Laboratory of Vehicle Emissions Control, School of Environment, Center of Modern Analysis, Nanjing University, Nanjing 210093, ChinaKey Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Key Laboratory of Vehicle Emissions Control, School of Environment, Center of Modern Analysis, Nanjing University, Nanjing 210093, ChinaKey Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Key Laboratory of Vehicle Emissions Control, School of Environment, Center of Modern Analysis, Nanjing University, Nanjing 210093, ChinaKey Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Key Laboratory of Vehicle Emissions Control, School of Environment, Center of Modern Analysis, Nanjing University, Nanjing 210093, ChinaKey Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Key Laboratory of Vehicle Emissions Control, School of Environment, Center of Modern Analysis, Nanjing University, Nanjing 210093, ChinaPt, as a common cocatalyst, has been widely used in photocatalytic H<sub>2</sub> evolution. However, the specific role of Pt in photocatalytic H<sub>2</sub> evolution has not been thoroughly studied. In this paper, by employing three Pt sources with different charges (positive, negative and neutral), we systematically studied the charge effect of Pt sources on photocatalytic H<sub>2</sub> evolution via TiO<sub>2</sub> catalyst. According to the results of Raman, X-ray photoelectron spectroscopy (XPS), recycle experiments and photocurrent characterizations, it was found that TiO<sub>2</sub> would produce electropositive defects during photocatalytic H<sub>2</sub> evolution, inevitably leading to the decline of H<sub>2</sub> production activity. Thanks to the electrostatic interaction, the electronegative Pt source not only promoted charge separation, but preferential deposited on electropositive defects, which acted as the defect repair agent, and thus resulted in the increased photocatalytic stability. This work may provide a new perspective for enhancing photocatalytic stability of hydrogen production.https://www.mdpi.com/2073-4344/10/9/1047photocatalytic stabilityelectropositive defectPt sourceselectrostatic interactiondefect repair
collection DOAJ
language English
format Article
sources DOAJ
author Zhan Shu
Yandi Cai
Jiawei Ji
Changjin Tang
Shuohan Yu
Weixin Zou
Lin Dong
spellingShingle Zhan Shu
Yandi Cai
Jiawei Ji
Changjin Tang
Shuohan Yu
Weixin Zou
Lin Dong
Pt Deposites on TiO<sub>2</sub> for Photocatalytic H<sub>2</sub> Evolution: Pt Is Not Only the Cocatalyst, but Also the Defect Repair Agent
Catalysts
photocatalytic stability
electropositive defect
Pt sources
electrostatic interaction
defect repair
author_facet Zhan Shu
Yandi Cai
Jiawei Ji
Changjin Tang
Shuohan Yu
Weixin Zou
Lin Dong
author_sort Zhan Shu
title Pt Deposites on TiO<sub>2</sub> for Photocatalytic H<sub>2</sub> Evolution: Pt Is Not Only the Cocatalyst, but Also the Defect Repair Agent
title_short Pt Deposites on TiO<sub>2</sub> for Photocatalytic H<sub>2</sub> Evolution: Pt Is Not Only the Cocatalyst, but Also the Defect Repair Agent
title_full Pt Deposites on TiO<sub>2</sub> for Photocatalytic H<sub>2</sub> Evolution: Pt Is Not Only the Cocatalyst, but Also the Defect Repair Agent
title_fullStr Pt Deposites on TiO<sub>2</sub> for Photocatalytic H<sub>2</sub> Evolution: Pt Is Not Only the Cocatalyst, but Also the Defect Repair Agent
title_full_unstemmed Pt Deposites on TiO<sub>2</sub> for Photocatalytic H<sub>2</sub> Evolution: Pt Is Not Only the Cocatalyst, but Also the Defect Repair Agent
title_sort pt deposites on tio<sub>2</sub> for photocatalytic h<sub>2</sub> evolution: pt is not only the cocatalyst, but also the defect repair agent
publisher MDPI AG
series Catalysts
issn 2073-4344
publishDate 2020-09-01
description Pt, as a common cocatalyst, has been widely used in photocatalytic H<sub>2</sub> evolution. However, the specific role of Pt in photocatalytic H<sub>2</sub> evolution has not been thoroughly studied. In this paper, by employing three Pt sources with different charges (positive, negative and neutral), we systematically studied the charge effect of Pt sources on photocatalytic H<sub>2</sub> evolution via TiO<sub>2</sub> catalyst. According to the results of Raman, X-ray photoelectron spectroscopy (XPS), recycle experiments and photocurrent characterizations, it was found that TiO<sub>2</sub> would produce electropositive defects during photocatalytic H<sub>2</sub> evolution, inevitably leading to the decline of H<sub>2</sub> production activity. Thanks to the electrostatic interaction, the electronegative Pt source not only promoted charge separation, but preferential deposited on electropositive defects, which acted as the defect repair agent, and thus resulted in the increased photocatalytic stability. This work may provide a new perspective for enhancing photocatalytic stability of hydrogen production.
topic photocatalytic stability
electropositive defect
Pt sources
electrostatic interaction
defect repair
url https://www.mdpi.com/2073-4344/10/9/1047
work_keys_str_mv AT zhanshu ptdepositesontiosub2subforphotocatalytichsub2subevolutionptisnotonlythecocatalystbutalsothedefectrepairagent
AT yandicai ptdepositesontiosub2subforphotocatalytichsub2subevolutionptisnotonlythecocatalystbutalsothedefectrepairagent
AT jiaweiji ptdepositesontiosub2subforphotocatalytichsub2subevolutionptisnotonlythecocatalystbutalsothedefectrepairagent
AT changjintang ptdepositesontiosub2subforphotocatalytichsub2subevolutionptisnotonlythecocatalystbutalsothedefectrepairagent
AT shuohanyu ptdepositesontiosub2subforphotocatalytichsub2subevolutionptisnotonlythecocatalystbutalsothedefectrepairagent
AT weixinzou ptdepositesontiosub2subforphotocatalytichsub2subevolutionptisnotonlythecocatalystbutalsothedefectrepairagent
AT lindong ptdepositesontiosub2subforphotocatalytichsub2subevolutionptisnotonlythecocatalystbutalsothedefectrepairagent
_version_ 1724675312196780032