Path of electron transfer created in S-doped NH2-UiO-66 bridged ZnIn2S4/MoS2 nanosheet heterostructure for boosting photocatalytic hydrogen evolution. Issue 8 (1st April 2020)
- Record Type:
- Journal Article
- Title:
- Path of electron transfer created in S-doped NH2-UiO-66 bridged ZnIn2S4/MoS2 nanosheet heterostructure for boosting photocatalytic hydrogen evolution. Issue 8 (1st April 2020)
- Main Title:
- Path of electron transfer created in S-doped NH2-UiO-66 bridged ZnIn2S4/MoS2 nanosheet heterostructure for boosting photocatalytic hydrogen evolution
- Authors:
- Ran, Qi
Yu, Zebin
Jiang, Ronghua
Qian, Lun
Hou, Yanping
Yang, Fei
Li, Fengyuan
Li, Mingjie
Sun, Qianqian
Zhang, Heqing - Abstract:
- Abstract : This work introduces the synthesis of ZnIn2 S4 /NH2 -UiO-66/MoS2 sheet heterostructure photocatalysts and their application to photocatalytic hydrogen evolution. Abstract : Developing well-designed architectures plays a decisive role in accelerating photo-generated carrier transport in composite photocatalysts. Herein, a microporous sulfur-doped (S-doped) NH2 -UiO-66 bridged ZnIn2 S4 /MoS2 sheet heterostructure photocatalyst is synthesized through thermolysis of sulfur rich precursors to functionalize the organic ligands of NH2 -UiO-66 to boost photocatalytic efficiency. XPS spectra confirm the existence of S-doped NH2 -UiO-66, and Raman spectra show transition metal-assisted sulfuration instead of carbonization. FT-IR spectra further confirm the formation of Zn–O–C covalent bonds at the interface between NH2 -UiO-66 and ZnIn2 S4 . In particular, the Zn–O–C bonds preserve the energy of photo-generated electrons and inhibit the energy relaxation of electrons at the interface of the heterostructure. In addition, NH2 -UiO-66 with a high photocatalytic response greatly facilitates the transport of photo-generated electrons not only as an electron transport bridge but also as an electron donor. Profiting from the unique design of the ternary composite, the sample exhibits excellent PHE performance. The obtained ZnIn2 S4 /NH2 -UiO-66/5%-MoS2 (5.69 mmol h −1 g −1 ) exhibits the highest H2 evolution rate, which is 15 and 1.9 times higher than those of ZnIn2 S4 (0.369 mmolAbstract : This work introduces the synthesis of ZnIn2 S4 /NH2 -UiO-66/MoS2 sheet heterostructure photocatalysts and their application to photocatalytic hydrogen evolution. Abstract : Developing well-designed architectures plays a decisive role in accelerating photo-generated carrier transport in composite photocatalysts. Herein, a microporous sulfur-doped (S-doped) NH2 -UiO-66 bridged ZnIn2 S4 /MoS2 sheet heterostructure photocatalyst is synthesized through thermolysis of sulfur rich precursors to functionalize the organic ligands of NH2 -UiO-66 to boost photocatalytic efficiency. XPS spectra confirm the existence of S-doped NH2 -UiO-66, and Raman spectra show transition metal-assisted sulfuration instead of carbonization. FT-IR spectra further confirm the formation of Zn–O–C covalent bonds at the interface between NH2 -UiO-66 and ZnIn2 S4 . In particular, the Zn–O–C bonds preserve the energy of photo-generated electrons and inhibit the energy relaxation of electrons at the interface of the heterostructure. In addition, NH2 -UiO-66 with a high photocatalytic response greatly facilitates the transport of photo-generated electrons not only as an electron transport bridge but also as an electron donor. Profiting from the unique design of the ternary composite, the sample exhibits excellent PHE performance. The obtained ZnIn2 S4 /NH2 -UiO-66/5%-MoS2 (5.69 mmol h −1 g −1 ) exhibits the highest H2 evolution rate, which is 15 and 1.9 times higher than those of ZnIn2 S4 (0.369 mmol h −1 g −1 ) and 5%-MoS2 /ZnIn2 S4 (2.93 mmol h −1 g −1 ), respectively. In addition, the apparent quantum efficiency of the ZnIn2 S4 /NH2 -UiO-66/5%-MoS2 composite (7.95%) is higher than that of the 5%-MoS2 /ZnIn2 S4 composite (3.12%) at 420 nm. This work provides new insight into designing novel and highly efficient photocatalysts for photocatalytic hydrogen evolution. … (more)
- Is Part Of:
- Catalysis science & technology. Volume 10:Issue 8(2020)
- Journal:
- Catalysis science & technology
- Issue:
- Volume 10:Issue 8(2020)
- Issue Display:
- Volume 10, Issue 8 (2020)
- Year:
- 2020
- Volume:
- 10
- Issue:
- 8
- Issue Sort Value:
- 2020-0010-0008-0000
- Page Start:
- 2531
- Page End:
- 2539
- Publication Date:
- 2020-04-01
- Subjects:
- Catalysis -- Periodicals
541.395 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/CY ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d0cy00127a ↗
- Languages:
- English
- ISSNs:
- 2044-4753
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3090.943100
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 13824.xml