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A Metal‐Organic‐Framework‐Derived g‐C 3 N 4 /α‐Fe 2 O 3 Hybrid for Enhanced Visible‐Light‐Driven Photocatalytic Hydrogen Evolution
Author(s) -
Liu Jing,
Zhao Xiuxia,
Jing Peng,
Shi Wei,
Cheng Peng
Publication year - 2019
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201805349
Subject(s) - photocatalysis , visible spectrum , materials science , water splitting , hydrogen , hydrogen production , metal , acceptor , semiconductor , photochemistry , excited state , optoelectronics , catalysis , atomic physics , physics , chemistry , organic chemistry , condensed matter physics , metallurgy
As one of the most efficient systems for photocatalytic hydrogen evolution, the Z‐Scheme system, consisting of different semiconductors with a reversible donor–acceptor pair, has attracted great attention. Considering the non‐toxicity and low cost of photocatalysts, a series of g‐C 3 N 4 /α‐Fe 2 O 3 hybrids were rationally constructed based on the Z‐Scheme mechanism for the first time, using a metal‐organic framework template approach that can fine tune the compositions and properties of the hybrids. An optimized hybrid, g‐C 3 N 4 /α‐Fe 2 O 3 ‐2, exhibited prominent photocatalytic water splitting performance with a visible light response. Under irradiation of visible light ( λ >420 nm), the hybrid shows a high durability and superior hydrogen production rate of 2066.2 μmol g −1  h −1 from water splitting, which is approximately three times greater than that of bulk g‐C 3 N 4 because of the effective separation of photo‐excited charge carriers by two narrow band gap semiconductors, tightly coupled with the Z‐Scheme structural feature.

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