A well-designed honeycomb CoO@CdS photocatalyst derived from cobalt foam for high-efficiency visible-light H evolution
Well-designed honeycomb Co 3 O 4 @CdS (H-Co 3 O 4 @CdS) was fabricated via a one-step strategy for efficient water splitting. During the decoration of CdS, honeycomb Co 3 O 4 (H-Co 3 O 4 ) with macropores was formed simultaneously. H-Co 3 O 4 could enhance CdS visible-light absorption capacity consp...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2021-05, Vol.9 (19), p.11665-11673 |
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Zusammenfassung: | Well-designed honeycomb Co
3
O
4
@CdS (H-Co
3
O
4
@CdS) was fabricated
via
a one-step strategy for efficient water splitting. During the decoration of CdS, honeycomb Co
3
O
4
(H-Co
3
O
4
) with macropores was formed simultaneously. H-Co
3
O
4
could enhance CdS visible-light absorption capacity conspicuously and narrow its band gap from 2.08 to 1.03 eV. Therefore, H-Co
3
O
4
@CdS presented a remarkable H
2
production of up to
ca.
16 320 μmol g
−1
h
−1
(
λ
> 420 nm), nearly 7.3 times higher than that of pristine CdS, indicating the excellent synergistic effect between H-Co
3
O
4
and CdS. Through various photoelectricity tests (
e.g.
, PL spectra, EPR, photoelectric responsiveness and impedance), it could be found that the distinguished H
2
evolution was attributed to the improved charge carrier separation and electron generation. What's more, the enhanced H
2
production of H-Co
3
O
4
@CdS is related to the improved specific surface area (83.49 m
2
g
−1
) and pore volume (0.247 cm
3
g
−1
) as well. Density Functional Theory (DFT) calculations confirmed that CdS has the function of diverting electrons, and the orbital energy level of absorbed H
2
O molecules showed obvious migration due to the accumulation of electrons. Besides, the d-band of Co could induce more electrons to traverse the Fermi level. Subsequently, more electrons could be transferred from Co
3
O
4
to CdS and break the O-H
1
bond. Compared to the H-Co
3
O
4
@CdS system, the d-band center of the Co atoms in H-Co
3
O
4
@CdS-H
2
O shifted from −5.83 to −2.58 eV, thereby demonstrating that Co
3
O
4
served as an electron reservoir for charge redistribution in the photocatalytic water splitting process. In the end, a practicable mechanism for H-Co
3
O
4
@CdS about H
2
O dissociation and H
2
desorption was proposed.
A well-designed honeycomb Co
3
O
4
@CdS photocatalyst derived from cobalt foam was synthesized for high-efficiency visible-light H
2
evolution (
ca.
16 320 μmol h
−1
g
−1
). |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d0ta11433b |