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The effective spatial separation of photogenerated charge carriers is essential for realizing efficient CO
2
conversion. Herein, a new CsPbBr
3
-Co
3
O
4
heterostructure photocatalyst was rationally developed for photocatalytic CO
2
reduction. A facile synthetic strategy based on electrostatic interactions was utilized. The results revealed that the CsPbBr
3
-Co
3
O
4
hybrid exhibited a boosted evolution rate of 64.6 μmol g
−1
h
−1
(CO: 35.40 μmol g
−1
h
−1
; CH
4
: 29.2 μmol g
−1
h
−1
) with an electron consumption rate (
R
electron
) of 304.4 μmol g
−1
h
−1
, surpassing pristine CsPbBr
3
or Co
3
O
4
. The high activity mainly arises from efficient charge separation and the directional transfer of electrons from CsPbBr
3
to Co
3
O
4
via
an intimately coupled heterointerface. Notably, the surface features (derived from the unique morphology) expedited the CO
2
adsorption and accumulation of electrons at the Co
3
O
4
site which ultimately facilitated the conversion of CO
2
over the CsPbBr
3
-Co
3
O
4
composite. This approach provides a strategy to design and modulate highly active metal oxide and perovskite-based photocatalysts and presents great potential for constructing a heterointerface for CO
2
reduction.
CsPbBr
3
quantum dots were precisely incorporated in Co
3
O
4
hexagonal platelets to construct a new CsPbBr
3
-Co
3
O
4
heterostructure, which exhibited efficient charge separation to achieve an improved photocatalytic reduction of CO
2
into CO and CH
4
.
Sprache
–
Identifikatoren
eISSN: 2052-1553
DOI: 10.1039/d3qi00527e
Titel-ID: cdi_rsc_primary_d3qi00527e
Format
–
Weiterführende Literatur
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