4 research outputs found
BiOBr<sub>0.75</sub>I<sub>0.25</sub>/BiOIO<sub>3</sub> as a Novel Heterojunctional Photocatalyst with Superior Visible-Light-Driven Photocatalytic Activity in Removing Diverse Industrial Pollutants
A series
of novel heterojunctional photocatalysts BiOBr<sub>0.75</sub>I<sub>0.25</sub>/BiOIO<sub>3</sub> were synthesized by a facile deposition–precipitation
method for the first time. In contrast to pristine BiOIO<sub>3</sub>, the photoabsorption of BiOBr<sub>0.75</sub>I<sub>0.25</sub>/BiOIO<sub>3</sub> composites in visible light region is greatly promoted. All
the BiOBr<sub>0.75</sub>I<sub>0.25</sub>/BiOIO<sub>3</sub> composite
photocatalysts exhibit highly enhanced photocatalytic activity in
decomposing bisphenol A under visible light (λ > 420 nm)
illumination,
and the 20% BiOIO<sub>3</sub>-BiOBr<sub>0.75</sub>I<sub>0.25</sub> sample possesses the optimal photoreactivity, which is 7.4, and
3.3 times higher than those of pure BiOIO<sub>3</sub> and BiOBr<sub>0.75</sub>I<sub>0.25</sub>. Moreover, the 20% BiOIO<sub>3</sub>-BiOBr<sub>0.75</sub>I<sub>0.25</sub> sample displays superior photocatalytic
performance against diverse industrial contaminants and pharmaceuticals,
including methyl orange, phenol, 2,4-dichlorophenol, chlortetracycline
hydrochloride, and tetracycline hydrochloride. The enhancement of
phototcatalytic activity is ascribed to the profoundly promoted transfer
and separation of photoexcited charge carriers, which is verified
by transient photocurrent response and photoluminescence emission.
In addition, the photocatalytic mechanism over composite photocatalyst
under visible light irradiation is systematically investigated by
active species trapping experiment and •OH quantification experiment.
This work may provide a new hint for fabrication of high-performance
heterojunctions by combining the narrow-band gap and wide-band gap
semiconductors
Fabrication of Heterogeneous-Phase Solid-Solution Promoting Band Structure and Charge Separation for Enhancing Photocatalytic CO<sub>2</sub> Reduction: A Case of Zn<i><sub>X</sub></i>Ca<sub>1–<i>X</i></sub>In<sub>2</sub>S<sub>4</sub>
Photocatalytic CO<sub>2</sub> reduction into solar fuels
illustrates huge charm for simultaneously settling energy and environmental
issues. The photoreduction ability of a semiconductor is closely correlated
to its conduction band (CB) position. A homogeneous-phase solid-solution
with the same crystal system always has a monotonously changed CB
position, and the high CB level has to be sacrificed to achieve a
benign photoabsorption. Herein, we report the fabrication of heterogeneous-phase
solid-solution Zn<i><sub>X</sub></i>Ca<sub>1–<i>X</i></sub>In<sub>2</sub>S<sub>4</sub> between trigonal ZnIn<sub>2</sub>S<sub>4</sub> and cubic CaIn<sub>2</sub>S<sub>4</sub>. The
Zn<i><sub>X</sub></i>Ca<sub>1–<i>X</i></sub>In<sub>2</sub>S<sub>4</sub> solid solutions with orderly tuned photoresponsive
range from 540 to 640 nm present a more negative CB level and highly
enhanced charge-separation efficiency. Profiting from these merits,
all of these Zn<i><sub>X</sub></i>Ca<sub>1–<i>X</i></sub>In<sub>2</sub>S<sub>4</sub> solid solutions exhibit
remarkably strengthened photocatalytic CO<sub>2</sub> reduction performance
under visible light (λ > 420 nm) irradiation. Zn<sub>0.4</sub>Ca<sub>0.6</sub>In<sub>2</sub>S<sub>4</sub>, bearing the most negative
CB position and highest charge-separation efficiency, casts the optimal
photocatalytic CH<sub>4</sub> and CO evolution rates, which reach
16.7 and 6.8 times higher than
that of ZnIn<sub>2</sub>S<sub>4</sub> and 7.2 and 3.9 times higher
than that of CaIn<sub>2</sub>S<sub>4</sub>, respectively. To verify
the crucial role of the heterogeneous-phase solid solution in promoting
the band structure and photocatalytic performance, another heterogeneous-phase
solid-solution Zn<i><sub>X</sub></i>Cd<sub>1–<i>X</i></sub>In<sub>2</sub>S<sub>4</sub> has been synthesized.
It also displays an upshifted CB level and promoted charge separation.
This work may provide a new perspective into the development of an
efficient visible-light driven photocatalyst for CO<sub>2</sub> reduction
and other photoreduction reactions
Nanocrystalline Cellulose Cures Constipation <i>via</i> Gut Microbiota Metabolism
Constipation can seriously affect the quality of life
and increase
the risk of colorectal cancer. The present strategies for constipation
therapy have adverse effects, such as causing irreversible intestinal
damage and affecting the absorption of nutrients. Nanocrystalline
cellulose (NCC), which is from natural plants, has good biocompatibility
and high safety. Herein, we used NCC to treat constipation assessed
by the black stool, intestinal tissue sections, and serum biomarkers.
We studied the effect of NCC on gut microbiota and discussed the correlation
of gut microbiota and metabolites. We evaluated the long-term biosafety
of NCC. NCC could effectively treat constipation through gut microbiota
metabolism, which required a small dosage and did not affect the organs
and intestines. NCC could be used as an alternative to medications
and dietary fiber for constipation therapy
Facile <i>In Situ</i> Self-Sacrifice Approach to Ternary Hierarchical Architecture Ag/AgX (X = Cl, Br, I)/AgIO<sub>3</sub> Distinctively Promoting Visible-Light Photocatalysis with Composition-Dependent Mechanism
Three
series of ternary hierarchical architecture photocatalysts Ag/AgX
(X = Cl, Br, I)/AgIO<sub>3</sub> were fabricated for the first time
by a facile <i>in situ</i> ion-exchange route. The novel
ternary architectures are confirmed by XRD, XPS, SEM, TEM, EDX, and
EDX mapping. In contrast to pristine AgIO<sub>3</sub>, the Ag/AgX
(X = Cl, Br, I)/AgIO<sub>3</sub> composites show extended absorption
edges and highly boosted photoabsorption in the visible region, which
are separately ascribed to the intrinsic absorption of AgX and the
surface plasmon resonance (SPR) effect of Ag species. The photocatalysis
activity of Ag/AgX (X = Cl, Br, I)/AgIO<sub>3</sub> composites is
studied and compared <i>via</i> photodegradation of methyl
orange (MO) under visible-light (λ > 420 nm) irradiation.
It is interesting to find that the activity enhancement levels are
different for Ag/AgX (X = Cl, Br, I)/AgIO<sub>3</sub> with four types
of photocatalytic mechanism, which are closely related to the type
of AgX or the component content in Ag/AgX (X = Cl, Br, I)/AgIO<sub>3</sub>. The separation behaviors of charge carrier were also systematically
investigated by the PL and EIS. The study may furnish new perspective
into controllable fabrication of hierarchical architecture photocatalysts
with multiform photocatalytic mechanism