Highly efficient hydrogen evolution catalysis based on MoS₂/CdS/TiO₂ porous composites

다국어 초록 (Multilingual Abstract)

<P><B>Abstract</B></P> <P>Efficient production of hydrogen through visible-light-driven water splitting mechanism using semiconductor-based composites has been identified as a promising strategy for converting light into clean H<SUB>2</SUB> fuel. However, researchers are facing lots of challenges such as light absorption and electron-hole pair recombination and so on. Here, new sheet-shaped MoS<SUB>2</SUB> and pyramid-shaped CdS <I>in-situ</I> co-grown on porous TiO<SUB>2</SUB> photocatalysts (MoS<SUB>2</SUB> CdSTiO<SUB>2</SUB>) are successfully obtained <I>via</I> mild sulfuration of MoO<SUB>3</SUB> and CdO coexisted inside porous TiO<SUB>2</SUB> monolith by a hydrothermal route. The scanning electron microscopy and transmission electron microscopy results exhibit that the MoS<SUB>2</SUB> CdSTiO<SUB>2</SUB> composites have average pore size about 500 nm. The 3%MoS<SUB>2</SUB> 10%CdSTiO<SUB>2</SUB> demonstrated excellent photocatalytic activity and high stability for a hydrogen production with a high H<SUB>2</SUB>-generation rate of 4146 μmol h<SUP>−1</SUP> g<SUP>−1</SUP> under visible light irradiation even without noble-metal co-catalysts. The super photocatalytic performance of the visible-light-driven hydrogen evolution is predominantly attributed to the synergistic effect. The conduction band of MoS<SUB>2</SUB> facilitates in transporting excited electrons from visible-light on CdS to the porous TiO<SUB>2</SUB> for catalytic hydrogen production, and holes to MoS<SUB>2</SUB> for inhibiting the photocorrosion of CdS, respectively, leading to enhancing the efficient separation of electrons and holes.</P> <P><B>Highlights</B></P> <P> <UL> <LI> MoS<SUB>2</SUB>-CT photocatalysts have been successfully synthesized by two-step method. </LI> <LI> The porous structure can enhance photogenerated electron-hole pairs separation. </LI> <LI> The 3% MoS<SUB>2</SUB>-CT shows an excellent H<SUB>2</SUB> evolution rate of 4146 μmol h<SUP>−1</SUP> g<SUP>−1</SUP>. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>