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Enhanced Visible-Light Driven Photocatalytic Performances Over LaFeO3/NiO Modified Porous g-C3N4 Nanosheets

机译:增强的可见光驱动光催化性能通过LafeO3 / NiO改性多孔G-C3N4纳米蛋白酶

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LaFeO3/NiO modified g-C3N4 nanosheets (L-N/CNS) were synthesized by a two-step method. HRTEM results showed that an intimate contact between LaFeO3, NiO and N-CNS was successfully established. Ninety percent of phenol was degraded within 120 min, and the hydrogen evolution rate of 171.2 mu mol h(-1) g(-1) was obtained over the L-N/CNS heterojunctions under the visible-light irradiation. It was higher than that of g-C3N4 nanosheets, NiO modified g-C3N4 and LaFeO3/g-C3N4. The center dot O-2(-) radicals acted the crucial role in the photocatalytic degradation reaction. EIS, PL and time-resolved fluorescence spectra demonstrated that L-N/CNS possessed the highest charge separation efficiency. The intimate contact between LaFeO3, NiO and g-C3N4 nanosheets promoted the separation and transfer of photo-induced electron-hole pairs and consequently prolonged the exciton lifetime, and implied more photo-induced electrons could be probably involved in the photocatalytic reactions on the surface of photocatalysts. Thus, the visible-light driven photocatalytic performances of L-N/CNS were effective. This work provided a feasible method to design and construct heterostructures for the exploitation of solar energy.
机译:通过两步法合成Lafeo3 / NiO改性G-C3N4纳米液(L-N / CNS)。 HRTEM结果表明,Lafeo3,NIO和N-CNS之间的密切接触已成功建立。在120分钟内降解百分之九十的苯酚,并在可见光照射下通过L-N / CNS杂谐振在L-N / CNS杂交中获得171.2μmolH(-1)的氢进化速率。它高于G-C3N4纳米片,NiO改性G-C3N4和LafeO3 / G-C3N4。中心点O-2( - )基团在光催化降解反应中作用了至关重要的作用。 EIS,PL和时间分辨荧光光谱表明L-N / CNS具有最高电荷分离效率。 Lafeo3,NiO和G-C3N4纳米片之间的紧密接触促进了光诱导的电子 - 空穴对的分离和转移,从而延长了激子寿命,并暗示了更多的光致电极可能参与表面上的光催化反应光催化剂。因此,L-N / CNS的可见光驱动的光催化性能是有效的。这项工作提供了一种可行的方法来设计和构建用于利用太阳能的异性结构。

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