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Oxygen vacancies and interfaces enhancing photocatalytic hydrogen production in mesoporous CNT/TiO2 hybrids

机译:氧空位和界面增强中孔CNT / TiO2杂化物的光催化制氢

摘要

We demonstrate a unique route towards hierarchical assemblies of mesoporous TiO2 and CNT/TiO2 photocatalysts by a combination of electrospinning and sol–gel methods. The resulting materials exhibit a mesoporous network of highly crystalline, well-connected inorganic nanocrystals with an order of magnitude higher photocatalytic activity than individualised TiO2 nanoparticles. The in-situ combination of small amounts of MWCNTs with TiO2 to form an electrospun CNT/TiO2 hybrid further enhanced the oxide photoactivity considerably, reaching hydrogen evolution rates of 1218 μmol/h in water splitting in the presence of sacrificial reagents under UV irradiation. We also discuss the effect of oxygen vacancies on the oxide crystallisation and phase transformation. These vacancies lead to inter-bandgap states and a lower flat band potential that facilitates the photocatalytic process.
机译:我们通过电纺丝和溶胶-凝胶方法的结合展示了一条通向介孔TiO2和CNT / TiO2光催化剂分层组装的独特途径。所得材料显示出高度结晶的,连接良好的无机纳米晶体的介孔网络,其光催化活性比单独的TiO2纳米颗粒高一个数量级。少量MWCNT与TiO2的原位结合形成静电纺丝CNT / TiO2杂化物进一步显着增强了氧化物的光活性,在牺牲剂存在下于紫外线照射下,水分解时氢的析出速率达到1218μmol/ h。我们还讨论了氧空位对氧化物结晶和相变的影响。这些空位导致带隙状态和较低的平坦带电势,从而促进光催化过程。

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