State Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University, Fuzhou, 350002, China.
Angew Chem Int Ed Engl. 2016 Sep 12;55(38):11512-6. doi: 10.1002/anie.201606102. Epub 2016 Aug 17.
The precise modification of redox species on the inner and outer surfaces of hollow nanostructures is relevant in catalysis, surface science, and nanotechnology, but has proven difficult to achieve. Herein, we develop a facile approach to specifically fabricate Pt and Co3 O4 nanoparticles (NPs) onto the interior and exterior surface of hollow carbon nitride spheres (HCNS), respectively, to promote the surface redox functions of the polymer semiconductors. The photocatalytic water splitting activities of HCNS with spatially separated oxidation and reduction centers at their nanodomains were enhanced. The origin of the enhanced activity was attributed to the spatially separated reactive sites for the evolution of H2 and O2 and also to the unidirectional migration of the electron and hole on the Janus surfaces, thereby preventing the unwanted reverse reaction of water splitting and decreasing charge recombination.
在内、外表面上精确修饰中空纳米结构中的氧化还原物种在催化、表面科学和纳米技术中具有重要意义,但这一目标一直难以实现。在此,我们开发了一种简便的方法,分别将 Pt 和 Co3 O4 纳米颗粒 (NPs) 特异性地组装到中空氮化碳球 (HCNS) 的内、外表面上,以增强聚合物半导体的表面氧化还原功能。具有纳米域内空间分离氧化还原中心的 HCNS 的光催化水分解活性得到了提高。活性增强的原因归因于 H2 和 O2 演化的空间分离反应位点,以及 Janus 表面上电子和空穴的单向迁移,从而防止了水分解的不期望的逆反应并减少了电荷复合。