Wang Jing, Song Jiayu, Kang Xin, Wang Dongxu, Tian Chungui, Zhang Qin, Zhao Hui, Liu Jiancong
Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education, Heilongjiang University, Harbin 150080, China.
Molecules. 2024 Apr 21;29(8):1890. doi: 10.3390/molecules29081890.
Carbon nitride (CN) has gained considerable attention and has been regarded as an ideal candidate for photocatalytic hydrogen evolution. However, its photocatalytic efficiency is still unsatisfactory due to the rapid recombination rate of photo-generated carriers and restricted surface area with few active sites. Herein, we successfully synthesized a single-atom Pt cocatalyst-loaded photocatalyst by utilizing the anchoring effect of carbon dots (CDs) on CN. The introduction of CDs onto the porous CN matrix can greatly enhance the specific surface area of CN to provide more surface-active sites, increase light absorption capabilities, as well as improve the charge separation efficiency. Notably, the functional groups of CDs can efficiently anchor the single-atom Pt, thus improving the atomic utilization efficiency of Pt cocatalysts. A strong interaction is formed via the connection of Pt-N bonds, which enhances the efficiency of photogenerated electron separation. This unique structure remarkably improves its H evolution performance under visible light irradiation with a rate of 15.09 mmol h g. This work provides a new approach to constructing efficient photocatalysts by using CDs for sustainable hydrogen generation, offering a practical approach to utilizing solar energy for clean fuel production.
氮化碳(CN)已引起广泛关注,并被视为光催化析氢的理想候选材料。然而,由于光生载流子的快速复合率以及活性位点少导致的受限表面积,其光催化效率仍不尽人意。在此,我们利用碳点(CDs)对CN的锚定作用成功合成了负载单原子Pt助催化剂的光催化剂。将CDs引入多孔CN基体可极大地提高CN的比表面积,以提供更多的表面活性位点,增强光吸收能力,并提高电荷分离效率。值得注意的是,CDs的官能团可有效锚定单原子Pt,从而提高Pt助催化剂的原子利用效率。通过Pt-N键的连接形成了强相互作用,增强了光生电子的分离效率。这种独特的结构在可见光照射下显著提高了其析氢性能,产氢速率为15.09 mmol h g。这项工作为利用CDs构建高效光催化剂以实现可持续制氢提供了一种新方法,为利用太阳能生产清洁燃料提供了一种切实可行的途径。