Jin Yanling, Wang Jiayi, Gao Xin, Ren Fang, Chen Zhengyan, Sun Zhenfeng, Ren Penggang
Faculty of Printing, Packaging Engineering and Digital Media Technology, Xi'an University of Technology, Jinhua South Road No. 5, Xi'an 710048, China.
School of Materials Science and Engineering, Xi'an University of Technology, Jinhua South Road No. 5, Xi'an 710048, China.
Materials (Basel). 2023 Jul 21;16(14):5137. doi: 10.3390/ma16145137.
Titanium dioxide (TiO) is an ideal photocatalyst candidate due to its high activity, low toxicity and cost, and high chemical stability. However, its practical application in photocatalysis is seriously hindered by the wide band gap energy of TiO and the prone recombination of electron-hole pairs. In this study, C, N doped TiO were supported on spent coffee grounds-derived carbon (ACG) via in situ formation, which was denoted as C, N-TiO@ACG. The obtained C, N-TiO@ACG exhibits increased light absorption efficiency with the band gap energy decreasing from 3.31 eV of TiO to 2.34 eV, a higher specific surface area of 145.8 m/g, and reduced recombination rates attributed to the synergistic effect of a spent coffee grounds-derived carbon substrate and C, N doping. Consequently, the optimal 1:1 C, N-TiO@ACG delivers considerable photocatalytic activity with degradation efficiencies for methylene blue (MB) reaching 96.9% within 45 min, as well as a high reaction rate of 0.06348 min, approximately 4.66 times that of TiO (0.01361 min). Furthermore, it also demonstrated greatly enhanced photocatalytic efficiency towards methyl orange (MO) in the presence of MB compared with a single MO solution. This work provides a feasible and universal strategy of synchronous introducing nonmetal doping and biomass-derived carbon substrates to promote the photocatalytic performance of TiO for the degradation of organic dyes.
二氧化钛(TiO₂)因其高活性、低毒性和成本以及高化学稳定性,是一种理想的光催化剂候选材料。然而,TiO₂的宽带隙能量以及电子 - 空穴对易于复合,严重阻碍了其在光催化中的实际应用。在本研究中,通过原位形成将C、N掺杂的TiO₂负载在废弃咖啡渣衍生的碳(ACG)上,记为C、N - TiO₂@ACG。所制备的C、N - TiO₂@ACG表现出光吸收效率提高,带隙能量从TiO₂的3.31 eV降至2.34 eV,比表面积高达145.8 m²/g,且由于废弃咖啡渣衍生的碳基底与C、N掺杂的协同作用,复合率降低。因此,最优的1:1 C、N - TiO₂@ACG具有可观的光催化活性,亚甲基蓝(MB)的降解效率在45分钟内达到96.9%,反应速率高达0.06348 min⁻¹,约为TiO₂(0.01361 min⁻¹)的4.66倍。此外,与单一甲基橙(MO)溶液相比,在MB存在下,其对MO的光催化效率也大大提高。这项工作提供了一种可行且通用的策略,即同步引入非金属掺杂和生物质衍生的碳基底,以促进TiO₂对有机染料降解的光催化性能。