Coward Luke T, Chu Thu T M, Li Xiaotong, Lyu Pin, Love Oksana
Department of Chemistry and Biochemistry, University of North Carolina Asheville, 1 University Heights, Asheville, North Carolina 28804, United States.
Department of Chemistry and Organic and Carbon Electronics Laboratories (ORaCEL), North Carolina State University, Raleigh, North Carolina 27695, United States.
ACS Nanosci Au. 2025 Jul 30;5(4):324-336. doi: 10.1021/acsnanoscienceau.5c00087. eCollection 2025 Aug 20.
Solar energy, as an alternative source to catalyze chemical reactions, has been rapidly utilized and developed over the past few decades, particularly with TiO-based semiconductor photocatalysts. Regulating the carrier dynamics under photoexcitation and controlling the interfacial reaction kinetics have been emphasized as fundamental approaches to increase the quantum yield of photocatalytic systems. Transition-metal-ion doping is a promising strategy to address these issues, although the precise roles and optimal spatial distribution of dopants remain unclear. In this systematic study, we designed surface-only, bulk-only, and surface-bulk-doped brookite TiO nanoparticles using Ni as dopants and evaluated the photocatalytic performance of these doped samples based on the apparent reaction rate constants. It is demonstrated that the crystal structure, morphology, and surface composition did not change significantly after doping, and the observed enhancement in photocatalysis can be correlated to the doping positions. Continuous doping from the bulk to surface, forming the trap-to-transfer centers to mediate interfacial electron transfer, proves to be the most effective pathway. This proof-of-concept work offers a unique perspective on the transition-metal-ion-induced photocatalysis mechanism of brookite TiO nanoparticles and will help us design more efficient photocatalytic systems.
太阳能作为一种催化化学反应的替代能源,在过去几十年中得到了迅速的利用和发展,特别是基于TiO的半导体光催化剂。调节光激发下的载流子动力学和控制界面反应动力学已被强调为提高光催化系统量子产率的基本方法。过渡金属离子掺杂是解决这些问题的一种有前途的策略,尽管掺杂剂的确切作用和最佳空间分布仍不清楚。在这项系统研究中,我们设计了仅表面掺杂、仅体相掺杂和表面-体相掺杂的板钛矿TiO纳米颗粒,以镍作为掺杂剂,并基于表观反应速率常数评估了这些掺杂样品的光催化性能。结果表明,掺杂后晶体结构、形态和表面组成没有明显变化,观察到的光催化增强与掺杂位置有关。从体相到表面的连续掺杂,形成陷阱到转移中心以介导界面电子转移,被证明是最有效的途径。这项概念验证工作为板钛矿TiO纳米颗粒的过渡金属离子诱导光催化机理提供了独特的视角,并将有助于我们设计更高效的光催化系统。