光催化
制氢
催化作用
纳米材料
材料科学
氢
纳米技术
电子顺磁共振
分解水
光化学
电子结构
光催化分解水
化学工程
化学
计算化学
物理
有机化学
工程类
生物化学
核磁共振
作者
Alberto Naldoni,Marco Altomare,Giorgio Zoppellaro,Ning Liu,Štěpán Kment,Radek Zbořil,Patrik Schmuki
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2018-11-30
卷期号:9 (1): 345-364
被引量:626
标识
DOI:10.1021/acscatal.8b04068
摘要
Black TiO2 nanomaterials have recently emerged as promising candidates for solar-driven photocatalytic hydrogen production. Despite the great efforts to synthesize highly reduced TiO2, it is apparent that intermediate degree of reduction (namely, gray titania) brings about the formation of peculiar defective catalytic sites enabling cocatalyst-free hydrogen generation. A precise understanding of the structural and electronic nature of these catalytically active sites is still elusive, as well as the fundamental structure–activity relationships that govern formation of crystal defects, increased light absorption, charge separation, and photocatalytic activity. In this Review, we discuss the basic concepts that underlie an effective design of reduced TiO2 photocatalysts for hydrogen production such as (i) defects formation in reduced TiO2, (ii) analysis of structure deformation and presence of unpaired electrons through electron paramagnetic resonance spectroscopy, (iii) insights from surface science on electronic singularities due to defects, and (iv) the key differences between black and gray titania, that is, photocatalysts that require Pt-modification and cocatalyst-free photocatalytic hydrogen generation. Finally, future directions to improve the performance of reduced TiO2 photocatalysts are outlined.
科研通智能强力驱动
Strongly Powered by AbleSci AI