Khasnabis Sutripto, Mesburis Cassandra, Godin Robert
Department of Chemistry, The University of British Columbia, 3247 University Way, Kelowna, BC, V1V 1V7, Canada.
Clean Energy Research Center, The University of British Columbia, 2360 East Mall, Vancouver, BC, V6T 1Z3, Canada.
ChemSusChem. 2025 Jul 1;18(13):e202500203. doi: 10.1002/cssc.202500203. Epub 2025 May 8.
This study aims to spatially understand the effect of Pt deposition on slow (μs-s) carrier dynamics in carbon nitride (CN) photocatalysts, using a homebuilt microsecond diffuse reflectance transient absorption microscopy setup. It is found that Pt deposition lengthens the overall charge half-lives about threefold, while having a spatial preference for binding with respect to defects that induce charge trapping in the μs-s timescale. The initial trapped charge population shows a slight decrease after Pt deposition, suggesting that the more reactive and mobile charges are extracted by Pt sites, leaving behind deeply trapped and long-lived charges. The results emphasize that spatial heterogeneity of surface cocatalysts likely plays a major role in controlling the charge carrier dynamics and activity of photocatalysts.
本研究旨在利用自制的微秒级漫反射瞬态吸收显微镜装置,从空间角度了解铂沉积对氮化碳(CN)光催化剂中慢(微秒至秒)载流子动力学的影响。研究发现,铂沉积使整体电荷半衰期延长了约三倍,同时在与导致微秒至秒时间尺度上电荷俘获的缺陷结合方面具有空间偏好性。铂沉积后,初始俘获电荷数量略有减少,这表明活性和移动性更强的电荷被铂位点提取,留下了深度俘获且寿命较长的电荷。结果强调,表面助催化剂的空间异质性可能在控制光催化剂的载流子动力学和活性方面起主要作用。