Penfold Thomas J, Szlachetko Jakub, Santomauro Fabio G, Britz Alexander, Gawelda Wojciech, Doumy Gilles, March Anne Marie, Southworth Stephen H, Rittmann Jochen, Abela Rafael, Chergui Majed, Milne Christopher J
Chemistry-School of Natural and Environmental Sciences, Newcastle University, Newcastle upon Tyne, NE1 7RU, UK.
SwissFEL, Paul Scherrer Institut, CH-5232, Villigen-PSI, Switzerland.
Nat Commun. 2018 Feb 2;9(1):478. doi: 10.1038/s41467-018-02870-4.
Nanostructures of transition metal oxides, such as zinc oxide, have attracted considerable interest for solar-energy conversion and photocatalysis. Both applications are sensitive to the transport and trapping of photoexcited charge carriers. The probing of electron trapping has recently become possible using time-resolved element-sensitive methods, such as X-ray spectroscopy. However, valence-band-trapped holes have so far escaped observation. Herein we use X-ray absorption spectroscopy combined with a dispersive X-ray emission spectrometer to probe the charge carrier relaxation and trapping processes in zinc oxide nanoparticles after above band-gap photoexcitation. Our results, supported by simulations, demonstrate that within 80 ps, photoexcited holes are trapped at singly charged oxygen vacancies, which causes an outward displacement by ~15% of the four surrounding zinc atoms away from the doubly charged vacancy. This identification of the hole traps provides insight for future developments of transition metal oxide-based nanodevices.
诸如氧化锌之类的过渡金属氧化物纳米结构在太阳能转换和光催化领域引起了广泛关注。这两种应用都对光激发电荷载流子的传输和俘获很敏感。最近,利用时间分辨元素敏感方法(如X射线光谱法)探测电子俘获已成为可能。然而,价带俘获空穴迄今为止仍未被观测到。在此,我们使用X射线吸收光谱法结合色散X射线发射光谱仪,来探测氧化锌纳米颗粒在带隙以上光激发后的电荷载流子弛豫和俘获过程。我们的结果在模拟的支持下表明,在80皮秒内,光激发空穴被俘获在单电荷氧空位处,这导致四个周围锌原子相对于双电荷空位向外位移约15%。这种对空穴陷阱的识别为基于过渡金属氧化物的纳米器件的未来发展提供了见解。