Ultrafast Charge and Exciton Diffusion in Monolayer Films of 9-Armchair Graphene Nanoribbons

被引:0
|
作者
Varghese, Sebin [1 ,2 ]
Mehew, Jake Dudley [1 ]
Wang, Hai I. [3 ,4 ]
Wuttke, Michael [3 ]
Zhou, Yazhou [3 ]
Muellen, Klaus [3 ]
Narita, Akimitsu [3 ,5 ]
Cummings, Aron W. [1 ]
Tielrooij, Klaas-Jan [1 ,2 ]
机构
[1] CSIC & BIST, Catalan Inst Nanosci & Nanotechnol ICN2, Campus UAB, Bellaterra 08193, Barcelona, Spain
[2] Eindhoven Univ Technol, Den Dolech 2, NL-5612 AZ Eindhoven, Netherlands
[3] Max Planck Max Planck Inst Polymer Res, Ackermannweg 10, D-55128 Mainz, Germany
[4] Univ Utrecht, Debye Inst Nanomat Sci, Princetonpl 1, NL-3584 CC Utrecht, Netherlands
[5] Okinawa Inst Sci & Technol Grad Univ, Organ & Carbon Nanomat Unit, 1919-1 Tancha, Onna, Okinawa 9040495, Japan
基金
欧盟地平线“2020”; 欧洲研究理事会;
关键词
charge mobility; excitons; graphene nanoribbons; spatiotemporal microscopy; LAYER;
D O I
10.1002/adma.202407796
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Determining the electronic transport properties of graphene nanoribbons is crucial for assessing their suitability for applications. So far, this has been highly challenging both through experimental and theoretical approaches. This is particularly the case for graphene nanoribbons that are prepared by chemical vapor deposition, which is a scalable and industry-compatible bottom-up growth method that results in closely packed arrays of ribbons with relatively short lengths of a few tens of nanometers. In this study, the experimental technique of spatiotemporal microscopy is applied to study monolayer films of 9-armchair graphene nanoribbons prepared using this growth method, and combined with linear-scaling quantum transport calculations of arrays of thousands of nanoribbons. Both approaches directly resolve electronic spreading in space and time through diffusion and give an initial diffusivity approaching 200 cm2 s-1 during the first picosecond after photoexcitation. This corresponds to a mobility up to 550 cm2 V-1 s-1. The quasi-free carriers then form excitons, which spread with a diffusivity of tens of cm2 s-1. The results indicate that this relatively large charge carrier mobility is the result of electronic transport not being hindered by defects nor inter-ribbon hopping. This confirms their suitability for applications that require efficient electronic transport.
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页数:8
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