Department of Materials Science and Engineering, ARC Centre of Excellence in Future Low-Energy Electronics Technologies (FLEET), Monash University, Clayton, Victoria, 3800, Australia.
College of Electronic Science and Technology and College of Optoelectronics Engineering, Shenzhen University, Shenzhen, 518000, P. R. China.
Adv Mater. 2018 Apr;30(15):e1705792. doi: 10.1002/adma.201705792. Epub 2018 Mar 1.
A semiconductor p-n junction typically has a doping-induced carrier depletion region, where the doping level positively correlates with the built-in potential and negatively correlates with the depletion layer width. In conventional bulk and atomically thin junctions, this correlation challenges the synergy of the internal field and its spatial extent in carrier generation/transport. Organic-inorganic hybrid perovskites, a class of crystalline ionic semiconductors, are promising alternatives because of their direct badgap, long diffusion length, and large dielectric constant. Here, strong depletion in a lateral p-n junction induced by local electronic doping at the surface of individual CH NH PbI perovskite nanosheets is reported. Unlike conventional surface doping with a weak van der Waals adsorption, covalent bonding and hydrogen bonding between a MoO dopant and the perovskite are theoretically predicted and experimentally verified. The strong hybridization-induced electronic coupling leads to an enhanced built-in electric field. The large electric permittivity arising from the ionic polarizability further contributes to the formation of an unusually broad depletion region up to 10 µm in the junction. Under visible optical excitation without electrical bias, the lateral diode demonstrates unprecedented photovoltaic conversion with an external quantum efficiency of 3.93% and a photodetection responsivity of 1.42 A W .
半导体 p-n 结通常具有掺杂诱导的载流子耗尽区,其中掺杂水平与内置电势呈正相关,与耗尽层宽度呈负相关。在传统的体材料和原子薄结中,这种相关性挑战了内部电场及其在载流子产生/输运中的空间扩展的协同作用。有机-无机杂化钙钛矿是一类晶态离子半导体,由于其直接带隙、长扩散长度和大介电常数,是很有前途的替代品。本文报道了在单个 CH3NH3PbI 钙钛矿纳米片表面通过局部电子掺杂诱导的横向 p-n 结中的强耗尽。与传统的弱范德华吸附的表面掺杂不同,MoO 掺杂剂与钙钛矿之间的共价键和氢键在理论上被预测并在实验上得到证实。强杂化诱导的电子耦合导致内置电场增强。由于离子极化率引起的大介电常数进一步有助于形成异常宽的耗尽区,在结中达到 10 µm。在没有外加偏压的可见光激发下,横向二极管表现出前所未有的光伏转换,外量子效率为 3.93%,光探测响应率为 1.42 A W-1。