Department of Materials and Interfaces, Weizmann Institute of Science, Rehovot, 76100, Israel.
Chemical Research Support, Weizmann Institute of Science, Rehovot, 76100, Israel.
Adv Mater. 2018 May;30(20):e1800413. doi: 10.1002/adma.201800413. Epub 2018 Mar 30.
1D core-shell heterojunction nanostructures have great potential for high-performance, compact optoelectronic devices owing to their high interface area to volume ratio, yet their bottom-up assembly toward scalable fabrication remains a challenge. Here the site-controlled growth of aligned CdS-CdSe core-shell nanowalls is reported by a combination of surface-guided vapor-liquid-solid horizontal growth and selective-area vapor-solid epitaxial growth, and their integration into photodetectors at wafer-scale without postgrowth transfer, alignment, or selective shell-etching steps. The photocurrent response of these nanowalls is reduced to 200 ns with a gain of up to 3.8 × 10 and a photoresponsivity of 1.2 × 10 A W , the fastest response at such a high gain ever reported for photodetectors based on compound semiconductor nanostructures. The simultaneous achievement of sub-microsecond response and high-gain photocurrent is attributed to the virtues of both the epitaxial CdS-CdSe heterojunction and the enhanced charge-separation efficiency of the core-shell nanowall geometry. Surface-guided nanostructures are promising templates for wafer-scale fabrication of self-aligned core-shell nanostructures toward scalable fabrication of high-performance compact photodetectors from the bottom-up.
1D 核壳异质结纳米结构由于具有高的比表面积与体积比,在高性能、紧凑型光电器件中有很大的应用潜力,但其自下而上的组装对于可扩展的制造仍然是一个挑战。在此,通过表面引导的气-液-固水平生长和选择性区域气-固外延生长的结合,实现了 CdS-CdSe 核壳纳米墙的定向生长,在无需后续生长转移、对准或选择性壳刻蚀步骤的情况下,将其集成到晶圆级的探测器中。这些纳米墙的光电流响应时间缩短至 200ns,增益高达 3.8×10^3,光响应率为 1.2×10^-3 A/W,这是基于化合物半导体纳米结构的探测器中,在如此高的增益下,最快的响应速度。亚微秒响应时间和高增益光电流的同时实现归因于外延 CdS-CdSe 异质结的优点和核壳纳米墙结构增强的电荷分离效率。表面引导的纳米结构是自对准核壳纳米结构的晶圆级制造的有前途的模板,可自下而上实现高性能紧凑型光探测器的可扩展制造。