Hot Carrier Enhancement of Dember Photorefractive Space-Charge Fields in Zincblende Semiconductors

W. Schroeder, T. S. Stark, Arthur L. Smir, G. Valley
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Abstract

We use a novel, nondegenerate, polarization-sensitive, transient-grating technique1 to monitor the picosecond dynamics of the photorefractive effect in undoped CdTe and InP:Fe at 960 nm. The technique circumvents the limited temporal resolution of the two-beam coupling geometry by using a time-delayed third probe pulse (with a duration of <5 psec) to read the gratings written in the semiconductor. The technique also exploits the crystal symmetry of zincblende semiconductors by using an optically induced anisotropy in the crystal index of refraction2 to separate the photorefractive gratings from the stronger, co-existing instantaneous bound-electronic and freecarrier gratings. In both semiconductors, the photorefractive effect is associated with the Dember field between mobile electron-hole pairs, in contrast to the more conventional photorefractive space-charge field connected with the separation of a mobile carriers species from a stationary, but oppositely charged, mid-gap state. In the undoped CdTe sample, which possesses no optically-active mid-gap levels, the electron-hole pairs are produced by two-photon absorption of 1.3 eV photons across the 1.44 eV band-gap of the semiconductor. The resultant ~1 eV excess carrier energy, which allows hot carrier transport to dominate the initial formation of the space-charge field, causes up to an order of magnitude enhancement in the photorefractive effect on picosecond timescales. After the carriers have cooled and the initial overshoot in the space-charge field has decayed, the photorefractive effect is observed to decay as the Dember field is destroyed by ambipolar diffusion of the electron-hole pairs across the grating period. In InP:Fe on the other hand, the electron-hole pairs are produced predominantly by direct single-photon band-to-band absorption into the band-tail of the semiconductor (band-gap ~1.35 eV), since the iron dopant only dominates the linear absorption at longer wavelengths. This means that the carriers are generated with little excess energy. Consequently, no hot carrier enhancement of the photorefractive effect was observed, and once formed, the Dember space-charge field decayed directly by ambipolar diffusion.
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锌闪锌矿半导体中Dember光折变空间电荷场的热载流子增强
我们使用一种新颖的、非简并的、偏振敏感的瞬态光栅技术1来监测960 nm处未掺杂CdTe和InP:Fe光折变效应的皮秒动态。该技术通过使用时间延迟的第三探针脉冲(持续时间<5 psec)来读取半导体中写入的光栅,从而绕过了双光束耦合几何结构的有限时间分辨率。该技术还利用锌闪锌矿半导体的晶体对称性,利用晶体折射率的光学诱导各向异性,将光折变光栅与更强的、共存的瞬时束缚电子和自由载流子光栅分开。在这两种半导体中,光折变效应都与移动电子-空穴对之间的Dember场有关,而传统的光折变空间电荷场则与移动载流子种与固定但相反电荷的中隙态分离有关。在未掺杂的CdTe样品中,没有光学活性的中隙能级,电子-空穴对是通过半导体的1.44 eV带隙中1.3 eV光子的双光子吸收产生的。由此产生的~1 eV多余载流子能量,使得热载流子输运在空间电荷场的初始形成中占主导地位,在皮秒时间尺度上导致光折变效应的数量级增强。当载流子冷却后,空间电荷场的初始超调衰减后,由于电子-空穴对在光栅周期内的双极性扩散破坏了Dember场,光折变效应也随之衰减。另一方面,在InP:Fe中,电子-空穴对主要是通过直接的单光子带对吸收到半导体的带尾(带隙~1.35 eV)产生的,因为铁掺杂剂仅在较长波长的线性吸收中占主导地位。这意味着载流子产生时几乎没有多余的能量。因此,没有观察到热载流子光折变效应的增强,并且一旦形成,Dember空间电荷场直接通过双极性扩散衰减。
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