用于开发光伏中高效载流子倍增的新材料的出现

IF 6.1 Q2 CHEMISTRY, PHYSICAL Chemical physics reviews Pub Date : 2020-08-18 DOI:10.1063/5.0025748
S. Maiti, M. van der Laan, D. Poonia, P. Schall, S. Kinge, L. Siebbeles
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引用次数: 12

摘要

在传统的太阳能电池半导体材料(主要是硅)中,能量高于带隙的光子最初产生热电子和空穴,随后通过声子发射冷却到带边缘。由于后一种过程,超过带隙的电荷载流子的能量以热量的形式损失,并且无助于将太阳能转化为电能。如果多余的能量大于带隙,原则上可以通过一个被称为载流子倍增(CM)的过程来利用,在这个过程中,一个被吸收的光子产生两(或更多)对电子和空穴。因此,通过CM,光子能量超过带隙的两倍,增强了太阳能电池的光电流。在本文中,我们从基本认识、高效CM新材料的出现以及基于CM的太阳能电池应用等方面讨论了CM研究的最新进展。根据我们目前的理解,CM阈值可以接近最小值的两倍带隙的材料,其中光子诱导从更深的价带或更高的导带的不对称电子跃迁。此外,材料必须具有低激子结合能和高电荷载流子迁移率,这样光激发就可以直接形成自由电荷,这些自由电荷可以很容易地在光伏器件的外部电极上提取出来。耦合的PbSe量子点、Sn/Pb基卤化物钙钛矿和过渡金属二硫族化合物(如MoTe2)的渗透网络在很大程度上满足了这些要求。这些发现为进一步开发高效光伏新材料指明了光明的前景。
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Emergence of new materials for exploiting highly efficient carrier multiplication in photovoltaics
In conventional solar cell semiconductor materials (predominantly Si) photons with energy higher than the band gap initially generate hot electrons and holes, which subsequently cool down to the band edge by phonon emission. Due to the latter process, the energy of the charge carriers in excess of the band gap is lost as heat and does not contribute to the conversion of solar to electrical power. If the excess energy is more than the band gap it can in principle be utilized through a process known as carrier multiplication (CM) in which a single absorbed photon generates two (or more) pairs of electrons and holes. Thus, through CM the photon energy above twice the band gap enhances the photocurrent of a solar cell. In this review, we discuss recent progress in CM research in terms of fundamental understanding, emergence of new materials for efficient CM, and CM based solar cell applications. Based on our current understanding, the CM threshold can get close to the minimal value of twice the band gap in materials where a photon induces an asymmetric electronic transition from a deeper valence band or to a higher conduction band. In addition, the material must have a low exciton binding energy and high charge carrier mobility, so that photoexcitation leads directly to the formation of free charges that can readily be extracted at external electrodes of a photovoltaic device. Percolative networks of coupled PbSe quantum dots, Sn/Pb based halide perovskites, and transition metal dichalcogenides such as MoTe2 fulfill these requirements to a large extent. These findings point towards promising prospects for further development of new materials for highly efficient photovoltaics.
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