论文标题
通过基于硫基于硫的2D钙钛矿的原位形成,改善光伏设备的性能和稳定性
Improvement of both performance and stability of photovoltaic devices by in situ formation of a sulfur-based 2D perovskite
论文作者
论文摘要
具有出色性能的钙钛矿太阳能电池(PSC)已被认为是光伏技术的潜在候选者。但是,活性钙钛矿层中的缺陷会诱导非辐射重组,从而限制了PSC的性能和稳定性。基于噻吩的2D结构的构建是杂交PSC表面钝化的重要方法之一,它可能将2D钙钛矿的稳定性与3D钙钛矿的高性能结合在一起。在这里,富含硫的间隔阳离子2-硫代氨基胺(TEAI)被合成为钝化剂,用于构建三维/二维(3D/2D)钙钛矿双层双层结构。与3D钙钛矿(MAFAPBI3)设备(17.42%)相比,TEAI处理的PSC具有更高的效率(20.06%)。时间分辨的光致发光(TRPL)和飞秒瞬时吸收(TA)光谱法用于研究表面钝化对3D钙钛矿的电荷载体动力学的影响。此外,TEAI处理的钙钛矿设备的稳定性测试显示,湿润(RH〜56%)和热稳定性的显着改善,就像基于硫的2D(TEA)2PBI4材料在3D表面上的材料自组成,从而使钙钛矿表面疏水性疏水。我们的发现提供了一种可靠的方法来连续提高设备稳定性和性能,从而为PSC的工业化铺平了道路。
Perovskite solar cells (PSCs) with superior performance have been recognized as a potential candidate in photovoltaic technologies. However, the defects in active perovskite layer induce non-radiative recombination which restricts the performance and stability of the PSCs. The construction of thiophene-based 2D structure is one of the significant approaches for surface passivation of hybrid PSCs that may combine the benefits of the stability of 2D perovskite with the high performance of 3D perovskite. Here, a sulfur-rich spacer cation 2-thiopheneethylamine iodide (TEAI) is synthesized as a passivation agent for the construction of three-dimensional/two-dimensional (3D/2D) perovskite bilayer structure. TEAI-treated PSCs possess a much higher efficiency (20.06%) compared to the 3D perovskite (MAFAPbI3) devices (17.42%). Time-resolved photoluminescence (TRPL) and femtosecond transient absorption (TA) spectroscopy are employed to investigate the effect of surface passivation on the charge carrier dynamics of the 3D perovskite. Additionally, the stability test of TEAI-treated perovskite devices reveals significant improvement in humid (RH ~ 56%) and thermal stability as the sulfur-based 2D (TEA)2PbI4 material self-assembles on the 3D surface making the perovskite surface hydrophobic. Our findings provide a reliable approach to improve device stability and performance successively, paving the way for industrialization of PSCs.