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用于高效钙钛矿太阳能电池的含水性前驱体溶液。

Aqueous-Containing Precursor Solutions for Efficient Perovskite Solar Cells.

作者信息

Liu Dianyi, Traverse Christopher J, Chen Pei, Elinski Mark, Yang Chenchen, Wang Lili, Young Margaret, Lunt Richard R

机构信息

Department of Chemical Engineering and Materials Science Michigan State University East Lansing Michigan 48824 USA.

Department of Physics and Astronomy Michigan State University East Lansing Michigan 48824 USA.

出版信息

Adv Sci (Weinh). 2017 Nov 10;5(1):1700484. doi: 10.1002/advs.201700484. eCollection 2018 Jan.

Abstract

Perovskite semiconductors have emerged as competitive candidates for photovoltaic applications due to their exceptional optoelectronic properties. However, the impact of moisture instability on perovskite films is still a key challenge for perovskite devices. While substantial effort is focused on preventing moisture interaction during the fabrication process, it is demonstrated that low moisture sensitivity, enhanced crystallization, and high performance can actually be achieved by exposure to high water content (up to 25 vol%) during fabrication with an aqueous-containing perovskite precursor. The perovskite solar cells fabricated by this aqueous method show good reproducibility of high efficiency with average power conversion efficiency (PCE) of 18.7% and champion PCE of 20.1% under solar simulation. This study shows that water-perovskite interactions do not necessarily negatively impact the perovskite film preparation process even at the highest efficiencies and that exposure to high contents of water can actually enable humidity tolerance during fabrication in air.

摘要

钙钛矿半导体因其卓越的光电性能,已成为光伏应用领域颇具竞争力的候选材料。然而,湿度不稳定性对钙钛矿薄膜的影响仍是钙钛矿器件面临的关键挑战。尽管大量工作聚焦于在制造过程中防止水分相互作用,但研究表明,在使用含水性钙钛矿前驱体制造过程中,通过暴露于高含水量(高达25体积%)的环境中,实际上可以实现低湿度敏感性、增强结晶和高性能。通过这种水性方法制造的钙钛矿太阳能电池显示出良好的高效再现性,在太阳模拟条件下,平均功率转换效率(PCE)为18.7%,最佳PCE为20.1%。这项研究表明,即使在最高效率下,水与钙钛矿的相互作用也不一定会对钙钛矿薄膜制备过程产生负面影响,而且在空气中制造过程中暴露于高含水量环境实际上可以实现湿度耐受性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdce/5770683/6371c316a3d0/ADVS-5-na-g001.jpg

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