Enhancement of Perovskite-Based Solar Cells Employing Core-Shell Metal Nanoparticles

被引:513
作者
Zhang, Wei [1 ]
Saliba, Michael [1 ]
Stranks, Samuel D. [1 ]
Sun, Yao [2 ]
Shi, Xian [2 ]
Wiesner, Ulrich [2 ]
Snaith, Henry J. [1 ]
机构
[1] Univ Oxford, Dept Phys, Clarendon Lab, Oxford OX1 3PU, England
[2] Cornell Univ, Dept Mat Sci & Engn, Ithaca, NY 14853 USA
基金
美国国家科学基金会; 英国工程与自然科学研究理事会;
关键词
Perovskites; thin-film solar cells; Au@SiO2 nanoparticles; exciton binding energy; free charge carriers; ENERGY-GAP; PHOTOLUMINESCENCE; EFFICIENCY; DEPENDENCE;
D O I
10.1021/nl4024287
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recently, inorganic and hybrid light absorbers such as quantum dots and organometal halide perovskites have been studied and applied in fabricating thin-film photovoltaic devices because of their low-cost and potential for high efficiency. Further boosting the performance of solution processed thin-film solar cells without detrimentally increasing the complexity of the device architecture is critically important for commercialization. Here, we demonstrate photocurrent and efficiency enhancement in mesosuperstructured organometal halide perovskite solar cells incorporating core shell Au@SiO2 nanoparticles (NPs) delivering a device efficiency of up to 11.4%. We attribute the origin of enhanced photocurrent to a previously unobserved and unexpected mechanism of reduced exciton binding energy with the incorporation of the metal nanoparticles, rather than enhanced light absorption. Our findings represent a new aspect and lever for the application of metal nanoparticles in photovoltaics and could lead to facile tuning of exciton binding energies in perovskite semiconductors.
引用
收藏
页码:4505 / 4510
页数:6
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