Enhancing Intrinsic Stability of Hybrid Perovskite Solar Cell by Strong, yet Balanced, Electronic Coupling

被引:44
作者
El-Mellouhi, Fedwa [1 ]
Bentria, El Tayeb [1 ]
Rashkeev, Sergey N. [1 ]
Kais, Sabre [1 ,2 ,3 ,4 ]
Alharbi, Fahhad H. [1 ,2 ]
机构
[1] Hamad Bin Khalifa Univ, QEERI, Doha, Qatar
[2] Hamad Bin Khalifa Univ, Coll Sci & Engn, Doha, Qatar
[3] Purdue Univ, Dept Chem, Phys, W Lafayette, IN 47907 USA
[4] Purdue Univ, Birck Nanotechnol Ctr, W Lafayette, IN 47907 USA
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
关键词
METAL-HALIDE PEROVSKITES; INORGANIC PEROVSKITES; HIGH-PERFORMANCE; BAND-GAP; LIGHT;
D O I
10.1038/srep30305
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the past few years, the meteoric development of hybrid organic-inorganic perovskite solar cells (PSC) astonished the community. The efficiency has already reached the level needed for commercialization; however, the instability hinders its deployment on the market. Here, we report a mechanism to chemically stabilize PSC absorbers. We propose to replace the widely used methylammonium cation (CH3NH3+) by alternative molecular cations allowing an enhanced electronic coupling between the cation and the PbI6 octahedra while maintaining the band gap energy within the suitable range for solar cells. The mechanism exploits establishing a balance between the electronegativity of the materials' constituents and the resulting ionic electrostatic interactions. The calculations demonstrate the concept of enhancing the electronic coupling, and hence the stability, by exploring the stabilizing features of CH3PH3+, CH3SH2+, and SH3+ cations, among several other possible candidates. Chemical stability enhancement hence results from a strong, yet balanced, electronic coupling between the cation and the halides in the octahedron. This shall unlock the hindering instability problem for PSCs and allow them to hit the market as a serious low-cost competitor to silicon based solar cell technologies.
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页数:8
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