期刊
ACS ENERGY LETTERS
卷 2, 期 8, 页码 1841-1847出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsenergylett.7b00525
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- U.S. Department of Energy Sunshot Initiative, Next Generation Photovoltaics 3 program [DE-EE0006710]
- University of Washington Clean Energy Institute
- Swiss National Science Foundation (SNSF) [P2EZP2_152168, P300P2_164660]
- Swiss National Science Foundation (SNF) [P2EZP2_152168, P300P2_164660] Funding Source: Swiss National Science Foundation (SNF)
Mixed halide hybrid perovskites are of significant interest because their bandgap can be tuned as a current-matched top-cell in tandem photovoltaics. However, several mixed halide perovskites phase segregate under illumination, exhibit large voltage deficits, and produce unstable photocurrents. We investigate the origin of phase segregation and implication for tandems with mixed halide large-bandgap (similar to 1.75 eV) perovskites. We show explicitly that MAPb(I0.6Br0.4)(3) and (MA(0.9),Cs-0.1)Pb(I-0.6,Br-0.4)(3), termed MA and MACs, respectively, rapidly phase segregate in the dark upon 1 sun equivalent current injection. This is direct experimental evidence that conduction band electrons or valence band holes are the culprit behind phase segregation. In contrast, (FA(0.83),Cs-0.17)Pb(I-0.66,Br-0.34)(3), or FACs, prepared at only 75 degrees C resists phase segregation below 4 sun injection. FACs prepared at 165 degrees C yields larger grains and withstands higher injected carrier concentrations before phase segregation. The FACs and MACs devices sustain near constant power output at 1 sun and do not affect the current output of a GIGS bottom cell when used as an incident light filter.
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