Mixed-halide perovskites solar cells through PbICl and PbCl2 precursor films by sequential chemical vapor deposition

卤化物 钙钛矿(结构) 碘化物 太阳能电池 材料科学 氯化铅 无机化学 化学气相沉积 钙钛矿太阳能电池 兴奋剂 氯化物 相(物质) 薄膜 化学工程 光伏系统 光电子学 能量转换效率 带隙 沉积(地质) 金属卤化物 化学 纳米技术 有机化学 冶金 古生物学 工程类 生物 沉积物
作者
Siphelo Ngqoloda,Christopher J. Arendse,S. Guha,T.F.G. Muller,Stephen C. Klue,Siphesihle S. Magubane,Clive J. Oliphant
出处
期刊:Solar Energy [Elsevier BV]
卷期号:215: 179-188 被引量:13
标识
DOI:10.1016/j.solener.2020.12.042
摘要

Mixed halide perovskites with chlorine (Cl) content have received significant interest due to better charge transport properties and longer diffusion length compared to pure iodine-based perovskites. The superior properties of Cl-doped perovskites improve solar cell device performance, although the quantification of Cl composition in the perovskite films remain difficult to achieve. Hence, it is difficult to correlate the Cl-quantity with the improved device performance. In this work, we deposited Cl-doped perovskite films through a facile three- and two-step sequential chemical vapor deposition (CVD) where lead halide films were deposited in the first steps of the process and subsequently converted to perovskites. No Cl substitution by iodine was observed during a sequential deposition of lead chloride and lead iodide films which reacted to form a lead chloride iodide phase (PbICl). The substitution of Cl by iodine ions only occurred during the conversion to perovskite phase. Large perovskite grains (greater than 2 µm) were realized when converting a PbI2 film to perovskite compared to chlorine containing lead halide films, contradicting literature. However, Cl doped perovskite solar cells showed improved device efficiencies as high as 10.87% compared to an un-doped perovskite solar cell (8.76%).
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