材料科学
非阻塞I/O
纳米网
钙钛矿(结构)
光电流
分析化学(期刊)
表面光电压
氧化镍
光致发光
能量转换效率
光谱学
钙钛矿太阳能电池
化学工程
光电子学
纳米技术
氧化物
石墨烯
化学
工程类
物理
量子力学
催化作用
冶金
生物化学
色谱法
作者
Ujwal Kumar Thakur,Pawan Kumar,Sergey Gusarov,Alexander E. Kobryn,Saralyn Riddell,Ankur Goswami,Kazi M. Alam,Spencer Savela,Piyush Kar,Thomas Thundat,A. Meldrum,Karthik Shankar
标识
DOI:10.1021/acsami.9b18197
摘要
Leading edge p-i-n type halide perovskite solar cells (PSCs) severely underperform n-i-p PSCs. p-i-n type PSCs that use PEDOT:PSS hole transport layers (HTLs) struggle to generate open-circuit photovoltage values higher than 1 V. NiO HTLs have shown greater promise in achieving high Voc values albeit inconsistently. In this report, a NiO nanomesh with Ni3+ defect grown by the hydrothermal method was used to obtain PSCs with Voc values that consistently exceeded 1.10 V (champion Voc = 1.14 V). A champion device photoconversion efficiency of 17.75% was observed. Density functional theory modeling was used to understand the interfacial properties of the NiO/perovskite interface. The PCE of PSCs constructed using the Ni3+-doped NiO nanomesh HTL was ∼34% higher than that of conventional compact NiO-based perovskite solar cells. A suite of characterization techniques such as transmission electron microscopy, field emission scanning electron microscopy, intensity-modulated photocurrent spectroscopy, intensity-modulated photovoltage spectroscopy, time-resolved photoluminescence, steady-state photoluminescence, and Kelvin probe force microscopy provided evidence of better film quality, enhanced charge transfer, and suppressed charge recombination in PSCs based on hydrothermally grown NiO nanostructures.
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