Department of Chemistry, University of Washington , Seattle, Washington 98105, United States.
ACS Nano. 2016 Nov 22;10(11):10258-10266. doi: 10.1021/acsnano.6b05825. Epub 2016 Oct 17.
We use high-resolution, spatially resolved, laser beam induced current, confocal photoluminescence, and photoconductive atomic force microscopy (pcAFM) measurements to correlate local solar cell performance with spatially heterogeneous local material properties in methylammonium lead triiodide (CHNHPbI) perovskite solar cells. We find that, for this material and device architecture, the photocurrent heterogeneity measured via pcAFM on devices missing a top selective contact with traditional Au-coated tips is significantly larger than the photocurrent heterogeneity observed in full devices with both electron- and hole-selective extraction layers, indicating that extraction barriers at the Au/perovskite interface are ameliorated by deposition of the organic charge extraction layer. Nevertheless, in completed, efficient device structures (PCE ≈ 16%) with state-of-the-art nickel oxide and [6,6]-phenyl-C61-butyric acid (PCBM) methyl ester contacts, we observe that the local photoluminescence (PL) is weakly anticorrelated with local photocurrent at both short-circuit and open-circuit conditions. We determine that the contact materials are fairly homogeneous; thus the heterogeneity stems from the perovskite itself. We suggest a cause for the anticorrelation as being related to local carrier extraction heterogeneity. However, we find that the contacts are still the dominating source of losses in these devices, which minimizes the impact of the material heterogeneity on device performance at present. These results suggest that further steps to prevent recombination losses at the interfaces are needed to help perovskite-based cells approach theoretical efficiency limits; only at this point will material heterogeneity become crucial.
我们使用高分辨率、空间分辨的激光束诱导电流、共焦光致发光和光电导原子力显微镜(pcAFM)测量来关联局部太阳能电池性能与局部材料特性在甲基碘化铵(CHNHPbI)钙钛矿太阳能电池中的空间不均匀性。我们发现,对于这种材料和器件结构,在没有传统 Au 涂层尖端的顶部选择性接触的器件上通过 pcAFM 测量的光电流不均匀性明显大于在具有电子和空穴选择性提取层的全器件中观察到的光电流不均匀性,这表明 Au/钙钛矿界面处的提取势垒通过沉积有机电荷提取层得到改善。然而,在具有先进的氧化镍和[6,6]-苯基-C61-丁酸甲酯(PCBM)接触的完整、高效的器件结构(PCE ≈ 16%)中,我们观察到在短路和开路条件下,局部光致发光(PL)与局部光电流弱反相关。我们确定接触材料相当均匀;因此,不均匀性源于钙钛矿本身。我们认为这种反相关的原因与局部载流子提取不均匀性有关。然而,我们发现这些器件中的接触仍然是损耗的主要来源,这使得材料不均匀性对器件性能的影响在目前最小化。这些结果表明,需要进一步采取措施来防止界面处的复合损失,以帮助基于钙钛矿的电池接近理论效率极限;只有在这一点上,材料不均匀性才会变得至关重要。