4.8 Article

High-Performance Perovskite Solar Cells Engineered by an Ammonia Modified Graphene Oxide Interfacial Layer

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 8, 期 23, 页码 14503-14512

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.6b02064

关键词

perovskite solar cells; ammonia modified graphene oxide; hole transfer layer; energy-level-match; perovskite structure; device performance

资金

  1. National Natural Science Foundation of China [11175239, 11405253, 11405257, 11505270, U1332205]
  2. Strategic Priority Research Program of the Chinese Academy of Sciences [XDA02040200]
  3. Science and Technology Commission of Shanghai Municipality [14DZ2261200]
  4. Shanghai Municipal Commission for Science and Technology [15ZR1448300]
  5. One Hundred Person Project of the Chinese Academy of Sciences

向作者/读者索取更多资源

The introduction of an ammonia modified graphene oxide (GO:NH3) layer into perovskite-based solar cells (PSCs) with a structure of indium tin oxide (ITO)/poly(3,4-ethylene-dioxythiophene):poly(4 styrenestilfonate) (PEDOT:PSS)-GO: NH3/CH3NH3PbI3-xClx/phenyl C61-butyric acid methyl ester (PCBM)/(solution Bphen) sBphen/Ag improves their performance and perovskite structure stability significantly. The fabricated devices with a champion PCE up to 16.11% are superior in all the performances in comparison with all the reference devices Go without the GO:NH3 layer. To understand the improved device performances, synchrotron-based grazing incidence Xray diffraction (GIXRD), scanning electron microscopy (SEM), ultraviolet photoelectron spectroscopy (UPS), X-ray photoelectron spectroscopy (XPS), and UV-visible absorption measurements have been conducted on perovskite films on different substrates. It was found that these improvements should be partially attributed to the improved crystallization and preferred orientation order of, peovskite structure, partially to the improved morphology with nearly complete coverage, partially to the enhanced optical absorption caused by the PEDOT:PSS-GO:NH3 layer, and partially to the better matched energy-level-alignment at the perovskite interface. Furthermore; the device was shown to be more stable in the ambient condition, which is clearly associated with the improved peovskite structure stability by the GO:NH3 layer observed by the GIXRD measurements. All these achievements will promote more applications of chemically modified graphene oxide interfacial layer in the PSCs as well as other organic multilayer devices.

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