Autor: |
Rajamanickam P; Department of Materials Science and Engineering, National Yang Ming Chiao Tung University, 1001 Ta-Hseuh Rd., Hsinchu 300093, Taiwan., Narra S; Department of Applied Chemistry and Institute of Molecular Science, National Yang Ming Chiao Tung University, 1001 Ta-Hseuh Rd., Hsinchu 300093, Taiwan.; Center for Emergent Functional Matter Science, National Yang Ming Chiao Tung University, 1001 Ta-Hseuh Rd., Hsinchu 300093, Taiwan., Seetharaman A; Department of Applied Chemistry and Institute of Molecular Science, National Yang Ming Chiao Tung University, 1001 Ta-Hseuh Rd., Hsinchu 300093, Taiwan., Diau EW; Department of Applied Chemistry and Institute of Molecular Science, National Yang Ming Chiao Tung University, 1001 Ta-Hseuh Rd., Hsinchu 300093, Taiwan.; Center for Emergent Functional Matter Science, National Yang Ming Chiao Tung University, 1001 Ta-Hseuh Rd., Hsinchu 300093, Taiwan. |
Abstrakt: |
The bottleneck in the rapid development of tin-based perovskite solar cells (TPSCs) is the inherent chemical instability. Although this is being addressed continuously, the device performance has not improved further due to the use of PEDOT:PSS as the hole-transport material (HTM), which has poor long-term stability. Herein we have applied commercial ITO nanoparticles over ITO glass substrates and altered the surface chemistry of the ITO electrode via a simple two-step thermal annealing, followed by a UV-ozone treatment. These surface-modified ITO electrodes display promising interfacial characteristics, such as a suitable band alignment owing to significantly reduced surface carbon contamination, increased In-O bonding, and reduced oxygen vacancies, that enabled fabrication of an HTM-free TPSC device according to a two-step method. The fabricated device possessed an outstanding power conversion efficiency (PCE) of 9.7%, along with a superior long-term stability by retaining over 90% of the initial PCE upon shelf storage in a glovebox for a period of over 10000 h. The application of ITO nanoparticles led to effective interfacial passivation, whose impacts on the long-term durability were assessed using electrochemical impedance spectroscopy, time-resolved photoluminescence decay profiles, and femtosecond transient absorption spectroscopy techniques. |