4.7 Article

Highly stable carbon-based perovskite solar cell with a record efficiency of over 18% via hole transport engineering

期刊

JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
卷 35, 期 6, 页码 987-993

出版社

JOURNAL MATER SCI TECHNOL
DOI: 10.1016/j.jmst.2018.12.025

关键词

Planar carbon-based perovskite solar cells; Hole transport engineering; Recorded efficiency; Excellent moisture and light stability

资金

  1. National Program for Support of Top-notch Young Professionals
  2. Australian Government through the Australian Renewable Energy Agency (ARENA)

向作者/读者索取更多资源

Carbon-based perovskite solar cells show great potential owing to their low-cost production and superior stability in air, compared to their counterparts using metal contacts. The photovoltaic performance ofcarbon based PSCs, however, has been progressing slowly in spite of an impressive efficiency when they were first reported. One of the major obstacles is that the hole transport materials developed for state-of-the-art Au-based PSCs are not suitable for carbon-based PSCs. Here, we develop a low-temperature, solution-processed Poly(3-hexylthiophene-2,5-diyl) (P3HT)/graphene composite hole transport layer(HTL), that is compatible with paintable carbon-electrodes to produce state-of-the-art perovskitedevices. Space-charge-limited-current measurements reveal that the as-prepared P3HT/graphene composite exhibits outstanding charge mobility and thermal tolerance, with hole mobility increasing from 8.3 x 10(-3) cm(2)V(-1)s(-1) (as-deposited) to 1.2 x 10(-2)cm(2)V(-1)s(-1) (after annealing at 100 degrees C)-two orders of magnitude larger than pure P3HT. The improved charge transport and extraction provided by the composite HTL provides a significant efficiency improvement compared to cells with a pure P3HT HTL. As aresult, we report carbon-based solar cells with a record efficiency of 17.8% (certified by Newport); and the first perovskite cells to be certified under the stabilized testing protocol. The outstanding device stabilityis demonstrated by only 3% drop after storage in ambient conditions (humidity: ca. 50%) for 1680 h (non-encapsulated), and retention of ca. 89% of their original output under continuous 1-Sun illumination atroomtemperature for 600 h (encapsulated) in a nitrogen environment. (c) 2019 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science & Technology.

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