石墨烯
材料科学
钙钛矿(结构)
氧化物
氧化铟锡
异质结
铟
光电子学
化学工程
基质(水族馆)
载流子
兴奋剂
纳米技术
薄膜
海洋学
地质学
工程类
冶金
作者
Efat Jokar,Zhong Huang,Sudhakar Narra,Chi‐Yung Wang,Vidya Kattoor,Chih‐Chun Chung,Eric Wei‐Guang Diau
标识
DOI:10.1002/aenm.201701640
摘要
Abstract Reduced graphene oxides (rGO) are synthesized via reduction of GO with reducing agents as a hole‐extraction layer for high‐performance inverted planar heterojunction perovskite solar cells. The best efficiencies of power conversion (PCE) of these rGO cells exceed 16%, much greater than those made of GO and poly(3,4‐ethenedioxythiophene):poly(styrenesulfonate) films. A flexible rGO device shows PCE 13.8% and maintains 70% of its initial performance over 150 bending cycles. It is found that the hole‐extraction period is much smaller for the GO/methylammonium lead‐iodide perovskite (PSK) film than for the other rGO/PSK films, which contradicts their device performances. Photoluminescence and transient photoelectric decays are measured and control experiments are performed to prove that the reduction of the oxygen‐containing groups in GO significantly decreases the ability of hole extraction from PSK to rGO and also retards the charge recombination at the rGO/PSK interface. When the hole injection from PSK to GO occurs rapidly, hole propagation from GO to the indium‐doped tin oxide (ITO) substrate becomes a bottleneck to overcome, which leads to a rapid charge recombination that decreases the performance of the GO device relative to the rGO device.
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