材料科学
掺杂剂
兴奋剂
光电流
钙钛矿(结构)
磁滞
带隙
能量转换效率
化学工程
分析化学(期刊)
纳米技术
光电子学
凝聚态物理
有机化学
工程类
化学
物理
作者
Jung Kyu Kim,Sung Uk Chai,Yongfei Ji,Ben Levy‐Wendt,Suk Hyun Kim,Yeonjin Yi,Tony F. Heinz,Jens K. No̸rskov,Jong Hyeok Park,Xiaolin Zheng
标识
DOI:10.1002/aenm.201801717
摘要
Abstract To further increase the open‐circuit voltage ( V oc ) of perovskite solar cells (PSCs), many efforts have been devoted to doping the TiO 2 electron transport/selective layers by using metal dopants with higher electronegativity than Ti. However, those dopants can introduce undesired charge traps that hinder charge transport through TiO 2 , so the improvement in the V oc is often accompanied by an undesired photocurrent density–voltage ( J–V ) hysteresis problem. Herein, it is demonstrated that the use of a rapid flame doping process (40 s) to introduce cobalt dopant into TiO 2 not only solves the J–V hysteresis problem but also increases the V oc and power conversion efficiency of both mesoscopic and planar PSCs. The reasons for the simultaneous improvements are two fold. First, the flame‐doped Co‐TiO 2 film forms Co‐O v (cobalt dopant‐oxygen vacancy) pairs and hence reduces the number density of Ti 3+ trap states. Second, Co doping upshifts the band structure of TiO 2 , facilitating efficient charge extraction. As a result, for planar PSCs, the flame doping of Co increases the efficiency from 17.1% to 18.0% while reducing the hysteresis from 16.0% to 1.7%. Similarly, for mesoscopic PSCs, the flame doping of Co increases the efficiency from 18.5% to 20.0% while reducing the hysteresis from 7.0% to 0.1%.
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