Wang Hanyu, Zou Wenjing, Ouyang Yukun, Liu Xingchong, Li Haimin, Luo Hu, Zhao Xiaopeng
School of New Energy and Materials, Southwest Petroleum University, Chengdu 610500, China.
J Phys Chem Lett. 2022 Sep 15;13(36):8573-8579. doi: 10.1021/acs.jpclett.2c02414. Epub 2022 Sep 8.
The disordered distribution of trap states and ion migration limit the commercial application of perovskite solar cells (PSCs). Herein, we apply an oxamic acid potassium salt (OAPS) as a bifunctional additive of perovskite film. The Lewis base group C=O of OAPS can interact with the uncoordinated Pb caused by the I site substitution by Pb and the dangling bonds of the perovskite, which is beneficial to reduce the nonradiative recombination loss. In addition, the countercation K of OAPS is confirmed to occupy the perovskite lattice interstitial sites and result in lattice expansion, inhibiting the formation of iodide Frenkel defects and I ion migration. As a result, the synergistic effect achieves enhanced power conversion efficiency (PCE) from 19.98 to 23.02%, with a fill factor reaching up to 81.90% and suppressed current-voltage hysteresis. The device also presents improved stability, maintaining 93% of the initial PCE after 2000 h of storage.
陷阱态的无序分布和离子迁移限制了钙钛矿太阳能电池(PSC)的商业应用。在此,我们将草酸钾盐(OAPS)用作钙钛矿薄膜的双功能添加剂。OAPS的路易斯碱基团C=O可与由Pb取代I位点以及钙钛矿的悬空键所导致的未配位Pb相互作用,这有利于减少非辐射复合损失。此外,证实OAPS的抗衡阳离子K占据钙钛矿晶格间隙位置并导致晶格膨胀,抑制碘化物弗伦克尔缺陷的形成和I离子迁移。结果,协同效应使功率转换效率(PCE)从19.98%提高到23.02%,填充因子高达81.90%,并抑制了电流-电压滞后现象。该器件还表现出 improved stability,在储存2000小时后仍保持初始PCE的93%。