Machado Pamela, Scigaj Mateusz, Gazquez Jaume, Rueda Estel, Sánchez-Díaz Antonio, Fina Ignasi, Gibert-Roca Martí, Puig Teresa, Obradors Xavier, Campoy-Quiles Mariano, Coll Mariona
Institut de Ciència de Materials de Barcelona ICMAB-CSIC, Campus UAB Bellaterra E-08193, Barcelona , Spain.
Chem Mater. 2019 Feb 12;31(3):947-954. doi: 10.1021/acs.chemmater.8b04380. Epub 2019 Jan 16.
Ferroelectric perovskite oxides are emerging as a promising photoactive layer for photovoltaic applications because of their very high stability and their alternative ferroelectricity-related mechanism for solar energy conversion that could lead to extraordinarily high efficiencies. One of the biggest challenges so far is to reduce their band gap toward the visible region while simultaneously retaining ferroelectricity. To address these two issues, herein an elemental composition engineering of BiFeO is performed by substituting Fe by Co cations, as a means to tune the characteristics of the transition metal-oxygen bond. We demonstrate by solution processing the formation of epitaxial, pure phase, and stable BiFe Co O thin films for ≤ 0.3 and film thickness up to 100 nm. Importantly, the band gap can be tuned from 2.7 to 2.3 eV upon cobalt substitution while simultaneously enhancing ferroelectricity. As a proof of concept, nonoptimized vertical devices have been fabricated and, reassuringly, the electrical photoresponse in the visible region of the Co-substituted phase is improved with respect to the unsubstituted oxide.
铁电钙钛矿氧化物因其极高的稳定性以及与铁电相关的太阳能转换替代机制(这可能带来极高的效率),正成为光伏应用中一种很有前景的光活性层。到目前为止,最大的挑战之一是在保持铁电性的同时,将其带隙向可见光区域减小。为了解决这两个问题,本文通过用Co阳离子替代Fe对BiFeO进行元素组成工程,以此作为调节过渡金属-氧键特性的一种手段。我们通过溶液处理证明,对于≤0.3且膜厚达100 nm的情况,可形成外延、纯相且稳定的BiFeCoO薄膜。重要的是,钴替代后带隙可从2.7 eV调至2.3 eV,同时增强了铁电性。作为概念验证,已制备出未优化的垂直器件,令人欣慰的是,与未替代的氧化物相比,Co替代相在可见光区域的电光响应得到了改善。