Zhong Hong-Xia, Liu Shi-Ming, Cen Yu-Lang, Zhang Min, Zhu Yao-Hui, Du Juan, He Yong, Guo Wen-Hui, Wang Xin-Qiang, Shi Jun-Jie
School of Mathematics and Physics, China University of Geosciences, Wuhan 430074, China.
School of Physics and Technology, Wuhan University, Wuhan 430072, China.
ACS Appl Mater Interfaces. 2021 Oct 20;13(41):48971-48980. doi: 10.1021/acsami.1c10318. Epub 2021 Oct 6.
Perovskite-perovskite tandem solar cells have bright prospects to improve the power conversion efficiency (PCE) beyond the Shockley-Queisser (SQ) limit of single-junction solar cells. The star lead-based halide perovskites are well-recognized as suitable candidates for the front cell, thanks to their suitable band gap (∼1.8 eV), strong optical absorption, and high certified PCE. However, the toxicity of lead for the front cell and the lack of a narrow band gap (∼1.1 eV) for the rear cell seriously restrict the development of the two-junction tandem cell. To break through this bottleneck, a novel Dion-Jacobson (DJ)-type ( = 2) chalcogenide perovskite CsLaMX (M = Ta, Nb; X = S, Se) has been found based on the powerful first-principles and advanced many-body perturbation GW calculations. Their excellent electronic, transport, and optical properties can be summarized as follows. (1) They are stable and environmentally friendly lead-free materials. (2) The direct band gap of CsLaTaSe (0.96-1.10 eV) is much smaller than those of lead-based halide perovskites and very suitable for the rear cell in the two-junction tandem cell. (3) The carrier mobility in CsLaTaSe reaches 1.6 × 10 cm V s at room temperature. (4) The absorption coefficients (3-5 × 10 cm) are 1 order higher than that of Si (10 cm). (5) The estimated PCEs of the CsSbBr-CsLaTaSe tandem cell (33.3%) and the concentrator solar cell (35.8% in 100 suns) are higher than those of the best recorded GaAs-Si tandem cell (32.8%) and the perovskite-perovskite tandem solar cell (24.8%). These energetic results strongly demonstrate that the novel lead-free chalcogenide perovskites CsLaMX are good candidates for the rear cell of tandem cells.
钙钛矿-钙钛矿串联太阳能电池有望提高功率转换效率(PCE),突破单结太阳能电池的肖克利-奎塞尔(SQ)极限。基于卤化铅的明星钙钛矿因其合适的带隙(约1.8 eV)、强烈的光吸收和高认证PCE,被公认为前电池的合适候选材料。然而,前电池中铅的毒性以及后电池缺乏窄带隙(约1.1 eV)严重限制了双结串联电池的发展。为了突破这一瓶颈,基于强大的第一性原理和先进的多体微扰GW计算,发现了一种新型的狄翁-雅各布森(DJ)型(= 2)硫族钙钛矿CsLaMX(M = Ta,Nb;X = S,Se)。它们优异的电子、传输和光学性质可总结如下。(1)它们是稳定且环保的无铅材料。(2)CsLaTaSe的直接带隙(0.96 - 1.10 eV)远小于基于卤化铅的钙钛矿,非常适合双结串联电池中的后电池。(3)CsLaTaSe在室温下的载流子迁移率达到1.6 × 10 cm V s。(4)吸收系数(3 - 5 × 10 cm)比Si(10 cm)高1个数量级。(5)CsSbBr - CsLaTaSe串联电池(33.3%)和聚光太阳能电池(100倍太阳光下为35.8%)的估计PCE高于最佳记录的GaAs - Si串联电池(32.8%)和钙钛矿-钙钛矿串联太阳能电池(24.8%)。这些能量结果有力地证明了新型无铅硫族钙钛矿CsLaMX是串联电池后电池的良好候选材料。