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效率超过15%的无铅、锡基全钙钛矿串联太阳能电池

Lead-Free, Sn-Based All-Perovskite Tandem Solar Cells with an Efficiency Over 15.

作者信息

Yoon Saemon, Ryu Jun, Cho SungWon, Kim Hyung Do, Lim Jongchul, Cho Jung Sang, Park Jongsung, Kang Dong-Won

机构信息

Department of Smart Cities, Chung-Ang University (CAU), Seoul, 06974, Republic of Korea.

Department of Polymer Chemistry, Graduate School of Engineering, Kyoto University, Katsura Campus, Kyoto, 615-8510, Japan.

出版信息

Small. 2025 Mar 25:e2501876. doi: 10.1002/smll.202501876.

Abstract

Recent advances in tin-based perovskite solar cells (TPSCs) have yielded significant gains in power conversion efficiency (PCE), yet progress on wide-bandgap (WBG) tin perovskites remains limited, primarily due to the complexities of halogen composition tuning and the associated phase segregation. Here, a halogen composition-independent strategy is presented for realizing WBG TPSCs by partially substituting formamidinium with dimethylammonium (DMA) in the A-site of the perovskite lattice. This substitution expands the lattice, widening the bandgap from 1.63 to 1.72 eV without requiring additional bromine. Comprehensive structural and optical analyses reveal enhanced crystallinity, reduced strain, and improved film morphology. Furthermore, ultraviolet photoelectron spectroscopy confirms enhanced band alignment with the hole transport layer, enabling more efficient charge extraction. By employing a dielectric/metal/dielectric transparent electrode, semi-transparent TPSCs (ST-TPSCs) are fabricated with a PCE of 10.37% and high near-infrared transmittance, which is well-suited for tandem applications. Stacking this ST-TPSC with a narrow-bandgap TPSC yields the first four-terminal, lead-free perovskite tandem device, achieving a combined PCE of 15.02%. These findings show that DMA incorporation effectively addresses the challenges of WBG TPSCs without relying on halogen adjustments, providing a robust pathway toward high-efficiency, eco-friendly photovoltaics and highlighting the promise of tin-based perovskites for next-generation tandem solar cells.

摘要

锡基钙钛矿太阳能电池(TPSCs)的最新进展在功率转换效率(PCE)方面取得了显著提升,但宽带隙(WBG)锡钙钛矿的进展仍然有限,主要是由于卤素组成调整的复杂性以及相关的相分离。在此,提出了一种与卤素组成无关的策略,通过在钙钛矿晶格的A位用二甲铵(DMA)部分替代甲脒来实现WBG TPSCs。这种替代扩大了晶格,在无需额外溴的情况下将带隙从1.63 eV拓宽至1.72 eV。全面的结构和光学分析表明结晶度提高、应变降低且薄膜形态得到改善。此外,紫外光电子能谱证实了与空穴传输层的能带排列得到增强,从而实现更高效的电荷提取。通过采用介电/金属/介电透明电极,制备出了半透明TPSCs(ST-TPSCs),其PCE为10.37%且具有高近红外透过率,非常适合串联应用。将这种ST-TPSC与窄带隙TPSC堆叠,得到了首个四端无铅钙钛矿串联器件,实现了15.02%的综合PCE。这些发现表明,引入DMA有效地解决了WBG TPSCs的挑战,而无需依赖卤素调整,为高效、环保的光伏提供了一条稳健的途径,并突出了锡基钙钛矿在下一代串联太阳能电池方面的前景。

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