材料科学
串联
甲脒
带隙
钙钛矿(结构)
能量转换效率
锡
结晶度
光电子学
X射线光电子能谱
光伏
纳米技术
化学工程
光伏系统
工程类
复合材料
生态学
冶金
生物
作者
Saemon Yoon,Jun Ryu,SungWon Cho,Hyung Do Kim,Jongchul Lim,Jung Sang Cho,Jong Sung Park,Dong‐Won Kang
出处
期刊:Small
[Wiley]
日期:2025-03-25
标识
DOI:10.1002/smll.202501876
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI