硫系化合物
材料科学
硫化铅
动力学
带隙
亚硫酸盐
沉积(地质)
光电子学
化学浴沉积
兴奋剂
太阳能电池
硒化铜铟镓太阳电池
纳米技术
能量转换效率
亚硫酸钠
离子键合
化学工程
化学气相沉积
太阳能燃料
石墨
硫化物
薄膜
光伏系统
纳米片
太阳能电池效率
混合太阳能电池
锑
作者
Lingjie Liu,Peng Tang,Hu Li,Jin‐Rui Cai,Limei Lin,Shuiyuan Chen,Jianmin Li,Guilin Chen
出处
期刊:ACS Photonics
[American Chemical Society]
日期:2025-10-14
卷期号:12 (12): 6752-6761
被引量:1
标识
DOI:10.1021/acsphotonics.5c01825
摘要
Antimony sulfide (Sb2S3) is a promising solar abosrber due to its excellent optoelectronic properties. However, efficiency improvements are hindered by a limited understanding of complex reaction mechanisms in solution-based deposition, particularly the unclear dynamic evolution of the ionic environment during sulfur-source decomposition. To address this, we modified conventional chemical bath deposition (CBD) by dynamically injecting sodium sulfite (Na2SO3) using a programmable peristaltic pump. This strategy achieved precise control over the release kinetics of S2– and Sb3+, yielding denser Sb2S3 films with enhanced crystallinity, reduced oxygen incorporation, and lower defect density. In full-inorganic FTO/TiO2/CdS/Sb2S3/PbS/graphite devices, the optimized dynamic injection approach delivered a power conversion efficiency (PCE) of 7.60%, surpassing the conventional CBD method (6.88%) and representing the highest reported value for Sb2S3 solar cells using graphite electrodes. Notably, all functional layers were synthesized via the inherently safe and tunable CBD process. This study elucidates Sb2S3 deposition kinetics and proposes a dynamic injection strategy with potential applications in doping control and bandgap engineering for broader chalcogenide materials.
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