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首页> 外文期刊>Materials Chemistry and Physics >Approach toward high efficiency CdTe/CdS heterojunction solar cells
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Approach toward high efficiency CdTe/CdS heterojunction solar cells

机译:高效CdTe / CdS异质结太阳能电池的方法

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CdTe solar cells were fabricated by depositing MOCVD grown CdTe films on CdS/SnO_2/glass substrates with varying Te:Cd mole ratios in the growth ambient. Cells grown in Te-rich ambient showed increased atomic interdiffusion at the CdS/CdTe interface and produced high-efficiency cells (11.9%) with an open-circuit voltage (V_(oc)) of 780 mV. Cd-rich cells were < 6% efficient. Carrier transport analysis showed that the transport mechanism switches from tunneling/interface recombination in the Cd-rich cells to depletion region recombination limited transport in the Te-rich cells. This suggests that the enhanced interdiffusion is beneficial for these cells and leads to reduced lattice mismatch or gradual transition from CdS to CdTe with fewer interface states. In order to understand the loss mechanisms associated with grain boundaries in polycrystalline CdTe cells, an attempt was made to fabricate thin film CdTe/CdS device structures using an epitaxial lift-off (ELO) process. Single crystal CdTe and CdTe/CdS epitaxial layers were separated from the GaAs substrate by selective etching and were then transferred and bonded to a SnO_2/glass substrate. SIMS analysis of CdTe/CdS cells, with Au/Cu ohmic contacts to CdTe, showed much less Cu diffusion in the single crystal CdTe films due to the absence of grain boundaries. X-ray diffraction measurements showed that the CdTe/CdS lattice structure and quality does not change appreciably after the lift-off process. A new methodology was developed, using XRD and the lift-off technique, to assess the lattice mismatch induced strain and defects at the heterojunction interface. The lattice constant of CdTe at the interface with GaAs was 6.317 A, which is smaller than the ideal lattice constant of 6.481 A for the CdTe bulk.
机译:通过在生长环境中以不同的Te:Cd摩尔比将MOCVD生长的CdTe膜沉积在CdS / SnO_2 /玻璃基板上来制造CdTe太阳能电池。在富含Te的环境中生长的细胞在CdS / CdTe界面处显示出更大的原子相互扩散,并产生了具有780 mV开路电压(V_(oc))的高效电池(11.9%)。富镉细胞的效率<6%。载流子转运分析表明,转运机制从富含Cd的细胞中的隧穿/界面重组转变为富含Te的细胞中的耗尽区重组限制了转运。这表明增强的相互扩散对这些细胞是有益的,并导致晶格失配减少或从CdS到CdTe的逐渐过渡,界面状态更少。为了了解与多晶CdTe电池中晶界相关的损耗机理,人们尝试使用外延剥离(ELO)工艺制造薄膜CdTe / CdS器件结构。通过选择性蚀刻从GaAs衬底分离单晶CdTe和CdTe / CdS外延层,然后将其转移并结合到SnO_2 /玻璃衬底上。具有与CdTe的Au / Cu欧姆接触的CdTe / CdS电池的SIMS分析表明,由于没有晶界,单晶CdTe膜中的铜扩散少得多。 X射线衍射测量表明,CdTe / CdS晶格结构和质量在剥离过程后没有明显变化。开发了一种使用XRD和剥离技术的新方法,以评估晶格失配引起的异质结界面处的应变和缺陷。在与GaAs的界面处CdTe的晶格常数为6.317 A,小于CdTe体的理想晶格常数6.481A。

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