在聚合物-富勒烯混合太阳能电池中,电荷转移状态与热激子解离相比
Jiye Lee1, Koen Vandewal, Shane R Yost
1Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Journal of the American Chemical Society
|August 10, 2010
概括
热激子解离对聚合物富勒烯太阳能电池的影响最小. 研究表明,对于激子和直接电荷转移激发,内部量子产量是相似的,这表明热过程并不重要.
科学领域:
- 材料科学 材料科学 材料科学
- 太阳能光伏发电是如何实现的
- 物理化学 物理化学
背景情况:
- 聚合物富勒烯太阳能电池是可再生能源的关键技术.
- 激发分离是将光转化为电力的关键步骤.
- 热激子解离是一种用于高效电荷生成的拟议机制.
研究的目的:
- 为了研究热激子解离在原型聚合物-富勒烯太阳能电池中的作用.
- 为了确定热过程是否对载体光生成有显著的贡献.
- 为了比较热激子解离与直接电荷转移激化的效率.
主要方法:
- 实验分析了两个原型的聚合物-富勒烯混合太阳能电池.
- 测量载体光生成的内部量子产量.
- 对电流-电压特征的温度依赖性的分析.
主要成果:
- 发现内部量子产量对于激子和直接电荷转移状态激发都是相似的.
- 电流-电压特征的温度依赖性表明热激子解离的影响是可以忽略不计的.
- 热激子解离似乎不是这些系统中电荷生成的主要途径.
结论:
- 在聚合物-富勒烯太阳能电池中热激子解离的意义是可以忽略不计的.
- 电荷生成主要通过既定的途径发生,而不是热激子解离.
- 可能需要进一步的研究来探索替代机制或材料系统.
更多相关视频
相关概念视频
P-N junction
A p-n junction is formed when p-type and n-type semiconductor materials are joined together. At the interface of the p-n junction, holes from the p-side and electrons from the n-side begin to diffuse into the opposite sides due to the concentration gradient. This diffusion of carriers leads to a region around the junction where there are no free charge carriers, known as the depletion region. The charge density within the depletion region for the n-side and p-side can be described by the...
Photochemical Electrocyclic Reactions: Stereochemistry
The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
Selection Rules: Photochemical Activation
Selection Rules: Photochemical Activation
Thermal and Photochemical Electrocyclic Reactions: Overview
Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.
Carrier Generation and Recombination
Carrier generation is the process by which electron-hole pairs (EHPs) are created within the semiconductor. In direct-bandgap semiconductors, such as gallium arsenide (GaAs), this occurs efficiently when energy absorption prompts valence electrons to leap into the conduction band, leaving behind holes.
This process is given by the generation rate G and is efficient due to the conservation of momentum between the valence band maximum and conduction band minimum.
Indirect generation involves an...
This process is given by the generation rate G and is efficient due to the conservation of momentum between the valence band maximum and conduction band minimum.
Indirect generation involves an...
The Electrical Double Layer
In the region where two bulk phases meet, an intricate electric charge distribution arises due to charge transfer, ion adsorption, molecular orientation, and charge distortion. This complex distribution is commonly referred to as the electrical double layer.When a solid electrode interfaces with ions in an electrolyte solution, the speed of electron transfer dictates the rates of oxidation and reduction. The electrode acquires a charge through the escape of atoms into the solution as cations or...
Thermal Electrocyclic Reactions: Stereochemistry
The stereochemistry of electrocyclic reactions is strongly influenced by the orbital symmetry of the polyene HOMO. Under thermal conditions, the reaction proceeds via the ground-state HOMO.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.


