富勒烯
材料科学
悬空债券
电子顺磁共振
聚合物
光化学
亚稳态
光降解
化学物理
光电子学
核磁共振
有机化学
硅
复合材料
光催化
化学
催化作用
物理
作者
Fadzai Fungura,William R. Lindemann,J. Shinar,Ruth Shinar
标识
DOI:10.1002/aenm.201601420
摘要
Intrinsic photodegradation of organic solar cells, theoretically attributed to CH bond rearrangement/breaking, remains a key commercialization barrier. This work presents, via dark electron paramagnetic resonance (EPR), the first experimental evidence for metastable C dangling bonds (DBs) formed by blue/UV irradiation of polymer:fullerene blend films in nitrogen. The DB density increases with irradiation and decreases ≈4‐fold after 2 weeks in the dark. The dark EPR also shows increased densities of other spin‐active sites in photodegraded polymer, fullerene, and polymer:fullerene blend films, consistent with broad electronic measurements of fundamental properties, including defect/gap state densities. The EPR and electronic measurements enable identification of defect states, whether in the polymer, fullerene, or at the donor/acceptor (D/A) interface. Importantly, the EPR results indicate that the DBs are at the D/A interface, as they were present only in the blend films. The role of polarons in interface DB formation is also discussed.
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