Local environment surrounding S and Cd in CdS:O thin film photovoltaic materials probed by x-ray absorption fine structures
Y. L. Soo, W. H. Sun, S. C. Weng, Y. S. Lin, S. L. Chang, Ling‐Yun Jang, Xin Li Wu, Yonggang Yan
Abstract
Y. L. Soo, W. H. Sun, S. C. Weng, Y. S. Lin, S. L. Chang, Ling‐Yun Jang, Xin Li Wu, Yonggang Yan
Abstract
Local environments surrounding Cd and S in CdS:O thin films have been determined using extended x-ray absorption fine structure (EXAFS) and near-edge x-ray absorption fine structure (NEXAFS). As indicated by the Cd EXAFS, Cd atoms remain predominantly bonded with S. The S EXAFS and NEXAFS clearly demonstrate the presence of S–O bonds. The oxygen atoms actually combine with S to form SO3 and SO4 complexes. Combined with the transmission electron micrograph, these x-ray results suggest formation of oxygen-free CdS nanocrystals and provide an unambiguous explanation for the mystery of increased band gap that appears to violate the band anticrossing model.
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Local environments surrounding Cd and S in CdS:O thin films have been determined using extended x-ray absorption fine structure (EXAFS) and near-edge x-ray absorption fine structure (NEXAFS). As indicated by the Cd EXAFS, Cd atoms remain predominantly bonded with S. The S EXAFS and NEXAFS clearly demonstrate the presence of S–O bonds. The oxygen atoms actually combine with S to form SO3 and SO4 complexes. Combined with the transmission electron micrograph, these x-ray results suggest formation of oxygen-free CdS nanocrystals and provide an unambiguous explanation for the mystery of increased band gap that appears to violate the band anticrossing model.
Key concepts: Extended X-ray absorption fine structure, XANES, Absorption (acoustics), X-ray absorption fine structure, Surface-extended X-ray absorption fine structure, Materials science, Band gap, Thin film