2011
DOI: 10.1088/1674-1056/20/5/053102
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The structure and the potential energy function of AlSO(CS,X2A″)

Abstract: Yang Ze-Jin(杨则金) a) † , Gao Qing-He(高清河) b) , Li Jin(李 劲) c) , Linghu Rong-Feng(令狐荣锋) d) , Guo Yun-Dong(郭云东) e) , Cheng Xin-Lu(程新路) f) , Zhu Zheng-He(朱正和) f) , and Yang Xiang-Dong(杨向东) f)

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Cited by 24 publications
(25 citation statements)
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“…For the samples of perovskite/PDT-T (τ = 65.92) and perovskite/PDTT-T (τ = 53.99), the shortened TRPL decay indicates a faster electron-transfer process and more efficient hole extraction from the perovskite into HTM. 55 PDTT-T accelerates charge transport more obviously, which agrees well with the trend in PL spectra.…”
Section: ■ Results and Discussionsupporting
confidence: 85%
“…For the samples of perovskite/PDT-T (τ = 65.92) and perovskite/PDTT-T (τ = 53.99), the shortened TRPL decay indicates a faster electron-transfer process and more efficient hole extraction from the perovskite into HTM. 55 PDTT-T accelerates charge transport more obviously, which agrees well with the trend in PL spectra.…”
Section: ■ Results and Discussionsupporting
confidence: 85%
“…All TiO 2 /FTO/glass and Nb-doped TiO 2 /FTO/glass substrates were treated by UV-ozone treatment for 15 min before deposition of the perovskite films. The perovskite solution containing 1 mmol of PbI 2 (99.99%, Alfar Aesar), 1 mmol of CH 3 NH 3 I (synthesized according to our earlier work 4,17,18 ), and 1 mmol of dimethyl sulfoxide (DMSO, 99.9%, Aldrich) was dissolved in 600 mg of N,N-dimethylformamide (DMF, 99.8%, Alfa Aesar). The mixed solution was spin-coated on top of the ETLs (TiO 2 and Nbdoped TiO 2 ) at 1000 rpm for 5 s and 4000 rpm for 45 s while dripping chlorobenzene onto the substrate during the second spinning step.…”
Section: Methodsmentioning
confidence: 99%
“…Recent experimental and computational studies suggested the existence of ordered phase of polymers near graphitic surfaces, known as the interphase we introduce earlier. [ 27,28 ] Although the high crystallinity of this polymer interface limits the density of chemical cross-links, the ordered structures allow cooperative physical cross-links between them and thus are stiffened compared to the uncross-linked polymers. The results from our simulations with a 5 nm polymer deposition clearly demonstrate the ordering near graphitic surface.…”
Section: Molecular Mechanisms Of the Self-stiffening Effectmentioning
confidence: 99%