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Bifunctional passivation by lewis-base molecules for efficient printable mesoscopic perovskite solar cells
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作者 Hang Yang Jianhong Zhao +8 位作者 Xiaodong Ren Tong Zhou Henbing Zhang Weilong Zhang Jin Zhang Guangzhi Hu Yuming Zhang Wen-Hua Zhang Qingju Liu 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2024年第9期177-184,共8页
Printable mesoscopic perovskite solar cells(PM-PSCs)possess notable merits in terms of cost-effectiveness,easy manufacturing,and large scale applications.Nevertheless,the absence of a hole transport layer contributes ... Printable mesoscopic perovskite solar cells(PM-PSCs)possess notable merits in terms of cost-effectiveness,easy manufacturing,and large scale applications.Nevertheless,the absence of a hole transport layer contributes to the exacerbation of carrier recombination,and the defects between the perovskite and electron transport layer(ETL)interfaces significantly decrease the efficiency of the devices.In this study,a bifunctional surface passivation approach is proposed by applying a thioacetamide(TAA)surfactant on the mesoporous TiO_(2)interface.The results demonstrate that TAA molecules could interact with TiO_(2),thereby diminishing the oxygen vacancy defects.Additionally,the amino group and sulfur atoms in TAA molecules act as Lewis base to effectively passivate the uncoordinated Pb^(2+)in perovskite and improve the morphology of perovskite,and decrease the trap-state density of perovskite.The TAA passivation mechanism improves the alignment of energy levels between TiO_(2)and perovskite,facilitating electron transport and reducing carrier recombination.Consequently,the TAA-passivated device achieved a champion power conversion efficiency(PCE)of 17.86%with a high fill factor(FF)of 79.16%and an open-circuit voltage(V_(OC))of 0.971 V.This investigation presents a feasible strategy for interfacial passivation of the ETL to further improve the efficiency of PM-PSCs. 展开更多
关键词 Perovskite solarcells Carbon electrode THIOACETAMIDE Interfacial passivation
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Synthesis,Crystal Structure and Photoluminescence Property of Potassium Terbium Polyphosphate KTb(PO3)4 被引量:1
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作者 钱伟 朱忠其 +1 位作者 张科 朱静 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2017年第2期236-241,共6页
The potassium terbium polyphosphate crystal KTb(PO3)4 has been synthesized using a high temperature solution reaction method. The structure and composition were characterized by single-crystal X-ray diffraction, pow... The potassium terbium polyphosphate crystal KTb(PO3)4 has been synthesized using a high temperature solution reaction method. The structure and composition were characterized by single-crystal X-ray diffraction, powder X-ray diffraction and elemental analysis. The compound crystallizes in the monoclinic space group P21/n with a=10.3182(6), b=8.9129(5), c=10.7940(6) , β=105.993(1)o, V=954.3 3, Z=4, Mr=513.91, Dc=3.577 g/cm3, μ=8.585 mm(-1), F(000)=960, S=0.955,(Δρ)max=1.380,(Δρ)min=–3.428 e/3, the final R=0.0301 and w R=0.0400 for 2301 observed reflections with I 〉 2σ(I). In addition, pure powder of isostructural Rb Tb(PO3)4 was synthesized in order to investigate the optical property. Photoluminescence measurements show that both crystals ATb(PO3)4(A=K(1), Rb(2)) are promising candidates to become solid-state visible green light-emitting sources. 展开更多
关键词 visible potassium monoclinic luminescence corner evaporation crystalline graphite transitions calcined
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