SnO2 nanosheet films about 200 nm in thickness are successfully fabricated on fluorine-doped tin oxide (FTO) glass by a facile solution-grown approach. The prepared SnO2 nanosheet film is appfied as an interfacial l...SnO2 nanosheet films about 200 nm in thickness are successfully fabricated on fluorine-doped tin oxide (FTO) glass by a facile solution-grown approach. The prepared SnO2 nanosheet film is appfied as an interfacial layer between the nanocrystalline TiO2 film and the FTO substrate in dye-sensitized solar cells (DSCs). Experimental results show that the introduction of a SnO2 nanosheet film not only suppresses the electron back-transport reaction at the electrolyte/FTO interface but also provides an efficient electron transition channel along the SnO2 nanosheets, and as a result, increasing the open circuit voltage and short current density, and finally improving the conversion efficiency for the DSCs from 3.89% to 4.62%.展开更多
Over the years,the efficiency of inorganic perovskite solar cells(PSCs)has increased at an unprecedented pace.However,energy loss in the device has limited a further increase in efficiency and commercialization.In thi...Over the years,the efficiency of inorganic perovskite solar cells(PSCs)has increased at an unprecedented pace.However,energy loss in the device has limited a further increase in efficiency and commercialization.In this work,we used(NH4)2C2O4·H2O to treat CsPbBrI2 perovskite film during spin-coating.The CsPbBrI2 underwent secondary crystallization to form high quality films with micrometer-scale and low trap density.(NH4)2C2O4·H2O treatment promoted charge transfer capacity and reduced the ideal factor.It also dropped the energy loss from 0.80 to 0.64 eV.The resulting device delivered a power conversion efficiency(PCE)of 16.55%with an open-circuit voltage(Voc)of 1.24 V,which are largely improved compared with the reference device which exhibited a PCE of 13.27%and a Voc of 1.10 V.In addition,the optimized treated device presented a record indoor PCE of 28.48%under a fluorescent lamp of 1000 lux,better than that of the reference device(19.05%).展开更多
Conventional titanium oxide(TiO2) as an electron transport layer(ETL) in hybrid organic-inorganic perovskite solar cells(PSCs) requires a sintering process at a high temperature to crystalize, which is not suitable fo...Conventional titanium oxide(TiO2) as an electron transport layer(ETL) in hybrid organic-inorganic perovskite solar cells(PSCs) requires a sintering process at a high temperature to crystalize, which is not suitable for flexible PSCs and tandem solar cells with their low-temperatureprocessed bottom cell. Here, we introduce a low-temperature solution method to deposit a TiO2/tin oxide(SnO2) bilayer towards an efficient ETL. From the systematic measurements of optical and electronic properties, we demonstrate that the TiO2/SnO2 ETL has an enhanced charge extraction ability and a suppressed carrier recombination at the ETL/perovskite interface, both of which are beneficial to photo-generated carrier separation and transport. As a result, PSCs with TiO2/SnO2 bilayer ETLs present higher photovoltaic performance of the baseline cells compared with their TiO2 and SnO2 single-layer ETL counterparts. The champion PSC has a power conversion efficiency(PCE) of 19.11% with an open-circuit voltage(Voc)of 1.15 V, a short-circuit current density(Jsc) of 22.77 mA cm^-2,and a fill factor(FF) of 72.38%. Additionally, due to the suitable band alignment of the TiO2/SnO2 ETL in the device, a high Vocof 1.18 V is achieved. It has been proven that the TiO2/SnO2 bilayer is a promising alternative ETL for high efficiency PSCs.展开更多
Reducing energy loss(V_(loss))is one of the most crucial challenges in organic photovoltaic cells.The V_(loss),determined by the differences between the optical band gap(E_(g))of the active layer material and the open...Reducing energy loss(V_(loss))is one of the most crucial challenges in organic photovoltaic cells.The V_(loss),determined by the differences between the optical band gap(E_(g))of the active layer material and the open-circuit voltage(V_(oc))of the device,is generally alleviated by lowering the energy difference between the lowest unoccupied molecular orbital(LUMO)and highest occupied molecular orbital(HOMO)level of the donor(D)and acceptor(A).In this work,we synthesized two A-π-D-π-A-type small-molecule donors(SMDs)SM-benzotriazole(BTz)-1 and SM-BTz-2 by introducing a BTzπ-bridge unit and terminal regulation.The BTzπ-bridge unit significantly lowers the HOMO energy level of SMDs,resulting in high V_(oc)and high mobility,achieving a balance of low energy loss(<0.5 eV)and high efficiency.Ultimately,the organic solar cells based on SM-BTz-2 as the donor and Y6 as the acceptor obtain a high V_(oc)of 0.91 V,J_(sc) of 22.8 mA cm^(−2),fill factor of 68%,and power conversion efficiency(PCE)of 14.12%,which is one of the highest efficiencies based on the SMDs with triazoleπ-bridges to date.What’s more,the BTzπ-bridge unit is a potential unit that can improve mobility and reduce energy loss.展开更多
Despite demonstrating remarkable power conversion efficiencies(PCEs), perovskite solar cells(PSCs) have not yet achieved their full potential. In particular, the interfaces between the perovskite and charge transport ...Despite demonstrating remarkable power conversion efficiencies(PCEs), perovskite solar cells(PSCs) have not yet achieved their full potential. In particular, the interfaces between the perovskite and charge transport layers account for the vast majority of the recombination losses.Interfacial contact and band alignment between the lowtemperature-processed TiO_(2) electron transport layer(ETL)and the perovskite are essential to minimize nonradiative recombination losses. In this study, a CeOx interlayer is employed to modify the perovskite/TiO_(2) interface, and the charge transport properties of the devices are investigated. The bilayer-structured TiO_(2)/CeOx ETL leads to the modification of the interface energetics, resulting in improved electron extraction and reduced nonradiative recombination in the PSCs.Devices based on TiO_(2)/CeOx ETL exhibit a high open-circuit voltage(Voc) of 1.13 V and an enhanced PCE of more than 20%as compared with Vocof 1.08 V and a PCE of approximately 18% for TiO^(2-)based devices. Moreover, PSCs based on TiO_(2)/CeOx ETL maintain over 88% of their initial PCEs after light illumination for 300 min, whereas PSCs based on TiO_(2) ETL almost failed. This study provides an efficient strategy to enhance the PCE and stability of PSCs based on a lowtemperature-processed TiO_(2) ETL.展开更多
基金supported by the National Natural Science Foundation of China (Nos.20903073 and 20671070)the Key Project of Education Ministry of China (No.207008)+1 种基金the Natural Science Foundation of Tianjin (No.09JCYBJC07000)the Science and Technology Developing Foundation for Tianjin Universities (No.20080309)
文摘SnO2 nanosheet films about 200 nm in thickness are successfully fabricated on fluorine-doped tin oxide (FTO) glass by a facile solution-grown approach. The prepared SnO2 nanosheet film is appfied as an interfacial layer between the nanocrystalline TiO2 film and the FTO substrate in dye-sensitized solar cells (DSCs). Experimental results show that the introduction of a SnO2 nanosheet film not only suppresses the electron back-transport reaction at the electrolyte/FTO interface but also provides an efficient electron transition channel along the SnO2 nanosheets, and as a result, increasing the open circuit voltage and short current density, and finally improving the conversion efficiency for the DSCs from 3.89% to 4.62%.
基金financial support from the National Key R&D Program of China(2016YFA0202400)the National Natural Science Foundation of China(61674109)+4 种基金the Natural Science Foundation of Jiangsu Province(BK20170059)funded by the Collaborative Innovation Center of Suzhou Nano Science and Technologythe Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD)the “111”Project of The State Administration of Foreign Experts Affairs of Chinathe Open Fund of the State Key Laboratory of Integrated Optoelectronics(IOSKL2018KF07)。
文摘Over the years,the efficiency of inorganic perovskite solar cells(PSCs)has increased at an unprecedented pace.However,energy loss in the device has limited a further increase in efficiency and commercialization.In this work,we used(NH4)2C2O4·H2O to treat CsPbBrI2 perovskite film during spin-coating.The CsPbBrI2 underwent secondary crystallization to form high quality films with micrometer-scale and low trap density.(NH4)2C2O4·H2O treatment promoted charge transfer capacity and reduced the ideal factor.It also dropped the energy loss from 0.80 to 0.64 eV.The resulting device delivered a power conversion efficiency(PCE)of 16.55%with an open-circuit voltage(Voc)of 1.24 V,which are largely improved compared with the reference device which exhibited a PCE of 13.27%and a Voc of 1.10 V.In addition,the optimized treated device presented a record indoor PCE of 28.48%under a fluorescent lamp of 1000 lux,better than that of the reference device(19.05%).
基金supported by the National Key Research and Development of China (2018YFB1500103 and 2018YFB0704100)the National Natural Science Foundation of China (61574145, 61874177, 51502315 and 61704176)+1 种基金Zhejiang Provincial Natural Science Foundation (LR16F040002)Zhejiang Energy Group (znkj-2018-118)
文摘Conventional titanium oxide(TiO2) as an electron transport layer(ETL) in hybrid organic-inorganic perovskite solar cells(PSCs) requires a sintering process at a high temperature to crystalize, which is not suitable for flexible PSCs and tandem solar cells with their low-temperatureprocessed bottom cell. Here, we introduce a low-temperature solution method to deposit a TiO2/tin oxide(SnO2) bilayer towards an efficient ETL. From the systematic measurements of optical and electronic properties, we demonstrate that the TiO2/SnO2 ETL has an enhanced charge extraction ability and a suppressed carrier recombination at the ETL/perovskite interface, both of which are beneficial to photo-generated carrier separation and transport. As a result, PSCs with TiO2/SnO2 bilayer ETLs present higher photovoltaic performance of the baseline cells compared with their TiO2 and SnO2 single-layer ETL counterparts. The champion PSC has a power conversion efficiency(PCE) of 19.11% with an open-circuit voltage(Voc)of 1.15 V, a short-circuit current density(Jsc) of 22.77 mA cm^-2,and a fill factor(FF) of 72.38%. Additionally, due to the suitable band alignment of the TiO2/SnO2 ETL in the device, a high Vocof 1.18 V is achieved. It has been proven that the TiO2/SnO2 bilayer is a promising alternative ETL for high efficiency PSCs.
基金the National Key Research and Development Program of China(2019YFA0705900)the National Natural Science Foundation of China(51820105003,21734008,61904181,52173188 and 52103243)+1 种基金the Key Research Program of the Chinese Academy of Sciences(XDPB13)the Basic and Applied Basic Research Major Program of Guangdong Province(2019B030302007).
文摘Reducing energy loss(V_(loss))is one of the most crucial challenges in organic photovoltaic cells.The V_(loss),determined by the differences between the optical band gap(E_(g))of the active layer material and the open-circuit voltage(V_(oc))of the device,is generally alleviated by lowering the energy difference between the lowest unoccupied molecular orbital(LUMO)and highest occupied molecular orbital(HOMO)level of the donor(D)and acceptor(A).In this work,we synthesized two A-π-D-π-A-type small-molecule donors(SMDs)SM-benzotriazole(BTz)-1 and SM-BTz-2 by introducing a BTzπ-bridge unit and terminal regulation.The BTzπ-bridge unit significantly lowers the HOMO energy level of SMDs,resulting in high V_(oc)and high mobility,achieving a balance of low energy loss(<0.5 eV)and high efficiency.Ultimately,the organic solar cells based on SM-BTz-2 as the donor and Y6 as the acceptor obtain a high V_(oc)of 0.91 V,J_(sc) of 22.8 mA cm^(−2),fill factor of 68%,and power conversion efficiency(PCE)of 14.12%,which is one of the highest efficiencies based on the SMDs with triazoleπ-bridges to date.What’s more,the BTzπ-bridge unit is a potential unit that can improve mobility and reduce energy loss.
基金supported by the National Key Research and Development Program of China (2018YFB1500101)the 111 Project (B16016)+1 种基金the National Natural Science Foundation of China (U1705256,51702096 and 61904053)the Fundamental Research Funds for the Central Universities (2019MS026,2019MS027 and 2020MS080)。
文摘Despite demonstrating remarkable power conversion efficiencies(PCEs), perovskite solar cells(PSCs) have not yet achieved their full potential. In particular, the interfaces between the perovskite and charge transport layers account for the vast majority of the recombination losses.Interfacial contact and band alignment between the lowtemperature-processed TiO_(2) electron transport layer(ETL)and the perovskite are essential to minimize nonradiative recombination losses. In this study, a CeOx interlayer is employed to modify the perovskite/TiO_(2) interface, and the charge transport properties of the devices are investigated. The bilayer-structured TiO_(2)/CeOx ETL leads to the modification of the interface energetics, resulting in improved electron extraction and reduced nonradiative recombination in the PSCs.Devices based on TiO_(2)/CeOx ETL exhibit a high open-circuit voltage(Voc) of 1.13 V and an enhanced PCE of more than 20%as compared with Vocof 1.08 V and a PCE of approximately 18% for TiO^(2-)based devices. Moreover, PSCs based on TiO_(2)/CeOx ETL maintain over 88% of their initial PCEs after light illumination for 300 min, whereas PSCs based on TiO_(2) ETL almost failed. This study provides an efficient strategy to enhance the PCE and stability of PSCs based on a lowtemperature-processed TiO_(2) ETL.