Although the performance of perovskite solar cells(PSCs)has been dramatically increased in recent years,stability is still the main obstacle preventing the PSCs from being commercial.PSC device instability can be caus...Although the performance of perovskite solar cells(PSCs)has been dramatically increased in recent years,stability is still the main obstacle preventing the PSCs from being commercial.PSC device instability can be caused by a variety of reasons,including ions diffusion,surface and grain boundary defects,etc.In this work,the cross-linkable tannic acid(TA)is introduced to modify perovskite film through post-treatment method.The numerous organic functional groups(–OH and C=O)in TA can interact with the uncoordinated Pb^(2+)and I^(-)ions in perovskite,thus passivating defects and inhibiting ions diffusion.In addition,the formed TA network can absorb a small amount of the residual moisture inside the device to protect the perovskite layer.Furthermore,TA modification regulates the energy level of perovskite,and reduces interfacial charge recombination.Ultimately,following TA treatment,the device efficiency is increased significantly from 21.31%to 23.11%,with a decreased hysteresis effect.Notably,the treated device shows excellent air,thermal,and operational stability.In light of this,the readily available,inexpensive TA has the potential to operate as a multipurpose interfacial modifier to increase device efficiency while also enhancing device stability.展开更多
It has been widely recognized that hole transporting materials(HTMs)play a key role in the rapid progress of perovskite solar cells(PVSCs).However,common organic HTMs such as spiro-OMe TAD not only suffer from high sy...It has been widely recognized that hole transporting materials(HTMs)play a key role in the rapid progress of perovskite solar cells(PVSCs).However,common organic HTMs such as spiro-OMe TAD not only suffer from high synthetic costs,but also usually require the additional chemical doping process to improve their hole transport ability,which unfortunately induces the terrible stability issue.Therefore,it is urgent to develop low-cost dopant-free HTMs for efficient and stable PVSCs.In this work,we have successfully developed a new class of efficient dopant-free fluoranthene-based HTMs(TPF1–5)with quite low lab synthetic costs by combining donor-acceptor and branched structure designs.The detailed structure-property study revealed that tuning the twisted arms at different substitution sites would regulate the intermolecular interactions and film-forming ability,thereby significantly affecting the performance of the HTMs.By applying these HTMs in conventional PVSCs,the dopant-free TPF1-based devices not only achieved the best efficiency of 21.76%,which is comparable to that of the doped spiro-OMeTAD control devices,but also showed much better operational stability,which maintained over 87%of the initial efficiency under maximum power point tracking after 1038 h.展开更多
Perovskite solar cells(PSCs)have been proven to be a promising option for photovoltaic conversion.With the aim to achieve efficient and stable PSCs,it is essential to explore dopant-free hole-transporting materials(HT...Perovskite solar cells(PSCs)have been proven to be a promising option for photovoltaic conversion.With the aim to achieve efficient and stable PSCs,it is essential to explore dopant-free hole-transporting materials(HTMs)with high hole mobility.Herein,HTMs bearing electron donor(D)-electron acceptor(A)-electron donor(D)structures have been constructed with strong intramolecular charge transfer(ICT)effect,based on rational combination of dibenzo[a,c]phenazine and pyridine as electronic acceptors and anchoring groups to perovskite layer.Accordingly,high hole mobility(7.31×10^(-5) cm^(2)·V^(-1)·s^(-1))and photoelectric conversion efficiency(20.45%)have been achieved by dopant-free DPyP-based PSC.It afforded an efficient way to design HTMs with high hole mobility by adjustment of molecular configurations and electronic property of conjugated systems.展开更多
Three new organic dyes were synthesized and characterized for applications in dye-sensitized solar cells (DSSCs). In these dyes, diarylmethylene-bridged triphenylarnine is the donor, and different acceptors and viny...Three new organic dyes were synthesized and characterized for applications in dye-sensitized solar cells (DSSCs). In these dyes, diarylmethylene-bridged triphenylarnine is the donor, and different acceptors and vinyl- thiophene are designed to get TBA-1, TBA-2 and TBA-3. Their photophysical, electrochemical and photovoltaic properties were investigated, and the effects of the acceptor structures as well as the linkage on these properties were evaluated. Results demonstrated that the vinylthiophene linkage between the donor and the acceptor is favor- able for improving light harvesting ability of TBA-2. In addition, the electrochemical impedance spectroscopy ex- periments suggest larger Rrec and longer electron lifetime of TBA-2. Therefore, it outperforms the other dyes, exhib- iting the highest power conversion efficiency of 3.87%, with Jsc of 8.25 mAocm-2 and Voc of 666 mV. Unfortunately, the TBA-3 with three acceptor groups only shows efficiency of 3.52%, indicating that the design of increasing ac- ceptor groups plays little role on enhancing the solar cell efficiency.展开更多
Organic hole-transporting materials(HTMs)are an essential component in conventional perovskite solar cells(PSCs).In this work,two sulfonyldibenzene-based molecules,named CS-04 and CS-05,are synthesized and employed as...Organic hole-transporting materials(HTMs)are an essential component in conventional perovskite solar cells(PSCs).In this work,two sulfonyldibenzene-based molecules,named CS-04 and CS-05,are synthesized and employed as HTMs in n-i-p PSCs.In comparison with CS-04,the carbazole-substituted methoxytriphenylamine(Cz MOTPA)group in CS-05 exhibits an increased degree of molecular distortion,thus endowing CS-05 with excellent solvent solubility and film-formation ability.Moreover,CS-05 shows a high hole mobility,superior hole extraction and hole transporting properties.As a result,CS-05 yields impressive device performances with a high power conversion efficiency(PCE)of 20.15%,while that of CS-04 based device is 19.50%,which is comparable to that of the Spiro-OMe TAD based control device(19.59%).This finding illustrates the potential of sulfonyldibenzene-based molecules for the applications in PSCs,and also provides a novel avenue to improve the performances and stability of PSCs by tailoring the sulfonyldibenzene-based molecules.展开更多
基金supported by the General Program of Chongqing Natural Science Foundation(CSTB2022NSCQMSX1227 and CSTB2022NSCQ-MSX0459)the supports from the Fundamental Research Funds for the Central Universities(SWU-XDJH202314)。
文摘Although the performance of perovskite solar cells(PSCs)has been dramatically increased in recent years,stability is still the main obstacle preventing the PSCs from being commercial.PSC device instability can be caused by a variety of reasons,including ions diffusion,surface and grain boundary defects,etc.In this work,the cross-linkable tannic acid(TA)is introduced to modify perovskite film through post-treatment method.The numerous organic functional groups(–OH and C=O)in TA can interact with the uncoordinated Pb^(2+)and I^(-)ions in perovskite,thus passivating defects and inhibiting ions diffusion.In addition,the formed TA network can absorb a small amount of the residual moisture inside the device to protect the perovskite layer.Furthermore,TA modification regulates the energy level of perovskite,and reduces interfacial charge recombination.Ultimately,following TA treatment,the device efficiency is increased significantly from 21.31%to 23.11%,with a decreased hysteresis effect.Notably,the treated device shows excellent air,thermal,and operational stability.In light of this,the readily available,inexpensive TA has the potential to operate as a multipurpose interfacial modifier to increase device efficiency while also enhancing device stability.
基金supported by National Key Research&Development Program of China(No.2023YFE0210900)National Natural Science Foundation of China(No.21975085)+1 种基金Excellent Youth Foundation of Hubei Scientific Committee(No.2021CFA065)open Fund of Hubei Key Laboratory of Material Chemistry and Service Failure(No.2023MCF02)。
文摘It has been widely recognized that hole transporting materials(HTMs)play a key role in the rapid progress of perovskite solar cells(PVSCs).However,common organic HTMs such as spiro-OMe TAD not only suffer from high synthetic costs,but also usually require the additional chemical doping process to improve their hole transport ability,which unfortunately induces the terrible stability issue.Therefore,it is urgent to develop low-cost dopant-free HTMs for efficient and stable PVSCs.In this work,we have successfully developed a new class of efficient dopant-free fluoranthene-based HTMs(TPF1–5)with quite low lab synthetic costs by combining donor-acceptor and branched structure designs.The detailed structure-property study revealed that tuning the twisted arms at different substitution sites would regulate the intermolecular interactions and film-forming ability,thereby significantly affecting the performance of the HTMs.By applying these HTMs in conventional PVSCs,the dopant-free TPF1-based devices not only achieved the best efficiency of 21.76%,which is comparable to that of the doped spiro-OMeTAD control devices,but also showed much better operational stability,which maintained over 87%of the initial efficiency under maximum power point tracking after 1038 h.
基金supported by the National Natural Science Foundation of China(51973162,22235006,and 22122504)Foundation of Hubei Scientific Committee(2022BAA015,2022EHB010)+1 种基金the Fundamental Research Funds for the Central Universities(2042020kf2058)the Knowledge Innovation Projectof Wuhan City(whkxjsjo14).
文摘Perovskite solar cells(PSCs)have been proven to be a promising option for photovoltaic conversion.With the aim to achieve efficient and stable PSCs,it is essential to explore dopant-free hole-transporting materials(HTMs)with high hole mobility.Herein,HTMs bearing electron donor(D)-electron acceptor(A)-electron donor(D)structures have been constructed with strong intramolecular charge transfer(ICT)effect,based on rational combination of dibenzo[a,c]phenazine and pyridine as electronic acceptors and anchoring groups to perovskite layer.Accordingly,high hole mobility(7.31×10^(-5) cm^(2)·V^(-1)·s^(-1))and photoelectric conversion efficiency(20.45%)have been achieved by dopant-free DPyP-based PSC.It afforded an efficient way to design HTMs with high hole mobility by adjustment of molecular configurations and electronic property of conjugated systems.
文摘Three new organic dyes were synthesized and characterized for applications in dye-sensitized solar cells (DSSCs). In these dyes, diarylmethylene-bridged triphenylarnine is the donor, and different acceptors and vinyl- thiophene are designed to get TBA-1, TBA-2 and TBA-3. Their photophysical, electrochemical and photovoltaic properties were investigated, and the effects of the acceptor structures as well as the linkage on these properties were evaluated. Results demonstrated that the vinylthiophene linkage between the donor and the acceptor is favor- able for improving light harvesting ability of TBA-2. In addition, the electrochemical impedance spectroscopy ex- periments suggest larger Rrec and longer electron lifetime of TBA-2. Therefore, it outperforms the other dyes, exhib- iting the highest power conversion efficiency of 3.87%, with Jsc of 8.25 mAocm-2 and Voc of 666 mV. Unfortunately, the TBA-3 with three acceptor groups only shows efficiency of 3.52%, indicating that the design of increasing ac- ceptor groups plays little role on enhancing the solar cell efficiency.
基金the National Natural Science Foundation of China(51733010,21672267,51973239 and52073316)the Science and Technology Planning Project of Guangdong(2015B090913003)the Fundamental Research Funds for the Central Universities(19lgpy118,XDJK2019B065 and XDJK2020B002)。
文摘Organic hole-transporting materials(HTMs)are an essential component in conventional perovskite solar cells(PSCs).In this work,two sulfonyldibenzene-based molecules,named CS-04 and CS-05,are synthesized and employed as HTMs in n-i-p PSCs.In comparison with CS-04,the carbazole-substituted methoxytriphenylamine(Cz MOTPA)group in CS-05 exhibits an increased degree of molecular distortion,thus endowing CS-05 with excellent solvent solubility and film-formation ability.Moreover,CS-05 shows a high hole mobility,superior hole extraction and hole transporting properties.As a result,CS-05 yields impressive device performances with a high power conversion efficiency(PCE)of 20.15%,while that of CS-04 based device is 19.50%,which is comparable to that of the Spiro-OMe TAD based control device(19.59%).This finding illustrates the potential of sulfonyldibenzene-based molecules for the applications in PSCs,and also provides a novel avenue to improve the performances and stability of PSCs by tailoring the sulfonyldibenzene-based molecules.