Graphene dispersions in low-boiling-point green solvents have wide applications in coatings,conducting inks,batteries,electronics and solar cells.Two three-dimensional(3D)cathode interfacial materials(CIMs)(1,3,5,7,9,...Graphene dispersions in low-boiling-point green solvents have wide applications in coatings,conducting inks,batteries,electronics and solar cells.Two three-dimensional(3D)cathode interfacial materials(CIMs)(1,3,5,7,9,11,13,15-octa-(9-bis(30-(N,N-dimethylamino)propyl)-2,7-fluorene)-vinylpentacyclo-octasiloxane)(POSSFN)and(1,3,5,7-tetra-(9-bis(30-(N,N-dimethylamino)propyl)-2,7-fluorene)-adamantane)(ADMAFN)are excellent surfactants for dispersing graphene in ethanol at the concentration of 0.97–1.18 mg mL−1,in agreement with their calculated large adsorption energies on graphene.The results of electron spin resonance,Raman,scanning Kelvin probe microscopy and X-ray photoelectron spectroscopy measurements indicate that the amino groups could n-dope graphene or form dipole interaction with graphene.The two 3D-surfactant-based graphene composites(POSSFN-G and ADMAFN-G)can work as high-performance CIMs in organic solar cells(OSCs),which improve the power conversion efficiency(PCE)of the OSCs based on PM6:Y6 to 15.9%–16.1%.ADMAFN forms dipole interaction with graphene in ADMAFN-G and the composite CIM delivers high PCE of 16.11%in the OSCs,while POSSFN forms n-doped composition with graphene in POSSFN-G which works well as thicker CIM film in the OSCs.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
Water electrolysis to produce H2 is a promising strategy for generating a renewable fuel.However,the sluggish-kinetics and low value-added anodic oxygen evolution reaction(OER)restricts the overall energy conversion e...Water electrolysis to produce H2 is a promising strategy for generating a renewable fuel.However,the sluggish-kinetics and low value-added anodic oxygen evolution reaction(OER)restricts the overall energy conversion efficiency.Herein we report a strategy of boosting H_(2)production at low voltages by replacing OER with a bioelectrochemical cascade reaction at a triphase bioanode.In the presence of oxygen,oxidase enzymes can convert biomass into valuable products,and concurrently generate H_(2)O_(2) that can be further electrooxidized at the bioanode.Benefiting from the efficient oxidase kinetics at an oxygen-rich triphase bioanode and the more favorable thermodynamics of H_(2)O_(2)oxidation than that of OER,the cell voltage and energy consumption are reduced by~0.70 V and~36%,respectively,relative to regular water electrolysis.This leads to an efficient H_(2)production at the cathode and valuable product generation at the bioanode.Integration of a bioelectrochemical cascade into the water splitting process provides an energy-efficient and promising pathway for achieving a renewable fuel.展开更多
基金the National Natural Science Foundation of China(51820105003,51863002 and 51973042)the Excellent Young Scientific and Technological Talents of Guizhou,China(QKHPTRC[2019]5652)。
文摘Graphene dispersions in low-boiling-point green solvents have wide applications in coatings,conducting inks,batteries,electronics and solar cells.Two three-dimensional(3D)cathode interfacial materials(CIMs)(1,3,5,7,9,11,13,15-octa-(9-bis(30-(N,N-dimethylamino)propyl)-2,7-fluorene)-vinylpentacyclo-octasiloxane)(POSSFN)and(1,3,5,7-tetra-(9-bis(30-(N,N-dimethylamino)propyl)-2,7-fluorene)-adamantane)(ADMAFN)are excellent surfactants for dispersing graphene in ethanol at the concentration of 0.97–1.18 mg mL−1,in agreement with their calculated large adsorption energies on graphene.The results of electron spin resonance,Raman,scanning Kelvin probe microscopy and X-ray photoelectron spectroscopy measurements indicate that the amino groups could n-dope graphene or form dipole interaction with graphene.The two 3D-surfactant-based graphene composites(POSSFN-G and ADMAFN-G)can work as high-performance CIMs in organic solar cells(OSCs),which improve the power conversion efficiency(PCE)of the OSCs based on PM6:Y6 to 15.9%–16.1%.ADMAFN forms dipole interaction with graphene in ADMAFN-G and the composite CIM delivers high PCE of 16.11%in the OSCs,while POSSFN forms n-doped composition with graphene in POSSFN-G which works well as thicker CIM film in the OSCs.
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.
基金supported by the National Key R&D Program of China(2019YFA0709200)the National Natural Science Foundation of China(21988102,51772198 and 21975171)。
文摘Water electrolysis to produce H2 is a promising strategy for generating a renewable fuel.However,the sluggish-kinetics and low value-added anodic oxygen evolution reaction(OER)restricts the overall energy conversion efficiency.Herein we report a strategy of boosting H_(2)production at low voltages by replacing OER with a bioelectrochemical cascade reaction at a triphase bioanode.In the presence of oxygen,oxidase enzymes can convert biomass into valuable products,and concurrently generate H_(2)O_(2) that can be further electrooxidized at the bioanode.Benefiting from the efficient oxidase kinetics at an oxygen-rich triphase bioanode and the more favorable thermodynamics of H_(2)O_(2)oxidation than that of OER,the cell voltage and energy consumption are reduced by~0.70 V and~36%,respectively,relative to regular water electrolysis.This leads to an efficient H_(2)production at the cathode and valuable product generation at the bioanode.Integration of a bioelectrochemical cascade into the water splitting process provides an energy-efficient and promising pathway for achieving a renewable fuel.
