The rapid development of communication technology and high-frequency electronic devices has created a need for more advanced electromagnetic interference(EMI)shielding materials.In response to this demand,a study has ...The rapid development of communication technology and high-frequency electronic devices has created a need for more advanced electromagnetic interference(EMI)shielding materials.In response to this demand,a study has been conducted to develop multifunctional carbon nanofibers(CNFs)/polyaniline(PANI)aerogels with excellent electromagnetic interference shielding,flame retardancy,and thermal insulation performance.The process involved freeze-drying of electrospun CNFs and PANI nanoparticles followed by in situ growth PANI to coat the CNFs,creating the core-shell structured CNFs/PANI composite fiber and its hybrid aerogels(CP-3@PANI).The interaction between PANI and aniline(ANI)provides attachment sites,allowing additional ANI adsorption into the aerogel for in situ polymerization.This results in PANI uniformly covering the surface of the CNFs,creating a core-shell composite fiber with a flexible CNF core and PANI shell.This process enhances the utilization rate of the ANI monomer and increases the PANI content loaded onto the aerogel.Additionally,effective connections are established between the CNFs,forming a stable,conductive three-dimensional network structure.The prepared CP-3@PANI aerogels exhibit excellent EMI shielding efficiency(SE)of 85.4 dB and specific EMI SE(SE d^(-1))of 791.2 dB cm^(3)g^(-1)in the X-band.Due to the synergistic flame-retardant effect of CNFs,PANI,and the dopant(phytic acid),the CP-3@PANI aerogels demonstrate outstanding flame-retardant and thermal insulation properties,with a peak heat release rate(PHRR)as low as 7.8 W g^(-1)and a total heat release of only 0.58 kJ g^(-1).This study provides an effective strategy for preparing multifunctional integrated EMI shielding materials.展开更多
For the further improvement of the power conversion efficiency(PCE)and stability of perovskite solar cells(PSCs),the buried interface between the perovskite and the electron transport layer is crucial.However,it is ch...For the further improvement of the power conversion efficiency(PCE)and stability of perovskite solar cells(PSCs),the buried interface between the perovskite and the electron transport layer is crucial.However,it is challenging to effectively optimize this interface as it is buried beneath the perovskite film.Herein,we have designed and synthesized a series of multifunctional organic-inorganic(OI)complexes as buried interfacial material to promote electron extraction,as well as the crystal growth of the perovskite.The OI complex with BF4−group not only eliminates oxygen vacancies on the SnO_(2) surface but also balances energy level alignment between SnO_(2) and perovskite,providing a favorable environment for charge carrier extraction.Moreover,OI complex with amine(−NH_(2))functional group can regulate the crystallization of the perovskite film via interaction with PbI2,resulting in highly crystallized perovskite film with large grains and low defect density.Consequently,with rational molecular design,the PSCs with optimal OI complex buried interface layer which contains both BF4−and−NH_(2) functional groups yield a champion device efficiency of 23.69%.More importantly,the resulting unencapsulated device performs excellent ambient stability,maintaining over 90%of its initial efficiency after 2000 h storage,and excellent light stability of 91.5%remaining PCE in the maximum power point tracking measurement(under continuous 100 mW cm−2 light illumination in N2 atmosphere)after 500 h.展开更多
Ultrathin Pd-based two-dimensional(2D)nanosheets(NSs)with tunable physicochemical properties have emerged as promising candidate for oxygen reduction reaction(ORR).Unfortunately,structurally ordered Pd-based NSs can b...Ultrathin Pd-based two-dimensional(2D)nanosheets(NSs)with tunable physicochemical properties have emerged as promising candidate for oxygen reduction reaction(ORR).Unfortunately,structurally ordered Pd-based NSs can be hardly prepared as high temperature annealing(>600℃)is necessary for disorder to order phase transition,making it a considerable challenge for morphology control.Herein,a new class of ultrathin structurally ordered Mo-doped L1_(0)-PdZn NSs with curved geometry and abundant defects/lattice distortions is reported as an efficient oxygen reduction electrocatalyst in alkaline solution.It is found that Mo(CO)_(6) serves as reducing agent and Mo source to generate the unique ordered 2D morphology,which leads to the significantly modified electronic structure.The developed L1_(0)-Mo-PdZn NSs exhibit excellent ORR mass activity of 2.6 A mg_(Pd)^(−1) at 0.9 V versus reversible hydrogen electrode,31.5 and 17.6 times higher than those of Pd/C and Pt/C,respectively,outperforming most of the reported Pdbased ORR electrocatalsyts.Impressively,L1_(0)-Mo-PdZn NSs is extremely stable for ORR,with only 2.3% activity loss after 10000 potential cycles.Density functional theory study suggests that ordered L1_(0) structure and Mo doping can raise the vacancy formation energy of Pd atom and thus promote the ORR stability.展开更多
基金the financial support from the Shenzhen Biodegradable Polymer Materials and Materials Genetic Evaluation Research Project Team (JCYJ20220818100217037)Science and Technology Program of Shenzhen (JSGG20200924171000001)+4 种基金the Key-Area Research and Development Program of Guangdong Province (2019B010941001)the Guangdong Provincial Key Laboratory of Energy Materials for Electric Power(2018B030322001)the National Key Research and Development Program of China (2018YFB0704100)Joint Laboratory of Radiation Protection and Material Genetic Engineering Applications in Nuclear Facilitiessupported by the Pico Center at SUSTech CRF which receives support from the Presidential Fund and Development and Reform Commission of Shenzhen Municipality。
文摘The rapid development of communication technology and high-frequency electronic devices has created a need for more advanced electromagnetic interference(EMI)shielding materials.In response to this demand,a study has been conducted to develop multifunctional carbon nanofibers(CNFs)/polyaniline(PANI)aerogels with excellent electromagnetic interference shielding,flame retardancy,and thermal insulation performance.The process involved freeze-drying of electrospun CNFs and PANI nanoparticles followed by in situ growth PANI to coat the CNFs,creating the core-shell structured CNFs/PANI composite fiber and its hybrid aerogels(CP-3@PANI).The interaction between PANI and aniline(ANI)provides attachment sites,allowing additional ANI adsorption into the aerogel for in situ polymerization.This results in PANI uniformly covering the surface of the CNFs,creating a core-shell composite fiber with a flexible CNF core and PANI shell.This process enhances the utilization rate of the ANI monomer and increases the PANI content loaded onto the aerogel.Additionally,effective connections are established between the CNFs,forming a stable,conductive three-dimensional network structure.The prepared CP-3@PANI aerogels exhibit excellent EMI shielding efficiency(SE)of 85.4 dB and specific EMI SE(SE d^(-1))of 791.2 dB cm^(3)g^(-1)in the X-band.Due to the synergistic flame-retardant effect of CNFs,PANI,and the dopant(phytic acid),the CP-3@PANI aerogels demonstrate outstanding flame-retardant and thermal insulation properties,with a peak heat release rate(PHRR)as low as 7.8 W g^(-1)and a total heat release of only 0.58 kJ g^(-1).This study provides an effective strategy for preparing multifunctional integrated EMI shielding materials.
基金The authors acknowledge the financial support from the Natural Science Foundation of China(Nos.21931002 and 22101123)the National Key Research and Development Program of China(2018YFB0704100)+4 种基金the Shenzhen Science and Technology Innovation Committee(no.JCYJ20200109140812302)the Leading talents of Guangdong province program(2016LJ06N507)the Guangdong Provincial Key Laboratory of Energy Materials for Electric Power(no.2018B030322001)the Guangdong Provincial Key Laboratory of Catalysis(no.2020B121201002)Outstanding Talents Training Fund in Shenzhen.
文摘For the further improvement of the power conversion efficiency(PCE)and stability of perovskite solar cells(PSCs),the buried interface between the perovskite and the electron transport layer is crucial.However,it is challenging to effectively optimize this interface as it is buried beneath the perovskite film.Herein,we have designed and synthesized a series of multifunctional organic-inorganic(OI)complexes as buried interfacial material to promote electron extraction,as well as the crystal growth of the perovskite.The OI complex with BF4−group not only eliminates oxygen vacancies on the SnO_(2) surface but also balances energy level alignment between SnO_(2) and perovskite,providing a favorable environment for charge carrier extraction.Moreover,OI complex with amine(−NH_(2))functional group can regulate the crystallization of the perovskite film via interaction with PbI2,resulting in highly crystallized perovskite film with large grains and low defect density.Consequently,with rational molecular design,the PSCs with optimal OI complex buried interface layer which contains both BF4−and−NH_(2) functional groups yield a champion device efficiency of 23.69%.More importantly,the resulting unencapsulated device performs excellent ambient stability,maintaining over 90%of its initial efficiency after 2000 h storage,and excellent light stability of 91.5%remaining PCE in the maximum power point tracking measurement(under continuous 100 mW cm−2 light illumination in N2 atmosphere)after 500 h.
基金National Natural Science Foundation of China,Grant/Award Numbers:22122202,21972051。
文摘Ultrathin Pd-based two-dimensional(2D)nanosheets(NSs)with tunable physicochemical properties have emerged as promising candidate for oxygen reduction reaction(ORR).Unfortunately,structurally ordered Pd-based NSs can be hardly prepared as high temperature annealing(>600℃)is necessary for disorder to order phase transition,making it a considerable challenge for morphology control.Herein,a new class of ultrathin structurally ordered Mo-doped L1_(0)-PdZn NSs with curved geometry and abundant defects/lattice distortions is reported as an efficient oxygen reduction electrocatalyst in alkaline solution.It is found that Mo(CO)_(6) serves as reducing agent and Mo source to generate the unique ordered 2D morphology,which leads to the significantly modified electronic structure.The developed L1_(0)-Mo-PdZn NSs exhibit excellent ORR mass activity of 2.6 A mg_(Pd)^(−1) at 0.9 V versus reversible hydrogen electrode,31.5 and 17.6 times higher than those of Pd/C and Pt/C,respectively,outperforming most of the reported Pdbased ORR electrocatalsyts.Impressively,L1_(0)-Mo-PdZn NSs is extremely stable for ORR,with only 2.3% activity loss after 10000 potential cycles.Density functional theory study suggests that ordered L1_(0) structure and Mo doping can raise the vacancy formation energy of Pd atom and thus promote the ORR stability.
