The photoreduction of CO_(2)into CH_(4)with simultaneous high activity and selectivity is a promising strategy to increase energy supply and alleviate global warming.However,the absence of the active sites that is res...The photoreduction of CO_(2)into CH_(4)with simultaneous high activity and selectivity is a promising strategy to increase energy supply and alleviate global warming.However,the absence of the active sites that is responsible for the adsorption and activation of CO_(2)and the generation of CO and H2via side reactions often lead to poor efficiency and low selectivity of the catalyst.Herein,Cu,Pd,and PdCu metal clusters cocatalyst-anchored defective TiO_(2)nanotubes(Cu/TiO_(2)-SBO,Pd/TiO_(2)-SBO,and Pd1Cu1/TiO_(2)-SBO)were designed via a simple solution impregnation reduction and applied for photocatalytic conversion of CO_(2)to CH_(4).The Pd1Cu1/TiO_(2)-SBO photocatalyst exhibits excellent catalytic performance among the other catalysts for photoreduction of CO_(2)into CH_(4).More interestingly,the product selectivity of CH_(4)reaches up to 100%with a rate of 25μmol g^(-1)h^(-1).In-situ diffuse reflectance infrared Fourier transform spectroscopy(DRIFTS)and density functional theory(DFT)simulations indicate that the main reasons for the high selectivity of CH_(4)are attributed to the PdCu alloy and oxygen vacancies,which jointly enhance the photoinduced carrier separation and lower energy barriers of key intermediates.Moreover,due to the tunable d-band center of the Cu site in the PdCu alloy,the generated intermediates can be well prevented from poisoning and promoted to participate in further reactions.Hopefully,the current study will provide insight into the development of new,highly selective photocatalysts for the visible light-catalytic reduction of CO_(2)into CH_(4).展开更多
Pd and Pd alloy membranes are of increasing interest for hydrogen separation and purification due to their good thermal stability, high permeability and perfect selectivity. PdCu alloy (60wt% Pd) membranes have simila...Pd and Pd alloy membranes are of increasing interest for hydrogen separation and purification due to their good thermal stability, high permeability and perfect selectivity. PdCu alloy (60wt% Pd) membranes have similar hydrogen permeability compared with PdAg alloy; meanwhile, it is cheaper than PdAg alloy. Furthermore, it has been reported that PdCu membrane has better resistance to poisoning and deactivation by H 2 S impurity. This paper reviews the properties and manufacturing methods of PdCu alloy membrane, finally, introduced some achievement made by us on PdCu alloy membrane.展开更多
The design of high-performance catalysts is the key to the efficient utilization of hydrogen energy.In this work,a PdCu nanoalloy was successfully anchored on TiO_(2)encapsulated with carbon to construct a catalyst.Ou...The design of high-performance catalysts is the key to the efficient utilization of hydrogen energy.In this work,a PdCu nanoalloy was successfully anchored on TiO_(2)encapsulated with carbon to construct a catalyst.Outstanding kinetics of the hydrolysis of ammonia borane(turnover frequency of 279 mol·min^(-1·)mol_(Pd)^(-1))ranking the third place among Pd-based catalysts was achieved in the absence of alkali.Both experimental research and theoretical calculations reveal a lower activation energy of the B-H bond on the PdCu nanoalloy catalyst than that on pristine Pd and a lower activation energy of the O-H bond than that on pristine Cu.The redistribution of d electron and the shift of the d-band center play a critical role in increasing the electron density of Pd and improving the catalytic performances of Pd_(0.1)Cu_(0.9)/TiO_(2)-porous carbon(Pd_(0.1)Cu_(0.9)/T-PC).This work provides novel insights into highly dual-active alloys and sheds light on the mechanism of dual-active sites in promoting borohydride hydrolysis.展开更多
Suzuki-Miyaura reactions, involving the activation of carbon-halogen bonds, especially C-C1 bonds, have drawn widespread attention because of their huge industrial potential. However, these reactions are dependent on ...Suzuki-Miyaura reactions, involving the activation of carbon-halogen bonds, especially C-C1 bonds, have drawn widespread attention because of their huge industrial potential. However, these reactions are dependent on the development of highly active and stable catalysts. Herein, we developed a convenient one-pot wet route to synthesize PdxCuy bimetallic nanocrystals for the Suzuki-Miyaura reaction. By introducing Cu, an earth-abundant element, the catalytic activity was greatly enhanced while the amount of Pd required was reduced. PdxCuy nanocrystals of different compositions, including PdBCu, Pd2Cu, PdCu, PdCu2, and PdCu3, were successfully synthesized by tuning the Pd：Cu ratio. Their catalytic performance in Suzuki-Miyaura reactions between phenylboronic acid and halobenzenes （iodo-, bromo-, or chlorobenzene） showed that PdCua nanocatalyst demonstrated the best efficacy.展开更多
Developing efficient and stable bimetallic Pdbased anode electrocatalysts toward formic acid oxidation(FAO)is of great significance for commercial applications of direct formic acid fuel cells(DFAFCs).Herein,we report...Developing efficient and stable bimetallic Pdbased anode electrocatalysts toward formic acid oxidation(FAO)is of great significance for commercial applications of direct formic acid fuel cells(DFAFCs).Herein,we report a facile synthesis approach to fabricate PdCu nanoclusters(NCs)catalysts with granular-film structure.The introduction of Cu can adjust the electronic structure and d-band center of Pd,which can improve the catalytic performance of the catalysts.Compared with Pd NCs catalyst,the catalytic durability and activity of PdCu NCs catalysts for FAO are greatly improved.The order for catalytic activity of NC metals is Pd_(85)Cu_(15)NCs>Pd_(70)Cu_(30)NCs>Pd NCs.The maximum mass activity can be acquired with the Pd_(85)Cu_(15)NCs catalyst,which is about1.7 times that of the Pd NCs catalyst.And Pd_(85)Cu_(15)NCs catalyst still maintains the highest catalytic current density after 50 cycles,indicating that Pd_(85)Cu_(15)NCs catalyst has the best durability and electrocatalytic activity for FAO.Our work provides a new prospect for the design of highly efficient anode catalysts materials for DFAFCs.展开更多
Transport of charge carriers in percolating nanocluster devices based on bimetallic PdCu nanoclusters was investigated in this work. The device was fabricated by self-assembly of the nanoclusters between electrical el...Transport of charge carriers in percolating nanocluster devices based on bimetallic PdCu nanoclusters was investigated in this work. The device was fabricated by self-assembly of the nanoclusters between electrical electrodes inside an ultra-high vacuum compatible system. The average size of the produced nanoclusters was 7.3 nm, and the composition was Pdo.77Cuo.23. Systematic in situ current-voltage measurements as a function of temperature were per- formed which provide a conductance-temperature profile. The results are explained in terms of the charge carriers＇ tunneling through small potential barriers at the junctions between nanoclusters. The results predict the size of the nanoclusters as well as the magnitude of the potential difference of the tunneling barriers. This investigation helps understanding the nature of the interface between the nanoclusters and the charge carrier transport within those devices to be utilized for optimizing gas sensing properties of PdCu nanocluster devices.展开更多
Improving the complete ethanol electrooxidation on Pd-based catalysts in alkaline media has drawn widely attention due to the high mass energy density.However,the weak adsorption energy of CH_(3)CO^(*) on Pd restricts...Improving the complete ethanol electrooxidation on Pd-based catalysts in alkaline media has drawn widely attention due to the high mass energy density.However,the weak adsorption energy of CH_(3)CO^(*) on Pd restricts the C–C bond cleavage.Inspired by the molecular orbital theory,we proposed the d-state-editing strategy to construct more unoccupied d-states of Pd for the enhanced interaction with CH_(3)CO^(*) to break C–C bonds.As expected,the reduced number of e_g electrons and more unoccupied d-states of Pd successfully formed on as-prepared porous Rh Au–Pd Cu nanosheets(PNSs).Theoretical calculations show that the optimized d-states of Rh Au–Pd Cu PNS can effectively improve the adsorption of CH_(3)CO^(*) and drastically reduce the energy barrier of C–C bond cleavage,thus boosting the complete oxidation of ethanol.The charge ratio of C_1 pathway on Rh Au–Pd Cu PNSs is 51.5%,more than 2 times higher than that of Pd NSs.Our finding provides an innovative perspective for the design of highly-efficient noble-based electrocatalysts.展开更多
基金the financial support from the Program for Innovative Research Team in University of Henan Province(21IRTSTHN009)Science and Technology Fund of Henan Province(225200810051)Natural Science Foundation of Henan Province(222300420406)。
文摘The photoreduction of CO_(2)into CH_(4)with simultaneous high activity and selectivity is a promising strategy to increase energy supply and alleviate global warming.However,the absence of the active sites that is responsible for the adsorption and activation of CO_(2)and the generation of CO and H2via side reactions often lead to poor efficiency and low selectivity of the catalyst.Herein,Cu,Pd,and PdCu metal clusters cocatalyst-anchored defective TiO_(2)nanotubes(Cu/TiO_(2)-SBO,Pd/TiO_(2)-SBO,and Pd1Cu1/TiO_(2)-SBO)were designed via a simple solution impregnation reduction and applied for photocatalytic conversion of CO_(2)to CH_(4).The Pd1Cu1/TiO_(2)-SBO photocatalyst exhibits excellent catalytic performance among the other catalysts for photoreduction of CO_(2)into CH_(4).More interestingly,the product selectivity of CH_(4)reaches up to 100%with a rate of 25μmol g^(-1)h^(-1).In-situ diffuse reflectance infrared Fourier transform spectroscopy(DRIFTS)and density functional theory(DFT)simulations indicate that the main reasons for the high selectivity of CH_(4)are attributed to the PdCu alloy and oxygen vacancies,which jointly enhance the photoinduced carrier separation and lower energy barriers of key intermediates.Moreover,due to the tunable d-band center of the Cu site in the PdCu alloy,the generated intermediates can be well prevented from poisoning and promoted to participate in further reactions.Hopefully,the current study will provide insight into the development of new,highly selective photocatalysts for the visible light-catalytic reduction of CO_(2)into CH_(4).
文摘Pd and Pd alloy membranes are of increasing interest for hydrogen separation and purification due to their good thermal stability, high permeability and perfect selectivity. PdCu alloy (60wt% Pd) membranes have similar hydrogen permeability compared with PdAg alloy; meanwhile, it is cheaper than PdAg alloy. Furthermore, it has been reported that PdCu membrane has better resistance to poisoning and deactivation by H 2 S impurity. This paper reviews the properties and manufacturing methods of PdCu alloy membrane, finally, introduced some achievement made by us on PdCu alloy membrane.
基金This work was financially supported by the National Natural Science Foundation of China(Nos.22279118,22279117,52071135,51871090,and U1804135)the Fundamental Research Funds for the Universities of Henan Province(No.NSFRF220201).
文摘The design of high-performance catalysts is the key to the efficient utilization of hydrogen energy.In this work,a PdCu nanoalloy was successfully anchored on TiO_(2)encapsulated with carbon to construct a catalyst.Outstanding kinetics of the hydrolysis of ammonia borane(turnover frequency of 279 mol·min^(-1·)mol_(Pd)^(-1))ranking the third place among Pd-based catalysts was achieved in the absence of alkali.Both experimental research and theoretical calculations reveal a lower activation energy of the B-H bond on the PdCu nanoalloy catalyst than that on pristine Pd and a lower activation energy of the O-H bond than that on pristine Cu.The redistribution of d electron and the shift of the d-band center play a critical role in increasing the electron density of Pd and improving the catalytic performances of Pd_(0.1)Cu_(0.9)/TiO_(2)-porous carbon(Pd_(0.1)Cu_(0.9)/T-PC).This work provides novel insights into highly dual-active alloys and sheds light on the mechanism of dual-active sites in promoting borohydride hydrolysis.
基金This research was supported in part by the National Natural Science Foundation of China （Nos. 21475007, 21275015 and 21505003）, and the Fundamental Research Funds for the Central Universities （Nos. YS1406, buctrc201507 and buctrc201608）. We also thank the support from the Innovation and Promotion Project of Beijing University of Chemical Technology, the Public Hatching Platform for Recruited Talents of Beijing University of Chemical Technology, the High- Level Faculty Program of Beijing University of Chemical Technology （No. buctrc201325）, and BUCT Fund for Disciplines Construction and Development （No. XK1526）.
文摘Suzuki-Miyaura reactions, involving the activation of carbon-halogen bonds, especially C-C1 bonds, have drawn widespread attention because of their huge industrial potential. However, these reactions are dependent on the development of highly active and stable catalysts. Herein, we developed a convenient one-pot wet route to synthesize PdxCuy bimetallic nanocrystals for the Suzuki-Miyaura reaction. By introducing Cu, an earth-abundant element, the catalytic activity was greatly enhanced while the amount of Pd required was reduced. PdxCuy nanocrystals of different compositions, including PdBCu, Pd2Cu, PdCu, PdCu2, and PdCu3, were successfully synthesized by tuning the Pd：Cu ratio. Their catalytic performance in Suzuki-Miyaura reactions between phenylboronic acid and halobenzenes （iodo-, bromo-, or chlorobenzene） showed that PdCua nanocatalyst demonstrated the best efficacy.
基金financially supported by the National Natural Science Foundation of China (No.51901197, 51971184 and 51771157)the Open Fund of Fujian Provincial Key Laboratory of Eco-Industrial Green Technology in Wuyi University (No.WYKF-EIGT2021-6)
文摘Developing efficient and stable bimetallic Pdbased anode electrocatalysts toward formic acid oxidation(FAO)is of great significance for commercial applications of direct formic acid fuel cells(DFAFCs).Herein,we report a facile synthesis approach to fabricate PdCu nanoclusters(NCs)catalysts with granular-film structure.The introduction of Cu can adjust the electronic structure and d-band center of Pd,which can improve the catalytic performance of the catalysts.Compared with Pd NCs catalyst,the catalytic durability and activity of PdCu NCs catalysts for FAO are greatly improved.The order for catalytic activity of NC metals is Pd_(85)Cu_(15)NCs>Pd_(70)Cu_(30)NCs>Pd NCs.The maximum mass activity can be acquired with the Pd_(85)Cu_(15)NCs catalyst,which is about1.7 times that of the Pd NCs catalyst.And Pd_(85)Cu_(15)NCs catalyst still maintains the highest catalytic current density after 50 cycles,indicating that Pd_(85)Cu_(15)NCs catalyst has the best durability and electrocatalytic activity for FAO.Our work provides a new prospect for the design of highly efficient anode catalysts materials for DFAFCs.
基金supported by the United Arab Emirates University under a Grant number FOS/IRG-23/11
文摘Transport of charge carriers in percolating nanocluster devices based on bimetallic PdCu nanoclusters was investigated in this work. The device was fabricated by self-assembly of the nanoclusters between electrical electrodes inside an ultra-high vacuum compatible system. The average size of the produced nanoclusters was 7.3 nm, and the composition was Pdo.77Cuo.23. Systematic in situ current-voltage measurements as a function of temperature were per- formed which provide a conductance-temperature profile. The results are explained in terms of the charge carriers＇ tunneling through small potential barriers at the junctions between nanoclusters. The results predict the size of the nanoclusters as well as the magnitude of the potential difference of the tunneling barriers. This investigation helps understanding the nature of the interface between the nanoclusters and the charge carrier transport within those devices to be utilized for optimizing gas sensing properties of PdCu nanocluster devices.
基金financially supported by the National Natural Science Foundation of China (22209039)Top-notch Personnel Fund of Henan Agricultural University (30500682)。
文摘Improving the complete ethanol electrooxidation on Pd-based catalysts in alkaline media has drawn widely attention due to the high mass energy density.However,the weak adsorption energy of CH_(3)CO^(*) on Pd restricts the C–C bond cleavage.Inspired by the molecular orbital theory,we proposed the d-state-editing strategy to construct more unoccupied d-states of Pd for the enhanced interaction with CH_(3)CO^(*) to break C–C bonds.As expected,the reduced number of e_g electrons and more unoccupied d-states of Pd successfully formed on as-prepared porous Rh Au–Pd Cu nanosheets(PNSs).Theoretical calculations show that the optimized d-states of Rh Au–Pd Cu PNS can effectively improve the adsorption of CH_(3)CO^(*) and drastically reduce the energy barrier of C–C bond cleavage,thus boosting the complete oxidation of ethanol.The charge ratio of C_1 pathway on Rh Au–Pd Cu PNSs is 51.5%,more than 2 times higher than that of Pd NSs.Our finding provides an innovative perspective for the design of highly-efficient noble-based electrocatalysts.
