Catalyst design relies heavily on electronic metal‐support interactions,but the metal‐support interface with an uncontrollable electronic or coordination environment makes it challenging.Herein,we outline a promisin...Catalyst design relies heavily on electronic metal‐support interactions,but the metal‐support interface with an uncontrollable electronic or coordination environment makes it challenging.Herein,we outline a promising approach for the rational design of catalysts involving heteroatoms as anchors for Pd nanoparticles for ethanol oxidation reaction(EOR)catalysis.The doped B and N atoms from dimethylamine borane(DB)occupy the position of the Ti_(3)C_(2) lattice to anchor the supported Pd nanoparticles.The electrons transfer from the support to B atoms,and then to the metal Pd to form a stable electronic center.A strong electronic interaction can be produced and the d‐band center can be shifted down,driving Pd into the dominant metallic state and making Pd nanoparticles deposit uniformly on the support.As‐obtained Pd/DB–Ti_(3)C_(2) exhibits superior durability to its counterpart(∼14.6% retention)with 91.1% retention after 2000 cycles,placing it among the top single metal anodic catalysts.Further,in situ Raman and density functional theory computations confirm that Pd/DB–Ti_(3)C_(2) is capable of dehydrogenating ethanol at low reaction energies.展开更多
Owing to their unique optical properties and nontoxicity,lead-free halide double perovskite nanocrystals are of interest for widespread applications.Herein,the colloid synthesis and photoluminescenc e property of Ag^(...Owing to their unique optical properties and nontoxicity,lead-free halide double perovskite nanocrystals are of interest for widespread applications.Herein,the colloid synthesis and photoluminescenc e property of Ag^(+)-Eu^(3+)codoped Cs_(2)NaInCl_(6)nanocrystals were investigated.The pe rovskite nanocrystals exhibit a broad warm-white photo luminescence with correlated color temperature(CCT)of 3447 K and color rendering index(CRI)of 90.2,and the means of codoping would improve its optical performance.A fast energy transfer and a long-lived self-trapped excitons state are unveiled by the femtosecond transient absorption spectra.The fast energy transfer from the self-trapped excitons of host nanocrystals to the Eu^(3+)ions is helpful to achieve a broad photoluminescence,and the quantum yield of Cs_(2)NaInCl_(6):0.05Ag^(+)-Eu^(3+)anocrystals can be enha nced to 69.5%.There is a large exciton binding energy and strong electron-phonon interaction in the codoped perovskite nanocrystals.The efficient and excellent air-stable double perovskite nanocrystals would be considered as a single-component phosphor for warm-white lighting.展开更多
In this study, we have performed first-principles screened exchanged hybrid density function theory with the HSE06 function calculations of the C-Mo, C-W, N-Nb and N-Ta codoped anatase TiO2 systems to investigate the ...In this study, we have performed first-principles screened exchanged hybrid density function theory with the HSE06 function calculations of the C-Mo, C-W, N-Nb and N-Ta codoped anatase TiO2 systems to investigate the effect of codoping on the electronic structure of TiO2. The calculated results demonstrate that （W（s）＋C（s）） codoped TiO2 narrows the band gap significantly, and have little influence on the position of conduction band edges, therefore, enhances the efficiency of the photocatalytic hydrogen generation from water and the photodegradation of organic pollutants. Moreover, the proper oxygen pressure and temperature are two key factors during synthesis which should be carefully under control so that the desired （W（s）＋C（s）） codoped TiO2 can be obtained.展开更多
Diamond crystals were synthesized with different doping proportions of N-H-O at 5.5 GPa-7.1 GPa and 1370℃-1450℃. With the increase in the N-H-O doping ratio, the crystal growth rate decreased, the temperature and pr...Diamond crystals were synthesized with different doping proportions of N-H-O at 5.5 GPa-7.1 GPa and 1370℃-1450℃. With the increase in the N-H-O doping ratio, the crystal growth rate decreased, the temperature and pressure conditions required for diamond nucleation became increasingly stringent, and the diamond crystallization process was affected. [111] became the dominant plane of diamonds;surface morphology became block-like;and growth texture,stacking faults, and etch pits increased. The diamond crystals had a two-dimensional growth habit. Increasing the doping concentration also increased the amount of N that entered the diamond crystals as confirmed via Fourier transform infrared spectroscopy. However, crystal quality gradually deteriorated as verified by the red-shifting of Raman peak positions and the widening of the Raman full width at half maximum. With the increase in the doping ratio, the photoluminescence property of the diamond crystals also drastically changed. The intensity of the N vacancy center of the diamond crystals changed, and several Ni-related defect centers, such as the NE1 and NE3 centers, appeared. Diamond synthesis in N-H-O-bearing fluid provides important information for deepening our understanding of the growth characteristics of diamonds in complex systems and the formation mechanism of natural diamonds, which are almost always N-rich and full of various defect centers. Meanwhile, this study proved that the type of defect centers in diamond crystals could be regulated by controlling the N-H-O impurity contents of the synthesis system.展开更多
Carbon-based materials have become a research hotspot in the field of energy storage devices in recent years due to their abundant resources,low cost,and environmental friendliness.However,the low capacity and poor hi...Carbon-based materials have become a research hotspot in the field of energy storage devices in recent years due to their abundant resources,low cost,and environmental friendliness.However,the low capacity and poor high rate performance still constitute great challenges.Metal organic framework-derived carbon has been widely researched because of its high porosity,tunable structure,and good conductivity.In this work,N/S codoped hierarchical porous carbon microspheres were prepared by a high-temperature heat treatment and atomic doping process using a zinc-based organic framework as the precursor.When used as a potassium-ion battery anode,it has a high reversible specific capacity(435.7 mAh g^(-1)),good rate performance(133.5 mAh g^(-1)at 10,000 m A g^(-1)),and long-term cycling stability(73.2%capacity retention after the 2500th cycle).The potassium storage mechanism of the derived carbon was explained by various electrochemical analysis methods and microstructure characterization techniques,and the relationship between the structural characteristics and electrochemical properties was researched.In a supercapacitor,the porous carbon material exhibits a specific capacitance of 307.2 F g^(-1)at a current density of 0.2 A g^(-1)in a KOH aqueous solution and achieves a retention rate of 99.88%after 10,000 cycles.The assembled symmetric supercapacitor device delivers a high energy density of 6.69 Wh kg^(-1),with a corresponding power density of 2500 W kg^(-1).In addition,density functional theory calculations further confirmed that N/S codoping can improve the adsorption capacities of potassium and hydroxyl ions in the derived carbon.展开更多
In the iron-based high-To bulk superconductors, Tc above 50 K was only observed in the electron-doped 1111-type compounds. Here we revisit the electron-doped SmFeAsO polycrystals to make a further investigation for th...In the iron-based high-To bulk superconductors, Tc above 50 K was only observed in the electron-doped 1111-type compounds. Here we revisit the electron-doped SmFeAsO polycrystals to make a further investigation for the highest Tc in these materials. To introduce more electron carriers and less crystal lattice distortions, we study the Th and F eodoping effects into the Sm-O layers with heavy electron doping. Dozens of Sm1-xThx FeAsO1-yFy samples are synthesized through the solid state reaction method, and these samples are carefully characterized by the structural, resistive, and magnetic measurements. We find that the codoping of Th and F clearly enhances the superconducting Tc more than the Th or F single-doped samples, with the highest record Tc up to 58.6K when x = 0.2 and y=0.225. Further element doping causes more impurities and lattice distortions in the samples with a weakened superconductivity.展开更多
Mg_(3)Sb_(2)has attracted intensive attention as a typical Zintl-type thermoelectric material.Despite the exceptional thermoelectric performance in n-type Mg_(3)Sb_(2),the dimensionless figure of merit(zT)of p-type Mg...Mg_(3)Sb_(2)has attracted intensive attention as a typical Zintl-type thermoelectric material.Despite the exceptional thermoelectric performance in n-type Mg_(3)Sb_(2),the dimensionless figure of merit(zT)of p-type Mg_(3)Sb_(2)remains lower than 1,which is mainly attributed to its inferior electrical properties.Herein,we synergistically optimize the thermoelectric properties of p-type Mg_(3)Sb_(2)materials via codoping of Cd and Ag,which were synthesized by high-energy ball milling combined with hot pressing.It is found that Cd doping not only increases the carrier mobility of p-type Mg_(3)Sb_(2),but also diminishes its thermal conductivity(κ_(tot)),with Mg_(2.85)Cd_(0.5)Sb_(2)achieving a lowκtot value of∼0.67 W m^(−1)K^(−1)at room temperature.Further Ag doping elevates the carrier concentration,so that the power factor is optimized over the entire temperature range.Eventually,a peak zT of∼0.75 at 773 K and an excellent average zT of∼0.41 over 300−773 K are obtained in Mg_(2.82)Ag_(0.03)Cd_(0.5)Sb_(2),which are∼240%and∼490%higher than those of pristine Mg_(3.4)Sb_(2),respectively.This study provides an effective pathway to synergistically improve the thermoelectric performance of p-type Mg_(3)Sb_(2)by codoping Cd and Ag,which is beneficial to the future applications of Mg_(3)Sb_(2)-based thermoelectric materials.展开更多
In this work, a simple method to modulate the crystal phase and morphology with a large amount of K＋ions codoping is proposed. The phase changes to the mixture of β-Na YF4 and β-KYF4 with increasing the content of...In this work, a simple method to modulate the crystal phase and morphology with a large amount of K＋ions codoping is proposed. The phase changes to the mixture of β-Na YF4 and β-KYF4 with increasing the content of K^＋ions to 80 mol%.When it exceeds 80 mol%, β-Na YF4 disappears gradually and β-KYF4 dominates with a poor crystalline. In addition, the morphology changes from nanosphere to nanoplate, and then to nanoprism, which indicates that a higher content of K^＋ions favors the growth rates along [0001] than the [10-10] of the nanocrystals. Additionally, the upconversion（UC） luminescence properties and the ratio of red/green（R/G） UC intensity of samples with different phases and morphologies are detected,which makes it possible to tune the UC fluorescence by varying the concentration of K^＋ions.展开更多
In this paper we present a novel report on the upconversion luminescence performance of NaY0.92Yb0.05Er0.03F4 enhanced by Zr^4＋ codoping. The luminescence intensity of the tridoped hexagonal NaYF_4 synthesized by a h...In this paper we present a novel report on the upconversion luminescence performance of NaY0.92Yb0.05Er0.03F4 enhanced by Zr^4＋ codoping. The luminescence intensity of the tridoped hexagonal NaYF_4 synthesized by a hydrothermal method increased to the maximum, about seven times of the non-Zr^4＋ sample when the Zr^4＋ codoping concentration rose to 6 mol%, while the luminescence lifetime was also prolonged by Zr^4＋ codoping. To explore the relationships between the microstructure and upconversion properties, X-ray powder diffraction, field emission scanning electron microscope, electron energy-dispersive spectroscopy and upconversion emission spectroscopy were employed. From these characterizations, we found that the codoping of Zr^4＋ could modulate the crystal microstructure of NaYF_4 for higher upconversion luminescence intensity and longer lifetime. This study may be helpful for the design and synthesis of high-performance upconversion materials.展开更多
The structural,electronic properties and formation energies of sulfur and alkaline earth codoped delafossite CuAlO_2 have been investigated using the first-principles density functional theory calculations.Our results...The structural,electronic properties and formation energies of sulfur and alkaline earth codoped delafossite CuAlO_2 have been investigated using the first-principles density functional theory calculations.Our results reveal that the volume of codoping systems increases with the increasing atomic radius of metal atoms.The formation energies under different growth conditions have been calculated,showing that the codoping systems are formed easily under O-rich growth conditions.Electronic band structures and density of states have been obtained.The decreased bandgaps,enhanced covalence and appearance of electron acceptors after codoping are all good for p-type conductivity.展开更多
本文基于密度泛函理论(DFT)的GGA+U方法,应用Materials Studio 5.0软件包中的CASTEP程序模拟计算了Al掺杂锐钛矿型TiO2和N-Al共掺杂锐钛矿型TiO2的电子结构。计算结果表明:Al掺杂和N-Al共掺杂均能够降低TiO2的带隙值。Al掺杂是由于Al的3...本文基于密度泛函理论(DFT)的GGA+U方法,应用Materials Studio 5.0软件包中的CASTEP程序模拟计算了Al掺杂锐钛矿型TiO2和N-Al共掺杂锐钛矿型TiO2的电子结构。计算结果表明:Al掺杂和N-Al共掺杂均能够降低TiO2的带隙值。Al掺杂是由于Al的3s和3p态使导带底端下移而导致TiO2的带隙变窄;而N-Al共掺杂由于在体系中引入了N2p态,使导带底端向能量更低的方向移动,比Al单独掺杂时具有更低的带隙值。该研究结果很好地解释了Al掺杂以及N-Al共掺杂诱使TiO2的导带底端下移,禁带宽度减小,导致光谱响应范围红移的内在原因。展开更多
基金Key Research and Development Program of Zhejiang,Grant/Award Number:2021C03022National Natural Science Foundation of China,Grant/Award Numbers:22002104,22272115,22202145,22202146,22102112,22202147。
文摘Catalyst design relies heavily on electronic metal‐support interactions,but the metal‐support interface with an uncontrollable electronic or coordination environment makes it challenging.Herein,we outline a promising approach for the rational design of catalysts involving heteroatoms as anchors for Pd nanoparticles for ethanol oxidation reaction(EOR)catalysis.The doped B and N atoms from dimethylamine borane(DB)occupy the position of the Ti_(3)C_(2) lattice to anchor the supported Pd nanoparticles.The electrons transfer from the support to B atoms,and then to the metal Pd to form a stable electronic center.A strong electronic interaction can be produced and the d‐band center can be shifted down,driving Pd into the dominant metallic state and making Pd nanoparticles deposit uniformly on the support.As‐obtained Pd/DB–Ti_(3)C_(2) exhibits superior durability to its counterpart(∼14.6% retention)with 91.1% retention after 2000 cycles,placing it among the top single metal anodic catalysts.Further,in situ Raman and density functional theory computations confirm that Pd/DB–Ti_(3)C_(2) is capable of dehydrogenating ethanol at low reaction energies.
基金Project supported by the National Natural Science Foundation of China(61805134,11974229,22303044)Fundamental Research Program of Shanxi Province(202203021221121)+3 种基金China Postdoctoral Science Foundation(2022M711898)Natural Science Fo undation of Shandong Province(ZR2023QB135)Postdoctoral Innovation Project of Shandong Province(SDCX-ZG-202201004)Graduate Innovation Project in Shanxi Province(2024KY450)。
文摘Owing to their unique optical properties and nontoxicity,lead-free halide double perovskite nanocrystals are of interest for widespread applications.Herein,the colloid synthesis and photoluminescenc e property of Ag^(+)-Eu^(3+)codoped Cs_(2)NaInCl_(6)nanocrystals were investigated.The pe rovskite nanocrystals exhibit a broad warm-white photo luminescence with correlated color temperature(CCT)of 3447 K and color rendering index(CRI)of 90.2,and the means of codoping would improve its optical performance.A fast energy transfer and a long-lived self-trapped excitons state are unveiled by the femtosecond transient absorption spectra.The fast energy transfer from the self-trapped excitons of host nanocrystals to the Eu^(3+)ions is helpful to achieve a broad photoluminescence,and the quantum yield of Cs_(2)NaInCl_(6):0.05Ag^(+)-Eu^(3+)anocrystals can be enha nced to 69.5%.There is a large exciton binding energy and strong electron-phonon interaction in the codoped perovskite nanocrystals.The efficient and excellent air-stable double perovskite nanocrystals would be considered as a single-component phosphor for warm-white lighting.
基金supported by the NKBRSF (2007CB815202)NKBRSF (No. 2009CB220010)+2 种基金NSFC (20833008)NSFC (No. 20973168)the Solar Energy Initiative of the Knowledge Innovation Program of the Chinese Academy of Science (No. KGCX2-YW-394-2)
文摘In this study, we have performed first-principles screened exchanged hybrid density function theory with the HSE06 function calculations of the C-Mo, C-W, N-Nb and N-Ta codoped anatase TiO2 systems to investigate the effect of codoping on the electronic structure of TiO2. The calculated results demonstrate that （W（s）＋C（s）） codoped TiO2 narrows the band gap significantly, and have little influence on the position of conduction band edges, therefore, enhances the efficiency of the photocatalytic hydrogen generation from water and the photodegradation of organic pollutants. Moreover, the proper oxygen pressure and temperature are two key factors during synthesis which should be carefully under control so that the desired （W（s）＋C（s）） codoped TiO2 can be obtained.
基金Project supported by the National Natural Science Foundation of China (Grant Nos. 51772120, 11604246, 51872112, and 11804305)the Project of Jilin Science and Technology Development Plan (Grant No. 20180201079GX)+1 种基金the Fundamental Research Funds for the Central Universities, the Natural Science Foundation of Chongqing, China (Grant No. cstc2019jcyj-msxm X0391)the Science and Technology Research Program of Chongqing Municipal Education Commission (Grant No. KJQN201901405)。
文摘Diamond crystals were synthesized with different doping proportions of N-H-O at 5.5 GPa-7.1 GPa and 1370℃-1450℃. With the increase in the N-H-O doping ratio, the crystal growth rate decreased, the temperature and pressure conditions required for diamond nucleation became increasingly stringent, and the diamond crystallization process was affected. [111] became the dominant plane of diamonds;surface morphology became block-like;and growth texture,stacking faults, and etch pits increased. The diamond crystals had a two-dimensional growth habit. Increasing the doping concentration also increased the amount of N that entered the diamond crystals as confirmed via Fourier transform infrared spectroscopy. However, crystal quality gradually deteriorated as verified by the red-shifting of Raman peak positions and the widening of the Raman full width at half maximum. With the increase in the doping ratio, the photoluminescence property of the diamond crystals also drastically changed. The intensity of the N vacancy center of the diamond crystals changed, and several Ni-related defect centers, such as the NE1 and NE3 centers, appeared. Diamond synthesis in N-H-O-bearing fluid provides important information for deepening our understanding of the growth characteristics of diamonds in complex systems and the formation mechanism of natural diamonds, which are almost always N-rich and full of various defect centers. Meanwhile, this study proved that the type of defect centers in diamond crystals could be regulated by controlling the N-H-O impurity contents of the synthesis system.
基金supported by the National Natural Science Foundation of China (51764029, 52004116)the National Key Research and Development Program of China (2019YFC1803501)+1 种基金the Applied Basic Research Plan of Yunnan Province(202001AU070039, 2018FB087)the Science Research Foundation of Yunnan Provincial Department of Education (2020J0070)
文摘Carbon-based materials have become a research hotspot in the field of energy storage devices in recent years due to their abundant resources,low cost,and environmental friendliness.However,the low capacity and poor high rate performance still constitute great challenges.Metal organic framework-derived carbon has been widely researched because of its high porosity,tunable structure,and good conductivity.In this work,N/S codoped hierarchical porous carbon microspheres were prepared by a high-temperature heat treatment and atomic doping process using a zinc-based organic framework as the precursor.When used as a potassium-ion battery anode,it has a high reversible specific capacity(435.7 mAh g^(-1)),good rate performance(133.5 mAh g^(-1)at 10,000 m A g^(-1)),and long-term cycling stability(73.2%capacity retention after the 2500th cycle).The potassium storage mechanism of the derived carbon was explained by various electrochemical analysis methods and microstructure characterization techniques,and the relationship between the structural characteristics and electrochemical properties was researched.In a supercapacitor,the porous carbon material exhibits a specific capacitance of 307.2 F g^(-1)at a current density of 0.2 A g^(-1)in a KOH aqueous solution and achieves a retention rate of 99.88%after 10,000 cycles.The assembled symmetric supercapacitor device delivers a high energy density of 6.69 Wh kg^(-1),with a corresponding power density of 2500 W kg^(-1).In addition,density functional theory calculations further confirmed that N/S codoping can improve the adsorption capacities of potassium and hydroxyl ions in the derived carbon.
基金Supported by the National Natural Science Foundation of China under Grant No 11474339the National Basic Research Program of China under Grant No 2016YFA0300301the Youth Innovation Promotion Association of the Chinese Academy of Sciences
文摘In the iron-based high-To bulk superconductors, Tc above 50 K was only observed in the electron-doped 1111-type compounds. Here we revisit the electron-doped SmFeAsO polycrystals to make a further investigation for the highest Tc in these materials. To introduce more electron carriers and less crystal lattice distortions, we study the Th and F eodoping effects into the Sm-O layers with heavy electron doping. Dozens of Sm1-xThx FeAsO1-yFy samples are synthesized through the solid state reaction method, and these samples are carefully characterized by the structural, resistive, and magnetic measurements. We find that the codoping of Th and F clearly enhances the superconducting Tc more than the Th or F single-doped samples, with the highest record Tc up to 58.6K when x = 0.2 and y=0.225. Further element doping causes more impurities and lattice distortions in the samples with a weakened superconductivity.
基金financially supported by the National Natural Science Foundation of China (Grant No. 52071041, 11874356, 51802034)supported by the Key Research Program of Frontier Sciences, CAS (Grant No.QYZDB-SSW-SLH016)
文摘Mg_(3)Sb_(2)has attracted intensive attention as a typical Zintl-type thermoelectric material.Despite the exceptional thermoelectric performance in n-type Mg_(3)Sb_(2),the dimensionless figure of merit(zT)of p-type Mg_(3)Sb_(2)remains lower than 1,which is mainly attributed to its inferior electrical properties.Herein,we synergistically optimize the thermoelectric properties of p-type Mg_(3)Sb_(2)materials via codoping of Cd and Ag,which were synthesized by high-energy ball milling combined with hot pressing.It is found that Cd doping not only increases the carrier mobility of p-type Mg_(3)Sb_(2),but also diminishes its thermal conductivity(κ_(tot)),with Mg_(2.85)Cd_(0.5)Sb_(2)achieving a lowκtot value of∼0.67 W m^(−1)K^(−1)at room temperature.Further Ag doping elevates the carrier concentration,so that the power factor is optimized over the entire temperature range.Eventually,a peak zT of∼0.75 at 773 K and an excellent average zT of∼0.41 over 300−773 K are obtained in Mg_(2.82)Ag_(0.03)Cd_(0.5)Sb_(2),which are∼240%and∼490%higher than those of pristine Mg_(3.4)Sb_(2),respectively.This study provides an effective pathway to synergistically improve the thermoelectric performance of p-type Mg_(3)Sb_(2)by codoping Cd and Ag,which is beneficial to the future applications of Mg_(3)Sb_(2)-based thermoelectric materials.
基金supported by the National High Technology Research and Development Program of China(Grant No.2013AA032205)the National Natural Science Foundation of China(Grant No.51272022)the Fundamental Research Funds for the Central Universities,China(Grant No.2012JBZ001)
文摘In this work, a simple method to modulate the crystal phase and morphology with a large amount of K＋ions codoping is proposed. The phase changes to the mixture of β-Na YF4 and β-KYF4 with increasing the content of K^＋ions to 80 mol%.When it exceeds 80 mol%, β-Na YF4 disappears gradually and β-KYF4 dominates with a poor crystalline. In addition, the morphology changes from nanosphere to nanoplate, and then to nanoprism, which indicates that a higher content of K^＋ions favors the growth rates along [0001] than the [10-10] of the nanocrystals. Additionally, the upconversion（UC） luminescence properties and the ratio of red/green（R/G） UC intensity of samples with different phases and morphologies are detected,which makes it possible to tune the UC fluorescence by varying the concentration of K^＋ions.
基金supported by the National Natural Science Foundation of China(No.51102047,51472050)State Key Laboratory of Photocatalysis on Energy and Environment Open Project
文摘In this paper we present a novel report on the upconversion luminescence performance of NaY0.92Yb0.05Er0.03F4 enhanced by Zr^4＋ codoping. The luminescence intensity of the tridoped hexagonal NaYF_4 synthesized by a hydrothermal method increased to the maximum, about seven times of the non-Zr^4＋ sample when the Zr^4＋ codoping concentration rose to 6 mol%, while the luminescence lifetime was also prolonged by Zr^4＋ codoping. To explore the relationships between the microstructure and upconversion properties, X-ray powder diffraction, field emission scanning electron microscope, electron energy-dispersive spectroscopy and upconversion emission spectroscopy were employed. From these characterizations, we found that the codoping of Zr^4＋ could modulate the crystal microstructure of NaYF_4 for higher upconversion luminescence intensity and longer lifetime. This study may be helpful for the design and synthesis of high-performance upconversion materials.
基金Supported by the National Natural Science Foundation of China under Grant Nos.11347199,51402244,and 11547311the Specialized Research Fund for Doctoral Program of Higher Education of China under Grant No.20130184120028+2 种基金the Fundamental Research Fund for the Central UniversitiesChina under Grant Nos.2682014CX084,2682014ZT30,and 2682014ZT31the fund of the State Key Laboratory of Solidification Processing in NWPU under Grant No.SKLSP201511
文摘The structural,electronic properties and formation energies of sulfur and alkaline earth codoped delafossite CuAlO_2 have been investigated using the first-principles density functional theory calculations.Our results reveal that the volume of codoping systems increases with the increasing atomic radius of metal atoms.The formation energies under different growth conditions have been calculated,showing that the codoping systems are formed easily under O-rich growth conditions.Electronic band structures and density of states have been obtained.The decreased bandgaps,enhanced covalence and appearance of electron acceptors after codoping are all good for p-type conductivity.
基金This work was supported by the National Natural Science Foundation of China （ No.：60671010, 20775045 ） and Natural Science Foundation of Shandong Province （Y2006B29）. The authors wish to thank Prof. D.R. Chen and Mr. H.F. Shao for the help in measurements of XRD and XPS, respectively.
文摘本文基于密度泛函理论(DFT)的GGA+U方法,应用Materials Studio 5.0软件包中的CASTEP程序模拟计算了Al掺杂锐钛矿型TiO2和N-Al共掺杂锐钛矿型TiO2的电子结构。计算结果表明:Al掺杂和N-Al共掺杂均能够降低TiO2的带隙值。Al掺杂是由于Al的3s和3p态使导带底端下移而导致TiO2的带隙变窄;而N-Al共掺杂由于在体系中引入了N2p态,使导带底端向能量更低的方向移动,比Al单独掺杂时具有更低的带隙值。该研究结果很好地解释了Al掺杂以及N-Al共掺杂诱使TiO2的导带底端下移,禁带宽度减小,导致光谱响应范围红移的内在原因。
