微量掺杂Mn改性Ni/ZSM-5用于等离子催化甲烷部分重整制氢

使用微量的Mn元素对浸渍法制备的Ni/ZSM-5催化剂进行了掺杂改性,并将其应用于低温等离子体催化甲烷重整制氢的反应中。研究结果表明,掺杂后的双金属催化剂可以有效提升甲烷转化率。同时利用XRD、EDS和H_(2)-TPR等技术手段对催化剂进行了表征,表征结果表明,催化剂改性后金属分散度得到改善、氧化还原能力提升。活性评价证实了改性催化剂在介质阻挡放电等离子中的制氢活性得到增强。

Effects of Ni doping contents on photocatalytic activity of B-BiVO_4 synthesized through sol-gel and impregnation two-step method

To enhance the photocatalytic activity of B-BiVO4,Ni-doped B?BiVO4photocatalyst(Ni-B-BiVO4)was synthesized through sol-gel and impregnation method.The photocatalysts were characterized by XPS,XRD,SEM,EDS,BET and UV-Vis DRS techniques.The results showed that single or double doping did not change the crystalline structure and morphology,but the particle size decreased with Ni doping.The band gap energy absorption edge of Ni-B-BiVO4shifted to a longer wavelength compared with undoped,B or Ni single doped BiVO4.More V4+and surface hydroxyl oxygen were observed in BiVO4after Ni-B co-doping.When the optimal mass fraction of Ni is0.30%,the degradation rate of MO in50min is95%for0.3Ni-B-BiVO4sample which also can effectively degrade methyl blue(MB),acid orange(AOII)II and rhodamine B(RhB).The enhanced photocatalytic activity is attributed to the synergistic effects of B and Ni doping.

Structural Analysis and Magnetic Properties of Gd-Doped Li-Ni Ferrites Prepared Using Rheological Phase Reaction Method

A series of Gd-doped Li-Ni ferrites with the formula of LiNi0.5GdxFe2-xO4 where x = 0.00 - 0.08 in steps of 0.02, were prepared by thermolysis of oxalate precursors obtained by rheological phase reaction. The structure, morphology, and the magnetic properties of the samples were characterized by powder X-ray diffraction （XRD）, atomic force microscopy （AFM） and a vibrating sample magnetometer （VSM）. A single spinel phase was obtained in the range of x = 0.00 - 0.04. The lattice parameters of the Gd-doped samples were larger than that of pure Li-Ni ferrite, and increased in the range of 0.00 ≤ x ≤ 0.04, then decreased up to x = 0.08, because of the formation of the secondary phase （Gd- FeO3）. All samples were spheric particles with an average size of about 100 nm, but agglomerated to some extent. The hysteresis loops indicated that the saturation magnetization decreased gradually with increasing Gd content, while the variation of coercivity was related to the microstructure of the Gd-doped samples.

Efficient splitting of alcohols into hydrogen and C–C coupled products over ultrathin Ni‐doped ZnIn_(2)S_(4) nanosheet photocatalyst

Integrating selective organic synthesis with hydrogen(H_(2))evolution in one photocatalytic redox reaction system sheds light on the underlying approach for concurrent employment of photogenerated electrons and holes towards efficient production of solar fuels and chemicals.In this work,a facile one‐pot oil bath method has been proposed to fabricate a noble metal‐free ultrathin Ni‐doped ZnIn_(2)S_(4)(ZIS/Ni)composite nanosheet for effective solar‐driven selective dehydrocoupling of benzyl alcohol into value‐added C–C coupled hydrobenzoin and H_(2) fuel,which exhibits higher performance than pure ZIS nanosheet.The remarkably improved photoredox activity of ZIS/Ni is mainly attributed to the optimized electron structure featuring narrower band gap and suitable energy band position,which facilitates the ability of light harvesting and photoexcited charge carrier separation and transfer.Furthermore,it has been demonstrated that it is feasible to employ ZIS/Ni for various aromatic alcohols dehydrocoupling to the corresponding C–C coupled products.It is expected that this work can stimulate further interest on the establishment of innovative photocatalytic redox platform coupling clean solar fuels synthesis and selective organic conversion in a sustainable manner.

Anomalous metastable hcp Ni nanocatalyst induced by non-metal N doping enables promoted ammonia borane dehydrogenation

Developing high-performing non-noble transition metal catalysts for H_(2) evolution from chemical hydrogen storage materials is of great significance for the hydrogen economy system, yet challenging. Herein,we present for the first time that anomalous metastable hexagonal close-packed Ni nanoparticles induced by heteroatom N doping encapsulated in carbon(N-hcp-Ni/C) can exhibit admirable catalytic performance for ammonia borane(AB) dehydrogenation, prominently outperforming conventional fcc Ni counterpart with similar morphology and favorably presenting the state-of-the-art level.Comprehensive experimental and theoretical studies unravel that unusual hcp phase engineering of Ni together with N doping could induce charge redistribution and modulate electronic structure, thereby facilitating H_(2)O adsorption and expediting H_(2)O dissociation(rate-determining step). As a result, AB dehydrogenation can be substantially boosted with the assistance of N-hcp-Ni/C. Our proposed strategy highlights that unconventional crystal phase engineering coupled with non-metal heteroatom doping is a promising avenue to construct advanced transition metal catalysts for future renewable energy technologies.

Effects of temperature and Nickel content on magnetic properties of Ni-doped ZnO

Magnetic properties of diluted magnetic semiconductors (DMSs), Ni-doped ZnO materials, prepared by sol-gel method were investigated by measuring magnetization as functions of magnetic field. The Ni content affects the magnetic properties at low sintered temperature but it has few effects on the magnetic properties at high sintered temperature. The sintered temperature has great effects on the magnetic properties of Ni/ZnO at high original mole ratio of Ni/Zn while it has slight effects on the magnetic properties of Ni/ZnO at low original mole ratio of Ni/Zn whatever low or high sintered temperature.

Metal-organic framework-derived Ni doped Co_(3)S_(4) hierarchical nanosheets as a monolithic electrocatalyst for highly efficient hydrogen evolution reaction in alkaline solution

Hierarchical nanostructure construction and electronic structure engineering are commonly employed to increase the electrocatalytic activity of HER electrocatalysts.Herein,Ni doped Co_(3)S_(4) hierarchical nanosheets on Ti mesh(Ni doped Co_(3)S_(4) HNS/TM)were successfully prepared by using metal organic framework(MOF)as precursor which was synthesized under ambient condition.Characterization results confirmed this structure and Ni incorporation into Co_(3)S_(4) lattice as well as the modified electronic structure of Co_(3)S_(4) by Ni doping.Alkaline HER performance showed that Ni doped Co_(3)S_(4) HNS/TM presented outstanding HER activity with 173 m V overpotential at-10 m A·cm^(-2),surpassing most of metal sulfide-based electrocatalysts.The hierarchical structure,superior electrical conductivity and electronic structure modulation contributed to the accelerated water dissociation and enhanced intrinsic activity.This work provides a new avenue for synthesizing hierarchical nanostructure and simultaneously tuning the electronic structure to promote HER performance,which has potential application in designing highly efficient and cost-effective HER nanostructured electrocatalyst.

Electronic Structures and Chemical Bonds of Cobaltite and Ni-Doped

The relation among electronic structure, chemical bond and thermoelectric property of Ca3 Co2 O6 and Ni-doped was studied by density function theory and discrete variation method（DFT-DVM）. The results indicate that the highest valence band（ HVB ）attd the lowest conduction band（ LCB ） are mainly attribuled to Co3d, Ni3d and O2p atomic orbitals. The property of a semiconductor is shown from the gap between HVB and LCB. The gap of Ni-doped one is less than that of Ca3 Co2 O6. The non-metal bond or ceramic characteristic of Ni-doped one is weaker than that of Ca3 Co2 O6, but the metal characteristics of Ni-doped one are stronger than those of Ca3 Co2 O6. The thermoelectric property should be improved by adding Ni element into the system of Ca3 Co2 O6 .

Iron-doped Ag/Ni_(2)(CO_(3))(OH)_(2)hierarchical microtubes for highly efficient water oxidation

Doping of foreign atoms and construction of unique structures are considered as effective approaches to design high-activity and strongdurability electrocatalysts.Herein,we report Fe-doped nickel hydroxide carbonate hierarchical microtubes with Ag nanoparticles(denoted Ag/NiFeHC HMTs)through hydrolysis precipitation process.Experimental tests and density functional theory calculations reveal that Fe doping can tune the electron configuration to enhance the conductivity,markedly improve the electrochemical surface area to expose more active sites,and act as reactive centers to lower the free energy of the rate determination step.In addition,the unique hierarchical structure can also offer active sites and excellent cycling stability.Benefitting from these advantages,the as-obtained Ag/NiFeHC HMTs show excellent oxygen evolution reaction activity,with an overpotential of 208 mV at 10 mA cm^(−2)in 1.0M KOH.Also,it could achieve long-term stability at a current density of 20 mA cm^(−2)for 24 h.

Doping Induced Gap Anisotropy in Iron-Based Superconductors:a Point-Contact Andreev Reflection Study of BaFe2-xNixAs2 Single Crystals

We report a systematic investigation on c-axis point-contact Andreev reflection （PCAR） in BaFe2-xNixAs2 superconducting single crystals from underdoped to overdoped regions （0.075≤ x ≤0.15）. At low temperatures, an in-gap sharp peak at low-bias voltage is observed in PCAR for overdoped samples, in contrast to the case of underdoped junctions, in which an in-gap plateau is observed. The variety of the conductance spectra with doping can be well described by using a generalized Blonder-Tinkham-Klapwijk formalism with an angle-dependent gap. This gap shows a clear crossover from a nodeless in the underdoped side to a nodal feature in the overdoped region. This result provides evidence of the doping-induced evolution of the superconducting order parameter when the inter-pocket and intra-pocket scattering are tuned through doping, as expected in the s± scenario.

Structure, photocatalytic and antibacterial activity study of Meso porous Ni and S co-doped TiO2 nano material under visible light irradiation

Undoped and Ni–S co-doped mesoporous TiO2 nano materials were synthesized by using sol–gel method.The characteristic features of as prepared catalyst samples were investigated using various advanced spectroscopic and analytical techniques.The characterization results of the samples revealed that all the samples exhibited anatase phase(XRD),decreasing band gap(2.68 eV)(UV–Vis-DRS),small particle size(9.2 nm)(TEM),high surface area(142.156 m^2·g^-1)(BET),particles with spherical shape and smooth morphology(SEM);there is a frequency shift observed for co-doped sample(FT-IR)and the elemental composition electronic states and position of the doped elements(Ni and S)in the TiO2 lattice analyzed by XPS and EDX.These results supported the photocatalytic degradation of Bismarck Brown Red(BBR)achieved with in 110 min and also exhibited the antibacterial activity on Staphylococcus aureus(MTCC-3160),Pseudomonas fluorescence(MTCC-1688)under visible light irradiation.

The Impact of Nickel Source/Doping Elements/Buffer on the Structure of Ni(OH)_2

The nano-nickel hydroxide samples were prepared by means of ultrasonic-assisted precipitation and the impact of source/doping element/buffer on the structure of Ni（OH）： was studied. The results of XRD, IR and TEM testing clearly revealed that larger anionic radius of the nickel sources or the buffer solution was conducive to the formation of α-Ni（OH）2. The proportion of α-Ni（OH）： samples doped with two elements was larger than that doped with single element. Additionally, speciation, valence as well as the radius of doping ions can directly affect the phase of Ni（OH）2.

Co掺杂富镍正极材料LiNi_(0.9)Mn_(0.1)O_(2)的制备及其性能

采用共沉淀法、结合两段式煅烧工艺制备富镍正极材料LiNi_(0.9)Mn_(0.1)O_(2),并探究最佳终烧温度以及最优Co掺杂量。结果表明:最佳终烧温度为740℃,最优Co掺杂量为10%(摩尔分数);此时制备的正极材料LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)不仅保持了原有层状结构,而且层状结构更加有序、Li^(+)/Ni^(2+)混排程度最低;采用该正极材料装配的电池电化学性能最优异,在0.1C电流密度下,首次放电比容量为250.92 mA·h/g,100次循环后容量保持率为91.82%;在5C大倍率电流密度下,放电比容量可达200.55 mA·h/g。Co掺杂可稳定富镍正极材料的层状结构,抑制Li^(+)/Ni^(2+)混排,提高富镍正极材料的综合电化学性能。

Ni doping effects in YBa_2Fe_3O_(8+w)

By doping Ni into YBa2Fe308＋w （YBFO） system, we obtained the phase YBa2Fe3-xNixO8＋w （YBFNO, x=0, 0.05, 0.10, 0.15, 0.30, 0.50, 1.00）. This paper discusses the changes in crystal structural, resistivity and magnetoresistivity （MR） of YBFO samples due to the incorporation of transition metal Ni. The results show that Ni substitution for partial Fe in YBFO does not substantially transform the structure of parent phase, but results in tiny changes in the lat- tice parameters. The YBFO crystal with Ni doped is semiconducting.

Effect of Ni-doping on electrochemical capacitance of MnO_2 electrode materials

Mn/Ni composite oxides as active electrode materials for supercapacitors were prepared by solid-state reaction through the reduction of KMnO4 with manganese acetate and nickel acetate at low temperature. The products were characterized by X-ray diffractometry(XRD) and transmission electron microscopy(TEM). The electrochemical characterizations were performed by cyclic voltammetry (CV) and constant current charge-discharge in a three-electrode system. The effects of different potential windows, scan rates, and cycle numbers on the capacitance behavior of Mn0.8Ni0.2Ox composite oxide were also investigated. The results show that the composite oxides are of nano-size and amorphous structure. With increasing the molar ratio of Ni, the specific capacitance goes through a maximum at molar fraction of Ni of 20%. The specific capacitance of Mn0.8Ni0.2Ox composite oxide is 194.5 F/g at constant current discharge of 5 mA.

Tuning Li/Ni mixing by reactive coating to boost the stability of cobalt-free Ni-rich cathode

Cobalt-free cathode materials are attractive for their high capacity and low cost,yet they still encounter issues with structural and surface instability.AlPO_(4),in particular,has garnered attention as an effective stabilizer for bulk and surface.However,the impact of interfacial reactions and elemental interdiffusion between AlPO_(4) and LiNi_(0.95)Mn_(0.05)O_(2) upon sintering on the bulk and surface remains elusive.In this study,we demonstrate that during the heat treatment process,AlPO_(4) decomposes,resulting in Al doping into the bulk of the cathode through elemental interdiffusion.Simultaneously,PO_(4)^(3-)reacts with the surface Li of material to form a Li_3PO_(4) coating,inducing lithium deficiency,thereby increasing Li/Ni mixing.The suitable Li/Ni mixing,previously overlooked in AlPO_(4) modification,plays a pivotal role in stabilizing the bulk and surface,exceeding the synergy of Al doping and Li_3PO_(4) coating.The presence of Ni^(2+)ions in the lithium layers contributes to the stabilization of the delithiated structure via a structural pillar effect.Moreover,suitable Li/Ni mixing can stabilize the lattice oxygen and electrode-electrolyte interface by increasing oxygen removal energy and reducing the overlap between the Ni^(3+/4+)e_g and O^(2-)2p orbitals.These findings offer new perspectives for the design of stable cobalt-free cathode materials.

Anion-cation dual doping: An effective electronic modulation strategy of Ni2P for high-performance oxygen evolution

Developing of high-performance and low-cost electrocatalysts is of great significance to reduce the overpotential and accelerated the reaction rate of oxygen evolution in water splitting and related energy conversion applications.Herein,Fe,O-dual doped Ni2P(Fe,O-Ni2P)nanoarray is successfully synthesized on carbon cloth demonstrating enhanced electrocatalytic activity and stability for oxygen evolution reaction(OER)under alkaline media.The as-synthesized Fe,O-Ni2P nanoarray exhibits obviously improved OER performance with a low overpotential of 210 mV at 10 mA cm^-2 current density and a Tafel slope of48 mV dec^-1,as well as long-term durability.The strong coupling interaction induced changes in electronic structure lead to relatively higher oxidation state and stronger oxidation ability of the Fe,O-Ni2P nanoarray,together with the high electrochemical surface area and good conductivity contribute to the superior OER performance.This work highlights the anion-cation dual doping strategy may be an effective method for fabrication of catalysts relating to energy conversion applications.

Modulating the CO methanation activity of Ni catalyst by nitrogen doped carbon

Nitrogen doping has been proved to be an effective way to modify the properties of graphene and other carbon materials. Herein, we explore a composite with nitrogen doped carbon overlayers wrapping Si C substrate as a support for Ni（Ni/CN-Si C） and evaluate its effects on the methanation activity. The results show that both the activity and stability of Ni are enhanced. Characterization with STEM, XRD, XPS, Raman and H2-TPR indicates that nitrogen doping generates more defects in the carbon overlayers, which benefit the dispersion of Ni. Furthermore, the reduction of Ni is facilitated.

Ni元素对Zn-22Al药芯钎料用于Cu/Al钎焊接头组织和力学性能的影响

目的:研究Ni元素对Zn-Al药芯焊丝熔化特性、铺展性能的影响。方法:在钎剂中添加一定比例的Ni粉,在钎焊过程中形成Cu/Al接头的Ni合金化,分析不同含量Ni元素添加对Zn-22Al钎料以及Cu/Al异种合金钎焊接头的性能及显微组织的影响。结果:Ni粉添加可使Zn-22Al钎料在Al板上的铺展性能得到提升,当添加量质量分数为5%时钎料铺展性能提升26.75%;当添加量质量分数为7%时,用于Cu/Al钎焊的接头抗拉强度相较于未添加Ni粉焊接接头强度提升61.79%。结论:Ni粉添加可有效改善Zn-22Al焊缝的显微组织,体现为主晶相的细化,富Zn边界相的减少,促进主晶团之间形成层片状共析组织,以及减小了Cu侧生成的铜铝金属间化合物脆性相的厚度。

重掺杂p型SiC晶片Ni/Al欧姆接触特性

系统研究了Al和Ni/Al两种金属体系在重掺杂p型SiC晶片上的欧姆接触特性和电学性质。利用X射线衍射、扫描电子显微镜和综合物性测量系统对这两种电极表面的微观结构和样品的电学性质进行了表征。结果表明:在真空环境下经过800℃退火后Al电极可呈现出欧姆接触行为,其比接触电阻率为1.98×10^(-3)Ω·cm^(2),退火处理后Al电极与SiC在接触界面形成化合物Al_(4)C_(3),有助于提高接触界面稳定性。在Ni/Al复合体系中,当Ni金属层厚度为50 nm时,其比接触电阻率显著降低至4.013×10^(-4)Ω·cm^(2)。退火后Ni与SiC在接触界面生成的Ni_(2)Si有利于欧姆接触的形成和降低比接触电阻率。研究结果可为开发液相法生长的p型SiC晶片电子器件提供参考。