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| 1 | In situ construction of porous hierarchical(Ni3-xFex)FeN/Ni heterojunctions toward efficient electrocatalytic oxygen evolution显示文摘As a choke point in water electrolysis,the oxygen evolution reaction(OER)suffers from the severe electrode polarization and large overpotential.Herein,the porous hierarchical hetero-(Nis Fe)FeN/Ni catalysts are in situ constructed for the eficient electrocatalytic OER.X-ray absorption fine structure characterizations reveal the strong Ni-Fe bimetallic interaction in(Niz Fex)FeN/Ni.Theoretical study indicates the heterojunction and bimetallic interaction decrease the free-energy change for the rate-limiting step of the OER and the overpotential thereof.In addition,the high conductivity and porous hierarchical morphology favor the electron transfer,electrolyte access and O2 release.Consequently,the optimized catalyst achieves a low overpotential of 223 mV at 10 mA.cm^-2,a small Tafel slope of 68 mV:dec^-1,and a high stability.The excellent performance of the optimized catalyst is also demonstrated by the overall water electrolysis with a low working voltage and high Faradaic efficiency.Moreover,the correlation between the structure and performance is well established by the experimental characterizations and theoretical calculations,which confirms the origin of the OER activity from the surface metal oxyhydroxide in situ generated upon applying the current.This study suggests a promising approach to the advanced OER electrocatalysts for practical applications by constructing the porous hierarchical metal-compound/metal heterojunctions. | Minglei Yan Kun Mao Peixin Cui Chi Chen Jie Zhao Xizhang Wang Lijun Yang Hui Yang Qiang Wu Zheng Hu | 2020 | Nano Research2020，13，2： | 8 |
| 2 | Lead-free thermochromic perovskites with tunable transition temperatures for smart window applications显示文摘The structural flexibility of hybrid perovskite materials allows for phase transition and consequently thermochromic properties.Here we investigate the thermochromic performance in a series of copper-based layered perovskites with organic cations having different alky chain lengths. Their transition temperature is found to be dependent on the organic cations due to molecular motion and hydrogen bond interaction, providing possibilities to prepare thermochromic semiconductors near room temperature for smart window applications. | Jingwen Li Xiaolong Liu Peixin Cui Junmeng Li Tao Ye Xi Wang Chuang Zhang Yong Sheng Zhao | 2019 | Science China Chemistry2019，62，9： | 6 |
| 3 | Discriminating characters of ore-forming intrusions in the super-large Chalukou porphyry Mo deposit,NE China显示文摘The Chalukou porphyry Mo deposit, located in the Great Hinggan Range, is the largest Mo deposit in northeast China, although the age and genesis of the associated magmatic intrusions remain debated.Here we report zircon U-Pb ages and trace elements, whole rock geochemistry and Sre Nd isotope data with a view to understand the relationship between the magmatism and molybdenum mineralization.Zircon U-Pb analysis yield an age of 475 Ma for rhyolite in the older strata, 168 Ma for the premineralization monzogranite, and 154 Ma for the syn-mineralization granite porphyry. The granite porphyry and quartz porphyry are considered as the ore-forming intrusions. These rocks are peraluminous, alkali-calcic, and belong to high-K to shoshonitic series with a strong depletion of Eu. They also display characteristics of I-type granites. The rocks exhibit wide variations of(87 Sr/86 Sr)iin the range of 0.705426 -0.707363, and ε_(Nd)(t) of -3.7 to 0.93. Zircon REE distribution patterns show characteristics between crust and the mantle, implying magma genesis through crust-mantle interaction. The Fe_2O_3/FeO values(average 1) for the whole rock and EuN/Eu*Nvalues(average 0.45), Ce^(4+)/Ce^(3+) values(average 301)for zircon grains from the granite porphyry are higher than those from other lithologies. These features suggest that the ore-forming intrusions(syn-mineralization porphyry) had higher oxygen fugacity conditions than those of the pre-mineralization and post-mineralization rocks. The Chalukou Mo deposit formed in relation to the southward subduction of the Mongol-Okhotsk Ocean. Our study suggests that the subduction-related setting, crust-mantle interaction, and the large-scale magmatic intrusion were favorable factors to generate the super-large Mo deposits in this area. | Peixin Duan Cui Liu Xuanxue Mo Jinfu Deng Jinhua Qin Yu Zhang Shipan Tian | 2018 | Geoscience Frontiers2018，9，5： | 3 |
| 4 | Jahn-Teller distortion assisted interstitial nitrogen engineering:Enhanced oxygen dehydrogenation activity of N-doped Mn_(x)Co_(3-x)O_(4) hierarchical micro-nano particles显示文摘Rational design of earth-abundant transition metal oxides catalysts is highly desirable for developing sustainable chemical processes.Herein,we demonstrate a prospective interstitial nitrogen engineering for fabricating oxygen vacancies(OVs)-rich nitrogen-doped-Mn_(x)Co_(3-x)O_(4)(N-Mn_(x)Co_(3-x)O_(4))oxide catalyst,in which the ratio of OVs concentration of N-Mn_(x)Co_(3-x)O_(4)to Mn species is as high as 1:1,according to the characterizations of X-ray absorption(XAS)and X-ray photoelectron(XPS)spectroscopies.The promising strategy of interstitial nitrogen engineering through lattice distortion caused by the Jahn-Teller effect can significantly increase the amount of interstitial nitrogen.The resulting catalyst enables an additive-free aerobic dehydrogenation coupling of aromatic amine to afford azo compounds with>99%yield and>99%selectivity at 60☆.We observed the superb catalytic activity is promoted by the enhanced oxygen mobility in OVs,which were created by the interstitial nitrogen in the catalyst matrix.The presence of interstitial nitrogen in transition metal oxides in this study shows how the manipulation of catalyst matrix can increase the OV sites to promote aerobic oxidation reaction. | Yangxin Jin Fengfeng Li Peixin Cui Yun Yang Qingping Ke Minh Ngoc Ha Wangcheng Zhan Fei Ruan Chao Wan Zhao Lei Van Noi Nguyen Wei Chen Jun Tang | 2021 | Nano Research2021，14，8： | 1 |
| 5 | Sulfur-linked carbonyl polymer as a robust organic cathode for rapid and durable aluminum batteries显示文摘Rechargeable aluminum batteries are believed as a promising next-generation energy-storage system due to abundant low-cost Al sources and high volumetric specific capacity.The Al-storage cathodes,however,are plagued by strong electrostatic interaction between host materials and carrier ions,leading to large overpotential and undesired cycling stability as well as sluggish ion diffusion kinetics.Herein,sulfur-linked carbonyl polymer based on perylene-3,4,9,10-tetracarboxylic dianhydride(PTCDA) as the cathode materials for ABs is proposed,which demonstrates a small voltage polarization(135 mV),a reversible capacity of 110 mAh g^(-1) at 100 mA g^(-1) even after 1200 cycles,and rapid Al-storage kinetics.Compared with PTCDA,the sulfide polymer possesses higher working voltage because of its lower LUMO energy level according to theoretical calculation.The ordered carbonyl active sites in sulfide polymer contribute to the maximized material utilization and rapid ion coordination and dissociation,resulting in superior rate capability.Besides,the bridged thioether bonds endow the polysulfide with robust and flexible structure,which inhibits the dissolution of active materials and improves cycling stability.This work implies the importance of ordered arrangement of redox active moieties for organic electrode,which provides the theoretical direction for the structural design of organic materials applied in multivalent-ion batteries. | Liang Fang Limin Zhou Lianmeng Cui Peixin Jiao Qinyou An Kai Zhang | 2021 | Journal of Energy Chemistry2021，30，12： | 1 |
| 6 | Dynamic evolution of nitrogen and oxygen dual-coordinated single atomic copper catalyst during partial oxidation of benzene to phenol显示文摘Single atom catalysts(SACs)with metal_(1)-N_(x)sites have shown promising activity and selectivity in direct catalytic oxidation of benzene to phenol.The reaction pathway is considered to be involving two steps,including a H_(2)O_(2)molecule dissociated on the metal single site to form the(metal_(1)-N_(x))=O active site,and followed by the dissociation of another H_(2)O_(2)on the other side of metal atom to form O=(metal_(1)-N_(x))=O intermediate center,which is active for the adsorption of benzene molecule via the formation of a C-O bond to form phenol.In this manuscript,we report a Cu SAC with nitrogen and oxygen dual-coordination(Cu1-N3O1 moiety)that doesn’t need the first H_(2)O_(2)activation process,as verified by both experimental and density function theory(DFT)calculations results.Compared with the counterpart nitrogen-coordinated Cu SAC(denoted as Cu1/NC),Cu SAC with nitrogen and oxygen dual-coordination(denoted as Cu1/NOC)exhibits 2.5 times higher turnover frequency(TOF)and 1.6 times higher utilization efficiency of H_(2)O_(2).Particularly,the coordination number(CN)of Cu atom in Cu1/NOC maintains four even after H_(2)O_(2)treatment and reaction.Combining DFT calculations,the dynamic evolution of single atomic Cu with nitrogen and oxygen dualcoordination in hydroxylation of benzene is proposed.These findings provide an efficient route to improve the catalytic performance through regulating the coordination environments of SACs and demonstrate a new reaction mechanism in hydroxylation of benzene to phenol reaction. | Weiming Chen Hongqiang Jin Feng He Peixin Cui Changyan Cao Weiguo Song | 2022 | Nano Research2022，15，4： | 1 |
| 7 | Revealing efficient catalytic performance of N-CuO_(x) for aerobic oxidative coupling of aliphatic alkynes:A Langmuir-Hinshelwood reaction mechanism显示文摘O_(x)idative couplings of aliphatic alkynes are crucial for the production of naturally occurring 1,3-diynes.Herein we report the novel approach for effective synthesis of unsaturated coordinated N doped copper oxides(N-CuO_(x))catalyst,and uncover that N-CuO_(x) catalyst as an additive-free and cost-effective heterogeneous catalyst has highly catalytic performance for directly oxidative coupling of aliphatic alkynes.The key to achieve efficient oxidative coupling of aliphatic alkynes is the synergistic effect of N species and uncoordinated O/Cu species caused by N dopants,which undergoes the Langmuir–Hinshelwood reaction mechanism.The N-CuO_(x) catalyst displays~89.1%yield for hexadeca-7,9-diyne under mild conditions and stable reusability(5 cycles),showing significant advances compared with the traditionally copper oxides.These findings highlight the heteroatom dopants that provide a new methodology for designing efficient copper catalysts in synthesis of naturally occurring 1,3-diynes. | Jun Tang Bowen Jiao Wei Chen Fei Ruan Fengfeng Li Peixin Cui Chao Wan Minh Ngoc Ha Van Noi Nguyen Qingping Ke | 2022 | Nano Research2022，15，7： | 0 |
| 8 | In-situ doping nickel single atoms in two-dimensional MXenes analogue support for room temperature NO_(2) sensing显示文摘MXenes are promising supports for anchoring metal single atoms due to their versatile composition,well-defined nanostructures,and suitable conductivity.However,metal single atoms are usually coordinated with surface terminal groups(-O,-OH,-Cl,etc.)of MXenes via conventional wet-impregnation,resulting in limited electronic structure modification.Through a NiCl2 molten salt etching method,we observed that Ni single atoms could be in-situ doped in the lattice of MXenes analogue TiC_(0.5)N_(0.5) support(denoted as Ni1/TiC0.5N0.5),resulting in much larger charge transfer from Ni atoms to adjacent Ti atoms,and thus increasing the electronic density of these Ti atoms.When used for NO_(2) sensing,Ni_(1)/TiC_(0.5)N_(0.5) exhibited excellent response sensitivity(ultra-low limit of detection~10 ppb),selectivity,and good stability at room temperature.This study provides an effective strategy for producing MXenes analogue supported metal single atoms for potential application in gas sensing. | Weiming Chen Peipei Li Jia Yu Peixin Cui Xiaohu Yu Weiguo Song Changyan Cao | 2022 | Nano Research2022，15，10： | 0 |
| 9 | Construction of hierarchical FeNi_(3)@(Fe,Ni)S_(2) core-shell heterojunctions for advanced oxygen evolution显示文摘The investigation of earth-abundant electrocatalysts for efficient water electrolysis is of central importance in renewable energy system, which is currently impeded by the large overpotential of oxygen evolution reaction (OER). NiFe sulfides show promising OER activity but are troubled by their low intrinsic conductivities. Herein, we demonstrate the construction of the porous core-shell heterojunctions of FeNi3@(Fe,Ni)S_(2) with tunable shell thickness via the reduction of hierarchical NiFe(OH)x nanosheets followed by a partial sulfidization. The conductive FeNi3 core provides the highway for electron transport, and the (Fe,Ni)S_(2) shell offers the exposed surface for in situ generation of S-doped NiFe-oxyhydroxides with high intrinsic OER activity, which is supported by the combined experimental and theoretical studies. In addition, the porous hierarchical morphology favors the electrolyte access and O_(2) liberation. Consequently, the optimized catalyst achieves an excellent OER performance with a low overpotential of 288 mV at 100 mA·cm^(−2), a small Tafel slope of 48 mV·dec^(−1), and a high OER durability for at least 1,200 h at 200 mA·cm^(−2). This study provides an effective way to explore the advanced earth-abundant OER electrocatalysts by constructing the heterojunctions between metal and corresponding metal-compounds via the convenient post treatment, such as nitridation and sulfidization. | Minglei Yan Zhiyang Zhao Peixin Cui Kun Mao Chi Chen Xizhang Wang Qiang Wu Hui Yang Lijun Yang Zheng Hu | 2021 | Nano Research2021，14，11： | 0 |
| 10 | Regulation of hydrogen evolution performance of titanium oxide-carbon composites at high current density with a Ti-O hybrid orbital显示文摘Rational design and controllable synthesis of practical electrodes with high sta bility and activity at high current density for a hydrogen evolution reaction(HER)are critical for renewable and sustainable energy conversion.However,high-performance TiO_(2)-based electrocatalysts for HER are quite limited,and the cat alytic active centers still remain elusive.Herein,a simple strategy is demonstrated for the synthesis of TiO_(2)-carbon composite(TiO_(2)/C)with high HER performance and stability.The remarkable HER performance of TiO_(2)/C can be ascribed to the doping of carbon atoms,which leads to stronger hybridization of Ti 3d and O 2p orbitals,thus substantially improving the electrocatalytic efficiency.This study elucidates that the hydrogen evolution activity of oxide electrocatalysts can be largely improved by regulating their electronic structures by doping carbon atoms and also provides an effective strategy for designing heterostructured electro catalysts with high catalytic activity and stability at high current density for HER. | Meichen Liu Zhiping Lei Qingping Ke Peixin Cui Jiancheng Wang Jingchong Yan Zhanku Li Hengfu Shui Shibiao Ren Zhicai Wang Ying Kong Shigang Kang | 2022 | Carbon Energy2022，4，3： | 0 |
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