APPLIED SURFACE SCIENCE
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2023
·
IF 6.7
Liming Dai,Chenchen Fang,Fanglei Yao,Xiaoyuan Zhang,Xuefeng Xu,Shangling Han,Jingyao Deng,Junwu Zhu,Jingwen Sun
In-situ generated hydroxides and oxyhydroxides have been gradually recognized as the real active sites of metal organic frameworks (MOFs) towards the oxygen evolution reaction (OER). Nevertheless, the fine phase evolution process is still less of concern and elusive. Herein, we successfully construct serious of Ni-MOFs with differing thickness ranging from 1 nm to 270 nm through a competitive coordination strategy. Utilizing the operando resonance spectroscopy, an accurate phase inversion behavior of the Ni-MOFs has been witnessed during the OER, and demonstrated as a thickness-dependent process. Ultrathin architecture is identified as a positive factor to promote the exchange between MOFs ligands and applied electrolyte during the electrochemical test. Hence, after removing most of the internal ligands, 2D MOFs favor to be transformed as β-NiOOH, which is more active than the generated γ-NiOOH in bulky system. The density function theory (DFT) calculation alongside with the in-situ electrochemistry tests further affirm the β/γ-NiOOH transformation behavior. This work offers a new understanding of the electrocatalytic mechanism from the view point of phase evolution in 2D MOFs.
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NEW JOURNAL OF CHEMISTRY
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2023
·Vol. 47
·期 15
·7305-7311
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IF 3.3
Jie Liu,Yu Chen,Yin Wang,Lu Liu,Qi Chen,Qingqing Shi,Luyi Huang,Xing Chen,Kun Xie
Cobalt phosphide has excellent electrical conductivity, metallic properties, and thermal stability. However, its application is limited due to the few active sites exposed in electrochemical reactions and poor structural stability. Herein, we adopt the strategies of material compounding and structural design to construct CoP@Ni(OH)2 bilayer nanosheets. The bilayer nanosheet structure can provide abundant transport paths for electrons and ions while also exposing more electroactive sites. In addition, the close contact and mutual support of the bilayer nanosheet structure can significantly alleviate material morphological collapse during charging/discharging processes, improving the cycle stability. The advantages of multiple components were combined in CoP@Ni(OH)2 to provide multiple valances for the faradaic redox reactions. The CoP@Ni(OH)2 manifested a specific capacity of 1697.8 C g−1 at 1 A g−1 and maintained a high rate capability of 35.0% even at 20 A g−1. Moreover, the electrode, had great cycling stability, retaining 83.9% of its capacity at 6 A g−1 after 7000 cycles. The asymmetric supercapacitor made of CoP@Ni(OH)2//activated carbon delivered 53.2 W h kg−1 at 800 W kg−1.
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
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2023
·Vol. 34
·期 7
·1-13
·
IF 2.8
Hu Qi,Teng Yuancheng,Zhao Xiaofeng,Zhou Fei,Arslanov Temirlan,Dai Bo
Zn 1− x Ni x ZrTa 2 O 8 ( x = 0.02, 0.04, 0.06, 0.08, 0.10, 0.12) microwave dielectric ceramics were synthesized by traditional solid-state method. The effect of introducing Ni–O bonds to replace part of Zn–O bonds on the ceramic lattice and microwave dielectric properties was systematically studied. An appropriate amount of Ni 2+ substitution improves the microscopic morphology of crystal, including the grain size, number of pores, number of grain boundaries, and the grain uniformity, giving rise to an increase in the compactness of ceramics and, thereby enhancing the microwave dielectric properties. The Raman analysis prove that the introduction of Ni 2+ is beneficial to enhance the vibrational peak intensity of the oxygen octahedron and effectively improve the Q × f value. However, the introduction of excessive Ni 2+ will lead to the decrease of lattice oxygen and the increase of adsorbed oxygen, and the crystal will become relatively active and unstable, and the microwave performance will decrease. In addition, the substitution of Ni 2+ can also effectively control the resonance temperature coefficient, which is beneficial to improve the τ f value. As a result, Zn 0.94 Ni 0.06 ZrTa 2 O 8 exhibits excellent microwave dielectric properties: ε r = 32.15, Q × f = 15,7500 GHz, τ f = − 33.1 ppm/°C, presenting as a potential candidate for low-loss microwave dielectric materials.
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CATALYSIS LETTERS
·
2023
·
IF 2.8
Zhao Liping,Wang Changzhen,Bai Juan,Wu Ruifang,Li Haitao,Zhao Yongxiang
2-Hydroxytetrahydrofuran (HTHF) is the main by-product of hydrogenation of 1,4-butynediol (BYD) to 1,4-butanediol (BDO) in industry, which is difficult to be effectively removed in the subsequent distillation process and seriously affects the product quality. Here, a series of silica-supported bimetallic Ni–Fe catalysts with different Fe/Ni weight ratios were prepared by using incipient wetness impregnation method and investigated the effect of Fe on the catalyst performance in the hydrogenation of HTHF to BDO. In comparison with monometallic Ni and Fe catalysts, bimetallic Ni–Fe catalysts exhibited better performance for HTHF hydrogenation due to the formation of Ni–Fe alloy phase identified by XRD, TEM, STEM-EDS, H 2 -TPR, NH 3 /H 2 -TPD, Pyridine FTIR and XPS, etc. A mechanism is proposed to explain the promoting effect of Fe, which can be assigned to the synergism between nickel sites with high ability to activate/overflow hydrogen and Fe-containing sites with strong oxophilicity for the activation of the O-C-O bond over the tetrahydrofuran ring. Graphical Abstract
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Inorganics
·
2023
·Vol. 11
·期 4
·170
·
IF 2.9
Zikang Lu,Rikai Liang,Yuqi Shao,Weiju Hao
Achieving high−efficiency and stable hydrogen evolution from water splitting is a great challenge. Herein, a facilely prepared two−dimenssional self−supported catalytic electrode with excellent stability is constructed for large−scale hydrogen production from alkaline simulated seawater. The bifunctional catalytic electrode is prepared by a fast and mild one−step of sodium borohydride etching on a nickel foam (NF) substrate without adding other additives (NF@NiBx−3h). The overpotential of the hydrogen/oxygen evolution reaction (HER/OER) in alkaline−simulated seawater at 10 mA cm−2is 96 mV and 261 mV. At 200 mA cm−2, the NF@NiBx−3h electrode shows good stability over 7 days throughout the water splitting process due to the corrosion resistance of the NF substrate, and strong adhesion between the Ni−B active material and the substrate. This work demonstrates a novel strategy for fabricating catalytic electrodes with high−performance, low cost and excellent stability.Keywords:mild and fast construction;chemical etching;HER;OER;industrial−grade water splitting
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SURFACE ENGINEERING
·
2023
·
IF 2.8
Hao Liu,Yuelan Di,Haidou Wang,Yuncai Zhao
Metal components in microelectromechanical systems are prone to failure and corrosion due to droplet adhesion in wet environments. Several multi-level structures on the micro-nano scale may induce effective superhydrophobicity to prevent such adhesion. This study proposes a hybrid manufacturing process to generate ‘frame-cone’ textures on the surfaces of metals by combining ultra-fast laser etching and electrodeposition. Periodically distributed frame recesses and pits were coated with nano-submicron Ni coatings with conical shapes, and the pit depth and cone height were controlled by tuning the laser scanning time and current density, respectively. The surface adhesion force was reduced to 22.8 μN, and the static contact angle was maintained at 156.7° using the hybrid process, while the adhesion forces of laser etched samples with the same depth were 164.7 μN. The multi-level ‘frame-cone’ structure stored more air and reduced the contact areas between the bottoms of the pits and droplets. The hybrid process of ultra-fast laser etching and electrodeposition aided in improving the superhydrophobicity, with less damage to the substrate.
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ChemSusChem
·
2019
·Vol. 12
·期 17
·3977-3987
·
IF 7.804
Qiying Liu,Haiyong Wang,Haosheng Xin,Chenguang Wang,Long Yan,Yingxiong Wang,Qi Zhang,Xinghua Zhang,Ying Xu,George W. Huber,Longlong Ma
Graphical Cellulose conversion into ethanol : Ethanol is obtained through one-pot cellulose hydrogenolysis over graphene-layers-encapsulated nickel catalysts with the aid of H 3 PO 4 in water. This work, for the first time, demonstrates a chemocatalytic approach for a high-yield production of ethanol from biomass using a non-noble metal catalyst. Ethanol is an important bulk chemical with diverse applications. Biomass-derived ethanol is traditionally produced by fermentation. Direct cellulose conversion to ethanol by chemocatalysis is particularly promising but remains a great challenge. Herein, a one-pot hydrogenolysis of cellulose into ethanol was developed by using graphene-layers-encapsulated nickel (Ni@C) catalysts with the aid of H 3 PO 4 in water. The cellulose was hydrolyzed into glucose, which was activated by forming cyclic di-ester bonds between the OH groups of H 3 PO 4 and glucose, promoting ethanol formation under the synergistic hydrogenation of Ni@C. A 69.1 % yield of ethanol (carbon mole basis) was obtained, which is comparable to the theoretical value achieved by glucose fermentation. An ethanol concentration of up to 8.9 wt % was obtained at an increased cellulose concentration. This work demonstrates a chemocatalytic approach for the high-yield production of ethanol from renewable cellulosic biomass at high concentration.
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Scientific Reports
·
2019
·Vol. 9
·期 1
·1-13
·
IF 4.011
Yuan Xiaoyu,Yin Chunyue,Zhang Yuanyuan,Chen Zengyue,Xu Yifan,Wang Jun
In this paper, a double hollow spherical shell composite modified with layered double hydroxide (C@Ni-Al LDH HSS) was fabricated for uranium(VI) (U(VI)) adsorption. Various batch experiments were carried out to investigate the influence of pH, concentration, time and coexistence ion on extraction. The results showed that the adsorption processes of U(VI) onto C@Ni-Al LDH HSS were spontaneous and endothermic and closely followed pseudo-second-order and Langmuir isotherm models. The equilibrium time and maximum adsorption capacity of C@Ni-Al LDH HSS was 360 min and 545.9 mg g −1 . FT-IR and XPS analyses proved that the adsorption behavior was primarily attributed to the strong interaction between oxygen-containing functional groups and U(VI). Moreover, the extraction of trace U(VI) (μg L −1 ) in artificial and natural seawater was also studied. The results showed that C@Ni-Al LDH HSS provided a promising application for the efficient extraction of U(VI) from seawater.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2019
·
IF 6.361
Fuqin Zheng,Ziwei Zhang,Dong Xiang,Ping Li,Cheng Du,Zhihua Zhuang,Xiaokun Li,Wei Chen
Electrochemical water-splitting is an ideal strategy to produce the promising substitutable energy source, hydrogen (H 2 ). However, the sluggish kinetics of electrochemical oxygen evolution reaction (OER) and the prohibitive cost, low reserves and easy oxidation of noble metal-based electrocatalysts force researchers to explore efficient and low-cost electrocatalysts . Bimetal nanostructred materials are proved to have enhanced OER catalytic performances. In this study, a series of bimetallic metal-organic frameworks (Fe/Ni-MOFs) are prepared by a solvothermal method . The prepared MOFs present abundant unsaturated metal active sites for OER. The optimized Fe/Ni bimetal-MOF has low overpotentials of 236 mV at 10 mA cm −2 and 284 mV at 100 mA cm −2 for OER. In addition, in comparison with most of the previously reported OER electrocatalysts, the present MOF shows a lower Tafel slope of 49 mV dec −1 . Besides, the MOF catalyst exhibits high electrochemical stability and the OER activity shows a negligible change after stability test for 15 h and 10,000 voltammetric cycles. Meanwhile, the Fe-doped Ni-MOFs show faster catalytic kinetics and higher conductivity than the monometallic Ni-MOF. This work paves a way to exploit bi- or multi-metallic MOFs with high conductivities and electrocatalytic performances for electrochemical energy conversion .
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ACS Applied Materials & Interfaces
·
2018
·
IF 8.097
Yan Xing,Jing Cheng,Mengfei Zhang,Meng Zhao,Liyan Ye,Wei Pan
Water-purifying materials are of vital importance for providing sanitary water, especially in epidemic and disaster areas and for wilderness survival. Here, we report a novel inorganic composite with a fast, reusable, and pleiotropic water purification ability. The composite of heterogeneous Ni–La2O3 nanofibers was developed using an easy, low-cost, and large-scale production process, i.e., an electrospinning technique. Because of the unique heterostructure formed by introducing nickel nanoparticles into the La2O3 host, the nanocomposite fibers can rapidly remove various detrimental micropollutants with absorption rate constants hundreds of times greater than those of inorganic materials and activated carbons. In addition, the nanocomposite can be recycled by a soft washing procedure at ambient temperature and demonstrates a much more stable performance than the state-of-the-art activated carbon materials. Furthermore, the nanofibers have an excellent germicidal effect against the high-risk human pathogen Escherichia coli. Our work introduces a promising inorganic absorbent suitable for purifying life-sustaining water supplies in emergency situations and alleviating worldwide water shortages.
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JOURNAL OF ALLOYS AND COMPOUNDS
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2019
·
IF 4.175
Chengbo Wei,Chuan Liu,Linna Gao,Yanfang Sun,Qingyun Liu,Xiao Zhang,Jinxue Guo
Integrating heterogeneous hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) electrocatalysts into compatible composite catalysts with specific interfaces and structures holds great promise for the development of efficient bifunctional catalysts for overall water splitting. Herein, heterogeneous MoS 2 -Ni(OH) 2 catalyst supported by Ni foam (MoS 2 @Ni(OH) 2 /NF) is developed, in which the Ni(OH) 2 nanorod array is grafted with MoS 2 nanosheets . The hierarchical 1D/2D structures benefit not only the exposure of catalytic site but also the facilitated charge transfer. The heterointerfaces allow the synergism of electric structure modulation for improved catalytic activity and kinetics towards HER, OER, and overall water splitting. MoS 2 @Ni(OH) 2 /NF achieves a current density of 10 mA cm −2 at low overpotentials of 134 and 233 mV for HER and OER in 1 M KOH, respectively. Moreover, a cell voltage as low as 1.46 V is obtained to afford 10 mA cm −2 in a tow-electrode electrolyzer using MoS 2 @Ni(OH) 2 /NF as bifunctional catalysts, assuring it superior to most of the reported noble-metal-free bifunctional electrocatalysts. Such heterogeneous design of composite catalyst should shed light on the exploration of functional materials for energy applications.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
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2018
·
IF 4.229
Changli Zhu,Shisheng Hou,Linxi Hou,Kui Xie
High temperature carbon dioxide electrolyzers are expected to play a key role on carbon-neutral energy cycle. Here we report a novel composite, namely perovskite SrFeO 3−δ with impregnated Ni nanoparticles , as an advanced cathode materials for solid oxide electrolysis cells (SOECs). The XRD , SEM and TEM together indicate that the homogeneously distributed Ni nanoparticles on SrFeO 3−δ substrate create sufficient and active triple-phase boundary (TPB) for electrochemical carbon dioxide splitting. Electrochemical measurements show that this tailored SrFeO 3−δ cathode demonstrates better performance, and then exhibits long-term stability after 100 h operation and 8 redox cycles.
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