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CHEMICAL ENGINEERING SCIENCE · 2022 · IF 4.889

Coke-resistant (Pt + Ni)/ZSM-5 catalyst for shape-selective alkylation of toluene with methanol to para-xylene

He Han,Anfeng Zhang,Limin Ren,Xiaowa Nie,Min Liu,Yi Liu,Chuan Shi,Hong Yang,Chunshan Song,Xinwen Guo

Shape-selective alkylation of toluene with methanol is one of the most attractive promising synthetic routes to para -xylene. To date, modified ZSM-5 zeolites are considered to be one of the best candidate catalysts for this reaction. Although the para -selectivity could be tuned to approaching 100% by modification of the zeolite and optimization of reaction conditions, at present, there is still a lack of effective means to inhibit the rapid deactivation of the catalysts due to coke formation. In this work, a coke-resistant (Pt + Ni)/ZSM-5 zeolite with excellent stability for shape-selective alkylation of toluene with methanol to para -xylene is developed. The pore structure and acid properties of the zeolite are effectively tuned to ensure high para -selectivity. Meanwhile, the co-existence of Pt and Ni species in this catalyst plays the critical role in inhibiting coke formation, as the two species concurrently impede the formation of olefins, the main coking precursors, via two distinctive mechanisms.

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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

Hydrothermal synthesis of MWCNT/Ni-Mn-S composite derived from bimetallic MOF for high-performance electrochemical energy storage

Yanrui Hao,Hao Guo,Fan Yang,Junye Zhang,Ning Wu,Mingyue Wang,Cuiliu Li,Wu Yang

Multi-walled carbon nanotube (MWCNT)/Ni-Mn-S composites are derived from MWCNT/Ni/Mn bimetallic metal-organic framework (MOF) for supercapacitor electrodes. Electroconductive MWCNT is introduced into Ni-Mn-S to form a three-dimensional interconnected structure due to the covalent interaction between Ni atoms and C atoms. During energy storage, MWCNT serves as miniature current collector to shorten pathway of electron collection and transmission. In addition, S 2- etching agent with Kirkendall effect makes edges and surfaces of the resulted sulfide structures rougher provide more active sites and improves electrochemical performance compared with precursors. By finely adjusting Ni/Mn molar ratio, the prepared MWCNT/Ni-Mn-S composite achieves excellent properties. As-prepared MWCNT/Ni-Mn-S(3:2) exhibits high specific capacitance of 1041 mAh g −1 at 1 A g −1 and good cyclic stability. The capacitance retention reaches 83.3% after 10,000 cycles. The assembled MWCNT/Ni-Mn-S(3:2)//AC hybrid supercapacitor (HSC) also shows high energy density of 25.33 Wh Kg −1 at power density of 829 W Kg −1 and outstanding cycling stability (93.3% after 20,000 cycles), which illustrates MWCNT/Ni-Mn-S(3:2) has important potential in supercapacitor.

CAS / MDL: 308068-56-6
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CHINESE JOURNAL OF CHEMICAL ENGINEERING · 2022 · IF 3.898

The superhydrophobic sponge decorated with Ni-Co double layered oxides with thiol modification for continuous oil/water separation

Xiaodong Yang,Na Yang,Ziqiang Gong,Feifei Peng,Bin Jiang,Yongli Sun,Luhong Zhang

In this paper, the superhydrophobic polyurethane sponge (SS-PU) was facilely fabricated by etching with Jones reagent to bind the nanoparticles of Ni-Co double layered oxides (LDOs) on the surface, and following modification with n -dodecyl mercaptan (DDT). This method provides a new strategy to fabricate superhydrophobic PU sponge with a water contact angle of 157° for absorbing oil with low cost and in large scale. It exhibits the strong absorption capacity and highly selective characteristic for various kinds of oils which can be recycled by simple squeezing. Besides, the as-prepared sponge can deal with the floating and underwater oils, indicating its application value in handling oil spills and domestic oily wastewater. The good self-cleaning ability shows the potential to clear the pollutants due to the ultra-low adhesion to water. Especially, the most important point is that the superhydrophobic sponge can continuously and effectively separate the oil/water mixture against the condition of turbulent disturbance by using our designed device system, which exhibit its good superhydrophobicity, strong stability. Furthermore, the SS-PU still maintained stable absorption performance after 150 cycle tests without losing capacity obviously, showing excellent durability in long-term operation and significant potential as an efficient absorbent in large-scale dispose of oily water.

CAS / MDL: 100-97-0
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CRYSTENGCOMM · 2022 ·Vol. 24 ·期 18 ·3369-3379 · IF 3.756

Increasing oxygen vacancies in CeO2 nanocrystals by Ni doping and reduced graphene oxide decoration towards electrocatalytic hydrogen evolution

Yang Xu,Xiaodong Hao,Xishuo Zhang,Tong Wang,Zhuangzhuang Hu,Yujiao Chen,Xinyi Feng,Wen Liu,Fangyuan Hao,Xingang Kong,Chaozheng He,Shufang Ma,Bingshe Xu

Oxygen vacancy (VO) engineering has proved to be an effective approach for improving the hydrogen evolution reaction (HER) performance of low-cost metal oxide electrocatalysts. Cerium dioxide (CeO2), an abundant rare-earth metal oxide, is famous for its easy formation of VO and high oxygen mobility, which is believed to be conducive to its application in electrocatalytic HER. Herein, this study reports a facile modification strategy using rGO as a conductive support for CeO2 nanocrystals and introducing the transition metal Ni as the active dopant, resulting in the construction of the Ni–rGO/CeO2 electrocatalyst. It is found that rGO decoration prevents the aggregation of CeO2 NCs and increases the VO concentration in the CeO2 nanocrystals as well, while the introduced Ni leads to further formation of VO and serves as the active site for the HER reaction. Thus, the Ni–rGO/CeO2 electrocatalyst shows relatively low overpotential, a low Tafel slope, and great stability for HER, which is attributed to the synergistic effect of rGO decoration and Ni doping. This kind of facile strategy is promising for the design of noble-metal-free and low-cost electrocatalysts by the functional modification of CeO2-based nanocatalysts.

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Nanomaterials · 2022 ·Vol. 12 ·期 19 ·3472 · IF 5.719

The Synergistic Effect of MoS2 and NiS on the Electrical Properties of Iron Anodes for Ni-Fe Batteries

Hongwei Tang,Mengyue Liu,Lingna Kong,Xiaoyan Wang,Yue Lei,Xige Li,Yan Hou,Kun Chang,Zhaorong Chang

In this paper, a series of Fe3O4/MoS2/NiS composite electrodes were synthesized by a simple coprecipitation method. The influence of different ratio additives (MoS2and NiS) on the performance of iron anodes for Ni-Fe batteries was systematically investigated. In this paper, the mixed alkaline solution of 6 mol/L NaOH and 0.6 mol/L LiOH was used as electrolyte, and sintered Ni(OH)2was used as counterelectrode. The experimental results show that the MoS2and NiS additives can effectively eliminate the passivation phenomena in iron electrodes, reduce the electrode polarization, and increase the reversibility capacity. As a result, the Fe3O4/MoS2/NiS composite electrodes exhibit a high specific capacity, good rate performance, and long cycling stability. Especially, the Fe3O4/MoS2(5%)/NiS (5%) electrode with a suitable ratio of additives can provide excellent electrochemical performance, with high discharge capacities of 657.9 mAh g−1, 639.8 mAh g−1, and 442.1 mAh g−1at 600 mA g−1, 1200 mA g−1, and 2400 mA g−1, respectively. This electrode also exhibits good cycling stability.Keywords:nickel-iron battery;iron anode;Fe3O4;sulfide additives

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Processes · 2022 ·Vol. 10 ·期 10 ·1970 · IF 3.352

Highly Selective Production of Valuable Aromatic Hydrocarbons/Phenols from Forestry and Agricultural Residues Using Ni/ZSM-5 Catalyst

Xuan Zhou,Hongling Pan,Shuixiang Xie,Guotao Li,Zhicai Du,Xiang Wang,Yan Luo

The aim of this research is to design and synthesize an efficient catalyst to enhance high value-added products, such as aromatic hydrocarbons and phenols, from the catalytic fast pyrolysis (CFP) of different types of forestry and agricultural residues. All three biomasses (rape straw, wheat straw, and bamboo powder) had no aromatic production via thermal pyrolysis alone; however, the aromatic selectivity and monocyclic aromatic selectivity were largely enhanced using ZSM-5, with suitable silica-alumina ratios and Ni loadings. Specifically, for rape straw, the optimum catalyst was 15 wt.% Ni/ZSM-5 (silica-aluminum ratios = 85), and the selectivity of aromatic hydrocarbons was achieved at 39%, of which 71% were monocyclic aromatic hydrocarbons. For wheat straw, the optimum catalyst was 10 wt.% Ni/ZSM-5 (silica-aluminum ratios = 18), and the selectivity of aromatic hydrocarbons was 67%, of which 55% were monocyclic aromatic hydrocarbons. For bamboo powder, the optimum catalyst was 10 wt.% Ni/ZSM-5 (silica-aluminum ratios = 18), and the selectivity of aromatic hydrocarbons was achieved at 21%, of which 80% were monocyclic aromatic hydrocarbons. Meanwhile, biomass types have significant effects on the pyrolyzed product distribution due to their different components. Cellulose and hemicellulose promoted the production of aromatic hydrocarbons, while lignin enhanced the production of phenols. The promotion of phenol by Ni was better and more efficient than that by the molecular sieve.Keywords:catalytic fast pyrolysis;forestry and agricultural residues;Ni/ZSM-5;aromatic hydrocarbons;phenols;Py-GC/MS

CAS / MDL: 13478-00-7
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ACS Applied Materials & Interfaces · 2022 · IF 10.383

Sol/Antisolvent Coating for High Initial Coulombic Efficiency and Ultra-stable Mechanical Integrity of Ni-Rich Cathode Materials

Xiaoqing Zhang,Jianwei Xiong,Fengzhen Chang,Zhuijun Xu,Zheng Wang,Philip Hall,Ya-Jun Cheng,Yonggao Xia

The Ni-rich cathode holds great promise for high energy density lithium-ion batteries because of its high capacity and operating voltage. However, crucial problems such as cation disorder, structural degradation, side reactions, and microcracks become serious with increasing nickel content. Herein, a novel and facile sol/antisolvent coating modification of Ni-rich layered oxide LiNi0.85Co0.1Mn0.05O2 (NCM) is developed where we use ethanol to disperse the nanosized LiBO2 to form the sol and adopt tetrahydrofuran (THF) as antisolvent to prepare the cluster of nanoparticles to be coated on the surface of NCM. The coating thickness can be tuned through the THF addition amount. The LiBO2 nanorod deposition is formed as well over the crack of the NCM cathode, likely acting as a patch to repair the original defect of the intrinsic crack. The uniform LiBO2 nanospherical particle coating together with LiBO2 nanorod wrapping provides a double protection against electrolytes. Compared with the raw material, LiBO2-coated LiNi0.85Co0.1Mn0.05O2 (LiBO2-coated NCM) exhibits a high initial Coulombic efficiency of 90.3% at 0.2 C between 2.8 and 4.3 V vs Li+/Li, a superior rate capability, enhanced fast charge property at 3 C, and restricted microcrack formation. This simple in-site modification and repairing technology guarantees a good mechanical integrity of the polycrystalline Ni-rich cathode.

CAS / MDL: 13453-69-5
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IONICS · 2022 ·Vol. 28 ·期 8 ·3945-3956 · IF 2.961

Co(OH)2-Ni(OH)xSy amorphous composite electrocatalysts prepared by electrodeposition method for efficient oxygen evolution reaction

Wei Xuedong,Chai Yudan,Chen Weifeng,Liu Nan,Qiao Shuangyan

In this paper, an amorphous composite electrocatalyst of Co(OH) 2 -Ni(OH) x S y was prepared by a simple and rapid electrochemical deposition method on nickel foam (NF). The electrochemical performance for oxygen evolution reaction (OER) was tested in 1 M KOH solution. The overpotential of Co(OH) 2 -Ni(OH) x S y (Co:Ni = 9:1) electrode was 423 mV at 50 mA cm −2 . The potential of the Co(OH) 2 -Ni(OH) x S y (Co:Ni = 9:1) sample remained essentially unchanged from the initial potential of 1.651 V after 12 h of stability test. In this catalyst, the strong synergistic effect between cobalt and nickel ions, the greatly increased amorphous defect sites and oxygen vacancies, and the abundant electrochemical specific surface area together lead to the increased electrocatalytic activity and high electrocatalyst stability. This amorphous CoNi-based composite electrocatalyst prepared by simple electrodeposition has certain significance for the preparation of hydrogen energy.

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FUEL · 2022 · IF 8.035

Boosting hydrogen production from steam reforming of glycerol via constructing moderate metal-support interaction in Ni@Al2O3 catalyst

Yunzhu Wang,Songshan Zhu,Jichang Lu,Jiangping Liu,Yi Zhao,Sufang He,Yuhui Zhao,Huihui Lu,Yongming Luo

In this manuscript, the relationship between metal-support interaction and the catalytic performance for hydrogen production from steam reforming of glycerol (GSR) over Ni-Al 2 O 3 based catalysts was studied. Pure core–shell structured Ni@Al 2 O 3 and supported Ni/Al 2 O 3 with a fixed medium-sized nickel particle were synthesized without the other additional components to eliminate the influence of other factors. And then the nickel-alumina interaction of Ni@Al 2 O 3 was tuned precisely and the regulatory mechanism of nickel-alumina interaction on catalytic activity was elaborated. The strong nickel-alumina interaction over Ni/Al 2 O 3 and Ni@Al 2 O 3 with high calcination temperature resulted in the formation of NiAl 2 O 4 , which was unfavorable to the reduction of nickel species to obtain the more active nickel. Consequently, the poor catalytic performance was caused. The moderate nickel-alumina interaction of Ni@Al 2 O 3 promoted the exposure of the maximum area of active nickel and obtained higher turnover frequency (TOF). Thus, Ni@Al 2 O 3 showed the high catalytic performance in GSR. Additionally, metal-support interaction affected the morphology and growth mechanism of coke deposition. For Ni@Al 2 O 3 with moderate nickel-alumina interaction, the formation of carbon deposition followed the ‘tip-growth’ pattern, and the filamentous coke was mainly formed on catalysts. Conversely, ‘base-growth’ pattern was followed on Ni/Al 2 O 3 with strong nickel-alumina interaction to form mainly encapsulated coke. The research findings of the regulatory role of interaction between nickel and alumina on catalytic performance will provide valuable guidelines for designing effective GSR catalysts.

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Nanomaterials · 2022 ·Vol. 12 ·期 17 ·2942 · IF 5.719

Insight into the Effect of Selenization Temperature for Highly Efficient Ni-Doped Cu2ZnSn(S,Se)4 Solar Cells

Fancong Zeng,Yingrui Sui,Meiling Ma,Na Zhao,Tianyue Wang,Zhanwu Wang,Lili Yang,Fengyou Wang,Huanan Li,Bin Yao

Cu2Ni0·05Zn0·95Sn(S,Se)4(CNZTSSe) films were synthesized on Mo-coated glass substrates by the simple sol–gel means combined with the selenization process, and CNZTSSe-based solar cells were successfully prepared. The effects of selenization temperature on the performance and the photoelectric conversion efficiency (PCE) of the solar cells were systematically studied. The results show that the crystallinity of films increases as the selenization temperature raises based on nickel (Ni) doping. When the selenization temperature reached 540 °C, CNZTSSe films with a large grain size and a smooth surface can be obtained. The Se doping level gradually increased, and Se occupied the S position in the lattice as the selenization temperature was increased so that the optical band gap (Eg) of the CNZTSSe film could be adjusted in the range of 1.14 to 1.06 eV. In addition, the Ni doping can inhibit the deep level defect of SnZnand the defect cluster [2CuZn+ SnZn]. It reduces the carrier recombination path. Finally, at the optimal selenization temperature of 540 °C, the open circuit voltage (Voc) of the prepared device reached 344 mV and the PCE reached 5.16%.Keywords:solar cell;selenidation temperature;CNZTSSe;sol gel

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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2022 · IF 9.965

Self-templated transformation of Co-ZIF-L into hierarchical porous CoS2/Co-Ni LDHs with improved electrochemical activities

Yuming Xie,Jingqiu Li,Mengjue Cao,Yi Feng,Jianfeng Yao

CoS 2 /Co-Ni layered double hydroxides (LDHs) with a rational tailored pore structure are developed by partial sulfurization of Co-ZIF-L and subsequent Ni 2+ etching for the transformation of zeolitic imidazolate frameworks (ZIFs) to layered double hydroxides . The as-synthesized CoS 2 /Co-Ni LDHs maintain the leaf-like structure and have rich hierarchical pores. More importantly, CoS 2 nanoparticles are uniformly embedded among Co-Ni LDH layers, facilitating mass diffusion and favorably exposing more active sites. Benefiting from these desirable compositional and structural features, a remarkable specific capacitance (capacity) of 1784 F/g (223 mAh/g) at 1 A/g is delivered by CoS 2 /Co-Ni LDHs. Furthermore, the as-assembled CoS 2 /Co-Ni LDH//activated carbon as the asymmetric supercapacitor device also exhibits a high energy density of 125 Wh/kg at a power density of 800 W/kg and a superb capacitance retention of 98 % after 5000 cycles, outperforming many Co-Ni LDH based electrode materials reported in the literature.

CAS / MDL: 693-98-1 13478-00-7
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ACS Catalysis · 2022 · IF 13.7

Catalytic Cleavage of the C–O Bond in Lignin and Lignin-Derived Aryl Ethers over Ni/AlPyOx Catalysts

Liang Jiang,Guangyue Xu,Yao Fu

The conversion of lignin into value-added chemicals is one of the important ways for sustainable development. Herein, phytic acid, a biomass-derived chemical, was used as the phosphorus source and pore former to synthesize the AlPyOx support. After loading Ni, the Ni/AlPyOx catalysts were found to be highly active in the catalytic conversion of lignin model compounds to high-value-added chemicals under mild conditions. The benzyl phenyl ether (α-O-4 lignin model compound) could be completely converted into toluene and phenol with near-equivalent selectivity at 30 °C and 3 MPa H2. Diphenyl ether and 2-phenoxy-1-phenylethanol were also used as 4-O-5 and β-O-4 model compounds of lignin, respectively. The unique activity of Ni/AlP0.5Ox could be attributed to metallic Ni that interacts with AlP0.5Ox and the unique adsorption of substrates on the carrier. Lignin can also be degraded over Ni/AlP0.5Ox via selective cleavage of the C–O bond, and 26.60 wt % yield of identified monomers was obtained.

CAS / MDL: 946-80-5 101-84-8
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