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Constructing a stable interface on Ni-rich LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2) cathode via lactic acid-assisted engineering strategy

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Journal of Energy Chemistry 2024年第3期90卷 412-422,I0010页

作者： Weijian Tang Chengzhi Hu AFei Li Xiaoqin Huang Zhangxian Chen Jianhui Su Weixin Zhang Institute of Energy Hefei Comprehensive National Science CenterHefei 230031AnhuiChina School of Chemistry and chemical engineering Hefei University of Technology and Anhui Key Laboratory of Controllable Chemical Reaction&Material Chemical EngineeringHefei 230009AnhuiChina School of Electrical engineering and Automation Hefei University of TechnologyHefei 230009AnhuiChina

Ni-rich layered oxides are potential cathode materials for next-generation high energy density Li-ion batteries due to their high capacity and low ***,the inherently unstable surface properties,including high levels of residual Li compounds,dissolution of transition metal cations,and parasitic side reactions,have not been effectively addressed,leading to significant degradation in their electrochemical *** this study,we propose a simple and effective lactic acid-assisted interface engineering strategy to regulate the surface chemistry and properties of Ni-rich LiNi_(0.8)Co_(0.1)Mr_(0.1)O_(2) *** novel surface treatment method successfully eliminates surface residual Li compounds,inhibits structural collapse,and mitigates cathode-electrolyte interface film *** a result,the lactic acidtreated LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2) achieved a remarkable capacity retention of 91.7% after 100 cycles at 0.5 C(25℃) and outstanding rate capability of 149.5 mA h g^(-1) at 10 C,significantly outperforming the pristine ***,a pouch-type full cell incorporating the modified LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2) cathode demonstrates impressive long-term cycle life,retaining 81.5% of its capacity after 500 cycles at 1 *** importantly,the thermal stability of the modified cathode is also dramatically *** study offers a valuable surface modification strategy for enhancing the overall performance of Ni-rich cathode materials.

关键词： Residual Li Lactic acid Surface modification Carbon coating Layered cathode Ni-rich

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controllable selective anchoring of subnanometric Ru clusters or single-atoms/clusters on tungsten nitride for the hydrogen oxidation

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Science China Chemistry 2024年第11期67卷 3749-3756页

作者： Qijiao Sun Chuanqiang Wu Yiqiang Sun Yuan Shen Lei Zhao Xiaodong Yang Li Yang Yunxiang Lin Keke Mao Kun Xu School of Chemistry and chemical engineering Key Laboratory of Functional Inorganic Material Chemistry of Anhui Province Anhui Province Key Laboratory of Chemistry for Inorganic/Organic Hybrid Functionalized Materials Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education Anhui University Information materials and Intelligent Sensing laboratory of anhui Province Institutes of Physical Science and Information TechnologyAnhui University School of Chemistry and chemical engineering University of Jinan School of Energy and Environment Anhui University of Technology

The impregnation method in the preparation of metal cluster catalysts typically inadvertently introduces single atoms（SAs） into the substrate. However, the question of whether the introduction of SAs will further improve the catalytic activity of cluster systems for specific reactions such as the hydrogen oxidation reaction（HOR） remains unraveled. Herein, we demonstrate Ru clusters anchored on WN nanowires（RuC/WN） show a higher alkaline HOR catalytic activity in comparison with Ru SAs and nanoclusters（NCs）-coupled catalyst anchored on WN nanowires system（RuC,S/WN）. Notably, the RuC/WN exhibits superb intrinsic catalytic activity with a mass-normalized exchange current density of 890 m A mg-1PGM, which is among the top level of well developed Ru-based HOR catalysts. Both theoretical simulation and experimental investigation suggest that RuC/WN owns an optimized H*and OH*reaction intermediates for the alkaline HOR, therefore resulting in the excellent intrinsic HOR catalytic performance.

关键词： hydrogen oxidation reaction Ru cluster catalyst Ru single atoms and nanoclusters coupled catalyst tungsten nitride substrate

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Tuning synergy between nickel and iron in Ruddlesden-Popper perovskites through controllable crystal dimensionalities towards enhanced oxygenevolving activity and stability

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Carbon Energy 2024年第6期6卷 113-123页

作者： Haijuan Zhang Daqin Guan Yuxing Gu Hengyue Xu Chunchang Wang Zongping Shao Youmin Guo School of materials Science and Technology Anhui UniversityHefeiAnhuiChina Department of Building and Real Estate The Hong Kong Polytechnic UniversityHung HomHong KongChina WA School of Mines:Minerals Energy and Chemical EngineeringCurtin UniversityPerthWestern AustraliaAustralia State key laboratory of materials-Oriented chemical engineering Nanjing Tech UniversityNanjingJiangsuChina Tsinghua Shenzhen International Graduate School Tsinghua UniversityShenzhenGuangdongChina

Ni-Fe-based oxides are among the most promising catalysts developed to date for the bottleneck oxygen evolution reaction(OER)in water ***,understanding and mastering the synergy of Ni and Fe remain ***,we report that the synergy between Ni and Fe can be tailored by crystal dimensionality of Ni,Fe-contained Ruddlesden-Popper(RP)-type perovskites(La_(0.125)Sr_(0.875))n+1(Ni_(0.25)Fe_(0.75))nO3n+1(n=1,2,3),where the material with n=3 shows the best OER performance in alkaline *** X-ray absorption spectroscopy spectra before and after OER reveal that the material with n=3 shows enhanced Ni/Fe-O covalency to boost the electron transfer as compared to those with n=1 and n=*** experimental investigations demonstrate that the Fe ion is the active site and the Ni ion is the stable site in this system,where such unique synergy reaches the optimum at n=***,as n increases,the proportion of unstable rock-salt layers accordingly decreases and the leaching of ions(especially Sr^(2+))into the electrolyte is suppressed,which induces a decrease in the leaching of active Fe ions,ultimately leading to enhanced *** work provides a new avenue for rational catalyst design through the dimensional strategy.

关键词： crystal dimensionalities oxygen evolution reaction Ruddlesden-Popper perovskites synergy

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Recovery of lithium using H_(4)Mn_(3.5)Ti_(1.5)O_(12)/reduced graphene oxide/polyacrylamide composite hydrogel from brine by Ads-ESIX process

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Chinese Journal of chemical engineering 2022年第4期35卷 20-28页

作者： Jingsi Cui Huanxi Xu Yanfeng Ding Jingjing Tian Xu Zhang Guanping Jin anhui key lab of controllable chemical reaction&material chemical engineering School of Chemistry and Chemical EngineeringHefei University of TechnologyHefei 230009China

Powdery Li^(+)-imprinted manganese oxides adsorbent was widely used to the recovery of Li^(+),but there are some difficulties,such as poor stability in acid solution,inconvenience of operation and *** this work,a useful hydrogel composite based H_(4)Mn_(3.5)Ti_(1.5)O_(12)/reduced graphene oxide/polyacrylamide(HMTO-rGO/PAM)was fabricated by thermal initiation method with promising stable,conductive and selective *** resulting materials were characterized by field emission scanning electron microscope,infrared absorption spectrum,X-ray diffraction,X-ray photoelectron spectroscopy and electrochemical *** recovery of Li^(+)was investigated using HMTO-rGO/PAM from brine by a separated two-stage sorption statically and electrically switched ion exchange desorption *** adsorption capacity of 51.5 mg·g^(-1)could be achieved with an initial Li^(+)concentration of 200 mg·L^(-1)in pH 10,at 45℃ for 12 ***^(+)ions could be quickly desorbed by cyclic voltammetry(CV)in pH 3,0.1 mol·L^(-1)HCl/NH;Cl accompanying the exchange of Li^(+)and H+(NH;)and the transfer of LMTO-rGO/PAM to HMTO-rGO/PAM.

关键词： Lithium recovery Titanium doped lithium ion sieve Hydrogel Adsorption-electrically switched ion exchange(Ads-ESIX)

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Potential-aided recovery of iodide using 2-D nanosheet CuxO coating polymer/graphene/carbon fibers composite

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Chinese Journal of chemical engineering 2020年第4期28卷 1046-1054页

作者： Yexiao Yu Guanping Jin Yuhong Fang Zheng Xu Xiaoyuan Lü Chunnian Chen anhui key lab of controllable chemical reaction&material chemical engineering School of Chemistry and Chemical EngineeringHefei University of TechnologyHefei 230009China

2-D nanosheet Cu2O doped CuO coating poly m-phenylenediamine and melamine/graphene/carbon fibers composite(CuxO/MPM/GFs)was firstly fabricated by compound electrochemical ***/MPM/GFs was successfully used to the recovery of iodide(I-)from salt water by lower potential-aided sorption and desorption *** potential-aided recovery of I-at CuxO/MPM/GFs was characterized by FE-SEM,XRD,IR,Raman,XPS,UV-vis and electrochemical techniques in *** maximal adsorption capacity of 86.82 mg·g^-1 could be obtained with a pseudo-second-order model at 0.8 V for 210 min in pH 5.0,0.1 mol·L^-1 NaCl,and the process accompanied the generation of CuI,CuO and I5-.The I-could be quickly desorbed from the electrode with a transfer of CuI to Cu2O by cycle voltammetry from-1.0 to 0.5 V for 90 cycles in pH 9.0,0.1 mol·L^-1 ***,CuxO/MPM/GFs was renewable in the continuous electrochemical-adsorption-desorption processes.

关键词： Potential-aided recovery Iodide Cu2O Carbon fibers composite

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Defective NH_(2)-UiO-66(Zr) effectively converting CO_(2) into cyclic carbonate under ambient pressure,solvent-free and co-catalyst-free conditions

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Chinese Journal of chemical engineering 2022年第3期35卷 222-229页

作者： Xueting Liu Chunhui Hu Jingjing Wu Peng Cui Fengyu Wei School of Chemistry and chemical engineering Hefei University of TechnologyAnhui Key Laboratory of Controllable Chemical Reaction&Material Chemical EngineeringHefei 230009China

In this study,a series of metal-organic frameworks(MOFs)NH_(2)-UiO-66-x HAc catalysts were synthesized by solvothermal method using acetic acid(HAc)as a modulator,and were applied to the cycloaddition of CO_(2)and epichlorohydrin(EPIC)under ambient *** of the modulation by HAc on morphologies and structures of the MOFs are demonstrated via PXRD,FESEM,FTIR,N_(2)adsorption-desorption,XPS and ^(1)H NMR *** results show that the MOFs containing mesoporous pores can be prepared by adjusting the concentration of *** optimizing the amount of HAc added,the specific surface area of NH_(2)-UiO-66-8 HAc is as high as 879.17 m^(2)·g^(-1),which is 28.3%higher than that of the original *** the evaluation of catalytic performance showed that HAc modulation enhanced the activity of NH_(2)-UiO-66-x HAc under mild *** exposure of Lewis acid sites,increased specific surface area and porosity via the modulation of HAc defective ligand can be supposed the key factors to determine the enhanced catalytic *** addition,considering the influence of gas concentration on the reaction,the concept of TOP(Turnover of Pressure,defined as the mass of conversions of a unit mass catalyst under unit pressure and unit time)was first proposed in this article.

关键词： CO_(2)conversion Metal-organic frameworks Acetic acid modulation Defect Mild conditions

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Novel hierarchical yolk-shell α-Ni(OH)_(2)/Mn_(2)O_(3) microspheres as high specific capacitance electrode materials for supercapacitors

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Frontiers of chemical Science and engineering 2021年第5期15卷 1322-1331页

作者： Xiqing Luo Miaomiao Jiang Kun Shi Zhangxian Chen Zeheng Yang Weixin Zhang School of Chemistry and chemical engineering Hefei University of Technology and Anhui Key Laboratory of Controllable Chemical Reaction&Material Chemical EngineeringHefei230009China

For high performance supercapacitors, novel hierarchical yolk-shell α-Ni(OH)_(2)/Mn_(2)O_(3) microspheres were controllably synthesized using a facile two-step method based on the solvothermal treatment. The unique α-Ni(OH)_(2) based yolk-shell microstructures decorated with numerous interconnected nanosheets and the heterocomposition features can synergistically enhance reactive site exposure and electron conduction within the microspheres, facilitate charge transfer between electrolyte and electrode materials, and release structural stress during OH− chemisorption/desorption. Moreover, the Mn2O3 sediments distributed over the α-Ni(OH)_(2) microspheres can serve as an effective protective layer for electrochemical reactions. Consequently, when tested in 1 mol·L^(−1) KOH aqueous electrolyte for supercapacitors, the yolk-shell α-Ni (OH)_(2)/Mn_(2)O_(3) microspheres exhibited a considerably high specific capacitance of 2228.6 F·g^(−1) at 1 A·g^(−1) and an impressive capacitance retention of 77.7% after 3000 cycles at 10 A·g^(−1). The proposed α-Ni(OH)_(2)/Mn_(2)O_(3) microspheres with hetero-composition and unique hierarchical yolk-shell microstructures are highly promising to be used as electrode materials in supercapacitors and other energy storage devices.

关键词： α-Ni(OH)_(2)/Mn_(2)O_(3) yolk-shell microspheres electrode material high specific capacitance supercapacitors

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Fast and highly reversible Na^(+)intercalation/extraction in Zn/Mg dual-doped P2-Na_(0.67)MnO_(2)cathode material for high-performance Na-ion batteries

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Nano Research 2021年第10期14卷 3531-3537页

作者： Xiaoqin Huang Deli Li Haijian Huang Xiao Jiang Zeheng Yang Weixin Zhang School of Chemistry and chemical engineering Hefei University of TechnologyHefei 230009China anhui key laboratory of controllable chemical reaction&material chemical engineering Hefei 230009China

P2-type layered Na_(0.67)MnO_(2)has been considered to be a promising candidate cathode material for sodium ion ***,the undesired phase transitions during operation and the large Na^(+)radius induced sluggish ion diffusion remain the stumbling blocks to realize its high ***,we propose a Zn/Mg co-doping strategy,which is proved to have bifunctional ***,relative to the pristine P2-Na_(0.67)MnO_(2)and the single-ion(Zn/Mg)doped samples,the Zn/Mg dual-doped P2-Na_(0.67)MnO_(2)demonstrates a lower Mn^(3+)/Mn^(4+)ratio and a higher lattice O content,which facilitate the structural stability of the cathode *** intriguingly,the Zn/Mg co-doping gives rise to enlarged interplanar spacing,which provides spacious ion diffusion channels for fast Na^(+)intercalation/*** a result,the Zn/Mg dual-doped sample exhibits a high Na^(+)diffusion coefficient and a solid-solution reaction during charge/discharge,with a cell volume change determined to be only 0.55%.Taking advantages of the above favorable features,the Zn/Mg dual-doped P2-Na_(0.67)MnO_(2)demonstrates a high rate performance with 67.2 mAh·g^(-1)delivered at 10 C and a decent cycling stability with a capacity retention of 93.8%achieved at 1 C after 100 *** work introduces the Zn/Mg co-doping strategy to simultaneously improve the cycling stability and rate capability of P2-Na_(0.67)MnO_(2),which may offer a promising avenue for further performance enhancement of the layered Na-ion batteries cathode materials.

关键词： Na-ion batteries cathode materials co-doping Na-ion diffusion structural stability

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Synthesis and characterization of uniform nanoparticles of γ-Mo_2N for supercapacitors

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中国有色金属学会会刊：英文版 2009年第3期19卷 620-625页

作者：李学良邢妍汪华王华林王维东陈祥迎 School of chemical engineering Hefei University of Technology anhui key laboratory of controllable chemical reaction and material chemical engineering Hefei University of Technology

Uniform nanoparticles of molybdenum nitride were synthesized by temperature-programmed reaction(TPR) using MoO3 and ammonia as reactants. This material was characterized by X-ray diffractometry(XRD), transmission electron microscopy(TEM), scanning electron microcopy(SEM) and cyclic voltammetry(CV). Results show that the material consists of a pure phase of γ-Mo2N nanoparticles with average diameter of about 16 nm. The material presents a specific capacitance of 172 F/g in 1 mol/L H2SO4 electrolyte at a scan rate of 1 mV/s and the potential window is broadened to 1.1 V (-0.6 to 0.5 V). At the 6 000th cycle, the material remains 94.9% and 94.7% of the initial capacitance in 1 mol/L H2SO4 and KCl solution, respectively. A possible mechanism comprising surface control and diffusion control is proposed to explain the effect of scan rates on specific capacitance.

关键词：超级电容器纳米粒子 Mo2N 合成程序升温反应透射电子显微镜扫描电子显微镜 X射线衍射

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A chemical etching route to controllable fabrication of TiO2 hollow nanospheres for enhancing their photocatalytic activity

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Frontiers of chemical Science and engineering 2013年第2期7卷 192-201页

作者： Weixin ZHANG Jie XING Zeheng YANG Mei KONG Hongxu YAO School of chemical engineering Hefei University of Technology Anhui 230009 China anhui key laboratory of controllable chemical reaction & material chemical engineering Anhui 230009 China

The TiO2 hollow nanospheres with diameters of about 230 nm were prepared by a simple and controllable route based on hydrolysis of Ti（OBu）4 on the surfaces of the Cu20 solid nanospheres followed by inward etching of the Cu20 nanospheres. The as-prepared samples were characterized by X-ray diffraction, transmis- sion electron microscopy and scanning electron micro- scopy. The further post-heat treatment led to the high crystallization of the TiO2 hollow nanospheres. The photocatalytic performances of these samples were evaluated for the photodegradation of rhodamine B （RhB） under UV-light irradiation. The as-prepared TiO2 hollow nanospheres showed higher photocatalytic activity than the CuO and the CuO/TiO2 hollow nanospheres. Effects of temperature and time for post-heat treatment of TiO2 as well as initial RhB concentrations on the RhB photodegradation have also been studied. The results show that the TiO2 hollow nanospheres have the good reusability as photocatalysts and are promising in waste water treatment.

关键词： TiO2 hollow nanospheres rhodamine B,photocatalytic activity

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