Jun Yang

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Name: 杨军; Jun Yang
Organization: Shanghai Jiao Tong University , China
Department: Department of Chemical Engineering
Title: Professor(PhD)

TOPICS

Co-reporter:Yitian Bie;Jiulin Wang;Jingjing Zhou;Yanna Nuli
Chemical Communications 2017 vol. 53(Issue 59) pp:8324-8327
Publication Date(Web):2017/07/20
DOI:10.1039/C7CC04646D
Commercially available Li2O2 was proposed as a cathode additive in commercialized LiNi0.33Co0.33Mn0.33O2 (NCM) cathodes to offset the initial Li loss. Li2O2 can be decomposed substantially under catalysis of NCM and leaves almost no remnants after the Li compensation.
Co-reporter:Jinhui Zhu, Jun Yang, Jingjing Zhou, Tao Zhang, Lei Li, Jiulin Wang, Yanna Nuli
Journal of Power Sources 2017 Volume 366(Volume 366) pp:
Publication Date(Web):31 October 2017
DOI:10.1016/j.jpowsour.2017.09.035
•An organic–inorganic hybrid layer (OIHL) was direct fabricated on Li metal.•The OIHL consists of Li alkyl carbonate and Li chloride.•The Li-O2 batteries with OIHL protected Li metal anode exhibit long cycle life.•The OIHL prevents the growth of Li dendrites and the corrosion of Li metal.A stable organic–inorganic hybrid layer (OIHL) is direct fabricated on lithium metal surface by the interfacial reaction of lithium metal foil with 1-chlorodecane and oxygen/carbon dioxide mixed gas. This favorable OIHL is approximately 30 μm thick and consists of lithium alkyl carbonate and lithium chloride. The lithium-oxygen batteries with OIHL protected lithium metal anode exhibit longer cycle life (340 cycles) than those with bare lithium metal anode (50 cycles). This desirable performance can be ascribed to the robust OIHL which prevents the growth of lithium dendrites and the corrosion of lithium metal.
Co-reporter:Jinhui Zhu;Zhixin Xu;Jiulin Wang;Yanna Nuli;Xiaodong Zhuang;Xinliang Feng
Nanoscale (2009-Present) 2017 vol. 9(Issue 25) pp:8871-8878
Publication Date(Web):2017/06/29
DOI:10.1039/C7NR01545C
Silicon (Si) anodes, which are among the most promising candidates for high-energy lithium-ion batteries (LIBs), have attracted considerable attention from both academic and industrial communities. However, Si anodes usually suffer from an inherently low conductivity and extremely large volume change during the lithiation and delithiation processes, and consequently exhibit an inferior rate capability and poor cycle life. In this paper, we report new porous polymer-derived carbon coated Si nanoparticles (NPs) as the next generation anodes for LIBs to overcome these serious problems. Specifically, a porous covalent triazine framework (CTF) polymer shell was synthesized by in situ trimerization of p-benzenedinitrile in molten ZnCl2. Then, core–shell structured Si/nitrogen-doped porous carbon (Si@NPC) spheres were easily produced after high-temperature annealing. As an anode for LIBs, Si@NPC delivers a high capacity of 1390 mA h g−1 at 0.5 A g−1, stable cycle performance (107% capacity retention at 1 A g−1 for 200 cycles), and excellent rate capability of up to approximately 420 mA h g−1 at 16 A g−1. Such an exciting performance can be attributed to the ultra-stable, highly conductive, N-doped, and porous carbon shell. This work not only offers a new solution to the large volume change of Si-based anodes, but also enables the synthesis of porous polymer-based core–shell structures for energy storage and conversion.
Co-reporter:Jingjing Zhou;Zhixin Xu;Tao Zhang;Zhenying Chen;Jiulin Wang
Journal of Materials Chemistry A 2017 vol. 5(Issue 19) pp:9350-9357
Publication Date(Web):2017/05/16
DOI:10.1039/C7TA01564J
Rechargeable lithium–selenium (Li–Se) batteries are promising electrochemical systems with higher energy density than traditional Li ion batteries. Nevertheless, the dissolution of high-order lithium selenides and the shuttle effect in electrolytes lead to low Se utilization, inferior capacity and poor cycling performance. This study proposes a combination of nanostructured Se cathode materials and compatible carbonate electrolytes for promoting the performance of Li–Se batteries. Se/MC composite nanoparticles (∼35 nm) with a moderate Se content (≈51.4 wt%) were prepared by embedding Se into a metal–organic framework derived microporous carbon. The resulting Se/MC cathode exhibits significantly high rate capability and cycling stability in LiDFOB/EC-DMC-FEC electrolyte. It delivers a capacity of 511 mA h gSe−1 after 1000 cycles at 5C, with an inappreciable capacity decay of 0.012% per cycle. Even at a very high rate of 20C, a large capacity of 569 mA h gSe−1 can be obtained, corresponding to a decrease of only 5.6% compared to that at 0.5C. The impressive high rate performance is attributed to the co-effect of selenium confined in ultra-small microporous carbon particles and excellent compatibility of the electrolyte with both the Li anode and selenium composite cathode.
Co-reporter:Jinzuan Wang;Wenyan Yin;Shin-ichi Hirano
Journal of Materials Chemistry A 2017 vol. 5(Issue 39) pp:20623-20630
Publication Date(Web):2017/10/10
DOI:10.1039/C7TA06770D
Sodium-ion batteries (SIBs) are considered to be one of the most promising alternatives to lithium-ion batteries (LIBs) for energy storage due to the low cost and large abundance of natural sodium resources. However, the search for suitable sodium storage anode materials with enhanced rate capability and cycling stability is much more difficult for SIBs, due to the larger ionic radius of the sodium-ion than that of the lithium-ion. In this work, we design and fabricate a new type of carbon coated graphene/antimony composite (G@Sb@C) with a unique sandwich-like structure. The graphene framework and carbon layer can enhance the electronic conductivity and disperse the Sb particles uniformly. In addition, the covered carbon layer can buffer the volume change, suppress the aggregation of Sb, and stabilize the integrated structure of the composite during the cycling processes. As an anode material for SIBs, the G@Sb@C electrode delivers a high reversible capacity of 569.5 mA h g−1 after 200 cycles at a current rate of 0.1 A g−1, and the coulombic efficiency is ca. 99%. Moreover, the capacity reaches 433 mA h g−1 even at a high current rate of 5.0 A g−1. We believe that the unique sandwich-like structure design could also be extended to develop other materials suffering from the large volume change during charge/discharge cycling.
Co-reporter:Jinhui Zhu;Xiaodong Zhuang;Xinliang Feng;Shin-ichi Hirano
Journal of Materials Chemistry A 2017 vol. 5(Issue 32) pp:16732-16739
Publication Date(Web):2017/08/15
DOI:10.1039/C7TA04752E
Two-dimensional (2D) soft materials have attracted much attention recently due to their unique carbon-rich structure and extensive potential applications for energy storage. Although the specific surface areas (SSAs) of 2D soft materials are theoretically high, practically maintaining both the uniform 2D morphology and high SSA of a single 2D soft material is still challenging. Herein, graphene-coupled covalent triazine-based frameworks (G-CTFs) with typical 2D features, large aspect ratio, and ultrahigh SSA of up to 1584 m2 g−1 were synthesized through polymerization of p-benzenedinitrile in molten salt in the presence of p-benzonitrile-functionalized reduced graphene oxide. After their direct pyrolysis, nitrogen-enriched porous carbon nanosheets (G-PCs) can be easily obtained, which had the frameworks' 2D morphology and exhibited a high nitrogen content and even higher SSA of up to 1982/3021 m2 g−1, as calculated using the Brunauer–Emmett–Teller and Langmuir methods, respectively. Benefiting from these features, the G-PCs exhibited excellent energy storage performance as electrode materials in both a Li-ion battery (235 mA h g−1 at 5 A g−1 for 3000 cycles), Na-ion battery (138 mA h g−1 at 1 A g−1 for 500 cycles), and supercapacitor (340 F g−1 at 0.1 A g−1 and 10 000 stable charge–discharge cycles at 5 A g−1). All these results indicate that the 2D sandwich-like porous carbon materials could be promising candidates for high-performance energy storage devices.
Co-reporter:Yitian Bie;Yanna Nuli;Jiulin Wang
Journal of Materials Chemistry A 2017 vol. 5(Issue 5) pp:1919-1924
Publication Date(Web):2017/01/31
DOI:10.1039/C6TA09522D
Natural karaya gum (KG), composed of polysaccharides and glycoproteins, is investigated as a binder for high-performance silicon-based anodes. Good mechanical properties provided by the multi-branched structure and glycoproteins and superior binding strength resulting from plentiful polar function groups lead to superior electrochemical performance of KG electrodes.
Co-reporter:Jinhui Zhu, Jun Yang, Rongrong Miao, Zhaoquan Yao, Xiaodong Zhuang and Xinliang Feng  
Journal of Materials Chemistry A 2016 vol. 4(Issue 6) pp:2286-2292
Publication Date(Web):11 Jan 2016
DOI:10.1039/C5TA09073C
Nitrogen-doped (N-doped) porous carbons have drawn increasing attention due to their high activity for electrochemical catalysis, and high capacity for lithium-ion (Li-ion) batteries and supercapacitors. So far, the controlled synthesis of N-enriched ordered mesoporous carbons (N-OMCs) for Li-ion batteries is rarely reported due to the lack of a reliable nitrogen-doping protocol that maintains the ordered mesoporous structure. In order to realize this, in this work, ordered mesoporous carbons with controllable N contents were successfully prepared by using melamine, F127 and phenolic resin as the N-source, template and carbon-source respectively via a solvent-free ball-milling method. The as-prepared N-OMCs which showed a high N content up to 31.7 wt% were used as anodes for Li-ion batteries. Remarkably, the N-OMCs with an N content of 24.4 wt% exhibit the highest reversible capacity (506 mA h g−1) even after 300 cycles at 300 mA g−1 and a capacity retention of 103.3%. N-OMCs were also used as electrode materials in supercapacitors and a capacity of 150 F g−1 at 0.2 A g−1 with stable cycling up to 2500 times at 1 A g−1 was achieved. These attractive results encourage the design and synthesis of high heteroatom content ordered porous carbons for applications in the field of energy storage and conversion.
Co-reporter:Yitian Bie, Jun Yang, Xiaolin Liu, Jiulin Wang, Yanna Nuli, and Wei Lu
ACS Applied Materials & Interfaces 2016 Volume 8(Issue 5) pp:2899
Publication Date(Web):January 25, 2016
DOI:10.1021/acsami.5b10616
A robust silicon electrode for lithium-ion battery has been developed via prepolymerizing dopamine on silicon particle surface and then chemical binding with poly(acrylic acid) (PAA). In this favorable electrode, silicon nanoparticles are covered by a thin layer of polydopamine (PD) through firm hydrogen bonds between phenolic hydroxyl and hydroxyl, while the elastic polymer layer reacts with PAA binder to form three-dimensional cross-linked binding system. The Si@PD/PAA electrode exhibits more stable cycle performance than conventional electrodes. In the case of thick electrode, a capacity of 3.69 mA h cm–2 and fairly good rechargeability for 80 cycles can be achieved.Keywords: binder; dopamine; lithium-ion batteries; polyacrylic acid; silicon
Co-reporter:Yitian Bie, Jun Yang, Wei Lu, Zhihong Lei, Yanna Nuli, Jiulin Wang
Electrochimica Acta 2016 Volume 212() pp:141-146
Publication Date(Web):10 September 2016
DOI:10.1016/j.electacta.2016.06.152
Silicon is regarded as one of the most promising anode materials for Li-ion batteries owing to its high theoretical capacity (4200 mA h g−1, Li22Si5), but the short cycle life mainly caused by the dramatic volume effect has hindered its practical application. To address this major issue, we report here an effective and scalable approach to fabricate a novel Si electrode via the addition of silane coupling agent, which not only connects silicon and polyacrylic acid (PAA) covalently but also crosslinks PAA, thus forming an entire 3D binding network. The dual functions of 3-amino-propyltriethoxysilane (APTES) in an electrode with 80% Si nanoparticles greatly improves the structural stability during the charge/discharge process, leading to excellent electrochemical performances, such as 1000 mA h g−1 over 1200 cycles and high silicon loading of ca. 4.2 mA h cm−2. Moreover, this binder system is also effective for the thick silicon/graphite electrodes towards practical application.
Co-reporter:Yanqiong Shi, Rongrong Miao, Lei Li, Jun Yang, Jiulin Wang and Yanna Nuli  
RSC Advances 2016 vol. 6(Issue 53) pp:47820-47823
Publication Date(Web):09 May 2016
DOI:10.1039/C6RA08318H
A novel LiFSI/TEGDME-DX electrolyte with good compatibility to a lithium anode is firstly proposed for the rechargeable non-aqueous Li–O2 battery, in which an improved performance with longer cycle life was achieved when compared with the conventional LiTFSI/TEGDME electrolyte.
Co-reporter:Zhixin Xu; Jiulin Wang; Jun Yang;Xiaowei Miao; Renjie Chen;Ji Qian;Rongrong Miao
Angewandte Chemie International Edition 2016 Volume 55( Issue 35) pp:10372-10375
Publication Date(Web):
DOI:10.1002/anie.201605931

Abstract

The lithium–sulfur battery is regarded as one of the most promising candidates for lithium–metal batteries with high energy density. However, dendrite Li formation and low cycle efficiency of the Li anode as well as unstable sulfur based cathode still hinder its practical application. Herein a novel electrolyte (1 m LiODFB/EC-DMC-FEC) is designed not only to address the above problems of Li anode but also to match sulfur cathode perfectly, leading to extraordinary electrochemical performances. Using this electrolyte, lithium|lithium cells can cycle stably for above 2000 hours and the average Coulumbic efficiency reaches 98.8 %. Moreover, the Li–S battery delivers a reversible capacity of about 1400 mAh g−1sulfur with retention of 89 % for 1100 cycles at 1 C, and a capacity above 1100 mAh g−1sulfur at 10 C. The more advantages of this cell system are its outstanding cycle stability at 60 °C and no self-discharge phenomena.

Co-reporter:Zhixin Xu; Jiulin Wang; Jun Yang;Xiaowei Miao; Renjie Chen;Ji Qian;Rongrong Miao
Angewandte Chemie 2016 Volume 128( Issue 35) pp:10528-10531
Publication Date(Web):
DOI:10.1002/ange.201605931

Abstract

The lithium–sulfur battery is regarded as one of the most promising candidates for lithium–metal batteries with high energy density. However, dendrite Li formation and low cycle efficiency of the Li anode as well as unstable sulfur based cathode still hinder its practical application. Herein a novel electrolyte (1 m LiODFB/EC-DMC-FEC) is designed not only to address the above problems of Li anode but also to match sulfur cathode perfectly, leading to extraordinary electrochemical performances. Using this electrolyte, lithium|lithium cells can cycle stably for above 2000 hours and the average Coulumbic efficiency reaches 98.8 %. Moreover, the Li–S battery delivers a reversible capacity of about 1400 mAh g−1sulfur with retention of 89 % for 1100 cycles at 1 C, and a capacity above 1100 mAh g−1sulfur at 10 C. The more advantages of this cell system are its outstanding cycle stability at 60 °C and no self-discharge phenomena.

Co-reporter:Jiulin Wang;Yu-Shi He
Advanced Materials 2015 Volume 27( Issue 3) pp:569-575
Publication Date(Web):
DOI:10.1002/adma.201402569

There is currently an urgent demand for highly efficient energy storage and conversion systems. Due to its high theoretical energy density, low cost, and environmental compatibility, the lithium sulfur (Li–S) battery has become a typical representative of the next generation of electrochemical power sources. Various approaches have been explored to design and prepare sulfur cathode materials to enhance their electrochemical performance. This Research News article summarizes and compares different sulfur materials for Li–S batteries and particularly focuses on the fine structures, electrochemical performance, and electrode reaction mechanisms of pyrolyzed polyacrylo­nitrile sulfur (pPAN@S) and microporous-carbon/small-sulfur composite materials.

Co-reporter:Yitian Bie, Jinglu Yu, Jun Yang, Wei Lu, Yanna Nuli, Jiulin Wang
Electrochimica Acta 2015 Volume 178() pp:65-73
Publication Date(Web):1 October 2015
DOI:10.1016/j.electacta.2015.07.173
•Porous Si/CNT/C microspheres are obtained via spray drying and carbonization.•The favorable composite structure leads to excellent cycling stability and rate performance.•Introduction of copper into the microspheres significantly enhances the mechanical stability and cycle performance.Nano/micro-structured Si/CNT/C and Si-Cu/CNT/C microspheres are prepared by two simple steps of spray drying and carbonization, which are efficient and easy to scale up. In the Si/CNT/C composites, silicon particles (about 50–200 nm) are covered by a layer of carbon formed by pyrolysis of phenol-formaldenhyde resin (PF), which, in turn, connects with the three-dimensional multiwall carbon nanotubes (MWCNTs) conductive network. Numerous open pores, which could buffer volume expansion of silicon and improve the electrode kinetics, are engendered in the microspheres due to the rapid evaporation of solvent and unfoldment of flexible MWCNTs. Moreover, introduction of small amount of copper (5 wt.%) into the microspheres as Cu3Si phase reinforces the mechanical stability and improves the electronic conductivity. The favorable Si/CNT/C composite structure leads to significantly improved cycling stability and rate performance (ca. 1250 mA h g−1 at 5 A g−1) compared to pristine Si particles. Addition of copper further enhances the capacity retention to 91.2% after 80 cycles.
Co-reporter:Qingwen Lu, Jun Yang, Wei Lu, Jiulin Wang, Yanna Nuli
Electrochimica Acta 2015 Volume 152() pp:489-495
Publication Date(Web):10 January 2015
DOI:10.1016/j.electacta.2014.11.176
•A new type of Semi-IPN GPE was prepared via UV-cured technology.•This electrolyte shows superior thermal stability and good mechanical properties.•The GPE membrane has excellent interface stability toward Li electrode.•Li/LiFePO4 cell using GPE membrane displays excellent electrochemical behavior.A new type of semi-interpenetrating polymer network (Semi-IPN) gel polymer electrolyte (GPE) membrane based on the cross-linked poly(ethylene glycol) diacrylate-co-poly(vinylene carbonate) P(EGDA-co-VC) and PVDF-HFP linear polymer is successfully synthesized by UV-cured technology. The cross-linked P(EGDA-co-VC) can accommodate a large amount of liquid electrolyte inside the non-porous membrane via its strong interaction with Li+ and solvents, which avoids the liquid electrolyte leakage. The ionic conductivity of the Semi-IPN GPE reaches 1.49 × 10−3 S cm−1 at 25 °C and the electrochemical stability window up to 4.2 V (versus Li/Li+). It demonstrates excellent interface stability to lithium metal electrode, superior thermal stability and good mechanical properties. A symmetric Li/Li cell with the above electrolyte displays a lower voltage polarization and longer valid cycle life than that based on conventional liquid electrolyte. Moreover, the Li/LiFePO4 cells using the Semi-IPN GPE show superior cycling stability and rate performance comparable to the cell based on conventional liquid electrolyte. This Semi-IPN GPE is promising for rechargeable lithium batteries with high safety and energy density.A semi-interpenetrating polymer network (Semi-IPN) gel polymer electrolyte (GPE) membrane based on the cross-linked PEGDA-co-PVC and linear PVDF-HFP has been prepared by UV-cured technology. It exhibits excellent interface stability to lithium metal electrode, superior thermal stability and mechanical properties. Its use in Li/LiFePO4 cell shows superior cycling stability and rate performance.
Co-reporter:Rongrong Miao, Jun Yang, Yanan Wu, Jiulin Wang, Yanna Nuli and Wei Lu  
RSC Advances 2015 vol. 5(Issue 70) pp:56772-56779
Publication Date(Web):22 Jun 2015
DOI:10.1039/C5RA08622A
Despite the fact that silicon materials can be synthesized from various sources, deriving them from earth-abundant resources is of strategic significance for industrial processing. Here nanoporous silicon (pSi) was derived from earth-abundant natural clinoptilolite (NCLI) without complicated pretreatment. After surface carbon coating, the pSi–C composite displayed a superior stable capacity of ca. 1257 mA h g−1 and good cycling stability with 87.5% capacity retention on the 200th cycle versus the 3rd one, which benefit from its nanoporous structure, very small primary particle size of ∼10 nm and highly conductive carbon-matrix.
Co-reporter:Wanjing Pan;Xiaolin Liu;Xiaowei Miao
Journal of Solid State Electrochemistry 2015 Volume 19( Issue 11) pp:3347-3353
Publication Date(Web):2015 November
DOI:10.1007/s10008-015-2971-z
A new type of hybrid battery has been assembled with magnesium metal anode, hollow MoO2 microsphere cathode, and dual-salt electrolyte containing Mg2+ and Li+ ions. This kind of hybrid battery not only avoids metallic dendrite formation, which occurs in rechargeable lithium battery, but also ensures high-capacity intercalation reaction in the cathode, which is still a bottleneck for rechargeable magnesium battery. It is found that the morphology of MoO2 electrode has a great effect on its electrochemical performance. The hollow MoO2 microsphere cathode delivers an initial discharge capacity of 217.2 mAh g−1 with the coulombic efficiency of ca. 88 %. In the following cycles, its coulombic efficiency reaches nearly 100 %. In contrast, MoO2 solid particles with a size of 1–10 μm exhibit a capacity less than 50 mAh g−1. Inductively coupled plasma (ICP) analysis reveals that both of Mg2+ and Li+ ions take part in the cathode intercalation reaction.
Co-reporter:Dr. Xiaolin Liu; Jun Yang; Wenhua Hou; Jiulin Wang;Yanna Nuli
ChemSusChem 2015 Volume 8( Issue 16) pp:2621-2624
Publication Date(Web):
DOI:10.1002/cssc.201500574

Abstract

Herein, MoO2 nanoplates have been facilely prepared through a hydrothermal process by using MoO3 microbelts as the intercalation host. The obtained MoO2 nanoplates manifest excellent electrochemical properties when the discharge cutoff voltage is simply set at 1.0 V to preclude the occurrence of conversion reactions. Its initial reversible capacity reaches 251 mAh g−1, which is larger than that of Li4Ti5O12, at a current rate of 0.2 C. The average capacity decay is only 0.0465 mAh g−1 per cycle, with a coulombic efficiency of 99.5 % (from the 50th cycle onward) for 2000 cycles at 1 C. Moreover, this MoO2 electrode demonstrates an outstanding high power performance. When the current rate is increased from 0.2 to 50 C, about 54 % of the capacity is retained. The superior electrochemical performance can be attributed to the metallic conductivity of MoO2, short Li+ diffusion distance in the nanoplates, and reversible crystalline phase conversion of the addition-type reaction of MoO2. The prepared MoO2 nanoplates may hopefully replace their currently used analogues, such as Li4Ti5O12, in high power lithium-ion batteries.

Co-reporter:Dongpo Xu, Zhehao Huang, Rongrong Miao, Yitian Bie, Jun Yang, Yuan Yao and Shunai Che  
Journal of Materials Chemistry A 2014 vol. 2(Issue 46) pp:19855-19860
Publication Date(Web):30 Sep 2014
DOI:10.1039/C4TA04088K
Mesoporous silicon nanofibers were synthesised by magnesiothermic reduction of earthworm-like, lamellar structured silica nanotubes for use in developing highly efficient lithium ion batteries. The silica nanotubes resulted from the single-molecular-layer arrangement of a bolaamphiphile surfactant. The calcined mesoporous silica nanotubes transformed into mesoporous silicon nanofibers (nf-Si) after magnesiothermic reduction. Finally, carbon-layer-coated silicon nanofibers (nf-Si@C) were obtained by chemical vapour deposition (CVD), which displayed a stable capacity of approximately 1141 mA h g−1 over 100 cycles at 0.2 C.
Co-reporter:Xuejiao Feng, Jun Yang, Yitian Bie, Jiulin Wang, Yanna Nuli and Wei Lu  
Nanoscale 2014 vol. 6(Issue 21) pp:12532-12539
Publication Date(Web):07 Aug 2014
DOI:10.1039/C4NR03948C
Nano/micro-structured pSi and pSi/CNT particles were synthesized from nano-SiO2 as both a template and silicon precursor via a combination of spray drying and magnesiothermic reduction, followed by a nano-layer carbon coating by chemical vapor deposition to obtain a nano/micro-structured pSi/C and pSi/CNT/C composite. In the hierarchical microstructure of the pSi/CNT/C composite, Si nanoparticles less than 20 nm in size were homogenously dispersed in an electronically conductive and porous network of multiwall carbon nanotubes, which can accommodate the volume changes in Si and improve the structural and conductive stability during repeated cycles leading to excellent electrochemical performance. The pSi/CNT/C presented reversible capacities of ca. 2100 mA h g−1 at 1 A g−1 and ca. 1370 mA h g−1 at a high current rate of 5 A g−1. Its capacity retention after 100 cycles was 95.5% at 1 A g−1.
Co-reporter:Qingwen Lu, Jianhua Fang, Jun Yang, Xuejiao Feng, Jiulin Wang and Yanna Nuli  
RSC Advances 2014 vol. 4(Issue 20) pp:10280-10283
Publication Date(Web):11 Feb 2014
DOI:10.1039/C3RA47694D
A novel ion-conductive polyimide nanoscale layer is formed on the Li4Ti5O12 anode material via a stepwise thermal imidization of polyamic acid to suppress the interfacial side reactions, and leads to a significant improvement in electrochemical performances at elevated temperature.
Co-reporter:Jinglu Yu, Jun Yang, Xuejiao Feng, Hao Jia, Jiulin Wang, and Wei Lu
Industrial & Engineering Chemistry Research 2014 Volume 53(Issue 32) pp:12697-12704
Publication Date(Web):2017-2-22
DOI:10.1021/ie5010465
A uniform carbon layer was coated on Si nanoparticles by the dynamic chemical vapor deposition (CVD) process with toluene as the carbon source. The carbon layer thickness could easily be adjusted by controlling the preparation conditions. Samples selected from different positions of the reaction tube showed a small deviation in carbon content. As an anode material for a lithium-ion battery, the resulting Si@C composites exhibited better cycle reversibility and rate capability than pristine Si. The Si@C-2 sample (carbon layer thickness ≈ 12 nm) delivered a relatively stable specific capacity of ca. 1600 mA h g–1 at 0.3 A g–1 for 70 cycles. Its capacity remained at 750 mA h g–1 at 5 A g–1, compared with 240 mA h g–1 for pristine Si. Acetylene as a carbon source can also lead to superior cycle stability. This reformative CVD process provides an avenue for the large-scale production of uniform carbon coating materials used for batteries and other devices.
Co-reporter:Qingwen Lu, Jianhua Fang, Jun Yang, Rongrong Miao, Jiulin Wang, Yanna Nuli
Journal of Membrane Science 2014 449() pp: 176-183
Publication Date(Web):
DOI:10.1016/j.memsci.2013.08.029
Co-reporter:Kai Wu, Jun Yang, Yang Liu, Yao Zhang, Chenyun Wang, Jinmei Xu, Feng Ning, Deyu Wang
Journal of Power Sources 2013 Volume 237() pp:285-290
Publication Date(Web):1 September 2013
DOI:10.1016/j.jpowsour.2013.03.057
•The key factors of gassing in Li4Ti5O12 cells are investigated by the accelerating measurement.•The chemically catalytic reaction related to moisture makes a minor contribution to Li4Ti5O12 cell gassing.•Graphite cells show a similar swelling behavior at over-discharge state as Li4Ti5O12 cells.•Electrolyte decomposition at elevated temperature should be dominated by the anode potential.The possible reasons and key factors on gas generation of Li4Ti5O12 (LTO) cells are investigated by the accelerating measurement baking at 80 °C for 120 h. It is found that the chemically catalytic reaction related to moisture makes a minor contribution to cell swelling. Our LTO-based 383450 cells (∼10 mL) before pre-charge (i.e. formation) only produce ∼1.5 mL gas during baking test and CO2, instead of H2, is the dominant species in EC/DMC electrolyte. By contrast, the swelling ratio of the charged LTO cells, which are re-sealed after formation, is kept at ∼97% regardless of states of charge. This severe decomposition of carbonates at elevated temperature should be dominated by the anode potential, rather than catalysis of LTO, since graphite/NMC cells show a similar swelling behavior at over-discharge state, where graphite anode shares the same potential as LTO. On the other hand, the electrolyte stability is also dependent on the type of solvent. Among the investigated systems, the mixture of PC + DMC (1:1) exhibits the best behavior to suppress the cell swelling. The swelling ratio diminishes from ∼100% of other electrolytes to 50%. This improvement probably roots in the high quality of protective films formed during solvents' decomposition.
Co-reporter:Fei Wang, Jun Yang, Yanna NuLi, Jiulin Wang
Electrochimica Acta 2013 Volume 103() pp:96-102
Publication Date(Web):30 July 2013
DOI:10.1016/j.electacta.2013.03.201
A series of xLiMnPO4·yLi3V2(PO4)3/C (x/y = 8:1, 4:1, 2:1, 1:1) composites have been successfully synthesized by spray drying followed by solid-state reaction. The morphology and crystalline structure are characterized by scanning electron microscope, transmission electron microscopy, energy dispersive spectroscopy and X-ray diffraction. The composites contain both LiMnPO4 and Li3V2(PO4)3 phases with nanosized dispersion, and Mn doping LVP and V doping LMP also coexist. The incorporation of Li3V2(PO4)3 with LiMnPO4 can effectively enhance electrochemical kinetics of LiMnPO4 phase via the structure modification and shortened Li-diffusion length in the LiMnPO4. Among these composites, 2LiMnPO4·Li3V2(PO4)3/C composite delivers a discharge capacity of 148 mAh g−1 at 0.1 C rate, against 105 mAh g−1 for the pristine LiMnPO4/C, and exhibits much better high/low-temperature performances than the latter.
Co-reporter:Xuejiao Feng, Jun Yang, Qingwen Lu, Jiulin Wang and Yanna Nuli  
Physical Chemistry Chemical Physics 2013 vol. 15(Issue 34) pp:14420-14426
Publication Date(Web):24 Jun 2013
DOI:10.1039/C3CP51799C
The m-SiOx/Si composite for lithium ion battery anode was prepared via a partial reduction reaction between ball-milled silicon monoxide and magnesium by high-energy mechanical milling. The m-SiOx/Si is composed of Si-suboxide and embedded Si nano-crystallites. The particles were further covered by a uniform carbon layer on the surface via a chemical vapor deposition process. The m-SiOx/Si/C composite shows a stable reversible capacity of ca. 1250 mA h g−1 and excellent cycling stability with 90.9% capacity retention on the 100th cycle versus the 6th one (compared at the same current rate). In contrast, SiO pre-milled for 25 h presents a reversible capacity of only ca. 900 mA h g−1 under the same carbon coating condition.
Co-reporter:Qingwen Lu, Jianhua Fang, Jun Yang, Gengwei Yan, Sisi Liu, Jiulin Wang
Journal of Membrane Science 2013 s 425–426() pp: 105-112
Publication Date(Web):
DOI:10.1016/j.memsci.2012.09.038
Co-reporter:Xuejiao Feng;Xiaolei Yu;Jiulin Wang
Journal of Solid State Electrochemistry 2013 Volume 17( Issue 9) pp:2461-2469
Publication Date(Web):2013 September
DOI:10.1007/s10008-013-2128-x
The influence of environmentally friendly aqueous binders and carbon coating on the electrochemical performance of SiO powder anodes for lithium ion batteries has been investigated in detail. The SiO anode with sodium alginate (Alg), styrene butadiene rubber/sodium carboxymethyl cellulose (SCMC) or polyacrylic acid binder exhibits fairly good cycling stability. However, use of polyvinyl alcohol as binder results in rapid capacity loss during cycling. The positive effect of the former binders could be attributed to the amorphous structures and ester-like bond, which were detected by X-ray diffraction and Fourier transform infrared. The cycling performance is further enhanced by carbon coating on the surface of the SiO. The reversible capacity of SiO/C electrode with either Alg or SCMC can retain ca. 940 mAh g−1 after 100 cycles. In particular, a long-term cycling stability can be achieved for SiO/C electrode using SCMC binder. Additionally, the high irreversibility of SiO/C electrode at the first cycle can be completely compensated by a simple pretreatment.
Co-reporter:Lichao Yin, Jiulin Wang, Fengjiao Lin, Jun Yang and Yanna Nuli  
Energy & Environmental Science 2012 vol. 5(Issue 5) pp:6966-6972
Publication Date(Web):29 Feb 2012
DOI:10.1039/C2EE03495F
Polyacrylonitrile/graphene (PAN/GNS) composites have been synthesized via an in situ polymerization method for the first time, which serve as a precursor to prepare a cathode material for high-rate rechargeable Li–S batteries. It is observed from scanning electron microscopy (SEM) and transmission electron microscopy (TEM) that the PAN nanoparticles, less than 100 nm in size, are anchored on the surface of the GNS and this unique structure is maintained in the sulfur composite cathode material. The electrochemical properties of the pyrolyzed PAN-S/GNS (pPAN-S/GNS) composite cathode have been evaluated by cyclic voltammograms, galvanostatic discharge–charge cycling and electrochemical impedance spectroscopy. The results show that the pPAN-S/GNS nanocomposite, with a GNS content of ca. 4 wt.%, exhibits a reversible capacity of ca. 1500 mA hg−1sulfur or 700 mA hg−1composite in the first cycle, corresponding to a sulfur utilization of ca. 90%. The capacity retention is relatively stable at 0.1 C. Even up to 6 C, a competitive capacity of ca. 800 mA hg−1sulfur is obtained. The superior performance of pPAN-S/GNS is attributed to the introduction of the GNS and the even composite structure. The GNS in the composite materials works as a three-dimensional (3-D) nano current collector, which could act not only as an electronically conductive matrix, but also as a framework to improve the electrochemical performance.
Co-reporter:Shaohua Liu;Haiping Jia;Lu Han;Jiulin Wang;Pengfei Gao;Dongdong Xu;Shunai Che
Advanced Materials 2012 Volume 24( Issue 24) pp:3201-3204
Publication Date(Web):
DOI:10.1002/adma.201201036
Co-reporter:Lichao Yin, Jiulin Wang, Xiaolei Yu, Charles W. Monroe, Yanna NuLi and Jun Yang  
Chemical Communications 2012 vol. 48(Issue 63) pp:7868-7870
Publication Date(Web):21 Jun 2012
DOI:10.1039/C2CC33333C
A novel dual-mode sulfur-based cathode material is prepared for the first time, in which sulfur is embedded in both the pyrolyzed PAN nanoparticles (pPAN) and mildly reduced graphene oxide nanosheets (mGO). The pPAN–S/mGO–S composite demonstrates outstanding electrochemical performances in the rechargeable Li–S batteries.
Co-reporter:Fei-fei Wang, Yong-sheng Guo, Jun Yang, Yanna Nuli and Shin-ichi Hirano  
Chemical Communications 2012 vol. 48(Issue 87) pp:10763-10765
Publication Date(Web):13 Sep 2012
DOI:10.1039/C2CC35857C
A new phenolate-based magnesium ion conducting electrolyte is prepared. The electrolyte exhibits air insensitive character and excellent electrochemical performances which make it highly promising for advanced rechargeable Mg battery systems.
Co-reporter:Yongsheng Guo, Fan Zhang, Jun Yang, Feifei Wang
Electrochemistry Communications 2012 Volume 18() pp:24-27
Publication Date(Web):2012
DOI:10.1016/j.elecom.2012.01.026
A novel boron based electrolyte system based on reaction of tri(3,5-dimethylphenyl)borane (Mes3B) and PhMgCl in THF solution is proposed for the potential application in rechargeable magnesium battery. The optimized composition of Mes3B-(PhMgCl)2/THF electrolyte solution presents high ionic conductivity(ca. 2 × 10− 3 S/cm in 0.5 M solution) at room temperature, excellent Mg deposition reversibility as well as the highest anodic potential to date (3.5 V vs. Mg RE). The initial results indicate that the high-performance of the Mes3B–(PhMgCl)2 electrolyte might be attributed to non-covalent interactions arising from the excess amount of Grignard reagent PhMgCl. This study opens the door to the development of boron based electrolyte chemistry for high-energy rechargeable Mg batteries.Highlights► We synthesized a novel boron based electrolyte system for rechargeable Mg batteries. ► We examined the electrochemical properties of this novel boron based electrolyte system. ► The electrolyte presents the highest anodic stability to date (3.5 V vs. Mg/Mg2+). ► It possesses high ionic conductivity (ca. 2 × 10− 3 S/cm) and Mg deposition reversibility. ► It paves the way to development high-energy rechargeable Mg batteries.
Co-reporter:Xuejiao Feng, Jun Yang, Pengfei Gao, Jiulin Wang and Yanna Nuli  
RSC Advances 2012 vol. 2(Issue 13) pp:5701-5706
Publication Date(Web):18 Apr 2012
DOI:10.1039/C2RA20107K
A new kind of nanoporous silicon/carbon composite with excellent electrochemical performance was prepared via a mechanochemical reaction between SiCl4 and Li13Si4 under ball milling. The whole process is mild and simple, using no corrosive acid. In particular, this method is suitable for large-scale synthesis of nanoporous silicon based composite for a potential anode material of lithium ion batteries. Different structures of silicon and carbon coating approaches were investigated. Compared with nano-Si/SP/C-D and np-Si/SP/C-S, the np-Si/SP/C-D exhibited a considerably high initial capacity of 1413.2 mAh g−1 and an excellent cycling stability with 91.1% capacity retention against at 2nd cycle after 100 cycles at a current density of 100 mA g−1. The superior electrochemical performance is attributed to the open nanoporous structure, which can accommodate the volume expansion, and the excellent electronic and ionic conductivity of a thin carbon layer.
Co-reporter:Kai Wu;Yao Zhang;Chenyun Wang;Deyu Wang
Journal of Applied Electrochemistry 2012 Volume 42( Issue 12) pp:989-995
Publication Date(Web):2012 December
DOI:10.1007/s10800-012-0442-0
Carbon-coated nano-Li4Ti5O12 (LTO) anode material was prepared and evaluated with 5.5 Ah pouch cells, paired with LiNi1/3Co1/3Mn1/3O2 cathode for potential hybrid electric vehicle (HEV) application. The as-prepared LTO batteries showed excellent electrochemical performance. They delivered a peak discharge power density of ca. 2,800 W kg−1, and featured a high power (94 and 92 % of discharge and charge capacity at 20 C, respectively) and a prolonged cycle life (89 % capacity retention after 5,000 cycles at 10 C charge and discharge rate). However, the severe capacity decay was observed at elevated temperatures because of loose (worse) interfaces caused by gas generation. It was found that H2 was the dominant gas component, and the inflation rate had an Arrhenius-type correlation with storage temperature. The battery inflation, arising from side reactions between electrolyte and LTO anode, is the major technical barrier for practical application of the LTO batteries in HEV.
Co-reporter:Haiping Jia;Pengfei Gao;Jiulin Wang;Yanna Nuli;Zhi Yang
Advanced Energy Materials 2011 Volume 1( Issue 6) pp:1036-1039
Publication Date(Web):
DOI:10.1002/aenm.201100485
Co-reporter:Lichao Yin, Jiulin Wang, Jun Yang and Yanna Nuli  
Journal of Materials Chemistry A 2011 vol. 21(Issue 19) pp:6807-6810
Publication Date(Web):08 Apr 2011
DOI:10.1039/C1JM00047K
A novel pPAN-S@MWCNT core-shell composite material is prepared via in situpolymerization of acrylonitrile on the surface of MWCNT, mixing with sulfur and final pyrolysis. The homogenous dispersion and integration of MWCNT in the composite create an electronically conductive network and reinforce the structural stability, leading to the outstanding electrochemical performances as a cathode material for rechargeable lithium/sulfur batteries.
Co-reporter:Fei Wang, Jun Yang, Pengfei Gao, Yanna NuLi, Jiulin Wang
Journal of Power Sources 2011 Volume 196(Issue 23) pp:10258-10262
Publication Date(Web):1 December 2011
DOI:10.1016/j.jpowsour.2011.08.090
Olivine-structured LiMnPO4 with uniform cluster-like and rod-like morphologies have been synthesized via a simple solvothermal process in water–organic solvent mixtures. The cluster-like LiMnPO4 microstructures are composed of numerous nanoplates in thickness of ca. 35 nm and width of ca. 400 nm. Carbon is coated on the LiMnPO4 surfaces by chemical vapor deposition (CVD) from methylbenzene and ball milling with acetylene black, respectively. The hierarchical LiMnPO4 nanoplates deliver much higher discharge capacity and rate capability than the nanorods due to the larger interfacial area for electrochemical reaction and shorter lithium ion diffusion depth. Furthermore, carbon-coating via CVD approach leads to a significant improvement in the electrochemical performances compared to the ball milling process.Highlights► Cluster-like LiMnPO4 composed of nanoplates is prepared by a solvothermal method. ► The thickness along the b-axis is about 35 nm for the LiMnPO4 nanoplate. ► A uniform carbon layer on the LiMnPO4 surface is obtained via a CVD process. ► The LiMnPO4/C nanoplates exhibit superior electrochemical activity to the nanorods.
Co-reporter:Fei Wang, Jun Yang, Yanna NuLi, Jiulin Wang
Journal of Power Sources 2011 Volume 196(Issue 10) pp:4806-4810
Publication Date(Web):15 May 2011
DOI:10.1016/j.jpowsour.2011.01.055
Hedgehog-like LiCoPO4 with hierarchical microstructures is first synthesized via a simple solvothermal process in water–benzyl alcohol mixed solvent at 200 °C. Morphology and crystalline structure of the samples are characterized by scanning electron microscope, transmission electron microscopy and X-ray diffraction. The hedgehog-like LiCoPO4 microstructures in the size of about 5–8 μm are composed of large numbers of nanorods in diameter of ca. 40 nm and length of ca. 1 μm, which are coated with a carbon layer of ca. 8 nm in thickness by in situ carbonization of glucose during the solvothermal reaction. As a 5 V positive electrode material for rechargeable lithium battery, the hedgehog-like LiCoPO4 delivers an initial discharge capacity of 136 mAh g−1 at 0.1 C rate and retains its 91% after 50 cycles, showing much better electrochemical performances than sub-micrometer LiCoPO4 synthesized by conventional high-temperature solid-state reaction.Graphical abstractResearch highlights► Hedgehog-like LiCoPO4 material composed of numerous nanorods is first prepared. ► Benzyl alcohol in water plays a key role in controlling the morphology and size. ► The LiCoPO4 cathode provides a high voltage around 4.8 V against lithium. ► The hierarchical microstructure favors superior electrochemical performances.
Co-reporter:Rongguan Lv, Jun Yang, Jiulin Wang, Yanna NuLi
Journal of Power Sources 2011 Volume 196(Issue 8) pp:3868-3873
Publication Date(Web):15 April 2011
DOI:10.1016/j.jpowsour.2010.12.101
A porous-microspheres Li–Si film (PMLSF) is prepared by multi-step constant current (MSCC) electrodeposition on Cu foil. Its structure and morphology are characterized using X-ray diffraction (XRD) and scanning electron microscope (SEM). As negative electrodes of lithium-ion batteries, the PMLSF electrode delivers the first gravimetric and geometric charge capacities of 2805.7 mA h g−1 and 621.9 μA h cm−2 at the current density of 25.5 μA cm−2, and its initial coulombic efficiency is as high as 98.2%. When the PMLSF electrode is cycled in VC-containing electrolyte, the superior cycling performance can be obtained. After 50 cycles, 96.0% of its initial capacity is retained at the current density of 50.0 μA cm−2. Electrochemical impedance spectra (EIS) research confirms the positive effect of VC additive on the behavior of the PMLSF electrode.Graphical abstractThe porous-microspheres Li–Si film (PMLSF) was first electrodeposited via multi-step constant current technique on Cu foil. This film was mainly composed of irregular and inter-connected porous-microspheres with different sizes ranging from several micrometers to several tens of micrometers. As negative electrodes for lithium-ion battery, the PMLSF electrode exhibited high initial coulombic efficiency and good cycling stability.Research highlights▶ Li and Si are co-deposited from a non-aqueous electrolyte solution. ▶ The porous-microspheres Li–Si film is first prepared via electrodeposition. ▶ Co-deposition of Li and Si leads to a high initial coulombic efficiency (>90%). ▶ The particular film morphology favors a superior cycling stability.
Co-reporter:Pengfei Gao, Haiping Jia, Jun Yang, Yanna Nuli, Jiulin Wang and Jun Chen  
Physical Chemistry Chemical Physics 2011 vol. 13(Issue 45) pp:20108-20111
Publication Date(Web):17 Oct 2011
DOI:10.1039/C1CP23062J
A novel three-dimensional porous Si–MWNT heterostructure was designed to meet the demand of high-capacity and long-life lithium storage. This material presented a stable capacity above 1000 mAh g−1 for nearly 200 cycles, which benefited from its highly porous structure combined with robust MWNT connections that accommodated the host volume change and improved the electric conductivity.
Co-reporter:Yu-Shi He, Pengfei Gao, Jun Chen, Xiaowei Yang, Xiao-Zhen Liao, Jun Yang and Zi-Feng Ma  
RSC Advances 2011 vol. 1(Issue 6) pp:958-960
Publication Date(Web):07 Sep 2011
DOI:10.1039/C1RA00429H
A novel bath lily-like graphene sheet-wrapped nano-Si composite synthesized via a simple spray drying process exhibits a high reversible capacity of 1525 mAh g−1 and superior cycling stability, which could be attributed to a synergistic effect between highly conductive graphene sheets and active nanoparticles in the open nano/micro-structure.
Co-reporter:Pengfei Gao, Yanna Nuli, Yu-Shi He, Jiazhao Wang, Andrew I. Minett, Jun Yang and Jun Chen  
Chemical Communications 2010 vol. 46(Issue 48) pp:9149-9151
Publication Date(Web):01 Nov 2010
DOI:10.1039/C0CC02870C
A novel Si-MWNT nanocomposite synthesized via a CVD process shows a high reversible capacity of over 1500 mAh g−1 and stable cycling performance, which can be ascribed to the maintenance of a good conductive network by means of the direct scattered growth and pinning of MWNTs on Si particles.
Co-reporter:Fei Wang, Jun Yang, Yanna NuLi, Jiulin Wang
Journal of Power Sources 2010 Volume 195(Issue 19) pp:6884-6887
Publication Date(Web):1 October 2010
DOI:10.1016/j.jpowsour.2010.04.071
Li1+0.5xCo1−xVx(PO4)1+0.5x/C (x = 0, 0.05, 0.10) composites with ordered olivine structure have been synthesized for use as cathode material in lithium ion batteries. The morphology and microstructure are characterized by scanning electron microscope, transmission electron microscopy and X-ray diffraction. The electrochemical test results show that addition of vanadium into LiCoPO4 remarkably improves its charge and discharge behavior. Li1.025Co0.95V0.05(PO4)1.025/C electrode gives its initial discharge capacity of 134.8 mAh g−1 at 0.1 C current rate, against 112.2 mAh g−1 for the pristine LiCoPO4/C, and exhibits much better cyclic stability than the latter. In particular, vanadium doping leads to an enhancement of the discharge voltage plateau for about 70 mV.
Co-reporter:Yongsheng Guo, Jun Yang, Yanna NuLi, Jiulin Wang
Electrochemistry Communications 2010 Volume 12(Issue 12) pp:1671-1673
Publication Date(Web):December 2010
DOI:10.1016/j.elecom.2010.08.015
The electrochemical behavior of three electrolyte solutions containing Grignard reagents (RMgBr) with different organic groups were investigated with regard to the potential application in rechargeable magnesium battery. It is found that the electrochemical reversibility of magnesium deposition and dissolution processes and the anodic stability of the Grignard electrolyte can be significantly improved by replacing alkyl group with more stable 4-Fluorophenyl group. In addition, the ionic conductivity of the Grignard electrolyte solution is enhanced by 1.5 times by such a replacement. The test results indicate that 4-Fluorophenyl-MgBr/THF solution could be promising for use in rechargeable magnesium battery systems.
Co-reporter:Pengfei Gao, Jianwei Fu, Jun Yang, Rongguan Lv, Jiulin Wang, Yanna Nuli and Xiaozhen Tang  
Physical Chemistry Chemical Physics 2009 vol. 11(Issue 47) pp:11101-11105
Publication Date(Web):29 Oct 2009
DOI:10.1039/B914959G
A microporous carbon coated core/shell Si@C nanocomposite prepared by in situpolymerization exhibits a stable capacity of over 1200 mAh g−1 with 95.6% retention even after 40 cycles, which makes it a promising anode material for lithium ion batteries.
Co-reporter:Hongbin Zhao, Jun Yang, Lei Li, Hong Li, Jiulin Wang, Yongming Zhang
International Journal of Hydrogen Energy 2009 Volume 34(Issue 9) pp:3908-3914
Publication Date(Web):May 2009
DOI:10.1016/j.ijhydene.2009.02.079
Bimetallic Pt–Co nanoparticles were co-deposited on polypyrrole (PPy)-multiwalled carbon nanotube (MWCNT) composite by formaldehyde reduction route to develop an anode catalyst for direct methanol fuel cells (DMFCs). PPy-MWCNT support was prepared by in situ polymerization of pyrrole on MWCNT. The electrochemical activity of this catalyst towards methanol oxidation and the important influencing factors have been investigated. The Pt–Co/PPy-MWCNT composite via over-oxidation treatment shows higher catalytic activity and potential application value for DMFCs.
Co-reporter:Yanna NuLi, Jun Yang, Jiulin Wang and Yun Li
The Journal of Physical Chemistry C 2009 Volume 113(Issue 28) pp:12594-12597
Publication Date(Web):June 22, 2009
DOI:10.1021/jp903188b
A study on electrochemical intercalation of bivalent cation Mg2+ in magnesium manganese silicate is reported. Reversible Mg2+ intercalation can be demonstrated and the process is enhanced by use of nanoscopic particles, resulted from a lower interfacial charge transfer resistance and a shorter solid-state diffusion distance of Mg2+ in the host. As a step toward novel rechargeable magnesium battery system, we have demonstrated the feasibility of the electrochemical oxidation, reduction, and cycling of magnesium manganese silicate. The results show that the silicate compound could be a good host for Mg2+ intercalation and a potential cathode material for high-energy rechargeable magnesium batteries.
Co-reporter:Hongbin Zhao, Lei Li, Jun Yang, Yongming Zhang
Journal of Power Sources 2008 Volume 184(Issue 2) pp:375-380
Publication Date(Web):1 October 2008
DOI:10.1016/j.jpowsour.2008.03.024
A novel catalyst support was synthesized by in situ chemical oxidative polymerization of pyrrole on Vulcan XC-72 carbon in naphthalene sulfonic acid (NSA) solution containing ammonium persulfate as oxidant at room temperature. Pt nanoparticles with 3–4 nm size were deposited on the prepared polypyrrole–carbon composites by chemical reduction method. Scanning electron microscopy and transmission electron microscopy measurements showed that Pt particles were homogeneously dispersed in polypyrrole–carbon composites. The Pt nanoparticles-dispersed catalyst composites were used as anodes of fuel cells for hydrogen and methanol oxidation. Cyclic voltammetry measurements of hydrogen and methanol oxidation showed that Pt nanoparticles deposited on polypyrrole–carbon with NSA as dopant exhibit better catalytic activity than those on plain carbon. This result might be due to the higher electrochemically available surface areas, electronic conductivity and easier charge-transfer at polymer/carbon particle interfaces allowing a high dispersion and utilization of deposited Pt nanoparticles.
Co-reporter:Zhenzhen Feng, Jun Yang, Yanna NuLi, Jiulin Wang
Journal of Power Sources 2008 Volume 184(Issue 2) pp:604-609
Publication Date(Web):1 October 2008
DOI:10.1016/j.jpowsour.2008.05.021
Magnesium manganese silicate (Mg1.03Mn0.97SiO4) was prepared by a sol–gel method and evaluated as an intercalation electrode material for rechargeable magnesium batteries. The crystalline Mg1.03Mn0.97SiO4 phase was obtained after heating at 900 °C and its electrochemical performance was characterized at room temperature. The pure magnesium manganese silicate exhibits a relatively low reversible specific capacity in the electrolyte comprising 0.25 mol L−1 Mg(AlCl2EtBu)2/THF owing to its poor electronic conductivity. Using a ball mill in the presence of acetylene black, and in situ carbon coating, the resulting composites present an improved discharge voltage plateau (1.6 V vs. Mg/Mg2+) and increased discharge specific capacity (92.9 mAh g−1 at a C/50 rate). The Mg lower price and its feasibility for rechargeable batteries make magnesium manganese silicate an attractive candidate for rechargeable magnesium based batteries.
Co-reporter:Zhenzhen Feng, Jun Yang, Yanna NuLi, Jiulin Wang, Xiaojian Wang, Zhaoxiang Wang
Electrochemistry Communications 2008 Volume 10(Issue 9) pp:1291-1294
Publication Date(Web):September 2008
DOI:10.1016/j.elecom.2008.06.021
Orthorhombic magnesium manganese silicate (Mg1.03Mn0.97SiO4) was prepared and evaluated as a new cathode material for rechargeable magnesium batteries. Although the electrochemical activity of the Mg1.03Mn0.97SiO4 synthesized by high-temperature solid-state reaction is low, the magnesium storage capacity of nanosized Mg1.03Mn0.97SiO4 prepared by modified sol–gel route and in situ carbon coating reaches 244 mAh g−1. The capacity increase mechanism during charge/discharge cycling was also preliminary studied.
Co-reporter:Ying Zheng, Jun Yang, Yanna NuLi, Jiulin Wang
Journal of Power Sources 2007 Volume 174(Issue 2) pp:624-627
Publication Date(Web):6 December 2007
DOI:10.1016/j.jpowsour.2007.06.116
Finely dispersed tin alloy/oxide composites were synthesized via the reduction of tin oxide by aluminum under high-energy ball-milling. The morphology and crystal structure of the resulting samples were investigated by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD). The electrochemical measurements reveal that Sn3Co/Al2O3 composite has higher initial efficiency and better cycle performance than Sn/Al2O3. The Sn3Co/Al2O3 composite electrode containing LA132 binder exhibited a reversible capacity about 540 mA h g−1 with good capacity retention. On the other hand, it is found that the influence of binder type on the electrode performance is remarkable.
Co-reporter:Zhenzhen Feng, Yanna Nuli, Jun Yang
Acta Physico-Chimica Sinica 2007 Volume 23(Issue 3) pp:327-331
Publication Date(Web):March 2007
DOI:10.1016/S1872-1508(07)60026-6
Conductive sulfur-containing material (CSM), synthesized by simply heating a mixture of polyacrylonitrile (PAN) and elemental sulfur, and its composite with polyaniline (PAn) were used as the cathode material for rechargeable magnesium batteries. X-ray diffraction (XRD) and Fourier-transform infrared (FT-IR) spectroscopy measurements showed that the CSM consisted of a graphite-like microcrystal phase and an amorphous phase, with a dehydrapyridine-type matrix containing S–S bonds. When polyaniline was incorporated with CSM and Cu(II) was doped into the CSM/PAn composite, the specific discharge capacity and electrochemical reversibility were enhanced significantly. The composite exhibited a discharge capacity of 117.3 mAh·g−1 and the capacity retention remained at about 78% after twenty-two cycles, based on the second cycle discharge capacity. Here PAn functioned as both electrocatalyst and cathode material. At the same time, it improved the conductivity of the active CSM at a molecular level. The results of this study provided a new thought for structure design and development of a potential cathode material for rechargeable magnesium batteries.
Co-reporter:Y. Wang;J. Wang;J. Yang;Y. Nuli
Advanced Functional Materials 2006 Volume 16(Issue 16) pp:
Publication Date(Web):19 SEP 2006
DOI:10.1002/adfm.200600442

A LiFePO4 material with ordered olivine structure is synthesized from amorphous FePO4 · 4H2O through a solid–liquid phase reaction using (NH4)2SO3 as the reducing agent, followed by thermal conversion of the intermediate NH4FePO4 in the presence of LiCOOCH3 · 2H2O. Simultaneous thermogravimetric–differential thermal analysis indicates that the crystallization temperature of LiFePO4 is about 437 °C. Ellipsoidal particle morphology of the resulting LiFePO4 powder with a particle size mainly in the range 100–300 nm is observed by using scanning electron microscopy and transmission electron microscopy. As an electrode material for rechargeable lithium batteries, the LiFePO4 sample delivers a discharge capacity of 167 mA h g–1 at a constant current of 17 mA g–1 (0.1 C rate; throughout this study n C rate means that rated capacity of LiFePO4 (170 mA h g–1) is charged or discharged completely in 1/n hours), approaching the theoretical value of 170 mA h g–1. Moreover, the electrode shows excellent high-rate charge and discharge capability and high electrochemical reversibility. No capacity loss can be observed up to 50 cycles under 5 C and 10 C rate conditions. With a conventional charge mode, that is, 5 C rate charging to 4.2 V and then keeping this voltage until the charge current is decreased to 0.1 C rate, a discharge capacity of ca. 134 mA h g–1 and cycling efficiency of 99.2–99.6 % can be obtained at 5 C rate.

Co-reporter:Xiaowei Miao, Zhenying Chen, Nan Wang, Yanna Nuli, Jiulin Wang, Jun Yang, Shin-ichi Hirano
Nano Energy (April 2017) Volume 34() pp:
Publication Date(Web):April 2017
DOI:10.1016/j.nanoen.2017.02.014
•V2MoO8 is firstly synthesized by electrospinning and used as a cathode material for rechargeable Mg batteries.•Adding LiCl to APC electrolyte significantly improves the cell performance.•The mechanism of cathode reaction in Mg2+/Li+ dual-salt electrolyte is studied.With the increasing global demand for large-scale electrical energy storage, rechargeable Mg-based batteries are preferable due to their substantial prospective benefits in terms of raw abundance, theoretical capacity, and operational safety. Herein, we demonstrate for the first time V2MoO8 synthesized by a facile electrospinning method as a cathode material for rechargeable magnesium batteries with the electrolytes containing Mg2+ or Mg2+/Li+ ions. SEM and HRTEM indicate that the V2MoO8 sample presents wedged-shaped cuboid, 300–500 nm (thickness) ×4–6 µm (length) and its monoclinic phase structure provides a interlayer distance of 4.20 Å. As cathode material, V2MoO8 is discharged/charged in a specially self-designed mould battery using Mg metal anode at current densities from 20 to 500 mA g−1. It delivers a high initial discharge capacity of 312 mA h g−1 with the initial coulombic efficiency of 87.2% at 20 mA g−1 in 0.4 M (PhMgCl)2-AlCl3/1.0 M LiCl/THF electrolyte and presents good cycling and rate performance. XPS analysis reveals that both Mg2+ and Li+ ions take part in the cathode intercalation reaction, along with the valence changes of Mo/V ions. Additionally, a reversible capacity of ca. 210 mA h g−1 is obtained in Mg2+ electrolyte with the 1st cycle efficiency of 94% at 60 °C. The poor capacity retention is partially attributed to the irreversible phase change to amorphous state of V2MoO8.Well crystalline layered V2MoO8 is synthesized by electrospinning combined with calcinations. As a multi-electrons cathode material in rechargeable magnesium batteries, it delivers a fairly stable capacity of ca. 150 mA h g−1 with a discharge voltage of 1.55 V in APC/1 M LiCl. The LiCl effect, phase evolution during cycling and the big initial capacity loss are examined and discussed.
Co-reporter:Yitian Bie, Jun Yang, Yanna Nuli and Jiulin Wang
Journal of Materials Chemistry A 2017 - vol. 5(Issue 5) pp:NaN1924-1924
Publication Date(Web):2016/12/30
DOI:10.1039/C6TA09522D
Natural karaya gum (KG), composed of polysaccharides and glycoproteins, is investigated as a binder for high-performance silicon-based anodes. Good mechanical properties provided by the multi-branched structure and glycoproteins and superior binding strength resulting from plentiful polar function groups lead to superior electrochemical performance of KG electrodes.
Co-reporter:Pengfei Gao, Haiping Jia, Jun Yang, Yanna Nuli, Jiulin Wang and Jun Chen
Physical Chemistry Chemical Physics 2011 - vol. 13(Issue 45) pp:NaN20111-20111
Publication Date(Web):2011/10/17
DOI:10.1039/C1CP23062J
A novel three-dimensional porous Si–MWNT heterostructure was designed to meet the demand of high-capacity and long-life lithium storage. This material presented a stable capacity above 1000 mAh g−1 for nearly 200 cycles, which benefited from its highly porous structure combined with robust MWNT connections that accommodated the host volume change and improved the electric conductivity.
Co-reporter:Jingjing Zhou, Jun Yang, Zhixin Xu, Tao Zhang, Zhenying Chen and Jiulin Wang
Journal of Materials Chemistry A 2017 - vol. 5(Issue 19) pp:NaN9357-9357
Publication Date(Web):2017/04/12
DOI:10.1039/C7TA01564J
Rechargeable lithium–selenium (Li–Se) batteries are promising electrochemical systems with higher energy density than traditional Li ion batteries. Nevertheless, the dissolution of high-order lithium selenides and the shuttle effect in electrolytes lead to low Se utilization, inferior capacity and poor cycling performance. This study proposes a combination of nanostructured Se cathode materials and compatible carbonate electrolytes for promoting the performance of Li–Se batteries. Se/MC composite nanoparticles (∼35 nm) with a moderate Se content (≈51.4 wt%) were prepared by embedding Se into a metal–organic framework derived microporous carbon. The resulting Se/MC cathode exhibits significantly high rate capability and cycling stability in LiDFOB/EC-DMC-FEC electrolyte. It delivers a capacity of 511 mA h gSe−1 after 1000 cycles at 5C, with an inappreciable capacity decay of 0.012% per cycle. Even at a very high rate of 20C, a large capacity of 569 mA h gSe−1 can be obtained, corresponding to a decrease of only 5.6% compared to that at 0.5C. The impressive high rate performance is attributed to the co-effect of selenium confined in ultra-small microporous carbon particles and excellent compatibility of the electrolyte with both the Li anode and selenium composite cathode.
Co-reporter:Dongpo Xu, Zhehao Huang, Rongrong Miao, Yitian Bie, Jun Yang, Yuan Yao and Shunai Che
Journal of Materials Chemistry A 2014 - vol. 2(Issue 46) pp:NaN19860-19860
Publication Date(Web):2014/09/30
DOI:10.1039/C4TA04088K
Mesoporous silicon nanofibers were synthesised by magnesiothermic reduction of earthworm-like, lamellar structured silica nanotubes for use in developing highly efficient lithium ion batteries. The silica nanotubes resulted from the single-molecular-layer arrangement of a bolaamphiphile surfactant. The calcined mesoporous silica nanotubes transformed into mesoporous silicon nanofibers (nf-Si) after magnesiothermic reduction. Finally, carbon-layer-coated silicon nanofibers (nf-Si@C) were obtained by chemical vapour deposition (CVD), which displayed a stable capacity of approximately 1141 mA h g−1 over 100 cycles at 0.2 C.
Co-reporter:Xuejiao Feng, Jun Yang, Qingwen Lu, Jiulin Wang and Yanna Nuli
Physical Chemistry Chemical Physics 2013 - vol. 15(Issue 34) pp:NaN14426-14426
Publication Date(Web):2013/06/24
DOI:10.1039/C3CP51799C
The m-SiOx/Si composite for lithium ion battery anode was prepared via a partial reduction reaction between ball-milled silicon monoxide and magnesium by high-energy mechanical milling. The m-SiOx/Si is composed of Si-suboxide and embedded Si nano-crystallites. The particles were further covered by a uniform carbon layer on the surface via a chemical vapor deposition process. The m-SiOx/Si/C composite shows a stable reversible capacity of ca. 1250 mA h g−1 and excellent cycling stability with 90.9% capacity retention on the 100th cycle versus the 6th one (compared at the same current rate). In contrast, SiO pre-milled for 25 h presents a reversible capacity of only ca. 900 mA h g−1 under the same carbon coating condition.
Co-reporter:Lichao Yin, Jiulin Wang, Jun Yang and Yanna Nuli
Journal of Materials Chemistry A 2011 - vol. 21(Issue 19) pp:NaN6810-6810
Publication Date(Web):2011/04/08
DOI:10.1039/C1JM00047K
A novel pPAN-S@MWCNT core-shell composite material is prepared via in situpolymerization of acrylonitrile on the surface of MWCNT, mixing with sulfur and final pyrolysis. The homogenous dispersion and integration of MWCNT in the composite create an electronically conductive network and reinforce the structural stability, leading to the outstanding electrochemical performances as a cathode material for rechargeable lithium/sulfur batteries.
Co-reporter:Pengfei Gao, Jianwei Fu, Jun Yang, Rongguan Lv, Jiulin Wang, Yanna Nuli and Xiaozhen Tang
Physical Chemistry Chemical Physics 2009 - vol. 11(Issue 47) pp:NaN11105-11105
Publication Date(Web):2009/10/29
DOI:10.1039/B914959G
A microporous carbon coated core/shell Si@C nanocomposite prepared by in situpolymerization exhibits a stable capacity of over 1200 mAh g−1 with 95.6% retention even after 40 cycles, which makes it a promising anode material for lithium ion batteries.
Co-reporter:Fei-fei Wang, Yong-sheng Guo, Jun Yang, Yanna Nuli and Shin-ichi Hirano
Chemical Communications 2012 - vol. 48(Issue 87) pp:NaN10765-10765
Publication Date(Web):2012/09/13
DOI:10.1039/C2CC35857C
A new phenolate-based magnesium ion conducting electrolyte is prepared. The electrolyte exhibits air insensitive character and excellent electrochemical performances which make it highly promising for advanced rechargeable Mg battery systems.
Co-reporter:Jinhui Zhu, Jun Yang, Rongrong Miao, Zhaoquan Yao, Xiaodong Zhuang and Xinliang Feng
Journal of Materials Chemistry A 2016 - vol. 4(Issue 6) pp:NaN2292-2292
Publication Date(Web):2016/01/11
DOI:10.1039/C5TA09073C
Nitrogen-doped (N-doped) porous carbons have drawn increasing attention due to their high activity for electrochemical catalysis, and high capacity for lithium-ion (Li-ion) batteries and supercapacitors. So far, the controlled synthesis of N-enriched ordered mesoporous carbons (N-OMCs) for Li-ion batteries is rarely reported due to the lack of a reliable nitrogen-doping protocol that maintains the ordered mesoporous structure. In order to realize this, in this work, ordered mesoporous carbons with controllable N contents were successfully prepared by using melamine, F127 and phenolic resin as the N-source, template and carbon-source respectively via a solvent-free ball-milling method. The as-prepared N-OMCs which showed a high N content up to 31.7 wt% were used as anodes for Li-ion batteries. Remarkably, the N-OMCs with an N content of 24.4 wt% exhibit the highest reversible capacity (506 mA h g−1) even after 300 cycles at 300 mA g−1 and a capacity retention of 103.3%. N-OMCs were also used as electrode materials in supercapacitors and a capacity of 150 F g−1 at 0.2 A g−1 with stable cycling up to 2500 times at 1 A g−1 was achieved. These attractive results encourage the design and synthesis of high heteroatom content ordered porous carbons for applications in the field of energy storage and conversion.
Co-reporter:Pengfei Gao, Yanna Nuli, Yu-Shi He, Jiazhao Wang, Andrew I. Minett, Jun Yang and Jun Chen
Chemical Communications 2010 - vol. 46(Issue 48) pp:NaN9151-9151
Publication Date(Web):2010/11/01
DOI:10.1039/C0CC02870C
A novel Si-MWNT nanocomposite synthesized via a CVD process shows a high reversible capacity of over 1500 mAh g−1 and stable cycling performance, which can be ascribed to the maintenance of a good conductive network by means of the direct scattered growth and pinning of MWNTs on Si particles.
Co-reporter:Yitian Bie, Jun Yang, Jiulin Wang, Jingjing Zhou and Yanna Nuli
Chemical Communications 2017 - vol. 53(Issue 59) pp:NaN8327-8327
Publication Date(Web):2017/06/30
DOI:10.1039/C7CC04646D
Commercially available Li2O2 was proposed as a cathode additive in commercialized LiNi0.33Co0.33Mn0.33O2 (NCM) cathodes to offset the initial Li loss. Li2O2 can be decomposed substantially under catalysis of NCM and leaves almost no remnants after the Li compensation.
Co-reporter:Lichao Yin, Jiulin Wang, Xiaolei Yu, Charles W. Monroe, Yanna NuLi and Jun Yang
Chemical Communications 2012 - vol. 48(Issue 63) pp:NaN7870-7870
Publication Date(Web):2012/06/21
DOI:10.1039/C2CC33333C
A novel dual-mode sulfur-based cathode material is prepared for the first time, in which sulfur is embedded in both the pyrolyzed PAN nanoparticles (pPAN) and mildly reduced graphene oxide nanosheets (mGO). The pPAN–S/mGO–S composite demonstrates outstanding electrochemical performances in the rechargeable Li–S batteries.
L-Glutamic acid,N-[4-[2-[(6R)-2-amino-3,4,5,6,7,8-hexahydro-4-oxopyrido[2,3-d]pyrimidin-6-yl]ethyl]benzoyl]-
L-Glutamic acid,N-[4-[2-(2-amino-3,4,5,6,7,8-hexahydro-4-oxopyrido[2,3-d]pyrimidin-6-yl)ethyl]benzoyl]-
Manganese vanadiumoxide (MnV2O6)