Co-reporter:Mengfan Wang, Tao Qian, Sisi Liu, Jinqiu Zhou, and Chenglin Yan
ACS Applied Materials & Interfaces June 28, 2017 Volume 9(Issue 25) pp:21216-21216
Publication Date(Web):June 5, 2017
DOI:10.1021/acsami.7b02346
The development of nonprecious metal catalysts with desirable bifunctional activities to supersede noble metal catalysts is of vital importance for high performance aqueous zinc–air batteries. Here, an unprecedented activity of bifunctional electrocatalyst is reported by in situ growth of nitrogen-enriched carbon nanotubes with transition metal composite. The resultant catalyst delivers surprisingly high OER (potential@10 mA cm–2 of 1.58 V) and ORR (onset potential of 0.97 V, half-wave potential of 0.86 V) performance. The overall oxygen electrode activity (overvoltage between ORR and OER) of the catalyst is as low as 0.72 V. In aqueous Zn–air battery tests, primary batteries demonstrate high maximum power density and two-electrode rechargeable batteries also exhibit good cycle performance. The unprecedented electrocatalyst opens up new avenues for developing highly active nitrogen-doped carbon nanotube-supported electrocatalysts and offers prospects for the next generation of fuel cells, metal–air batteries, and photocatalysis applications.Keywords: carbon nanomaterial; nitrogen-doping; non-noble metal catalysts; oxygen evolution reaction; oxygen reduction reaction; zinc−air battery;
Co-reporter:Jie Liu, Tao Qian, Mengfan Wang, Xuejun Liu, Na Xu, Yizhou You, and Chenglin Yan
Nano Letters August 9, 2017 Volume 17(Issue 8) pp:5064-5064
Publication Date(Web):July 10, 2017
DOI:10.1021/acs.nanolett.7b02332
Using molecularly imprinted polymer to recognize various target molecules emerges as a fascinating research field. Herein, we applied this strategy for the first time to efficiently recognize and trap long-chain polysulfides (Li2Sx, x = 6–8) in lithium sulfur battery to minimize the polysulfide shuttling between anode and cathode, which enables us to achieve remarkable electrochemical performance including a high specific capacity of 1262 mAh g–1 at 0.2 C and superior capacity retention of over 82.5% after 400 cycles at 1 C. The outstanding performance is attributed to the significantly reduced concentration of long-chain polysulfides in electrolyte as evidenced by in situ UV/vis spectroscopy and Li2S nucleation tests, which were further confirmed by density functional theory calculations. The molecular imprinting is demonstrated as a promising approach to effectively prevent the free diffusion of long-chain polysulfides, providing a new avenue to efficiently recognize and trap lithium polysulfides for high-performance lithium sulfur battery with greatly suppressed shuttle effect.Keywords: in situ UV/vis spectroscopy; Li2S nucleation test; lithium sulfur battery; long-chain polysulfides; Molecularly imprinted polymer;
Co-reporter:Xuejun Liu, Na Xu, Tao Qian, Jie Liu, Xiaowei Shen, Chenglin Yan
Nano Energy 2017 Volume 41(Volume 41) pp:
Publication Date(Web):1 November 2017
DOI:10.1016/j.nanoen.2017.10.032
•Stabilize sulfur cathodes by the formation of low-solubility lithium polysulfides.•The resulted cathodes exhibited nearly 100% CE at current rates from 0.2C to 6 C.•The proposed mechanism was clearly revealed by in-situ UV/vis and DFT calculations.The long-chain lithium polysulfides that are soluble in ether-based electrolyte for lithium sulfur battery are regarded as one of reason for their low Coulumbic efficiency and low rate capability. In this work, we reported a new strategy to stabilize sulfur cathodes with alkylene radicals to covalently connect sulfur through the formation of low-solubility lithium polysulfides, which enables high Coulombic efficiencies of 99.9% at 0.2 C, 99.9% at 0.5 C, 100% at 1 C, 100% at 2 C, 100% at 4 C, 100% at 6 C as well as outstanding rate capability with a high capacity of 702 mAh g−1 at 6 C. The proposed mechanism was clearly revealed by in-situ UV/vis spectroscopy, demonstrating that short chain polysulfides as discharge products with low solubility are mainly produced during charging and discharging process. Moreover, DFT calculations confirmed that the bond breakage of the linear sulfur chains preferentially takes place in the center of the linear polysulfane, resulting in the formation of short-chain polysulfides, which could effectively avoid the production of soluble long-chain polysulfide and suppress the shuttling effect for high Coulumbic efficiency and high-rate capability lithium sulfur batteries.A new strategy is reported to stabilize sulfur cathodes with alkylene radicals through the formation of weakly soluble lithium polysulfides, which enables nearly 100% Columbic efficiency at current rates from 0.2C to 6 C as well as outstanding rate capability with a high capacity of 702 mAh g−1 at 6 C.Download high-res image (301KB)Download full-size image
Co-reporter:Yihao Xie;Yu Chen;Lei Liu;Peng Tao;Mouping Fan;Na Xu;Xiaowei Shen
Advanced Materials 2017 Volume 29(Issue 35) pp:
Publication Date(Web):2017/09/01
DOI:10.1002/adma.201702268
An ultrahigh pyridinic N-content-doped porous carbon monolith is reported, and the content of pyridinic N reaches up to 10.1% in overall material (53.4 ± 0.9% out of 18.9 ± 0.4% N content), being higher than most of previously reported N-doping carbonaceous materials, which exhibit greatly improved electrochemical performance for potassium storage, especially in term of the high reversible capacity. Remarkably, the pyridinic N-doped porous carbon monolith (PNCM) electrode exhibits high initial charge capacity of 487 mAh g−1 at a current density of 20 mA g−1, which is one of the highest reversible capacities among all carbonaceous anodes for K-ion batteries. Moreover, the K-ion full cell is successfully assembled, demonstrating a high practical energy density of 153.5 Wh kg−1. These results make PNCM promising for practical application in energy storage devices and encourage more investigations on a similar potassium storage system.
Co-reporter:Jinqiu Zhou;Tao Qian;Na Xu;Mengfan Wang;Xuyan Ni;Xuejun Liu;Xiaowei Shen
Advanced Materials 2017 Volume 29(Issue 33) pp:
Publication Date(Web):2017/09/01
DOI:10.1002/adma.201701294
For the first time a new strategy is reported to improve the volumetric capacity and Coulombic efficiency by selenium doping for lithium–organosulfur batteries. Selenium-doped cathodes with four sulfur atoms and one selenium atom (as the doped heteroatom) in the confined structure are designed and synthesized; this structure exhibits greatly improved volumetric/areal capacities, and a Coulombic efficiency of almost 100% for highly stable lithium–organosulfur batteries. The doping of Se significantly enhances the electronic conductivity of battery electrodes by a factor of 6.2 compared to pure sulfur electrodes, and completely restricts the production of long-chain lithium polysulfides. This allows achievement of a high gravimetric capacity of 700 mAh g−1 close to its theoretical mass capacity, an exceptional volumetric capacity of 2457 mAh cm−3, and excellent capacity retention of 92% after 400 cycles. Shuttle effect is efficiently weakened since no long-chain polysulfides are detected from in situ UV/vis results throughout the entire cycling process arising from selenium doping, which is theoretically confirmed by density functional theory calculations.
Co-reporter:Na Xu, Tao Qian, Xuejun Liu, Jie Liu, Yu ChenChenglin Yan
Nano Letters 2017 Volume 17(Issue 1) pp:
Publication Date(Web):December 15, 2016
DOI:10.1021/acs.nanolett.6b04610
The high solubility of long-chain lithium polysulfides and their infamous shuttle effect in lithium sulfur battery lead to rapid capacity fading along with low Coulombic efficiency. To address above issues, we propose a new strategy to suppress the shuttle effect for greatly enhanced lithium sulfur battery performance mainly through the formation of short-chain intermediates during discharging, which allows significant improvements including high capacity retention of 1022 mAh/g with 87% retention for 450 cycles. Without LiNO3-containing electrolytes, the excellent Coulombic efficiency of ∼99.5% for more than 500 cycles is obtained, suggesting the greatly suppressed shuttle effect. In situ UV/vis analysis of electrolyte during cycling reveals that the short-chain Li2S2 and Li2S3 polysulfides are detected as main intermediates, which are theoretically verified by density functional theory (DFT) calculations. Our strategy may open up a new avenue for practical application of lithium sulfur battery.Keywords: in situ UV/vis analysis; Lithium sulfur battery; short chain intermediates; shuttle effect;
Co-reporter:Mengfan Wang, Tao QianJinqiu Zhou, Chenglin Yan
ACS Applied Materials & Interfaces 2017 Volume 9(Issue 6) pp:
Publication Date(Web):January 20, 2017
DOI:10.1021/acsami.6b12197
Efficient bifunctional electrocatalysts with desirable oxygen activities are closely related to practical applications of renewable energy systems including metal–air batteries, fuel cells, and water splitting. Here a composite material derived from a combination of bimetallic zeolitic imidazolate frameworks (denoted as BMZIFs) and Fe/N/C framework was reported as an efficient bifunctional catalyst. Although BMZIF or Fe/N/C alone exhibits undesirable oxygen reaction activity, a combination of these materials shows unprecedented ORR (half-wave potential of 0.85 V as well as comparatively superior OER activities (potential@10 mA cm–2 of 1.64 V), outperforming not only a commercial Pt/C electrocatalyst but also most reported bifunctional electrocatalysts. We then tested its practical application in Zn–air batteries. The primary batteries exhibit a high peak power density of 235 mW cm–2, and the batteries are able to be operated smoothly for 100 cycles at a curent density of 10 mA cm–2. The unprecedented catalytic activity can be attritued to chemical coupling effects between Fe/N/C and BMZIF and will aid the development of highly active electrocatalysts and applications for electrochemical energy devices.
Co-reporter:Xianfu Wang, Yu Chen, Oliver G. Schmidt and Chenglin Yan
Chemical Society Reviews 2016 vol. 45(Issue 5) pp:1308-1330
Publication Date(Web):21 Dec 2015
DOI:10.1039/C5CS00708A
Engineered nanomembranes are of great interest not only for large-scale energy storage devices, but also for on-chip energy storage integrated microdevices (such as microbatteries, microsupercapacitors, on-chip capacitors, etc.) because of their large active surfaces for electrochemical reactions, shortened paths for fast ion diffusion, and easy engineering for microdevice applications. In addition, engineered nanomembranes provide a lab-on-chip electrochemical device platform for probing the correlations of electrode structure, electrical/ionic conductivity, and electrochemical kinetics with device performance. This review focuses on the recent progress in engineered nanomembranes including tubular nanomembranes and planar nanomembranes, with the aim to provide a systematic summary of their fabrication, modification, and energy storage applications in lithium-ion batteries, lithium–oxygen batteries, on-chip electrostatic capacitors and micro-supercapacitors. A comprehensive understanding of the relationship between engineered nanomembranes and electrochemical properties of lithium ion storage with engineered single-tube microbatteries is given, and the flexibility and transparency of micro-supercapacitors is also discussed. Remarks on challenges and perspectives related to engineered nanomembranes for the further development of energy storage applications conclude this review.
Co-reporter:Tingzhou Yang;Tao Qian;Mengfan Wang;Xiaowei Shen;Na Xu;Zhouzhou Sun
Advanced Materials 2016 Volume 28( Issue 3) pp:539-545
Publication Date(Web):
DOI:10.1002/adma.201503221
Co-reporter:Mouping Fan;Yu Chen;Yihao Xie;Tingzhou Yang;Xiaowei Shen;Na Xu;Haiying Yu
Advanced Functional Materials 2016 Volume 26( Issue 28) pp:5019-5027
Publication Date(Web):
DOI:10.1002/adfm.201601323
Sodium-ion battery (SIB) is especially attractive in cost-effective energy storage device as an alternative to lithium-ion battery. Particularly, metal phosphides as potential anodes for SIBs have recently been demonstrated owing to their higher specific capacities compared with those of carbonaceous materials. Unfortunately, most reported metal phosphides consist of irregular particles ranged from several hundreds nanometers to tens of micrometers, thus delivering limited cyclic stability. This paper reports the sodium storage properties of additive-free Cu3P nanowire (CPNW) anode directly grown on copper current collector via an in situ growth followed by phosphidation method. Therefore, as a result of its structure features, CPNW anode demonstrates highly stable cycling ability with an ≈70% retention in capacity at the 260th cycle, whereas most reported metal phosphides have limited cycle numbers ranged between 30 and 150. Besides, the reaction mechanism between Cu3P and Na is investigated by examining the intermediate products at different charge/discharge stages using ex situ X-ray diffraction measurements. Furthermore, to explore the practical application of CPNW anode, a pouch-type Na+ full cell consisting of CPNW anode and Na3V2(PO4)3 cathode is assembled and characterized. As a demonstration, a 10 cm × 10 cm light-emmiting diode (LED) screen is successfully powered by the Na+ full cell.
Co-reporter:Jinqiu Zhou, Tao Qian, Mengfan Wang, Na Xu, Qi Zhang, Qun Li, and Chenglin Yan
ACS Applied Materials & Interfaces 2016 Volume 8(Issue 8) pp:5358
Publication Date(Web):February 10, 2016
DOI:10.1021/acsami.5b12392
In situ core–shell coating was used to improve the electrochemical performance of Si-based anodes with polypyrrole-Fe coordination complex. The vast functional groups in the organometallic coordination complex easily formed hydrogen bonds when in situ modifying commercial Si nanoparticles. The incorporation of polypyrrole-Fe resulted in the conformal conductive coating surrounding each Si nanoparticle, not only providing good electrical connection to the particles but also promoting the formation of a stable solid-electrolyte-interface layer on the Si electrode surface, enhancing the cycling properties. As an anode material for Li-ion batteries, modified silicon powders exhibited high reversible capacity (3567 mAh/g at 0.3 A/g), good rate property (549.12 mAh/g at 12 A/g), and excellent cycling performance (reversible capacity of 1500 mAh/g after 800 cycles at 1.2 A/g). The constructed novel concept of core–shell coating Si particles presented a promising route for facile and large-scale production of Si-based anodes for extremely durable Li-ion batteries, which provided a wide range of applications in the field of energy storage of the renewable energy derived from the solar energy, hydropower, tidal energy, and geothermal heat.Keywords: coordination complex; cycling performance; lithium-ion battery; PPy-Fe; silicon
Co-reporter:Xueyi Lu, Wenping Si, Xiaolei Sun, Bo Liu, Long Zhang, Chenglin Yan, Oliver G. Schmidt
Nano Energy 2016 Volume 19() pp:428-436
Publication Date(Web):January 2016
DOI:10.1016/j.nanoen.2015.10.027
•Pd-functionalized MnOx-GeOy nanomembranes were used as catalyst of Li-O2 batteries.•Rolled-up technology and organic colloid method were applied for preparation.•The materials exhibits extremely low charge voltage of ~3.14 V and high efficiency.•The synergy among membrane, Pd and oxygen vacancies contributes to the performance.Li–O2 batteries have the potential to be the candidate for the power source to drive electric-vehicles and portable electronics. Recent studies have been focused on searching for stable electrode materials for rechargeable Li–O2 batteries with high efficiency and long cycle life. Here Pd-functionalized MnOx–GeOy nanomembranes were fabricated as the cathode materials of Li–O2 batteries. The incorporation of Pd nanoparticles on the nanomembranes matrix enables the fast transportation of both electrons and lithium ions as well as oxygen-containing species, thus efficiently lowering the charge voltage and greatly prolonging the cycle life of Li–O2 batteries to 160 cycles without apparent degradation. More importantly, Li–O2 batteries using such as-prepared Pd-functionalized MnOx–GeOy nanomembranes can be cycled repeatedly with extremely low charge voltage of only ~3.14 V. The presence of small amounts of Pd nanoparticles contributes to the formation of toroid-like Li2O2 during the oxygen reduction reaction which is efficiently decomposed afterwards by the oxygen evolution reaction. The encouraging performance suggests that such nanomembrane-based materials are promising cathode architectures for the future Li–O2 batteries.
Co-reporter:Xiaopeng Li;Junna Wang;Andreas Graff;Stefan L. Schweizer;Alexer Sprafke;Oliver G. Schmidt;Ralf B. Wehrspohn
Advanced Energy Materials 2015 Volume 5( Issue 4) pp:
Publication Date(Web):
DOI:10.1002/aenm.201401556
Co-reporter:Yu Chen;Lifeng Liu;Jie Xiong;Tingzhou Yang;Yong Qin
Advanced Functional Materials 2015 Volume 25( Issue 43) pp:6701-6709
Publication Date(Web):
DOI:10.1002/adfm.201503206
In the quest to develop next generation lithium ion battery anode materials, satisfactory electrochemical performance and low material/fabrication cost are the most desirable features. In this article, porous Si nanowires are synthesized by a cost-effective metal-assisted chemical etching method using cheap metallurgical silicon as feedstock. More importantly, a thin oxide layer (≈3 nm) formed on the surface of porous Si nanowires stabilizes the cycling performance of lithium ion batteries. Such an oxide coating is able to constrain the huge volume expansion of the underlying Si, yet it is thin enough to ensure good permeability for both lithium ions and electrons. Therefore, the extraordinary storage capacity of Si can be well retained in prolonged electrochemical cycles. Specifically, Si/SiOx nanowires deliver a reversible capacity of 1503 mAh g−1 at the 560th cycle at a current density of 600 mA g−1, demonstrating an average of only 0.04% drop per cycle compared with its initial capacity. Furthermore, the highly porous structure and thin Si wall facilitate the electrolyte penetration and shorten the solid-state lithium transportation path, respectively. As a result, stable and satisfactory reversible capacities of 1297, 976, 761, 548, and 282 mAh g−1 are delivered at current densities of 1200, 2400, 3600, 4800, and 7200 mA g−1, respectively.
Co-reporter:Tingzhou Yang, Tao Qian, Mengfan Wang, Jie Liu, Jinqiu Zhou, Zhouzhou Sun, Muzi Chen and Chenglin Yan
Journal of Materials Chemistry A 2015 vol. 3(Issue 12) pp:6291-6296
Publication Date(Web):16 Feb 2015
DOI:10.1039/C4TA07208A
A new approach using polypyrrole as the nitrogen source has been demonstrated for the fabrication of nitrogen-doped graphene, which subsequently served as nucleation centers for the growth of metal oxides. The thin layers of the nitrogen-doped graphene are not only used as conductive pathways accelerating the electrical conductivity of metal oxides but also serve as buffer layers to improve the electrical contact with metal oxide nanostructures during the delithiation/lithiation of lithium ions. As anodes for lithium ion batteries, the nitrogen-doped graphene and their hybrids with MnO2 nanorods exhibit exceptionally excellent capacity retention for 3000 cycles at 2500 mA g−1, and ultrafast rate capability, which pave the way for developing electrode materials for long cycle-life energy storage devices.
Co-reporter:Jinqiu Zhou, Tao Qian, Tingzhou Yang, Mengfan Wang, Jun Guo and Chenglin Yan
Journal of Materials Chemistry A 2015 vol. 3(Issue 29) pp:15008-15014
Publication Date(Web):22 Jun 2015
DOI:10.1039/C5TA03312H
Fe/Fe3C homogeneously dispersed in 2D porous nitrogen-doped graphitic carbon nanomeshes (N-Fe/Fe3C@C nanomeshes) was prepared by a novel template-free method using the polypyrrole–Fe (PPy–Fe) coordination complex as a precursor. The designed architecture is beneficial to electron transport and accommodation of the strains of Li insertion/extraction. As an anode material for Li-ion batteries, the as-prepared composite exhibits a reversible capacity of 1316 mA h g−1 (normalized to the mass of Fe/Fe3C in the composite) with extremely excellent cycling performance at high rate (nearly 100% capacity retention after 500 cycles) and good rate capability. The synthesis approach presents a promising route for a large-scale production of N-Fe/Fe3C@C nanomesh composites as an extremely durable high-rate anode material for Li-ion batteries.
Co-reporter:Tao Qian, Na Xu, Jinqiu Zhou, Tingzhou Yang, Xuejun Liu, Xiaowei Shen, Jiaqi Liang and Chenglin Yan
Journal of Materials Chemistry A 2015 vol. 3(Issue 2) pp:488-493
Publication Date(Web):21 Nov 2014
DOI:10.1039/C4TA05769D
Supercapacitor electrodes composed of a 3D V2O5 network with polypyrrole (PPy) uniformly decorated onto each nanowire were fabricated to enhance their pseudocapacitive performance. The continuous 3D network creates channels for better ion transport, and the high degree of pore connectivity in the network enhances the mass transport. The PPy shell could enhance the electric conductivity and prevent the dissolution of vanadium. These merits together with the ideal synergy between V2O5 and PPy lead to a high specific capacitance of 448 F g−1, which is three times higher than that of the stacked V2O5. The all-solid-state symmetric supercapacitor device assembled by the V2O5/PPy core/shell 3D network exhibits a high energy density (14.2 W h kg−1) at a power density of 250 W kg−1 and good cyclic stability (capacitance retention of 81% after 1000 cycles). Furthermore, the prepared device could power a red light-emitting diode indicator efficiently after charging for only 10 s.
Co-reporter:Xiaowei Shen, Tao Qian, Jinqiu Zhou, Na Xu, Tingzhou Yang, and Chenglin Yan
ACS Applied Materials & Interfaces 2015 Volume 7(Issue 45) pp:25298
Publication Date(Web):November 2, 2015
DOI:10.1021/acsami.5b07145
Flexible/bendable electronic equipment has attracted great interest recently, while the development is hindered by fabricating flexible/bendable power sources due to the lack of reliable materials that combine both electronically superior conductivity and mechanical flexibility. Here, a novel structure of manganese oxide, like fabric foam, was constructed, which was then cocooned with a carbon shell via chemical vapor deposition. Serving as a binder-free anode, the self-knitted MnO2@Carbon Foam (MCF) exhibits high specific capacitance (850–950 mAh/g), excellent cycling stability (1000 cycles), and good rate capability (60 C, 1 C = 1 A/g). Moreover, a flexible full lithium battery was designed based on an MCF anode and a LiCoO2/Al cathode, and the outstanding performance (energy density of 2451 Wh/kg at a power density of 4085 W/kg) demonstrates its promising potential of the practical applications.Keywords: flexible devices; full cell; high energy density; lithium-ion battery; α-MnO2 fabric foam
Co-reporter:Xueyi Lu, Wenping Si, Xiaolei Sun, Junwen Deng, Lixia Xi, Bo Liu, Chenglin Yan, Oliver G. Schmidt
Journal of Power Sources 2015 Volume 295() pp:197-202
Publication Date(Web):1 November 2015
DOI:10.1016/j.jpowsour.2015.07.018
•MnOx nanomembranes were used as the catalysts of Li–O2 batteries.•We reported a novel method—rolled-up technology to prepare MnOx catalysts.•The MnOx nanomembranes show higher capacity and stability than pure carbon black.•Oxygen vacancies of the MnOx nanomembranes contribute to the high performance.Two-dimensional MnOx nanomembranes prepared by electron beam evaporation are rolled up into three-dimensional hybrid micro/nano-tubes by strain release. The material is characterized with Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), cyclic voltammetry and used as the cathode catalysts for lithium–oxygen (Li–O2) batteries. The Li–O2 battery using such curly MnOx nanomembranes as the cathode delivers a specific discharge capacity of 4610 mAhgC−1 at a current density of 70 mAgC−1 which is higher than that of carbon black. Moreover, the MnOx nanomembrane electrode gains improved stability, being capable of cycling 112 times at a current density of 200 mAgC−1. The encouraging performance is ascribed to the unique superiorities of nanomembranes and those inner oxygen vacancies, indicating that nanomembranes are promising materials for Li–O2 batteries.
Co-reporter:Xueyi Lu;Junwen Deng;Wenping Si;Xiaolei Sun;Xianghong Liu;Bo Liu;Lifeng Liu;Steffen Oswald;Stefan Baunack;Hans Joachim Grafe;Oliver G. Schmidt
Advanced Science 2015 Volume 2( Issue 9) pp:
Publication Date(Web):
DOI:10.1002/advs.201500113
Co-reporter:Xianghong Liu, Jun Zhang, Wenping Si, Lixia Xi, Barbara Eichler, Chenglin Yan, and Oliver G. Schmidt
ACS Nano 2015 Volume 9(Issue 2) pp:1198
Publication Date(Web):February 3, 2015
DOI:10.1021/nn5048052
The large capacity loss and huge volume change of silicon anodes severely restricts their practical applications in lithium ion batteries. In this contribution, the sandwich nanoarchitecture of rolled-up Si/reduced graphene oxide bilayer nanomembranes was designed via a strain released strategy. Within this nanoarchitecture, the inner void space and the mechanical feature of nanomembranes can help to buffer the strain during lithiation/delithiation; the alternately stacked conductive rGO layers can protect the Si layers from excessive formation of SEI layers. As anodes for lithium-ion batteries, the sandwiched Si/rGO nanoarchitecture demonstrates long cycling life of 2000 cycles at 3 A g–1 with a capacity degradation of only 3.3% per 100 cycles.Keywords: lithium-ion batteries; nanoarchitecture; nanomembranes; reduced graphene oxide; silicon;
Co-reporter:Lin Zhang;Junwen Deng;Lifeng Liu;Wenping Si;Steffen Oswald;Lixia Xi;Manab Kundu;Guozhi Ma;Thomas Gemming;Stefan Baunack;Fei Ding;Oliver G. Schmidt
Advanced Materials 2014 Volume 26( Issue 26) pp:4527-4532
Publication Date(Web):
DOI:10.1002/adma.201401194
Co-reporter:Wenping Si;Ingolf Mönch;Junwen Deng;Shilong Li;Gungun Lin;Luyang Han;Yongfeng Mei;Oliver G. Schmidt
Advanced Materials 2014 Volume 26( Issue 47) pp:7973-7978
Publication Date(Web):
DOI:10.1002/adma.201402484
Co-reporter:Jiangfeng Ni;Yang Zhao;Tingting Liu;Honghe Zheng;Lijun Gao;Liang Li
Advanced Energy Materials 2014 Volume 4( Issue 16) pp:
Publication Date(Web):
DOI:10.1002/aenm.201400798
Co-reporter:Xiaolei Sun, Wenping Si, Xianghong Liu, Junwen Deng, Lixia Xi, Lifeng Liu, Chenglin Yan, Oliver G. Schmidt
Nano Energy 2014 Volume 9() pp:168-175
Publication Date(Web):October 2014
DOI:10.1016/j.nanoen.2014.06.022
•Ni/NiO hybrid nanomembranes anodes are designed for Li-ion batteries.•The anodes can be discharged and charged at an ultrahigh rate of ~115 C.•The anodes exhibit long-term cycling stability with excellent Coulombic efficiency.Herein we present the preparation of novel multifunctional metallic nickel/oxide (Ni/NiO) hybrid nanomembranes with rough and undulating surface morphologies, by a physical deposition method combined with chemical etching and thermal oxidation. Benefiting from the advantages of intrinsic architecture and electrochemical catalysis of metallic nickel, the anodes can be discharged and charged at an ultrahigh rate of ~115 C (1 C=718 mA g−1) if only the mass of NiO is taken into calculation or 60 C if the total mass of Ni/NiO nanomembranes is considered. To our knowledge, this is the best reported rate performance for NiO-based anodes in Li-ion batteries to date. Furthermore, excellent cycling stability is also demonstrated.
Co-reporter:Jinqiu Zhou, Tao Qian, Tingzhou Yang, Mengfan Wang, Jun Guo and Chenglin Yan
Journal of Materials Chemistry A 2015 - vol. 3(Issue 29) pp:NaN15014-15014
Publication Date(Web):2015/06/22
DOI:10.1039/C5TA03312H
Fe/Fe3C homogeneously dispersed in 2D porous nitrogen-doped graphitic carbon nanomeshes (N-Fe/Fe3C@C nanomeshes) was prepared by a novel template-free method using the polypyrrole–Fe (PPy–Fe) coordination complex as a precursor. The designed architecture is beneficial to electron transport and accommodation of the strains of Li insertion/extraction. As an anode material for Li-ion batteries, the as-prepared composite exhibits a reversible capacity of 1316 mA h g−1 (normalized to the mass of Fe/Fe3C in the composite) with extremely excellent cycling performance at high rate (nearly 100% capacity retention after 500 cycles) and good rate capability. The synthesis approach presents a promising route for a large-scale production of N-Fe/Fe3C@C nanomesh composites as an extremely durable high-rate anode material for Li-ion batteries.
Co-reporter:Xianfu Wang, Yu Chen, Oliver G. Schmidt and Chenglin Yan
Chemical Society Reviews 2016 - vol. 45(Issue 5) pp:NaN1330-1330
Publication Date(Web):2015/12/21
DOI:10.1039/C5CS00708A
Engineered nanomembranes are of great interest not only for large-scale energy storage devices, but also for on-chip energy storage integrated microdevices (such as microbatteries, microsupercapacitors, on-chip capacitors, etc.) because of their large active surfaces for electrochemical reactions, shortened paths for fast ion diffusion, and easy engineering for microdevice applications. In addition, engineered nanomembranes provide a lab-on-chip electrochemical device platform for probing the correlations of electrode structure, electrical/ionic conductivity, and electrochemical kinetics with device performance. This review focuses on the recent progress in engineered nanomembranes including tubular nanomembranes and planar nanomembranes, with the aim to provide a systematic summary of their fabrication, modification, and energy storage applications in lithium-ion batteries, lithium–oxygen batteries, on-chip electrostatic capacitors and micro-supercapacitors. A comprehensive understanding of the relationship between engineered nanomembranes and electrochemical properties of lithium ion storage with engineered single-tube microbatteries is given, and the flexibility and transparency of micro-supercapacitors is also discussed. Remarks on challenges and perspectives related to engineered nanomembranes for the further development of energy storage applications conclude this review.
Co-reporter:Tingzhou Yang, Tao Qian, Mengfan Wang, Jie Liu, Jinqiu Zhou, Zhouzhou Sun, Muzi Chen and Chenglin Yan
Journal of Materials Chemistry A 2015 - vol. 3(Issue 12) pp:NaN6296-6296
Publication Date(Web):2015/02/16
DOI:10.1039/C4TA07208A
A new approach using polypyrrole as the nitrogen source has been demonstrated for the fabrication of nitrogen-doped graphene, which subsequently served as nucleation centers for the growth of metal oxides. The thin layers of the nitrogen-doped graphene are not only used as conductive pathways accelerating the electrical conductivity of metal oxides but also serve as buffer layers to improve the electrical contact with metal oxide nanostructures during the delithiation/lithiation of lithium ions. As anodes for lithium ion batteries, the nitrogen-doped graphene and their hybrids with MnO2 nanorods exhibit exceptionally excellent capacity retention for 3000 cycles at 2500 mA g−1, and ultrafast rate capability, which pave the way for developing electrode materials for long cycle-life energy storage devices.
Co-reporter:Tao Qian, Na Xu, Jinqiu Zhou, Tingzhou Yang, Xuejun Liu, Xiaowei Shen, Jiaqi Liang and Chenglin Yan
Journal of Materials Chemistry A 2015 - vol. 3(Issue 2) pp:NaN493-493
Publication Date(Web):2014/11/21
DOI:10.1039/C4TA05769D
Supercapacitor electrodes composed of a 3D V2O5 network with polypyrrole (PPy) uniformly decorated onto each nanowire were fabricated to enhance their pseudocapacitive performance. The continuous 3D network creates channels for better ion transport, and the high degree of pore connectivity in the network enhances the mass transport. The PPy shell could enhance the electric conductivity and prevent the dissolution of vanadium. These merits together with the ideal synergy between V2O5 and PPy lead to a high specific capacitance of 448 F g−1, which is three times higher than that of the stacked V2O5. The all-solid-state symmetric supercapacitor device assembled by the V2O5/PPy core/shell 3D network exhibits a high energy density (14.2 W h kg−1) at a power density of 250 W kg−1 and good cyclic stability (capacitance retention of 81% after 1000 cycles). Furthermore, the prepared device could power a red light-emitting diode indicator efficiently after charging for only 10 s.