Browsing by Author "Wu, Hongliang"

Now showing 1 - 7 of 7
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    Construction of porous hierarchical NiCo2S4 toward high rate performance supercapacitor
    (Springer, 2019-11-11) Zhao, Fenglin; Huang, Wanxia; Sial, Muhammad Aurang Z. G.; Xie, Dong; Wu, Hongliang; Zhang, Qi; Zou, Jizhao; Zeng, Xierong
    Developing high-performance supercapacitors is an effective way to satisfy the ever-increasing energy storage demand for emerging devices, but the inferior rate performance of battery-type supercapacitors limits their large-scale utilization. Herein, porous hierarchical nickel cobalt sulfide (NiCo2S4) was constructed by a novel strategy that the synthesized nickel cobalt oxide nanosheets as chemical template for hydrothermal method. Furthermore, the backbone of nickel cobalt oxide nanosheets can finally convert to NiCo2S4, which both plays the role of matrix to buffer the volume variation and enhances entire conductivity. Benefiting from high specific area (79.9 m2 g−1), suitable nanopores for KOH electrolyte, high conductivity, and multiple Co/Ni valence, the hierarchical NiCo2S4 electrode delivers a high specific capacity of 1035.1 F g−1 at the current density of 1 A g−1, and an ultrahigh rate performance of 80.9% capacitance retention at 20 A g−1 was obtained. The assembled asymmetric supercapacitor device could achieve the maximum capacity of 102.4 F g−1 at 5 mV s−1 and maintain at 80.5 F g−1 at 50 mV s−1, indicating its superior rate ability. In addition, the highest energy density of 35.4 Wh kg−1 can be obtained at a power density of 0.4 kW kg−1. These results indicate that the porous hierarchical NiCo2S4 could be served as high rate performance electrode materials for advanced supercapacitors.
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    CoSe2/Co nanoheteroparticles embedded in Co, Nco-doped carbon nanopolyhedra/nanotubes as anefficient oxygen bifunctional electrocatalyst for Zn–air batteries
    (Royal Society of Chemistry, 2020-06-30) Zou, Jizhao; Luo, Qi; Wu, Hongliang; Liu, Shiyu; Lan, Tongbin; Yao, Yuechao; Sial, Muhammad Aurang Zeb Gul; Zhao, Fenglin; Zhang, Qi; Zenga, Xierong
    Transition metal selenide-based materials have been demonstrated as promising electrocatalysts for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER), yet the actual design of a highly efficient and stable electro-catalyst based on these materials still remains a long and arduous challenge. Herein, a predesigned hybrid Zn/Co zeolitic imidazole framework was used to fabricate CoSe2/Co nanoheteroparticles embedded within hierarchically porous Co, N co-doped carbonnanopolyhedra/nanotubes (CoSe2/Co@NC-CNTs) through a facile approach involving controlled carbonization and selenization procedures. As expected, the optimized CoSe2/Co@NC-CNT-1 displayed outstanding electrocatalytic performance for the ORR and OER, with an onset potential of 0.95 V vs. RHE, a half-wave potential of 0.84 V vs. RHE for ORR, and a potential of 1.69 V vs. RHE for OER at 10 mA cm−2. It also exhibited excellent long-term stability and methanol resistance ability, which were superior to commercial IrO2 and the commercial 20 wt% Pt/C catalyst. Notably, the assembled Zn–air battery with CoSe2/Co@NC-CNT-1 showed a low charge–discharge voltage gap (0.696 V at 10 mA cm−2) and a high peak power density (100.28 mW cm−2) with long-term cycling stability. These superior performances can be ascribed to the synergistic effects of the highly active CoSe2/Co nanoheterostructure, hierarchically porous structure with a large surface area, high electrical conductivity and uniform doping of the Co and N
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    Facile synthesis of 2D ultrathin and ultrahigh specific surface hierarchical porous carbon nanosheets for advanced energy storage
    (Elsevier, 2019-09-10) Yao, Yuechao; Xiao, Zunqin; Liu, Peng; Zhang, Shengjiao; Niu, Yuan; Wu, Hongliang; Liu, Shiyu; Tu, Wenxuan; Luo, Qi; Sial, Muhammad Aurang Zeb Gul; Zeng, Shao-Zhong; Zhang, Qi; Zou, Jizhao; Zeng, Xierong; Zhang, Wenjing
    Two dimensional (2D) porous carbon nanosheets (CNS) have attracted tremendous research interests in energy storage and conversion, such as supercapacitors (SCs) and lithium-sulfur batteries, because of their unique micromorphology, chemical stability and high specific surface area (SSA). Rational design and facile scalable synthesis of CNS with high SSA, low cost and ultrathin nanosheet structure is highly desired but hitherto remains a big challenge. Here, we report a novel synthesis method of 2D hierarchical porous CNS with ultrahigh SSA (2687 m2 g−1) and ultrathin structure by directly pyrolysing and activating a unique and abundant biomass sheet. The electrochemical characterisations show that the prepared CNS-4-1 materials as electrodes creates a good energy-storage capability, with the energy density being 91 Wh kg−1 for symmetric SCs in ionic liquids, which is the highest in the reported biomass-derived CNS materials for SCs applications so far. Besides, the CNS-5-1 also exhibits a high initial capacity of 1078 mAh g−1 at 0.1 C when it acted as a sulfur hosting material for lithium-sulfur batteries. More importantly, it also shows a 586 mAh g−1 reversible capacity and an approaching 100% coulombic efficiency after 500 cycles at a high rate of 1 C. These superior electrochemical properties of the CNS are mainly attributed to their unique 2D ultrathin nanosheet structure, large SSA, and reasonable hierarchical porous structure. This work not only provides a new strategy to fabricate the ultrathin CNS in large scale and low cost but also enlarges CNS materials potential applications in energy storage.
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    Facile synthesis of ultrahigh-surface-area hollow carbon nanospheres and their application in lithium-sulfur batteries
    (Wiley-VCH, 2017-12-13) Zeng, Shao-Zhong; Yao, Yuechao; Huang, Lin; Wu, Hongliang; Peng, Biaolin; Zhang, Qi; Li, Xiaohua; Yu, Liang; Liu, Shiyu; Tu, Wenxuan; Lan, Tongbin; Zeng, Xierong; Zou, Jizhao
    Hollow carbon nanospheres (HCNs) with specific surface areas up to 2949 m2 g−1 and pore volume up to 2.9 cm3 g−1 were successfully synthesized from polyaniline‐co‐polypyrrole hollow nanospheres by carbonization and CO2 activation. The cavity diameter and wall thickness of HCNs can be easily controlled by activation time. Owing to their large inner cavity and enclosed structure, HCNs are desirable carriers for encapsulating sulfur. To better understand the effects of pore characteristics and sulfur contents on the performances of lithium‐sulfur batteries, three composites of HCNs and sulfur are prepared and studied in detail. The composites of HCNs with moderate specific surface areas and suitable sulfur content present a better performance. The first discharge capacity of this composite reaches 1401 mAh g−1 at 0.2 C. Even after 200 cycles, the discharge capacity remains at 626 mAh g−1.
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    High-performance supercapacitors based on hierarchically porous carbons with a three-dimensional conductive network structure
    (Royal Society of Chemistry, 2019-03-27) Zou, Jizhao; Tu, Wenxuan; Zeng, Shao-Zhong; Yao, Yuechao; Zhang, Qi; Wu, Hongliang; Lan, Tongbin; Liua, Shiyu; Zeng, Xierong
    Clews of polymer nanobelts (CsPNBs) have the advantages of inexpensive raw materials, simple synthesis and large output. Novel clews of carbon nanobelts (CsCNBs) have been successfully prepared by carbonizing CsPNBs and by KOH activation subsequently. From the optimized process, CsCNBs*4, with a specific surface area of 2291 m2 g−1 and a pore volume of up to 1.29 cm3 g−1, has been obtained. Fundamentally, the CsCNBs possess a three-dimensional conductive network structure, a hierarchically porous framework, and excellent hydrophilicity, which enable fast ion diffusion through channels and a large enough ion adsorption/desorption surface to improve electrochemical performance of supercapacitors. The product exhibits a high specific capacitance of 327.5 F g−1 at a current density of 0.5 A g−1 in a three-electrode system. The results also reveal a high-rate capacitance (72.2% capacitance retention at 500 mV s−1) and stable cycling lifetime (95% of initial capacitance after 15 000 cycles). Moreover, CsCNBs*4 provides a high energy density of 29.8 W h kg−1 at a power density of 345.4 W kg−1 in 1 M tetraethylammonium tetrafluoroborate/acetonitrile (TEABF4/AN) electrolyte. These inspiring results imply that this carbon material with a three-dimensional conductive network structure possesses excellent potential for energy storage.
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    Optimized synthesis of ultrahigh-surface-area and oxygen-doped carbon nanobelts for high cycle-stability lithium-sulfur batteries
    (Electrochemical Society, 2019-10-14) Zou, Jizhao; Niu, Yuan; Tu, Wenxuan; Zhang, Qi; Yao, Yuechao; Zeng, Shao-Zhong; Lan, Tongbin; Wu, Hongliang; Zeng, Xierong; Zeng, Xierong
    Hierarchical clews of carbon nanobelts (CsCNBs) with ultrahigh specific surface area (2300 m2 g−1) and large pore volume (up to 1.29 cm3 g−1) has been successfully fabricated through carbonization and KOH activation of phenolic resin based nanobelts. The product possesses hierarchically porous structure, three-dimensional conductive network framework, and polar oxygen-rich groups, which are very befitting to load sulfur leading to excellent cycling stability of lithium-sulfur batteries. The composites of CsCNBs/sulfur exhibit an ultrahigh initial discharge capacity of 1245 mA h g−1 and ultralow capacity decay rate as low as 0.162% per cycle after 200 cycles at 0.1 C. Even at high current rate of 4 C, the cells still display a high initial discharge capacity (621 mA h g−1) and ultralow capacity decay rate (only 0.039% per cycle) after 1000 cycles. These encouraging results indicate that polar oxygen-containing functional groups are important for improving the electrochemical performance of carbons. The oxygen-doped carbon nanobelts have excellent energy storage potential in the field of energy storage.
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    Ultrahigh-content nitrogen-decorated nanoporous carbon derived from metal organic frameworks and its application in supercapacitors
    (Elsevier, 2018-04-03) Zou, Jizhao; Liu, Peng; Huang, Lin; Zhang, Qi; Lan, Tongbin; Zeng, Shao-Zhong; Zeng, Xierong; Yu, Liang; Liu, Shiyu; Wu, Hongliang; Tu, Wenxuan; Yao, Yuechao
    Single electric double-layer capacitors cannot meet the growing demand for energy due to their insufficient energy density. Generally speaking, the supercapacitors introduced with pseudo-capacitance by doping heteroatoms (N, O) in porous carbon materials can obtain much higher capacitance than electric double-layer capacitors. In view of above merits, in this study, nanoporous carbon materials with ultrahigh N enrichment (14.23 wt%) and high specific surface area (942 m2 g−1) by in situ introduction of N-doped MOF (ZTIF-1, Organic ligands 5-methyltetrazole/C2H4N4) were produced. It was found that as supercapacitors' electrode materials, these nanoporous carbons exhibit a capacitance as high as 272 F g-1 at 0.1 A g−1, and an excellent cycle life (almost no attenuation after 10,000 cycles.). Moreover, the symmetric supercapacitors were assembled to further investigate the actual capacitive performance, and the capacitance shows up to 154 F g-1 at 0.1 A g−1. Such excellent properties may be attributed to a combination of a high specific surface area, ultrahigh nitrogen content and hierarchically porous structure. The results shown in this study fully demonstrate that the nanoporous carbon materials containing ultrahigh nitrogen content can be used as a potential electrode material in supercapacitors.