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1.
Yifan Xu Yang Zhao Jing Ren Ye Zhang Huisheng Peng 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2016,128(28):8111-8114
Owing to the high theoretical energy density of metal–air batteries, the aluminum–air battery has been proposed as a promising long‐term power supply for electronics. However, the available energy density from the aluminum–air battery is far from that anticipated and is limited by current electrode materials. Herein we described the creation of a new family of all‐solid‐state fiber‐shaped aluminum–air batteries with a specific capacity of 935 mAh g−1 and an energy density of 1168 Wh kg−1. The synthesis of an electrode composed of cross‐stacked aligned carbon‐nanotube/silver‐nanoparticle sheets contributes to the remarkable electrochemical performance. The fiber shape also provides the aluminum–air batteries with unique advantages; for example, they are flexible and stretchable and can be woven into a variety of textiles for large‐scale applications. 相似文献
2.
Ye Zhang Lie Wang Ziyang Guo Yifan Xu Prof. Yonggang Wang Prof. Huisheng Peng 《Angewandte Chemie (International ed. in English)》2016,55(14):4487-4491
The lithium–air battery has been proposed as the next‐generation energy‐storage device with a much higher energy density compared with the conventional lithium‐ion battery. However, lithium–air batteries currently suffer enormous problems including parasitic reactions, low recyclability in air, degradation, and leakage of liquid electrolyte. Besides, they are designed into a rigid bulk structure that cannot meet the flexible requirement in the modern electronics. Herein, for the first time, a new family of fiber‐shaped lithium–air batteries with high electrochemical performances and flexibility has been developed. The battery exhibited a discharge capacity of 12 470 mAh g?1 and could stably work for 100 cycles in air; its electrochemical performances were well maintained under bending and after bending. It was also wearable and formed flexible power textiles for various electronic devices. 相似文献
3.
Realizing both High Energy and High Power Densities by Twisting Three Carbon‐Nanotube‐Based Hybrid Fibers 下载免费PDF全文
Ye Zhang Yang Zhao Dr. Xunliang Cheng Dr. Wei Weng Jing Ren Xin Fang Yishu Jiang Peining Chen Zhitao Zhang Prof. Yonggang Wang Prof. Huisheng Peng 《Angewandte Chemie (International ed. in English)》2015,54(38):11177-11182
Energy storage devices, such as lithium‐ion batteries and supercapacitors, are required for the modern electronics. However, the intrinsic characteristics of low power densities in batteries and low energy densities in supercapacitors have limited their applications. How to simultaneously realize high energy and power densities in one device remains a challenge. Herein a fiber‐shaped hybrid energy‐storage device (FESD) formed by twisting three carbon nanotube hybrid fibers demonstrates both high energy and power densities. For the FESD, the energy density (50 mWh cm?3 or 90 Wh kg?1) many times higher than for other forms of supercapacitors and approximately 3 times that of thin‐film batteries; the power density (1 W cm?3 or 5970 W kg?1) is approximately 140 times of thin‐film lithium‐ion battery. The FESD is flexible, weaveable and wearable, which offers promising advantages in the modern electronics. 相似文献
4.
Core–Shell Carbon‐Coated CuO Nanocomposites: A Highly Stable Electrode Material for Supercapacitors and Lithium‐Ion Batteries 下载免费PDF全文
Dr. Tao Wen Dr. Xi‐Lin Wu Dr. Shouwei Zhang Prof. Xiangke Wang Prof. An‐Wu Xu 《化学:亚洲杂志》2015,10(3):595-601
Herein we present a simple method for fabricating core–shell mesostructured CuO@C nanocomposites by utilizing humic acid (HA) as a biomass carbon source. The electrochemical performances of CuO@C nanocomposites were evaluated as an electrode material for supercapacitors and lithium‐ion batteries. CuO@C exhibits an excellent capacitance of 207.2 F g?1 at a current density of 1 A g?1 within a potential window of 0–0.46 V in 6 M KOH solution. Significantly, CuO electrode materials achieve remarkable capacitance retentions of approximately 205.8 F g?1 after 1000 cycles of charge/discharge testing. The CuO@C was further applied as an anode material for lithium‐ion batteries, and a high initial capacity of 1143.7 mA h g?1 was achieved at a current density of 0.1 C. This work provides a facile and general approach to synthesize carbon‐based materials for application in large‐scale energy‐storage systems. 相似文献
5.
Superior Rechargeability and Efficiency of Lithium–Oxygen Batteries: Hierarchical Air Electrode Architecture Combined with a Soluble Catalyst 下载免费PDF全文
Hee‐Dae Lim Hyelynn Song Jinsoo Kim Hyeokjo Gwon Youngjoon Bae Kyu‐Young Park Jihyun Hong Haegyeom Kim Taewoo Kim Prof. Yong Hyup Kim Xavier Lepró Raquel Ovalle‐Robles Prof. Ray H. Baughman Prof. Kisuk Kang 《Angewandte Chemie (International ed. in English)》2014,53(15):3926-3931
The lithium–oxygen battery has the potential to deliver extremely high energy densities; however, the practical use of Li‐O2 batteries has been restricted because of their poor cyclability and low energy efficiency. In this work, we report a novel Li‐O2 battery with high reversibility and good energy efficiency using a soluble catalyst combined with a hierarchical nanoporous air electrode. Through the porous three‐dimensional network of the air electrode, not only lithium ions and oxygen but also soluble catalysts can be rapidly transported, enabling ultra‐efficient electrode reactions and significantly enhanced catalytic activity. The novel Li‐O2 battery, combining an ideal air electrode and a soluble catalyst, can deliver a high reversible capacity (1000 mAh g?1) up to 900 cycles with reduced polarization (about 0.25 V). 相似文献
6.
Liwei Cheng Yanhong Liang Qiaonan Zhu Dandan Yu Mengxue Chen Junfei Liang Hua Wang 《化学:亚洲杂志》2020,15(8):1290-1295
Organic electrode materials hold great potential for fabricating sustainable energy storage systems, however, the development of organic redox‐active moieties for rechargeable aqueous zinc‐ion batteries is still at an early stage. Here, we report a bio‐inspired riboflavin‐based aqueous zinc‐ion battery utilizing an isoalloxazine ring as the redox center for the first time. This battery exhibits a high capacity of 145.5 mAh g?1 at 0.01 A g?1 and a long‐life stability of 3000 cycles at 5 A g?1. We demonstrate that isoalloxazine moieties are active centers for reversible zinc‐ion storage by using optical and photoelectron spectroscopies as well as theoretical calculations. Through molecule‐structure tailoring of riboflavin, the obtained alloxazine and lumazine molecules exhibit much higher theoretical capacities of 250.3 and 326.6 mAh g?1, respectively. Our work offers an effective redox‐active moiety for aqueous zinc batteries and will enrich the valuable material pool for electrode design. 相似文献
7.
Di Wang Fan Zhang Ping He Haoshen Zhou 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(8):2377-2381
Li‐O2 batteries are promising candidates for next‐generation high‐energy‐density battery systems. However, the main problems of Li–O2 batteries include the poor rate capability of the cathode and the instability of the Li anode. Herein, an ester‐based liquid additive, 2,2,2‐trichloroethyl chloroformate, was introduced into the conventional electrolyte of a Li–O2 battery. Versatile effects of this additive on the oxygen cathode and the Li metal anode became evident. The Li–O2 battery showed an outstanding rate capability of 2005 mAh g?1 with a remarkably decreased charge potential at a large current density of 1000 mA g?1. The positive effect of the halide ester on the rate capacity is associated with the improved solubility of Li2O2 in the electrolyte and the increased diffusion rate of O2. Furthermore, the ester promotes the formation of a solid–electrolyte interphase layer on the surface of the Li metal, which restrains the loss and volume change of the Li electrode during stripping and plating, thereby achieving a cycling stability over 900 h and a Li capacity utilization of up to 10 mAh cm?2. 相似文献
8.
Wenchao Zhang Chuangang Hu Zaiping Guo Liming Dai 《Angewandte Chemie (International ed. in English)》2020,59(9):3470-3474
Metal–CO2 batteries have attracted much attention owing to their high energy density and use of greenhouse CO2 waste as the energy source. However, the increasing cost of lithium and the low discharge potential of Na–CO2 batteries create obstacles for practical applications of Li/Na–CO2 batteries. Recently, earth‐abundant potassium ions have attracted considerable interest as fast ionic charge carriers for electrochemical energy storage. Herein, we report the first K–CO2 battery with a carbon‐based metal‐free electrocatalyst. The battery shows a higher theoretical discharge potential (E?=2.48 V) than that of Na–CO2 batteries (E?=2.35 V) and can operate for more than 250 cycles (1500 h) with a cutoff capacity of 300 mA h g?1. Combined DFT calculations and experimental observations revealed a reaction mechanism involving the reversible formation and decomposition of P121/c1‐type K2CO3 at the efficient carbon‐based catalyst. 相似文献
9.
Engineering Fast Ion Conduction and Selective Cation Channels for a High‐Rate and High‐Voltage Hybrid Aqueous Battery 下载免费PDF全文
Chunyi Liu Xusheng Wang Wenjun Deng Chang Li Prof. Jitao Chen Prof. Mianqi Xue Prof. Rui Li Prof. Feng Pan 《Angewandte Chemie (International ed. in English)》2018,57(24):7046-7050
The rechargeable aqueous metal‐ion battery (RAMB) has attracted considerable attention due to its safety, low costs, and environmental friendliness. Yet the poor‐performance electrode materials lead to a low feasibility of practical application. A hybrid aqueous battery (HAB) built from electrode materials with selective cation channels could increase the electrode applicability and thus enlarge the application of RAMB. Herein, we construct a high‐voltage K–Na HAB based on K2FeFe(CN)6 cathode and carbon‐coated NaTi2(PO4)3 (NTP/C) anode. Due to the unique cation selectivity of both materials and ultrafast ion conduction of NTP/C, the hybrid battery delivers a high capacity of 160 mAh g?1 at a 0.5 C rate. Considerable capacity retention of 94.3 % is also obtained after 1000 cycles at even 60 C rate. Meanwhile, high energy density of 69.6 Wh kg?1 based on the total mass of active electrode materials is obtained, which is comparable and even superior to that of the lead acid, Ni/Cd, and Ni/MH batteries. 相似文献
10.
N,P‐Codoped Carbon Networks as Efficient Metal‐free Bifunctional Catalysts for Oxygen Reduction and Hydrogen Evolution Reactions 下载免费PDF全文
Dr. Jintao Zhang Prof. Liangti Qu Prof. Gaoquan Shi Jiangyong Liu Prof. Jianfeng Chen Prof. Liming Dai 《Angewandte Chemie (International ed. in English)》2016,55(6):2230-2234
The high cost and scarcity of noble metal catalysts, such as Pt, have hindered the hydrogen production from electrochemical water splitting, the oxygen reduction in fuel cells and batteries. Herein, we developed a simple template‐free approach to three‐dimensional porous carbon networks codoped with nitrogen and phosphorus by pyrolysis of a supermolecular aggregate of self‐assembled melamine, phytic acid, and graphene oxide (MPSA/GO). The pyrolyzed MPSA/GO acted as the first metal‐free bifunctional catalyst with high activities for both oxygen reduction and hydrogen evolution. Zn–air batteries with the pyrolyzed MPSA/GO air electrode showed a high peak power density (310 W g?1) and an excellent durability. Thus, the pyrolyzed MPSA/GO is a promising bifunctional catalyst for renewable energy technologies, particularly regenerative fuel cells. 相似文献
11.
Dongliang Chao Wanhai Zhou Chao Ye Qinghua Zhang Yungui Chen Lin Gu Kenneth Davey Shi‐Zhang Qiao 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(23):7905-7910
Zinc‐based electrochemistry is attracting significant attention for practical energy storage owing to its uniqueness in terms of low cost and high safety. However, the grid‐scale application is plagued by limited output voltage and inadequate energy density when compared with more conventional Li‐ion batteries. Herein, we propose a latent high‐voltage MnO2 electrolysis process in a conventional Zn‐ion battery, and report a new electrolytic Zn–MnO2 system, via enabled proton and electron dynamics, that maximizes the electrolysis process. Compared with other Zn‐based electrochemical devices, this new electrolytic Zn–MnO2 battery has a record‐high output voltage of 1.95 V and an imposing gravimetric capacity of about 570 mAh g?1, together with a record energy density of approximately 409 Wh kg?1 when both anode and cathode active materials are taken into consideration. The cost was conservatively estimated at <US$ 10 per kWh. This result opens a new opportunity for the development of Zn‐based batteries, and should be of immediate benefit for low‐cost practical energy storage and grid‐scale applications. 相似文献
12.
Zhenyou Li Bhaghavathi P. Vinayan Piotr Jankowski Christian Njel Ananyo Roy Tejs Vegge Julia Maibach Juan Maria García Lastra Maximilian Fichtner Zhirong Zhao‐Karger 《Angewandte Chemie (International ed. in English)》2020,59(28):11483-11490
The development of multivalent metal (such as Mg and Ca) based battery systems is hindered by lack of suitable cathode chemistry that shows reversible multi‐electron redox reactions. Cationic redox centres in the classical cathodes can only afford stepwise single‐electron transfer, which are not ideal for multivalent‐ion storage. The charge imbalance during multivalent ion insertion might lead to an additional kinetic barrier for ion mobility. Therefore, multivalent battery cathodes only exhibit slope‐like voltage profiles with insertion/extraction redox of less than one electron. Taking VS4 as a model material, reversible two‐electron redox with cationic–anionic contributions is verified in both rechargeable Mg batteries (RMBs) and rechargeable Ca batteries (RCBs). The corresponding cells exhibit high capacities of >300 mAh g?1 at a current density of 100 mA g?1 in both RMBs and RCBs, resulting in a high energy density of >300 Wh kg?1 for RMBs and >500 Wh kg?1 for RCBs. Mechanistic studies reveal a unique redox activity mainly at anionic sulfides moieties and fast Mg2+ ion diffusion kinetics enabled by the soft structure and flexible electron configuration of VS4. 相似文献
13.
Flexible,Stretchable, and Rechargeable Fiber‐Shaped Zinc–Air Battery Based on Cross‐Stacked Carbon Nanotube Sheets 下载免费PDF全文
Yifan Xu Ye Zhang Ziyang Guo Jing Ren Prof. Yonggang Wang Prof. Huisheng Peng 《Angewandte Chemie (International ed. in English)》2015,54(51):15390-15394
The fabrication of flexible, stretchable and rechargeable devices with a high energy density is critical for next‐generation electronics. Herein, fiber‐shaped Zn–air batteries, are realized for the first time by designing aligned, cross‐stacked and porous carbon nanotube sheets simultaneously that behave as a gas diffusion layer, a catalyst layer, and a current collector. The combined remarkable electronic and mechanical properties of the aligned carbon nanotube sheets endow good electrochemical properties. They display excellent discharge and charge performances at a high current density of 2 A g?1. They are also flexible and stretchable, which is particularly promising to power portable and wearable electronic devices. 相似文献
14.
Shaoxuan Yang Yihuan Yu Meiling Dou Zhengping Zhang Liming Dai Feng Wang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(41):14866-14872
Two‐dimensional conjugated aromatic networks (CAN) with ultra‐thin conjugated layers (ca. 3.5 nm) and high single‐metal‐atom‐site density (mass content of 10.7 wt %, and 0.73 metal atoms per nm2) are prepared via a facile pyrolysis‐free route involving a one‐step ball milling of the solid‐phase‐synthesized polyphthalocyanine. These materials display outstanding oxygen reduction reaction (ORR) mass activity of 47 mA mgcat.?1 represents 1.3‐ and 6.4‐fold enhancements compared to Pt and Pt/C in benchmark Pt/C, respectively. Moreover, the primary Zn‐air batteries constructed with CAN as an air electrode demonstrate a mass/volume power density of 880 W gcat.?1/615 W cmcat.?3 and stable long‐term operation for 100 h. This strategy offers a new way to design high‐performance electrocatalysts with atomic precision for use in other energy‐storage and conversion applications. 相似文献
15.
《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2017,129(26):7562-7567
Nonaqueous redox‐flow batteries are an emerging energy storage technology for grid storage systems, but the development of anolytes has lagged far behind that of catholytes due to the major limitations of the redox species, which exhibit relatively low solubility and inadequate redox potentials. Herein, an aluminum‐based deep‐eutectic‐solvent is investigated as an anolyte for redox‐flow batteries. The aluminum‐based deep‐eutectic solvent demonstrated a significantly enhanced concentration of circa 3.2 m in the anolyte and a relatively low redox potential of 2.2 V vs. Li+/Li. The electrochemical measurements highlight that a reversible volumetric capacity of 145 Ah L−1 and an energy density of 189 Wh L−1 or 165 Wh kg−1 have been achieved when coupled with a I3−/I− catholyte. The prototype cell has also been extended to the use of a Br2‐based catholyte, exhibiting a higher cell voltage with a theoretical energy density of over 200 Wh L−1. The synergy of highly abundant, dendrite‐free, multi‐electron‐reaction aluminum anodes and environmentally benign deep‐eutectic‐solvent anolytes reveals great potential towards cost‐effective, sustainable redox‐flow batteries. 相似文献
16.
Zengxia Pei Ziwen Yuan Chaojun Wang Shenlong Zhao Jingyuan Fei Li Wei Junsheng Chen Cheng Wang Rongjie Qi Zongwen Liu Yuan Chen 《Angewandte Chemie (International ed. in English)》2020,59(12):4793-4799
Flexible zinc–air batteries (ZAB) are a promising battery candidate for emerging flexible electronic devices, but the catalysis‐based working principle and unique semi‐opened structure pose a severe challenge to their overall performance at cold temperature. Herein, we report the first flexible rechargeable ZAB with excellent low‐temperature adaptability, based on the innovation of an efficient electrocatalyst to offset the electrochemical performance shrinkage caused by decreased temperature and a highly conductive hydrogel with a polarized terminal group to render the anti‐freezing property. The fabricated ZABs show excellent electrochemical performances that outperform those of many aqueous ZABs at room temperature. They also deliver a high capacity of 691 mAh g?1 and an energy density of 798 Wh kg?1 at ?20 °C (92.7 % and 87.2 % retention of the room temperature counterparts, respectively), together with excellent flexibility and reverting capability. 相似文献
17.
Lisi Xie Xialiang Li Bin Wang Jia Meng Haitao Lei Wei Zhang Rui Cao 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(52):19059-19063
Electrodes for oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) are required in energy conversion and storage technologies. An assembly strategy involves covalently grafting Co corrole 1 onto Fe3O4 nanoarrays grown on Ti mesh. The resulted electrode shows significantly improved activity and durability for OER and ORR in neutral media as compared to Fe3O4 alone and with directly adsorbed 1 . It also displays higher atom efficiency (at least two magnitudes larger turnover frequency) than reported electrodes. Using this electrode in a neutral Zn‐air battery, a small charge–discharge voltage gap of 1.19 V, large peak power density of 90.4 mW cm?2, and high rechargeable stability for >100 h are achieved, opening a promising avenue of molecular electrocatalysis in a metal–air battery. This work shows a molecule‐engineered electrode for electrocatalysis and demonstrates their potential applications in energy conversion and storage. 相似文献
18.
Dr. Dong Zhou Yi Chen Prof. Baohua Li Prof. Hongbo Fan Prof. Faliang Cheng Dr. Devaraj Shanmukaraj Prof. Teofilo Rojo Prof. Michel Armand Prof. Guoxiu Wang 《Angewandte Chemie (International ed. in English)》2018,57(32):10168-10172
Ambient‐temperature sodium–sulfur (Na–S) batteries are considered a promising energy storage system due to their high theoretical energy density and low costs. However, great challenges remain in achieving a high rechargeable capacity and long cycle life. Herein we report a stable quasi‐solid‐state Na‐S battery enabled by a poly(S‐pentaerythritol tetraacrylate (PETEA))‐based cathode and a (PETEA‐tris[2‐(acryloyloxy)ethyl] isocyanurate (THEICTA))‐based gel polymer electrolyte. The polymeric sulfur electrode strongly anchors sulfur through chemical binding and inhibits the shuttle effect. Meanwhile, the in situ formed polymer electrolyte with high ionic conductivity and enhanced safety successfully stabilizes the Na anode/electrolyte interface, and simultaneously immobilizes soluble Na polysulfides. The as‐developed quasi‐solid‐state Na‐S cells exhibit a high reversible capacity of 877 mA h g?1 at 0.1 C and an extended cycling stability. 相似文献
19.
Dr. Xiaofei Hu Jianchao Sun Zifan Li Qing Zhao Chengcheng Chen Prof. Jun Chen 《Angewandte Chemie (International ed. in English)》2016,55(22):6482-6486
Developing rechargeable Na–CO2 batteries is significant for energy conversion and utilization of CO2. However, the reported batteries in pure CO2 atmosphere are non‐rechargeable with limited discharge capacity of 200 mAh g?1. Herein, we realized the rechargeability of a Na–CO2 battery, with the proposed and demonstrated reversible reaction of 3 CO2+4 Na?2 Na2CO3+C. The battery consists of a Na anode, an ether‐based electrolyte, and a designed cathode with electrolyte‐treated multi‐wall carbon nanotubes, and shows reversible capacity of 60000 mAh g?1 at 1 A g?1 (≈1000 Wh kg?1) and runs for 200 cycles with controlled capacity of 2000 mAh g?1 at charge voltage <3.7 V. The porous structure, high electro‐conductivity, and good wettability of electrolyte to cathode lead to reduced electrochemical polarization of the battery and further result in high performance. Our work provides an alternative approach towards clean recycling and utilization of CO2. 相似文献
20.
Congxin Xie Prof. Huamin Zhang Wenbin Xu Prof. Wei Wang Prof. Xianfeng Li 《Angewandte Chemie (International ed. in English)》2018,57(35):11171-11176
A zinc–iodine flow battery (ZIFB) with long cycle life, high energy, high power density, and self‐healing behavior is prepared. The long cycle life was achieved by employing a low‐cost porous polyolefin membrane and stable electrolytes. The pores in the membrane can be filled with a solution containing I3? that can react with zinc dendrite. Therefore, by consuming zinc dendrite, the battery can self‐recover from micro‐short‐circuiting resulting from overcharging. By using KI, ZnBr2, and KCl as electrolytes and a high ion‐conductivity porous membrane, a very high power density can be achieved. As a result, a ZIFB exhibits an energy efficiency (EE) of 82 % at 80 mA cm?2, which is 8 times higher than the currently reported ZIFBs. Furthermore, a stack with an output of 700 W was assembled and continuously run for more than 300 cycles. We believe this ZIFB can lead the way to development of new‐generation, high‐performance flow batteries. 相似文献