Facile fabrication of MoP nanodots embedded in porous carbon as excellent anode material for potassium-ion batteries

Molybdenum phosphide(MoP),owing to its abundant reserve and high theoretical capacity,is regarded as a promising anode material for potassium-ion batteries.However,it still suffers from the problems of acute volume expansion and weak diffusion kinetics.This study reports a simple method to synthesize a composite of molybdenum phosphide and porous carbon(MoP@PC)through simple mixing and annealing treatment.In the MoP@PC,lots of MoP nanodots with an average diameter of about 4 nm uniformly embedded in the petal-like porous carbon.The MoP@PC shows reversible capacities of 330 mAh g^-1 at100 mA g^-1 after 100 cycles,and ultra-long cycling stability with a capacity of 240 mAh g^-1 after 1000 cycles at 1 A g^-1 and 161 mAh g^-1 after 1000 cycles at 5 A g^-1.The structure of MoP@PC after charging-discharging cycles is also investigated by high resolution transmission electron microscope(HRTEM)and the result shows that MoP can still maintain the nanodot morphology without any agglomeration after 1000 cycles at 5 A g^-1.The storage mechanism of potassium ions was studied as well,which reveals that MoP and potassium ion have a conversion reaction.     

A high-performance potassium-ion capacitor based on a porous carbon cathode originated from the Aldol reaction product

Potassium-ion capacitors (KICs) emerge as a promising substitute for the well-developed lithium-ion capacitors (LICs), however, the energy density of KICs is below expectations because of lacking a suitable electrical double-layer positive electrode. Using chemical activation of the Aldol reaction product of acetone with KOH, we synthesized a porous carbon with a Brunauer-Emmett-Teller surface area of up to 2947 m²/g and a narrow pore size distribution ranging from 1 nm to 3 nm. Half-cell (versus potassium metal) test demonstrates that this porous carbon has high capacitive performance in K⁺ based organic electrolytes. Furthermore, a novel KIC fabricated by this porous carbon as the cathode, yields high values of energy density and power density. The processes used to make this porous carbon are readily low-cost to fabricate metal-ion capacitors.     

Freestanding film formed with Sb-nanoplates embedded in flexible porous carbon nanofibers as a binder-free anode for high-performance wearable potassium-ion battery

Antimony-based materials are considered as promising anodes for potassium ion batteries due to their high theoretical capacity and low electrode potential. However, the aggregation and bulk expansion of Sb particles in cycling will cause capacity attenuation and poor rate performance. In this paper, Sb nanoplates were designed to be embedded in flexible porous N-dopped carbon nanofibers (Sb@PCNFs) by a simple electrospinning deposition (ESD) method. In this structural design, Sb nanoplates of high capacity were employed as active materials, N-dopped carbon nanofibers were used to improve conductivity and structural stability. The introduction of pore-forming agent enables the nanofibers to possess porous structure, thus buffering the huge volume change and promoting the transfer of electrolyte/ions. More importantly, the freestanding film can be directly used as a working electrode, reducing the redundancy in the battery and the cost. Benefitting from the favorable structure, the freestanding flexible Sb@PCNFs electrode shows excellent potassium storage performance with a capacity of 314 mAh/g after 2000 cycles at 500 mA/g. This strategy of employing active material with high capacity in porous and conductive flexible nanofibers represents an effective method of achieving binder-free electrode with good electrochemical performance towards wearable energy storage devices.     

Cotton-derived oxygen/sulfur co-doped hard carbon as advanced anode material for potassium-ion batteries

Hard carbon is regarded as promising anode materials for potassium-ion batteries(KIBs)owing to their low price and easy availability.However,the limited rate capability still needs to be improved.Herein,we demonstrate the fabrication of oxygen/sulfur co-doped hard carbon through a facile hydrolyzationsulfuration process of skimmed cotton.The simultaneous dopants significantly improve potassium ion diffusion rate.When served as the anode for KIBs,this hydrolyzed hard carbon delivered a high reversible capacity(409 mAh/g at 0.1 A/g),superior rate capability(135 mAh/g at 2 A/g)and excellent cyclability(about 120 mAh/g overt 500 cycles at 2 A/g).This work provides a facile strategy to prepare low-cost doped-hard carbon with superior potassium storage property.     

用于高性能钠离子电容器的高氮掺杂多孔碳纳米纤维的简易合成

选择合适的生物质材料是获得功能碳材料的有效途径之一。通过柠檬酸钾和三聚氰胺一步热解法制备高氮掺杂多孔碳纳米纤维(NPCF)。在电流密度为0.1和1.0 A·g^-1时,NPCF电极的容量分别为218和140 mAh·g^-1。同时,具有NPCF阳极的钠离子电容器(SIC)在1.0 A·g^-1下表现出优异的倍率性能和超长的使用寿命,可循环超过2 500次。     

用于高性能钠离子电容器的高氮掺杂多孔碳纳米纤维的简易合成

选择合适的生物质材料是获得功能碳材料的有效途径之一。通过柠檬酸钾和三聚氰胺一步热解法制备高氮掺杂多孔碳纳米纤维(NPCF)。在电流密度为0.1和1.0 A·g^-1时,NPCF电极的容量分别为218和140 mAh·g^-1。同时,具有NPCF阳极的钠离子电容器(SIC)在1.0 A·g^-1下表现出优异的倍率性能和超长的使用寿命,可循环超过2 500次。     

用于高性能钠离子电容器的高氮掺杂多孔碳纳米纤维的简易合成

选择合适的生物质材料是获得功能碳材料的有效途径之一。通过柠檬酸钾和三聚氰胺一步热解法制备了高氮掺杂多孔碳纳米纤维(NPCF)。在电流密度为0.1和1.0 A·g^-1时,NPCF电极的容量分别为218和140 mAh·g^-1。同时,具有NPCF阳极的钠离子电容器(SIC)在1.0 A·g^-1下表现出优异的倍率性能和超长的使用寿命,可循环超过2 500次。     

CoS/N-doped carbon core/shell nanocrystals as an anode material for potassium-ion storage

Journal of Solid State Electrochemistry - Potassium-ion batteries (KIBs) are attracting tremendous attention due to the abundant potassium resources and their low price and high safety. However,...     

Interconnected carbon nanocapsules with high N/S co-doping as stable and high-capacity potassium-ion battery anode

Carbonaceous materials have drawn much attention in potassium-ion batteries (PIBs) due to their low price and superior physicochemical properties. However, the application of carbonaceous materials in PIB anodes is hindered by sluggish kinetics and large volume expansion. Herein, N/S co-doped carbon nanocapsule (NSCN) is constructed for superior K⁺storage. The NSCN possesses 3D nanocapsule framework with abundant meso/macropores, which guarantees structural robustness and accelerates ...     

Scalable synthesis of activated carbon with superparamagnetic properties

Magnetic activated carbons were obtained by in situ formation of coated superparamagnetic iron nanoparticles in the pores of carbons initially impregnated with ferric salt solution.     

Agar-derived nitrogen-doped porous carbon as anode for construction of cost-effective lithium-ion batteries

Balancing cost and performance of porous carbon (PC) as anode for lithium-ion battery (LIBs) is the key to effectively promote commercial application. Herein, low-cost N-doped PC (NPC-Ts, T = 600, 750 and 900 °C) were facilely prepared in batches via one-pot pyrolysis of agar with different carbonization temperature. The NPC-750 with specific surface area of 2914 m²/g and N content of 2.84% exhibits an ultrahigh reversible capacity of 1019 mAh/g at 0.1 A/g after 100 cycles and 837 mAh/g at 1 A/g after 500 cycles. Remarkably, the resulting LIBs exhibit an ultrafast charge-discharge feature with a remarkable capacity of 281 mAh/g at 10 A/g and a superlong cycle life with a capacity retention of 87% after 5000 cycles at 10 A/g. Coupling with LiFePO₄ cathode, the fabricated lithium-ion full cells possess high capacity, excellent rate and cycling performances (125 mAh/g at 100 mA/g, capacity retention of 95%, after 220 cycles), highlighting the practicability of this NPC-750 as the anode materials.     

Recent advances in anode materials for sodium - and potassium-ion hybrid capacitors

With the advent of the post–lithium-ion era, sodium- and potassium-based energy storage devices are intensively focused in the recent years. The novel sodium- and potassium-ion hybrid capacitors couple with the merits of supercapacitors and secondary batteries and thus are widely explored. A typical hybrid capacitor is generally constructed by combining a battery-type anode and a capacitive-type cathode, which presents both high energy density and power features. The design and fabrication of anode materials with high rate capability and long life to match the capacitive cathode is a critical issue. In this short review, the newly developed anode materials in nonaqueous capacitors are systematically analyzed. Based on a comprehensive summarization, the challenges for further practical applications of anode materials are prospected.     

Manganese oxide nanoparticle-loaded porous carbon nanofibers as anode materials for high-performance lithium-ion batteries

Mn-based oxide-loaded porous carbon nanofiber anodes, exhibiting large reversible capacity, excellent capacity retention, and good rate capability, are fabricated by carbonizing electrospun polymer/Mn(CH₃COO)₂ composite nanofibers without adding any polymer binder or electronic conductor. The excellent electrochemical performance of these organic/inorganic nanocomposites is a result of the unique combinative effects of nano-sized Mn-based oxides and carbon matrices as well as the highly-developed porous composite nanofiber structure, which make them promising anode candidates for high-performance rechargeable lithium-ion batteries.     

Metal-organic framework as a template for porous carbon synthesis

Porous carbon was synthesized by heating the precursor FA within the pores of MOF-5. The resultant carbon displayed a high specific surface area (BET, 2872 m2.g-1) and important hydrogen uptake (2.6 wt % at 760 Torr, -196 degrees C) as well as excellent electrochemical properties as an electrode material for electrochemical double-layered capacitor (EDLC).     

Uniform-dispersed ZnS quantum dots loading on graphene as a promising anode for potassium-ion batteries

The potassium-ion batteries(PIBs) have become the promising energy storage devices due to their relatively moderate cost and plenteous potassium resources.Whereas,the main drawback of PIBs is unsatisfacto ry electrochemical perfo rmance induced by the larger ionic radius of potassium ion.Herein,we report a well-designed,uniform-dispersed,and morphology-controllable zinc sulfide(ZnS) quantum dots loading on graphene as an anode in the PIBs.The directed uniform dispersion of the in-situ growing ZnS quantum dots(～2.8 nm in size) on graphene can mitigate the volume effect during the insertionextraction process and shorten the migration path of potassium ions.As a result,the battery exhibits superior cycling stability(350.4 mAh/g over 200 cycles at 0.1 A/g) and rate performance(98.8 mAh/g at2.0 A/g).We believe the design of active material with quantum dot-minimized size provides a novel route into PIBs and contributes to eliminating the major electrode failure issues of the system.     

Facile synthesis of biomass-derived hierarchical porous carbon microbeads for supercapacitors

Using the facile method of solvent evaporation, the leonardite fulvic acids (LFA)-based porous carbon microbeads (PCM) have been successfully prepared at ambient pressure, followed by carbonization and KOH activation (a low mass ratio alkali/LFA = 1.5) in an inert atmosphere. The effects of KOH treatment on pore structures and the formation mechanism of the PCM were discussed. The results showed that the sample exhibited remarkable improvement in textural properties. The activated carbon microbeads had high surface area (2269 m² g^?1), large pore volume (1.97 cm³ g^?1), and displayed excellent capacitive performances, compared with carbon powder. The porous carbon material electrodes with the “porous core structure” behaved superiorly at a specific capacitance of 320 F g^?1 at a current density of 0.05 A g^?1 in 6 M KOH electrolyte, which could still remain 193 F g^?1 when the current density increased to 100 A g^?1. Remarkably, in the 1 M TEABF₄/PC electrolyte, the PCM samples could reach 156 F g^?1 at 0.05 A g^?1, possess an outstanding energy density of 39.50 Wh kg^?1, and maintain at 22.05 Wh kg^?1 even when the power density rose up to 5880 W kg^?1. The balance of structural characteristic and high performance makes the porous carbon microbeads a competitive and promising supercapacitor electrode material.     

3D multicore-shell CoSn nanoboxes encapsulated in porous carbon as anode for lithium-ion batteries

Due to its high theoretical capacity and appropriate potential platform, tin-based alloy materials are expected to be a competitive candidate for the next-generation high performance anodes of lithium-ion batteries. Nevertheless, the immense volume change during the lithium-ion insert process leads to severe disadvantages of structural damage and capacity fade, which limits its practical application. In this work, a three-dimensional (3D) multicore-shell hollow nanobox encapsulated by carbon layer is obtained via a three-step method of hydrothermal reaction, annealing and alkali etching. During the electrochemical reactions, the CoSn@void@C nanoboxes provide internal space to compensate the volumetric change upon the lithiation of Sn, while the inactive component of Co acts as chemical buffers to withstand the anisotropic expansion of nanoparticles. Owing to the above-mentioned advantages, the elaborated anode delivers an excellent capacity of 788.2 mAh/g at 100 mA/g after 100 cycles and considerable capacity retention of 519.2 mAh/g even at a high current density of 1 A/g after 300 cycles. The superior stability and high performance indicate its capability as promising anodes for lithium-ion batteries.     

A porous silicon–carbon anode with high overall capacity on carbon fiber current collector

A porous silicon–carbon anode on a lightweight carbon fiber current collector is reported here for lithium-ion batteries. This Si–C anode was synthesized through a one-step carbonization of a Si-poly(acrylonitrile-co-methyl acrylate) precursor, which was directly deposited on a carbon fiber mat. The carbon fiber curent collector allows higher loading of active materials, resulting in high energy to mass and area ratios. The obtained Si–C electrode demonstrated superior overall capacity, cyclability, and rate capacity.     

The effect of electrolyte additives on the rate performance of hard carbon anode at low temperature for lithium-ion capacitor

Lithium-ion capacitor (LIC), which combines the advantages of lithium-ion battery (LIB) and electrical double layer capacitor (EDLC), has a rapid development during last decade, however, the poor low temperature performance still limits its application. In this paper, three electrolyte additives including vinylene carbonate (VC), fluoroethylene carbonate (FEC) and 1,3,2-dioxathiolane 2,2-dioxide (DTD) have been utilized and their effects on the rate performance of hard carbon (HC) anode of LIC at various temperatures ranging from 25 °C to ?40 °C have been well evaluated. The cell containing FEC shows the best rate performance at various temperatures and has the charge and discharge capability even at ?40 °C. For HC anode, the charge transfer impedance (R_CT) increases exponentially at low temperature, while the equivalent series resistance (Rs) and the impedance of solid electrolyte interface (SEI) increase relatively few. At low temperatures, the effect of FEC may be mainly reflected in its effect on the charge transfer process.     

Nanosized anatase titanium dioxide loaded porous carbon nanofiber webs as anode materials for lithium-ion batteries

Nanosized anatase titanium dioxide loaded porous carbon nanofibers (TiO₂/PCNFs) were prepared from electrospun TiO(OAc)₂/PAN/PMMA composite precursor fibers with different amount of PMMA porogen, which were sequentially heat-treated in different environments. Electrochemical measurement results show that these as-prepared TiO₂/PCNFs present higher cyclic reversible capacity than the TiO₂/CNFs counterpart (without PMMA porogen in its precursor fibers). Among the as-prepared TiO₂/PCNFs samples, the representative TiO₂/PCNFs (the mass ratio of PAN to PMMA is 3:1) exhibits the best high-rate performance with a high stable capacity retention about 200 mAhg^{− 1} at a current density as high as 800 mAg^{− 1}. This novel TiO₂/PCNFs composite material opens up a promising application in high-power lithium-ion batteries.