吳明鉑, 李玲燕,2, 劉 軍, 李 楊, 艾培培, 吳文婷, 鄭經(jīng)堂

(1.中國(guó)石油大學(xué)重質(zhì)油國(guó)家重點(diǎn)實(shí)驗(yàn)室,山東青島 266580；2.中建安裝工程有限公司,江蘇南京 210046)

稻殼基介孔炭的制備及其在超級(jí)電容器中的應(yīng)用

吳明鉑1, 李玲燕1,2, 劉 軍1, 李 楊1, 艾培培1, 吳文婷1, 鄭經(jīng)堂1

(1.中國(guó)石油大學(xué)重質(zhì)油國(guó)家重點(diǎn)實(shí)驗(yàn)室,山東青島 266580；2.中建安裝工程有限公司,江蘇南京 210046)

以量大價(jià)廉的稻殼為原料,先后經(jīng)NaOH脫硅處理、預(yù)氧化、磷酸活化,在無(wú)模板的情況下制備出介孔炭材料。NaOH脫硅處理可有效除去稻殼中的硅并破壞纖維素的晶體結(jié)構(gòu),脫硅過(guò)程中形成的孔隙亦有利于高比表面積和高中孔率介孔炭的制備。所制介孔炭比表面積和中孔率分別高達(dá)2 009 m2·g-1和90.8%。其在50 mA·g-1電流密度下的比電容達(dá)176 F·g-1,即使在1 000 mA·g-1的大電流下,其比電容仍保持在126 F·g-1,表現(xiàn)出優(yōu)異的倍率能力。所制介孔炭具有良好的循環(huán)穩(wěn)定性,在200·mA g-1電流密度下的比電容高達(dá)150 F·g-1,1 000次循環(huán)無(wú)容量衰減。稻殼基介孔炭在超級(jí)電容器領(lǐng)域具有良好的應(yīng)用前景。

稻殼；介孔炭；堿預(yù)處理；超級(jí)電容器

Received date:2015-04-05； Revised date:2015-09-28

Foundation item:National Natural Science Foundation of China(51172285,51372277,21302224)；Fundamental Research Funds for the Central Universities(CX-1217,14CX06045A,14CX02060A).

Author introduction:WU Ming-bo,Professor,Ph D.E-mail:wumb@upc.edu.cn.

English edition available online ScienceDirect(http://www.sciencedirect.com/science/journal/18725805).

1 Introduction

Supercapacitors are attracting much attention as a kind of promising energy storage devices owing to their high power density,high energy efficiency, long cycle life and environmental-friendly nature［1-4］. Porous carbons have been widely used as the electrode materials for commercial supercapacitors owing to their high surface area and low cost.It is noted that only the pores that electrolyte ions can access contribute to the double layer capacitance,and only the mesopores can facilitate the transport of electrolyte ions and exhibit high ion-accessible surface area of the spectrum of pores in porous carbon［5-9］.Therefore, mesoporous carbons(MCs)always show better rate performance than microporous carbons［10,11］.MCs are mainly made by the template method,during which the template needs to be synthesized beforehand andto be removed by acid or base washing after the synthesis of MCs,resulting in a high production cost,tedious and environment-hazardous preparative process of the templated MCs［12-14］.Thus facile and templatefree methods to prepare MCs are highly desired.

In this paper,the abundant and renewable rice husk(RH)with low cost has been selected as precursor of MC.Silicon-free MC was obtained by a method combining a H3PO4activation with a pretreatment with NaOH solution and a pre-oxidation in air.Symmetric supercapacitors were fabricated with the resulting MC as electrode material.Their electrochemical performance was evaluated by a two-electrode configuration.

2 Experimental

2.1 Preparation and characterization of mesoporous carbon

The synthesis schematic of MC is described in Fig.1.NaOH,RH and deionized water were sufficiently mixed at a mass ratio of 1∶5∶12.5,the resulting mixture was heated to 110℃ and then kept for 24 h.Then the mixture was fully washed by deionized water and dried.The obtained material was grinded and mixed with a H3PO4solution(85 wt%)and deionized water at a mass ratio of 1∶2∶2.5,the mixture was first heated to 200℃ and kept for 6 h in air, and then activated at 800℃ for 1 h.After the product was washed with deionized water and dried at 110℃for 1 h,the MC was obtained.For a comparison,activated carbon(AC) was prepared by the same process except without the treatment of RH with NaOH solution.

X-ray fluorescence(XRF,EIGAKS,Japan) was used to characterize the contents of silicon in RH and the MC.The surface morphology and microstructure of the samples were investigated by field emission scanning electron microscopy(FE-SEM,S4800,Japan)and transmission electron microscopy(TEM, JEM-2100UHR,Japan).The pore structure characterization was performed on the basis of low temperature nitrogen adsorption-desorption isotherms on a sorptometer(Micromeritics,ASAP 2020,America).

Fig.1 A schematic illustration of MC synthesis from rice husk.

2.2 Preparation of electrodes and electrochemical measurements

The samples were mixed with acetylene black and polytetrafluoroethylene(PTFE)binder at a mass ratio of 85∶5∶10 in ethanol to form a slurry.The slurry was coated onto the nickel foam to make the electrodes,which was finally dried at 100℃ for 1 h under vacuum.Two symmetric electrodes separated by a thin porous polymer separator(Celgard 2400)in a 6 mol/L KOH aqueous electrolyte were sandwichedin a CR2032 coin cell.The electrochemical properties of supercapacitors were studied by cyclic voltammetry (CV)on a Princeton electrochemical workstation (PARSTAT 4000,Princeton,USA)and galvanostatic charge-discharge test on a Land cell tester(Land, CT-2001A,China).

3 Results and discussion

The content of silicon in RH was evaluated by X-ray fluorescence(XRF).The silicon content of raw RH is 6.65 wt% whilethesilicon content is 0.33 wt%for the NaOH treated one,indicating that the silicon can be effectively removed by the NaOH treatment.

The N2adsorption-desorption isotherms and pore size distributions of the samples are shown in Fig.2. Both of the nitrogen adsorption-desorption isotherms show clearly hysteresis loops,indicating the existence of abundant mesopores.The pore structure parameters of the samples are presented in Table 1.The SBETand mesoporosity of MC are 2 009 m2·g-1and 90.8%, respectively,much higher than those of AC,illustrating that the NaOH treatment benefits the formation of mesopores.

Fig.2 (a)N2adsorption-desorption isotherms and(b)pore size distributions of AC and MC.

Table 1 Pore structural parameters of MC and AC.

Fig.3(a)shows the SEM image of RH.Fig.3 (b)and Fig.3(c)are SEM and TEM images of the prepared MC,respectively.MC in Fig.3(b)has a cracked and pitted surface,indicating that RH has been seriously corroded by H3PO4.A great deal of mesopores centering at 2-10 nm can be seen in Fig.3 (c),which is consistent with averaged pores of 3.3 nm given in Table 1.

Fig.3 SEM images of(a)RH and(b)MC,(c)TEM image of MC.

Fig.4 gives the discharge curves of MC electrode at different current densities.The charge-discharge curve at the current density of 50 mA·g-1exhibits a symmetrical triangular shape and all discharge curves are nearly linear,implying a good capacitive behavior［15-17］.

Fig.5 presents the CV curves of MC electrode at different scan rates in the 6 mol/L KOH aqueous electrolyte.The CV curves show rectangular shapes without redox peaks,denoting that the capacitancecomes from electric double layer capacitance.The CV curve keeps high rectangular degree even at high scan of 10 mV·s-1,which should be attributed to the high ion diffusion rate in mesopores［18-20］.

Fig.4 Discharge curves of MC electrode at different current densities.

Fig.5 CV curves of MC electrode at different scan rates.

Fig.6 shows the variation in the specific capacitance vs.current density.It can be observed that the specific capacitance of MC can reach as high as 176 F·g-1at the current density of 50 mA·g-1,and retains 126 F·g-1even at 1 000 mA·g-1,indicating an excellent rate capability of the MC electrode.The high capacitive behavior of MC electrode is originated from its high mesoporosity and large specific surface area as shown in Table 1,both of which benefit the formation of double-layer capacitance.

Fig.6 Specific capacitance of MC electrode at different current densities.

Electrochemical cycling stability is well known a key requirement for the application of supercapacitors,the specific capacitance change of MC under 1 000 cycles at 200 mA·g-1is shown in Fig.7.It can be easily seen that MC electrode has a good cycle stability,it has a stable specific capacitance of about 150 F/g,no capacitance fading is observed even after 1 000 cycles,indicating a good electrochemical stability of MC electrode.

Fig.7 Specific capacitance of MC electrode at a constant current density of 200 mA·g-1as a function of cycle number.

4 Conclusions

MC with a specific surface area of 2 009 m2·g-1and a mesoporosity of 90.8%was prepared from RH by a facile and template-free method.This templatefree method combines a H3PO4activation with a pretreatment of RH with a hot NaOH solution and a preoxidation in air.The pretreatment of RH with a hot NaOH solution can remove silicon and damage the crystal structure of cellulose in RH,which are crucial and beneficial to the preparation of MC with a high electrochemical performance.The specific capacitance of MC electrode can reach 176 F·g-1at 50 mA·g-1, and the electrode exhibits an excellent rate capability and cycle stability.

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Template-free preparation of mesoporous carbon from rice husks for use in supercapacitors

WU Ming-bo1, LI Ling-yan1,2, LIU Jun1, LI Yang1, AI Pei-pei1, WU Wen-ting1, ZHENG Jing-tang1
(1.State Key Laboratory of Heavy Oil Processing,China University of Petroleum,Qingdao 266580,China; 2.China Construction Installation Engineering Co.,Ltd,Nanjing 210046,China)

Mesoporous carbon(MC)was prepared from rice husk(RH)by a simple and template-free method which combines H3PO4activation with a pretreatment of the RH with a NaOH solution and pre-oxidation in air.The pretreatment of RH with NaOH removes silicon and damages the crystal structure of the cellulose in the RH,both of which are beneficial to the preparation of MC with a high surface area and high mesoporosity.The MC has a specific surface area of 2 009 m2·g-1and a mesoporosity of 90.8%. Its specific capacitance can reach 176 F·g-1at a current density of 50 mA·g-1,and a value of 126 F·g-1is retained at 1 000 mA·g-1,indicating an excellent rate capability.A MC electrode has a stable specific capacitance of about 150 F/g at 200 mA·g-1with no apparent capacitance fade after 1 000 cycles,indicating good electrochemical stability.

Rice husk；Mesoporous carbon；Alkali pretreatment；Supercapacitor

TQ127.1+1

A

國(guó)家自然科學(xué)基金(51172285,51372277,21302224);中央高?；究蒲袠I(yè)務(wù)費(fèi)專項(xiàng)資金(CX-1217,14CX06045A, 14CX02060A).

吳明鉑,教授,博士.E-mail:wumb@upc.edu.cn.

1007-8827(2015)05-0471-05

10.1016/S1872-5805(15)60201-3