Micro-ultracapacitors with highly doped silicon nanowires electrodes
© Thissandier et al.; licensee Springer. 2013
Received: 14 September 2012
Accepted: 31 October 2012
Published: 21 January 2013
Highly n-doped silicon nanowires (SiNWs) with several lengths have been deposited via chemical vapor deposition on silicon substrate. These nanostructured silicon substrates have been used as electrodes to build symmetrical micro-ultracapacitors. These devices show a quasi-ideal capacitive behavior in organic electrolyte (1 M NEt4BF4 in propylene carbonate). Their capacitance increases with the length of SiNWs on the electrode and has been improved up to 10 μFcm−2 by using 20 μm SiNWs, i.e., ≈10-fold bulk silicon capacitance. This device exhibits promising galvanostatic charge/discharge cycling stability with a maximum power density of 1.4 mW cm−2.
KeywordsUltracapacitor Electrochemical capacitor Silicon nanowires electrodes Chemical vapor deposition Cyclic voltammetry Galvanostatic charge/discharge Microdevice
Nowadays, electronic devices invade strongly our daily life. In the race to efficiency, they have to be faster and faster, smaller and smaller, and with better and better performance [1–4]. One way to reach this goal is to integrate supercapacitors in their microelectronic circuit. Supercapacitors are commonly used to complete batteries whenever pulse power, long term cycling, and high charge/discharge are required [5–9]. Many studies are currently dedicated to the design of micro-ultracapacitors with different types of carbons [5–7] or pseudo-capacitive materials (RuO2, MnO2 …) [8, 9]. However, their integration in microelectronic circuit is still a challenge. Elaborate silicon based micro-ultracapacitors should facilitate it. Moreover, such devices could directly be manufactured on chips. Recently, porous silicon nanowires (SiNWs) , porous silicon coated with gold [11, 12], SiNWs coated with NiO [13, 14], or SiC  have been studied as potential materials for supercapacitor electrodes. Si/SiC core-shell nanowires-based electrodes show the most promising performances and cycling stability, but no studies have been performed in the two electrode devices. More recently, we proved that chemical vapor deposition (CVD)-grown, SiNWs-based electrodes show a promising cycling stability in an organic electrolyte and a quasi-ideal pure capacitive behavior, i.e., the energy that is stored thanks to electrolyte ions accumulation at the polarized electrode/electrolyte interface . As pure capacitive supercapacitor capacitance is proportional to the developed surface area on the electrode, increasing the SiNWs length should improve the device capacitance. SiNWs length and doping level can easily be tuned by CVD, thanks to the vapor–liquid-solid (VLS) mechanism [17, 18], using a metal catalyst as seed to the SiNWs growth [19–21]. The SiNWs diameter and density can also be monitored.
This work underlines the importance of HCl use during the SiNWs growth by CVD to obtain very long nanowires and investigates the influence of SiNWs length on SiNWs/SiNWs micro-ultracapacitors devices capacitance.
Doped silicon nanowires growth
Several SiNWs electrodes with each different SiNWs length have been made. The SiNWs were grown in a CVD reactor by VLS method via gold catalysis on highly doped n-Si (111) substrate (doping level (i.e., the number of doping atoms per cubic centimeter of materials, Nd = 5.1018 cm−3). Gold colloids with size of 50 nm are used as catalysts, H2 as carrier gas, silane (SiH4) as silicon precursor, phosphine (PH3) as n-doping gas, and HCl as additive gas. As shown in our previous work [19–21], the use of HCl in our process enables us to reduce the gold surface migration. Thus, the nanowires (NWs) morphology is improved and their length is not limited.
Prior to the growth, the substrates surface has been prepared by successive dipping in (a) acetone, isopropanol and caro (H2SO4/H2O2, 3:1) to remove organic impurities followed by (b) 10% HF and NH4F solution to remove the native oxide layer. Then, 50-nm gold colloids are deposited on the surface with 10% HF from an aqueous gold colloid solution (British Bio Cell International Ltd., Llanishen, Cardiff, UK).
The growth has been performed at 600°C, under 3 Torr total pressure, with 40 sccm (standard cubic centimeters) of SiH4, 100 sccm of PH3 gas (0.2% PH3 in H2), 100 sccm of HCl gas and 700 sccm of H2 as supporting gas . Our VLS-CVD method enables an easier control of SiNWs parameters (length, density, diameter, doping type, and doping level) and growth on low cost substrates. The doping level of the SiNWs is managed by the pressure ratio: dopant gas/SiH4. In our setup the ratio can vary from 10−6 to 10−2 to obtain doping level from Nd ≈1016 to ≈1020 cm−3. It was checked by resistivity measurements in four probes configuration [21, 22]. The SiNWs length is monitored by the gas injection time. The growth rate is about 500 nm/min under these conditions.
SiNWs morphologies are checked by scanning electron microscopy (SEM) before and after electrochemical cycling. SiNWs density is estimated by counting the number of gold colloids per square centimeters on several SEM images.
SiNWs electrochemical characterization
All experiments were performed in a glove box at room temperature. The electrolyte was 1 M NEt4BF4 (Fluka Chemika, Buchs, Switzerland) in propylene carbonate (Sigma Aldrich, St. Louis, MO, USA). Nanostructured silicon (n-SiNWs) and bulk silicon substrates (n-Si) were always directly used as electrodes.
Results and discussion
SiNWs growth by CVD
Electrochemical characterization of SiNWs/SiNWs micro-ultracapacitors
All devices show a quasi-ideal capacitive behavior. Cyclic voltammetry curves are rectangular. Galvanostatic charge/discharge curves are triangular and symmetrical, which indicates that only very few losses occur between the charge and the discharge. An unexpected lower voltage for 1 M NEt4BF4 in PC is used to stay in the system electrochemical stability window (ESW) and avoid side reactions. In fact, the system ESW is smaller than the one obtained on platinum for this electrolyte due to silicon oxidation at a potential below the electrolyte one [15, 16].
SiNWs/SiNWs micro-ultracapacitors surface capacitances obtained from the galvanostatic charge/discharge (Formula 2) at 5 and 10 μA cm −2
SiNWs length (μm)
j = 5 μA cm−2
j = 10 μA cm−2
C (μF cm−2)
C (i μm)/C (5 μm)
C (μF cm−2)
C (i μm)/C (5 μm)
with Δj as the current density differences inside the cyclic voltammetry curve and v as the scan rate.
with j the current density used for the galvanostatic charge/discharge.
Devices with the same SiNWs length show similar capacitance values for both current densities. As noticed on the curves, capacitance increases with SiNWs length. This increase is proportional to the length increase between 5 (≈3.5 μF cm−2) and 10 μm SiNWs (≈7 μF cm−2), but not between 5 and 20 μm (≈9.5 μF cm−2). This can be explained by accessible surface losses due to SiNWs constriction when substrates are stacked together. New devices avoiding this constriction will be designed and evaluated. Although previous works on the use of silicon-based electrodes for supercapacitor [10–15] reported better capacitance values, the SiNWs length influence in two electrodes devices has never been investigated. Moreover, it could be improved up to the capacitance wanted by increasing the SiNWs length and density and by improving the device design. In fact, SiNWs growth by CVD enables to tune the NWs lengths without any limitation.
Choi et al.  reported the use of porous SiNWs as electrode for supercapacitor in such devices but with Li+ containing electrolyte. Their capacitance is expressed only in force per gram, so no accurate comparison with our results is possible. Desplobain et al.  have obtained devices with 320 μF cm−2 capacitance by using gold-coated porous silicon but in aqueous electrolyte. SiNWs coated with NiO [13, 14] or SiC  shows promising performances and cycling ability, but silicon is not the active material and their performances have not been evaluated in the two electrodes devices.
After 250 cycles at ±5 μA cm−2, each device shows less than 2% capacitance loss (1.8% for 20-μm SiNWs, 0.5% for 10-μm SiNWs, 0.7% for 5-μm SiNWs, and 0.5% for bulk silicon) (Figure 3). Whatever the length, SiNWs are stable after these cycling experiments, as observed on post-experimental SEM images (Figure 4). The top bending that can be observed is due to electrostatic forces occurring during the sample washing with organic solvents before the SEM observation.
Due to the moderate surface capacitance, 20-μm SiNWs-based microdevice only stores 5 μJ cm−2, i.e., few milliwatts per square centimeter. However, the interest of the device is more directed toward the power density which reaches 1.4 mWcm−2, which is close to the one of the 5-μm thick activated carbon supercapacitor (5 mW cm−2) .
Highly doped SiNWs/SiNWs micro-ultracapacitors show a quasi-ideal capacitive behavior in organic electrolyte (1 M NEt4BF4 in PC). Current density used for galvanostatic charge/discharge cycling does not seem to have a major influence on the device capacitance. Devices capacitance increase with the length of the SiNWs on the electrode has been improved up to 10 μF cm−2 by using 20-μm SiNWs, i.e., ≈10-fold bulk silicon capacitance. This device exhibits 1.8% capacitance loss in 250 cycles with a maximum power density of 1.4 mW cm−2. As SiNWs growth by CVD with HCl gas enables to tune the NWs lengths without any limitation, the capacitance can be improved up to the wanted values by increasing the SiNWs length and density and by improving device design to avoid SiNWs constriction.
Chemical vapor deposition
Standard cubic centimeters
Scanning electron microscopy
The authors thank the “Délégation Générale pour l’Armement” DGA and CEA for the financial support of this work.
- Simon P, Gogotsi Y: Materials for electrochemical capacitors. Nat Mater 2008, 7: 845–854. 10.1038/nmat2297View Article
- Aricò AS, Bruce P, Scrosati B, Tarascon J-M, Van Schalkwijk W: Nanostructured materials for advanced energy conversion and storage devices. Nat Mater 2005, 4: 366–377. 10.1038/nmat1368View Article
- Miller JR, Simon P: Electrochemical capacitors for energy management. Science 2008, 321: 651–652. 10.1126/science.1158736View Article
- Rogers JA, Huang Y: A curvy, stretchy future for electronics. Proc Nat Acad Sci USA 2009, 106: 10875–10876. 10.1073/pnas.0905723106View Article
- Kaempgen M, Chan CK, Ma J, Cui Y, Gruner G: Printable thin film supercapacitors using single-walled carbon nanotubes. Nano Lett 2009, 9: 1872–1876. 10.1021/nl8038579View Article
- Chmiola J, Largeot C, Taberna P-L, Simon P, Gogotsi Y: Monolithic carbide-derived carbon films for micro-supercapacitors. Science 2010, 328: 480–483. 10.1126/science.1184126View Article
- Pech D, Brunet M, Durou H, Huang P, Mochalin V, Gogotsi Y, Taberna PL, Simon P: Ultrahigh-power micrometre-sized supercapacitors based on onion-like carbon. Nat Nanotechnol 2010, 5: 651–654. 10.1038/nnano.2010.162View Article
- Kim HK, Seong TY, Lee SM, Yoon YS: Charge–discharge induced phase transformation of RuO 2 electrode for thin film supercapacitor. Met Mater Int 2003, 9: 239–246. 10.1007/BF03027042View Article
- Moser F, Athouel L, Crosnier O, Favier F, Bélanger D, Brousse T: Transparent electrochemical capacitor based on electrodeposited MnO2 thin film electrodes and gel-type electrolyte. Electrochem Comm 2009, 11: 1259–1261. 10.1016/j.elecom.2009.04.023View Article
- Choi JW, McDonough J, Jeong S, Yoo JS, Chan CK, Cui Y: Stepwise nanopore evolution in one-dimensional nanostructures. Nano Lett 2010, 10: 1409–1413. 10.1021/nl100258pView Article
- Rowlands SE, Latham RJ: Supercapacitor devices using porous silicon electrodes. Ionics 1999, 5: 144–149. 10.1007/BF02375918View Article
- Desplobain S, Gautier G, Semai J, Ventura L, Roy M: Investigations on porous silicon as electrode material in electrochemical capacitors. Phys Stat Sol (C) 2007, 4: 2180–2184. 10.1002/pssc.200674418View Article
- Lu F, Qiu M, Qi X, Yang L, Yin J, Hao G, Feng X, Li J, Zhang J: Electrochemical properties of high-power supercapacitors using ordered NiO coated Si nanowire array electrodes. Appl Phys A 2011, 104: 545–550. 10.1007/s00339-011-6412-2View Article
- Tao B, Zhang J, Miao F, Hui S, Wan L: Preparation and electrochemistry of NiO/SiNW nanocomposite electrodes for electrochemical capacitors. Electrochim Acta 2010, 55: 5258–5262. 10.1016/j.electacta.2010.04.057View Article
- Alper JP, Vincent M, Carraro C, Maboudian R: Silicon carbide coated silicon nanowires as robust electrode material for aqueous micro-supercapacitor. Appl Phys Lett 2012, 100: 163901. 10.1063/1.4704187View Article
- Thissandier F, Le Comte A, Crosnier O, Gentile P, Bidan G, Hadji E, Brousse T, Sadki S: Highly doped silicon nanowires based electrodes for micro-electrochemical capacitors application. Electrochem Comm 2012, 25: 109–111.View Article
- Wagner RS, Ellis WC: Vapor–liquid-solid mechanism of single crystal growth. Phys Lett 1964, 4: 89–90.
- Morales AM, Lieber CM: A laser ablation method for the synthesis of crystalline semiconductor nanowires. Science 1998, 279: 208–211. 10.1126/science.279.5348.208View Article
- Oehler F, Gentile P, Baron T, Ferret P: The effects of HCl on silicon nanowire growth: surface chlorination and existence of a “diffusion-limited minimum diameter”. Nanotechnology 2009, 20: 475307. 10.1088/0957-4484/20/47/475307View Article
- Oehler F, Gentile P, Baron T, Ferret P, Den Hertog M, Rouvière J: The importance of the radial growth in the faceting of silicon nanowires. Nano Lett 2010, 10: 2335–2341. 10.1021/nl904081gView Article
- Gentile P, Solanki A, Pauc N, Oehler F, Salem B, Rosaz G, Baron T, Den Hertog M, Calvo V: Effect of HCl on the doping and shape control of silicon nanowires. Nanotechnol 2012, 23: 215702. 10.1088/0957-4484/23/21/215702View Article
- Rosaz G, Salem B, Pauc N, Gentile P, Potié A, Baron T: High-performance silicon nanowire field-effect transistor with silicided contacts. Semicond Sci Technol 2011, 26: 085020. 10.1088/0268-1242/26/8/085020View Article
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