Fabrication of (Co,Mn)3O4/rGO Composite for Lithium Ion Battery Anode by a One-Step Hydrothermal Process with H2O2 as Additive
Fabrication of (Co,Mn)3O4/rGO Composite for Lithium Ion Battery Anode by a One-Step Hydrothermal Process with H2O2 as Additive
Zuohua Li 0 1
Yanhui Cui 1
Jun Chen 1
Lianlin Deng 1
Junwei Wu 1
0 School of Civil and Environmental Engineering, Harbin Institute of Technology Shenzhen Graduate School , Shenzhen , China , 2 IoT Application Technology Center of NDT, Shenzhen Graduate School, Harbin Institute of Technology , Shenzhen , China , 3 School of Materials Science and Engineering, Harbin Institute of Technology Shenzhen Graduate School, Shenzhen Key Laboratory of Advanced Materials , Shenzhen , China
1 Editor: Jun Xu, Beihang University , CHINA
Binary transition metal oxides have been regarded as one of the most promising candidates for high-performance electrodes in energy storage devices, since they can offer high electrochemical activity and high capacity. Rational designing nanosized metal oxide/carbon composite architectures has been proven to be an effective way to improve the electrochemical performance. In this work, the (Co,Mn)3O4 spinel was synthesized and anchored on reduced graphene oxide (rGO) nanosheets using a facile and single hydrothermal step with H2O2 as additive, no further additional calcination required. Analysis showed that this method gives a mixed spinel, i.e. (Co,Mn)3O4, having 2+ and 3+ Co and Mn ions in both the octahedral and tetrahedral sites of the spinel structure, with a nanocubic morphology roughly 20 nm in size. The nanocubes are bound onto the rGO nanosheet uniformly in a single hydrothermal process, then the as-prepared (Co,Mn)3O4/rGO composite was characterized as the anode materials for Li-ion battery (LIB). It can deliver 1130.6 mAh g-1 at current density of 100 mA g-1 with 98% of coulombic efficiency after 140 cycles. At 1000 mA g-1, the capacity can still maintain 750 mAh g-1, demonstrating excellent rate capabilities. Therefore, the one-step process is a facile and promising method to fabricate metal oxide/rGO composite materials for energy storage applications.
Data Availability Statement: All relevant data are
within the paper and its Supporting Information
Recently more attention has been paid to environment friendly, sustainable, and efficient
device for energy conversion and storage devices.[
] Li-ion batteries (LIBs) with high specific
capacity have received worldwide interest and an increase in research output.[
the conventional graphite anode fails to meet the requirements for the fast-growing markets,
for example in portable electronics and hybrid vehicles, due to limited power and energy
Transition metal oxides, especially M3O4 (M = Mn, Co or Fe) with a spinel structure, are
one of the most promising anode materials for lithium ion batteries, due to availability of the
elements and high capacity, which is more than twice that of traditional intercalation graphite
anode. Metal oxide (M3O4) behaves as anode materials for LIB based on conversion (redox)
] The mechanism can be described by M3O4 + 8Li+ + 8e- ! 4Li2O + 3M. Normally
lithium oxide Li2O is stable and does not decompose to the metallic lithium, however, in the
presence of nanosized transition metal (nano-M), the reaction can proceed as nano-M + Li2O
$ 2Li+ + nano-MO, and thus the function as lithium ion battery anode can be achieved.
Moreover, engineering the metal oxides at nanoscale offers further advantages, such as increased
active surface areas, short ion diffusion pathways, and better accommodation of the reaction
strains, which enhance the energy storage capacity or rate capabilities.
However, poor electronic conductivity and agglomeration of nanoparticles restricts the
direct utilization of nanosized transition metal oxide and graphene nanosheets. Carbon nano
fiber or other carbon source, which have better electronic conductivity,[
] can connect with
each other to provide a fast electronic conduction path and offer a space framework for metal
oxide nucleation to avoid agglomeration of the nanoparticles. As anode materials for lithium
ion battery, the M3O4/C composites can also accommodate the volume expansion of active
materials to achieve long term stable performances.[
] Yang et al.[
] reported that NiCo2O4/
carbon nanocomposite was prepared using a hydrothermal method and achieved a high
reversible capacity (958.4 mA h g-1 at a current of 40 mA g-1 after 50 cycles) as LIB anode. Composite
materials of nano transition metal oxides with graphene had been reported extensively to have
better electronic conductivity and electrochemical performances, such as nanomaterials of
] Mn3O4, CoMn2O4,[
] etc. However these
reported synthesis methods typically involve a two-steps process, and a facile and simple
method to synthesize M3O4/graphene composites with excellent lithium storage behavior is
still a challenge, especially for binary oxides.
In this work, we demonstrate a one-step hydrothermal route to synthesize nanocube (Co,
Mn)3O4 of about 20 nm in size, which are anchored on rGO. Unlike traditional processes, no
post annealing is necessary to crystallize the nanocubes. The as-prepared (Co,Mn)3O4/rGO
composite has been characterized as anode materials for a LIB. The obtained results show the
(Co,Mn)3O4/rGO composite exhibits a high discharge capacity, long term cycling stability and
an excellent rating capability. The optimum discharge capacity can reach 1130.6 mAh g-1 at
100 mA g-1 and a reversible capacity 939.1 mAh g-1 can be achieved after 140 cycles at 200 mA
g-1, with capacity retention 98.8%.
Synthesis of (Co,Mn)3O4/rGO composite
Graphene oxide (GO) was prepared by modified Hummers method.[
] In a typical procedure,
120 mg GO was dispersed in 30 ml deionized (DI) water by placing in an ultrasonic bath for 2
hours, 1.7 mmol Co(OAc)2 and 1 ml ammonium hydroxide (NH3 H2O), 3.5mmol Mn(OAc)2
were dissolved in 15 ml deionized (DI) water. The two solutions were then mixed and 2 ml
H2O2 was added before the solution was transferred into 100 ml Teflon-lined stainless steel
autoclave. The autoclave was kept at 200°C for 6 h before cooling down to room temperature.
The precipitate was washed and then placed in a centrifuge with DI water, this procedure was
repeated several times, until a pH 7 was obtained followed by freeze-drying to obtain a (Co,
Mn)3O4/rGO composite. For comparison, rGO was attained to remove (Co,Mn)3O4 from (Co,
Mn)3O4/rGO composite, which was conducted in 1M HCl solution with sonication, and
followed by freeze-drying.
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The crystalline structure of the (Co,Mn)3O4/rGO was characterized by X-ray diffraction
(XRD) by Rigaku D/max 2500PC system (Cu-Ka 40 kV, 200 mA) in the range between 10° and
80° with the scan rate of 8°/min. Field emission scanning electron microscopy (FE-SEM,
Hitachi S4700, 15kV) and transmission electron microscope (TEM, JEOL JEM-2100F) were used to
observe surface morphology and identify the phase composition of as-prepared (Co,Mn)3O4/
rGO composite. Raman spectroscopy was obtained using a Renishaw inVia Raman
spectrometer with 415 nm diode laser excitation to access the state of the GO. The X-ray photoelectron
spectroscopy (XPS) analysis was performed on a VG ESCALAB MKII with Al Kα (1486.6 eV)
as X-ray source.
For Li-ion battery measurement, the working electrodes was prepared by mixing the (Co,
Mn)3O4/rGO composite material with acetylene black and polymer binder (polyvinylidene
fluoride; PVDF) in a weight ratio of 70:20:10. The slurry was cast on a copper foil by a standard
laboratory scale doctor-blade technique followed by drying in air for 1 h at 80°C, and then
further dried in a vacuum oven (<0.1 mbar) at 120°C for 24 h. CR2032 coin-type cells were
directly fabricated in an Ar-filled glove box for electrochemical tests, using an electrolyte of 1
mol L-1 LiPF6 in a mixture of ethylene carbonate (EC) and diethyl carbonate (DEC) (1: 1 in
volume, battery grade, from Dongguan Shanshan Battery Materials Co. Ltd, China), with 10%
vinylene carbonate (VC, 99% purity, from Aladdin Reagents Co., Ltd, Shanghai) as an additive.
A metallic lithium foil served as the counter electrode. The cycle performance was performed
on a Maccor 4300 battery test system (accuracy: 0.1%) at 25°C with the potential window from
0.01 to 3.0 V. Cyclic voltammetry (CV) tests were conducted on a CHI760D electrochemical
workstation at a scan rate of 0.5 mV s-1.
Results and Discussion
Morphology and Structure Analysis
A reaction process and the resulting novel anode material developed in this work are
schematically illustrated in Fig 1.
In the first stage metal ions connect with ammonium hydroxide molecules to form metal
amine complex, which are likely adsorbed on the surface of GO sheet with hydroxyl and
carboxyl groups to form a GO + Co/Mn complex (left hand side of Fig 1). The introduction of
H2O2 into the system oxidizes the transition metal ions (Mn2+, Co2+) partially to Mn3+, Co3+
and then in the hydrothermal process becomes well crystallized (Co,Mn)3O4 on rGO (right
hand side of Fig 1). It is anticipated that the strongest adsorption sites result in (Co,Mn)3O4
and these sites have a even distribution on the GO. The reactions can be described by the
following equations [
Fig 1. Schematic show of the synthesis of the (Co,Mn)3O4/rGO nanocubes.
The as-synthesized (Co,Mn)3O4/rGO composite was first characterized by XRD to identify
its crystallographic structure. As shown in Fig 2A, the main diffraction peaks of the composite
material can be indexed to the spinel (Co,Mn)3O4 (JCPDF Card NO. 18–0408), and the sharp
peaks prove that the (Co,Mn)3O4 spinel is well crystallized. A detailed analysis shows that the
as-prepared product has two additional peaks around 24° and 31° matching well with MnCO3
(JCPDF Card No. 44–1472), suggesting a little amount of impurity. The accurate content of
(Co,Mn)3O4/rGO composite shown in Figure A in S1 File reveals accordant element
proportion with the raw material. The carbon state of the rGO was analysed by Raman spectroscopy.
Clear D and G peaks are observed at 1350 cm-1 and 1590 cm-1 respectively (see Figure B in S1
File), which is consistent with standard spectrum seen for rGO.[
] And ID/IG of rGO is
1.08, lower than 1.16 of GO that is matching with the reference (Figure C Panel A in S1 File)
. The XRD profile comparison was shown in Figure C Panel B in S1 File, the XRD pattern
of rGO also matches with the reference well [
], suggesting rGo was well prepared. A further
comparison with other Co-Mn spinel oxides has been made as shown in Figure D and Table A
in S1 File, and it is further verified that the product obtained here is a tetragonal mixed spinel
with the composition (Co,Mn)3O4.
A mixed spinel with the composition (Co,Mn)3O4 suggests that both tetragonal and
octahedral sites in the spinel are occupied by both 2+ and 3+ oxidation states. Detailed elemental
composition and oxidation state of as-synthesized product were characterized by XPS. The
spectrum obtained in Fig 2B indicates the presence of Co, Mn, and O, as well as C from the
rGO. In order to identify the oxidation state of Co and Mn, the XPS spectra in the Co 2p and
Mn 2p region were analyzed and fitted (Fig 2C and 2D).[
] For Co (Fig 2C), based on the
wide Co 2p3/2 and Co 2p1/2 peaks, it is reasonable to assume that Co2+ and Co3+ species
] Whereas, two main peaks of Co 2p3/2 and 2p1/2 are fitted well with two
spinorbit doublets, characteristic of Co2+ and Co3+,[
] and two additional satellite peaks
shown at 786.8 and 802.9 eV (indicarted by an inverted triangle) correspond to Co 2p3/2, Co
2p1/2 are respectively. The Mn 2p spectrum can be deconvolved into four peaks and assigned to
the co-existence of Mn2+ and Mn3+ cations[
] as shown in Fig 2D. It is reasonable, therefore,
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Fig 2. XRD and XPS characterizations (Co,Mn)3O4/rGO. (A) XRD patterns. (B) XPS survey spectrum. (C)
Highresolution XPS spectra of Co 2p. (D) High-resolution XPS spectra of Mn 2p.
to conclude that both of the Co and Mn elements have 2+ and 3+ valence states that agree well
with the results of XRD test. And the solid-state redox couples Mn3+/Mn2+ and Co3+/Co2+ are
present in the spinel structure, which may provide a notable electrochemical activity.
Previously, CoMn2O4 microspheres[
] and hierarchical porous CoMn(CoMn)2O4/rGO nanoplates
] had been synethesized as electrode materials for supercapacitor applications. However,
without any oxidant addition, such as H2O2, crystalline structure can only be obtained after
calcinations at least 300°C.
The morphology of the as-prepared composite was examined by SEM and TEM. Fig 3A
shows a SEM image of the (Co,Mn)3O4/rGO composite, showing a large number of (Co,
Mn)3O4 particles are anchored on the rGO nanosheets and Fig 3B shows that these
nanoparticles distribute uniformly without any obvious agglomeration. Because the rGO sheets provide
numerous nucleation sites, and as shown by the Fig 1 these are distributed on a scale of around
0.75 nm, but as seen in Fig 3C the distance between the cubic nanoparticles on the rGO sheet is
around 30 nm, so there must be sites that are preferred for (Co,Mn)3O4 growth.
In addition, the higher magnification (scale bar = 20nm) in Fig 3C shows that the (Co,
Mn)3O4 nanoparticles are ~20 nm with a cubic morphology. The HRTEM image shown in Fig
3D further reveals the (Co,Mn)3O4 nanocubes grown on rGO sheet have a lattice spacing of
0.49 nm, which corresponds well to the theoretical interplane spacing of spinel (Co,Mn)3O4
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Fig 3. SEM and TEM images of (Co,Mn)3O4/rGO composite. (A) SEM images. (B) and (C) TEM images. (D)
Li-Ion Batteries Performance
Coin-type cell was used to evaluate the lithium storage properties of (Co,Mn)3O4/rGO
composite as lithium anode. Fig 4A shows the first three charge-discharge profiles of as-synthesized
sample at a current density of 100 mA g-1 in the rage of 0.01~3.0 V (vs. Li/Li+).
The first discharge capacity is 1452 mAh g-1, and the first charge one is 1027 mAh g-1,
showing an irreversible capacity loss of 400 mA h g-1, and a coulombic efficiency of 70.7%. The
irreversible capacity loss arising during the first cycle is likely due to the incomplete
decomposition of Li2O and the difficult dissolution of the SEI layer.[
] In the 2nd cycle, the discharge
and charge capacity are 1082 mAh g-1 and 1026 mAh g-1 and in the 3rd cycle the discharge and
charge capacity are 1076 mAh g-1 and 1028 mAh g-1, respectively. It is noted that the charge
capacity are almost the same for the initial three cycles. The CV curves for LIBs at a scan rate of
0.5 mV s-1 in the potential range of 0.01~3V (vs. Li/Li+) are shown in Fig 4B. It is easily seen
that the first cycle exhibits differs from the following 2 cycles which almost overlaps with each
other, demonstrating that the electrode exhibit good stability and cyclability after 1st cycle. In
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Fig 4. Electrochemical performances of (Co,Mn)3O4/rGO composite as lithium ion battery anode. (A)
Charge-discharge voltage profiles of (Co,Mn)3O4/rGO composite for the first three cycles at a current density of
100 mA g−1. (B) CV curves for LIBs in the potential region of 0 ~ 3.0 V (vs. Li/Li+) at a scanning rate of 0.5 mV s−1.
(C) A comparison of the specific capacity as a function of current density. (D) Cycling performance at current
densities of 200 mA g−1 of (Co,Mn)3O4/rGO composite.
the first cycle, there is a broad peak at ~1.3 V and a sharp peak at ~0.3 V in the cathodic
process, which corresponds to the reduction of Mn3+, Co3+ to Mn2+, Co2+ as well as Mn2+, Co2+ to
metallic Mn, Co, respectively.[
] And it was also believed that the formation of SEI layer in
the first discharge process will contribute to discharge capacity, which accounts for the larger
discharge capacity and different CV shape with the next two cycles. Upon charge, two broad
oxidation peaks are shown at 1.5 V and 2.0 V, which can be assigned to the oxidation of Mn
and Co to Mn2+ and to Co2+, respectively. In the following two cycles, the reduction peak
moves to about 0.5 V, which is different from the irreversible electrochemical reaction during
the first discharge cycle.[
] On the basis of the cyclic voltammetry curves, the entire
electrochemical process can be described as follows:
Co; Mn3O4 8Li 8e
! 3Co 3Mn 4Li2O
Previously, Qiang Shen and co-workers[
] found that MnCO3 spindle–GO composites
and flower like MnCO3 could act as lithium ion battery anode materials. And the reaction
mechanism can be expressed as:
MnCO3 2Li ! Li2CO3 Mn
4 0:5xLi $ 3Li2O 0:5LixC2;
x 0; 1or2
However, when we make a comparison of the CV test (Fig 4B) in this work with those
results of MnCO3 LIB anode[
], no extra peaks of MnCO3 was founded. Therefore, the
MnCO3 impurity is neglectable to the electrode.
Fig 4C shows the rate capability of as-prepared (Co,Mn)3O4/rGO composite. The electrode
delivers a specific capacity of 1131 mAh g-1 at 100 mA g-1, 951 mAh g-1 at 200mA g-1, 877
mAh g-1 at 400 mA g-1, 720 mAh g-1 at 600mA g-1, 546 mAh g-1 at 1000 mA g-1 and 212 mAh
g-1 at 2000 mA g-1, respectively. When the current density turned back to 100 mA g-1, a specific
capacity of 1105 mAh g-1 with a capacity retention of 97.8%, demonstrating excellent rate
capabilities of the synthesized composite materials. Fig 4D shows cycling performances at the
current density of 200 mA g-1. After 140 cycles, a reversible capacity 939 mAh g-1 can be obtained
without any obvious degradation, with the capacity retention of 98.8%. In addition, the
coulombic efficiency retains 98% after 140 cycles. The slight capacity increase after 50th cycle is
due to the improvement of Li+ accessibility and accommodation behavior in the electrode, the
transformation of crystalline structure to an amorphous structure of (Co, Mn)3O4, and the
formation of a gel-like surface film during the initial activation process[
Co-Mn oxides had been studied extensively as anode materials for lithium ion batteries.
Here we made a comparison of the Co-Mn oxides in electrochemical performance and
synthesis method, as summarized in Table 1. It is obvious that the (Co,Mn)3O4/rGO composites in
this work exhibits outstanding cycling performance and highest reversible capacity. It is also
noted that two steps process is the most popular way to prepare crystalline Co-Mn oxides in
previous works, which prepared the precursor firstly followed by heat treatment to obtain the
oxide. However in this work, we report a simple and facile route to achieve (Co,Mn)3O4/rGO
hybrid without any following heat treatment. To the best of our knowledge, this is the first time
to report one-step hydrothermal synthesize (Co,Mn)3O4/rGO composite as an anode for LIBs
with outstanding performances. The excellent performance is attributed to synthetic effect of
well distributed nanocubes and strong adherence on rGO, which guarantees rapid lithium
conversion reaction and high electronic conductivity. Therefore, the one-step process is a facile
and promising method to fabricate metal oxide/rGO composites for LIB applications. It can be
Current density (mA
further used to synthesize other transition metal oxide/rGO composites for various
applications, such as electrochemical capacitor, and catalysts.
In summary, we firstly demonstrated an one-step route synthesis for binary transition metal
oxide (Co,Mn)3O4 nanocubes on the surface of rGO. With the introduction of oxidant H2O2 in
the synthesis process, the (Co,Mn)3O4/rGO composites can be obtained by a single
hydrothermal process. As anode materials for LIBs, as-prepared composites delivered reversible capacity
of 1100 mA h g-1 at a current density of 100 mA g-1. Also, excellent electrochemical stability is
revealed with nearly 98.8% retention of initial capacity after 140 cycles at 200 mA g-1. We
believe such good performance results from nano sized and uniform growth of cube (Co,
Mn)3O4 particles on rGO, which would shorten the transfer distance of ions and increase the
active contact area with electrolyte. Therefore, the one-step process is a simple and promising
method to fabricate high performance binary metal oxide/rGO composites for LIB
applications. Furthermore, the one-step route can be expanded to synthesize other binary transition
oxides for various applications.
S1 File. Figure A. The EDS spectrum and results of (Co, Mn)3O4/rGO composite; Figure B.
Raman spectra of the (Co,Mn)3O4/rGO composite; Figure C. The Raman spectra and XRD
patterns of GO and rGO. (A) The Raman spectra. (B) XRD patterns of GO and rGO. The rGO
is obtained by removing the metal oxide of (Co, Mn)3O4/rGO; Figure D. (Co,Mn)3O4 XRD
spectra comparison. (A) (Co,Mn)3O4 with CoMn2O4, MnCo2O4. (B) (Co,Mn)3O4 with Co3O4,
Mn3O4; Table A. Detailed information of Co-Mn oxides.
The work was supported by Shenzhen Peacock Plan Program (KQCX20140521144358003),
Fundamental Research Program of Shenzhen (JCYJ20140417172417144), International
Collaboration Program of Shenzhen (GJHZ20150312114008636), Shenzhen Technology
Innovation Program—Technology Development Projects (Grant No. CXZZ20140904154839135).
Data curation: JC LD.
Formal analysis: ZL YC JC LD.
Funding acquisition: ZL JW.
Investigation: ZL YC JC LD.
Methodology: ZL YC JC.
Project administration: ZL JW.
Writing – original draft: ZL YC JC.
Writing – review & editing: JW.
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