NiCuCo2O4 Supported NiâCu Ion-Exchanged ... - ACS Publications

Subscriber access provided by UNIV OF DURHAM

Article

NiCuCo2O4 Supported Ni-Cu Ion-exchanged Mesoporous Zeolite Heteronano Architecture: An Efficient, Stable, and Economical Non-precious Electrocatalyst for Methanol Oxidation Subhajyoti Samanta, Kousik Bhunia, Debabrata Pradhan, Biswarup Satpati, and Rajendra Srivastava ACS Sustainable Chem. Eng., Just Accepted Manuscript • DOI: 10.1021/ acssuschemeng.7b03444 • Publication Date (Web): 02 Jan 2018 Downloaded from http://pubs.acs.org on January 3, 2018

Just Accepted “Just Accepted” manuscripts have been peer-reviewed and accepted for publication. They are posted online prior to technical editing, formatting for publication and author proofing. The American Chemical Society provides “Just Accepted” as a free service to the research community to expedite the dissemination of scientific material as soon as possible after acceptance. “Just Accepted” manuscripts appear in full in PDF format accompanied by an HTML abstract. “Just Accepted” manuscripts have been fully peer reviewed, but should not be considered the official version of record. They are accessible to all readers and citable by the Digital Object Identifier (DOI®). “Just Accepted” is an optional service offered to authors. Therefore, the “Just Accepted” Web site may not include all articles that will be published in the journal. After a manuscript is technically edited and formatted, it will be removed from the “Just Accepted” Web site and published as an ASAP article. Note that technical editing may introduce minor changes to the manuscript text and/or graphics which could affect content, and all legal disclaimers and ethical guidelines that apply to the journal pertain. ACS cannot be held responsible for errors or consequences arising from the use of information contained in these “Just Accepted” manuscripts.

ACS Sustainable Chemistry & Engineering is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society. Copyright © American Chemical Society. However, no copyright claim is made to original U.S. Government works, or works produced by employees of any Commonwealth realm Crown government in the course of their duties.

Page 1 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

ACS Sustainable Chemistry & Engineering

NiCuCo2O4 Supported Ni-Cu Ion-exchanged Mesoporous Zeolite Heteronano Architecture: An Efficient, Stable, and Economical Nonprecious Electrocatalyst for Methanol Oxidation Subhajyoti Samanta†, Kousik Bhuniaǂ, Debabrata Pradhanǂ, Biswarup Satpati┴ and Rajendra Srivastava†* †

Department of Chemistry, Indian Institute of Technology Ropar, Nangal Road, Rupnagar-140001,

India ǂ

Materials Science Centre, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal-

721302, India ┴

Surface Physics and Material Science Division, Saha Institute of Nuclear Physics, 1/AF,

Bidhannagar, Kolkata 700 064, India

_____________________________________________________________________ Corresponding Author E-mail: [email protected] Phone: +91-1881-242175; Fax: +91-1881-223395

1 ACS Paragon Plus Environment

ACS Sustainable Chemistry & Engineering 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 2 of 40

___________________________________________________________________________

ABSTRACT A unique strategy to obtain highly efficient electrocatalyst based on the spinel Ni0.5Cu0.5Co2O4 and mesoporous ZSM-5 (Zeolite Socony Mobil-5) is reported here for methanol oxidation in an alkaline medium. To develop an efficient catalyst, Ni2+-Cu2+ ionexchanged mesoporous ZSM-5 and Ni0.5Cu0.5Co2O4 are prepared. 30 weight % of Ni0.5Cu0.5Co2O4

decorated

Ni2+-Cu2+

ion-exchanged

mesoporous

ZSM-5

exhibits

exceptionally higher catalytic activity with reasonably low onset potential than that of Ni0.5Cu0.5Co2O4, NiCo2O4, CuCo2O4, and Ni2+-Cu2+ ion-exchanged mesoporous ZSM-5. Electrochemical oxidation of HCHO and HCOOH also takes place over this catalyst at the same condition.

The material exhibits high current density (21.4 mA/cm2) and stable

electrocatalytic activity (with 99% retention) even after 1000 potential cycles. However, the benchmark catalyst Pt(20%)/C exhibits low activity (1.6 mA/cm2) and significant deactivation phenomenon (with 25% activity retention) at the identical condition. The cooperative contributions provided by Ni0.5Cu0.5Co2O4 and Ni2+-Cu2+ ion-exchanged mesoporous ZSM-5 support having Brönsted acidity, large external surface area, and intercrystalline mesoporosity deliver excellent electrocatalytic activity. The ease of synthesis, scale-up, stable & exceptional electrocatalytic activity paves the path towards the development of highly efficient alkaline direct methanol fuel cells.

KEYWORDS: Methanol fuel cell, Spinel, Mesoporous zeolite, Noble metal free electrocatalyst, Multi-functional catalyst __________________________________________________________________________


Page 3 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


INTRODUCTION To meet the energy demand and overcome the environmental pollution associated with the fossil fuels and biomass based fuels, efforts are in progress to develop eco-friendly and inexhaustible energy systems such as fuel cells, photoelectrochemical production of H2, Liion batteries, and so on.1-3 The use of H2 as a fuel is a major limitation associated with the highly efficient proton exchange membrane fuel cells because H2 is highly flammable and its storage and transportation is not safe.4 The use of methanol as an economical and easily available fuel is attractive and safer than hydrogen because the simple and sustainable storage system for methanol is already in practice.4 These facts have encouraged researchers to design and develop electrode materials and membranes for direct methanol fuel cells (DMFC).

4-6

Activity of the anode catalyst defines the efficiency of DMFC. At the

conventional electrode, methanol oxidation takes place at high over potential, which demands the development of an efficient anode catalyst.7-10 At present, commercial DMFC uses Platinum (Pt) based anode catalyst.7 The high cost, a limited reserve of Noble metals, and poor CO tolerance hinder the practical application of Pt based DMFC.8 During the methanol oxidation at Pt electrode, CO forms at the electrode surface and deactivates the Pt based catalysts. Noble metal-Pt based alloys have been developed to minimize the deactivation associated with conventional Pt catalysts.11-14 While the use of noble metal-Pt alloys has undoubtedly curtailed this catalyst-deactivation problem, their limited reserves and high costs still continue to restrict their sustainable commercial applications. Alkaline electrolyte based DMFC electrode systems are being developed since last 10 years. Methanol oxidation is kinetically faster in the alkaline medium than in the acidic medium under electrochemical condition.15,16 The alkaline medium provides many advantages that include retardation in the catalyst poisoning, improved efficiency and stability of the catalyst, and an economical and sustainable choice of electrode materials based on Pd, Ni, Cu, Co and other economical and easily available transition metals.17-20 To develop a highly efficient and economical catalyst for methanol electro-oxidation, transition metal based systems need to be explored. Literature reports suggest that Ni and Cu based catalysts are good choices for this reaction.19-25 The electrocatalytic oxidation of methanol has been compared at NiCo2O4, NiO, and Co3O4 modified electrodes in alkaline medium at the identical condition.23 The methanol oxidation at NiCo2O4 surface is mediated by the similar species (NiOOH and CoOOH) to that of NiO and CuO catalysts. With increase in the Ni content in Ni-Co hydroxides, response current corresponding to the methanol oxidation 3 ACS Paragon Plus Environment


was increased.24 Further, to increase the performance of NiCo2O4, Ni(OH)2 was loaded on the external surface of NiCo2O4.25,26 These studies suggest that the incorporation of an optimum amount of Nickel in the resultant catalytic system would be important to achieve the best result. Industrially robust zeolites are well explored for their applications as heterogeneous catalysts in energy sectors (especially petrochemical industry) and biomass conversion.27-31 Very recently, Ni/Cu-exchanged mesoporous ZSM-5 and SnO2/CeO2 supported mesoporous ZSM-5 have been explored for the electrochemical oxidation of methanol.32-34 Methanol transportation rate, oxidized products, electrons at the electrode surface and an effective contact at the electrode/electrolyte interface facilitate the electrocatalytic activity of DMFC. 35 Therefore, preparation of electrode materials with better textural properties and suitable conductivity is important for DMFC application. Very recently, WO3 based support materials have been reported for their applications in the development of fuel cell electrocatalysts.36,37 Mesoporous ZSM-5 zeolite has all those textural properties which are optimum for its DMFC application, except the required redox property. Applications of mesoporous zeolites in electrochemistry are being explored by our group.38-41 Besides the costly metal (Pd, Pt) based catalysts, systematic design and development of the economical transition metal (Co, Ni and Cu) based catalysts would be a viable strategy for its practical applications. Integration of suitable redox active metal oxides and metal ionexchanged Brönsted acidic mesoporous zeolites could provide enhanced activity in the methanol electrooxidation. In this study, a novel electrode material based on the nanocomposite of spinel (MCo2O4) and mesoporous ZSM-5 (Zeolite Socony Mobil-5) zeolite is reported for the DMFC application. The ion-exchange process was selected to obtain a suitable composition of Ni2+-Cu2+ ions in the mesoporous ZSM-5 (MesoZ). To enhance and fine tune the electrocatalytic activity, spinels were supported on the external surface of the Ni2+-Cu2+ ion-exchanged MesoZ. In this study, NiCo2O4, CuCo2O4, and Ni0.5Cu0.5Co2O4 materials were prepared. Among these spinels, highly active Ni0.5Cu0.5Co2O4 with optimized amount was supported on the external surface of Ni2+-Cu2+ ion-exchanged MesoZ to develop highly efficient electrocatalyst for methanol oxidation. Further, the activity and stability of the developed catalyst (Ni0.5Cu0.5Co2O4(30%)/Ni2Cu1-MesoZ) was compared with the benchmark (20%)Pt/C catalyst under the identical condition to adjudge the efficiency of the presently investigated electrocatalyst. We believe that such a systematic and strategic study for the development of Ni0.5Cu0.5Co2O4 supported Ni2+-Cu2+ ion-exchanged MesoZ is reported here for the first time. 4 ACS Paragon Plus Environment

Page 4 of 40

Page 5 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


MATERIALS AND METHOD Materials, procedure for the catalyst synthesis, details of characterization techniques, electrode fabrication, and electrochemical techniques are provided in the Supporting Information, SI.

RESULTS AND DISCUSSION As indicated in the introduction section, the content of Nickel plays an important role in the enhancement of the electrocatalytic methanol oxidation activity. Mesoporous ZSM-5 (MesoZ) is not only chosen for the efficient adsorption of methanol at the Bronsted acidic sites42 and enhanced methanol diffusion but also to incorporate active metal ions into the zeolite matrix. First a range of Ni, Cu, and Ni-Cu ions exchanged MesoZ materials were prepared and investigated for electrocatalytic methanol oxidation. Among these materials, Ni2Cu1-MesoZ exhibited the best electrocatalytic activity. The details of electrocatalytic oxidation leading to the optimized support material are not included in this manuscript. Further, spinels with different compositions of Ni and Cu were prepared and investigated to achieve the highly active Ni0.5Cu0.5Co2O4 spinel for the methanol oxidation. A part of the electrocatalytic activities exhibited by these spinels are provided in this section. Finally, highly active Ni0.5Cu0.5Co2O4 was supported on the best support material Ni2Cu1-MesoZ with different compositions and the complete details of the electrocatalytic methanol oxidation with these heterojunction materials are provided in this study.

PHYSICOCHEMICAL CHARACTERIZATION Powder X-ray diffraction patterns were recorded to ascertian the framework structure of the material. Diffraction planes (designated in Figure 1a) recorded for NiCo2O4 belong to the cubic NiCo2O4 spinel structure (JCPDS Card no. 43-1003) (Figure 1a).23 Diffraction planes recorded for CuCo2O4 belong to the face centered cubic (FCC) lattices of CuCo2O4 (JCPDS Card no. 78-2177) (Figure 1a).41 Ni0.5Cu0.5Co2O4 exhibits reflections similar to that of NiCo2O4/CuCo2O4 which confirms that the material is crystallized in the FCC structure (Figure 1a). Diffraction planes (designated in Figure 1b) recorded for MesoZ belong to the MFI framework structure.40 XRD patterns of Ni2Cu1-MesoZ and MesoZ are similar which confirms that the ion-exchange process did not alter the framework structure of the parent material. Diffraction peaks associated with Ni0.5Cu0.5Co2O4 and Ni2Cu1-MesoZ phases are observed in the XRD pattern recorded for Ni0.5Cu0.5Co2O4(30%)/Ni2Cu1-MesoZ (Figure 1b), 5 ACS Paragon Plus Environment


Page 6 of 40

which suggests that during the loading and heat treatment process, the individual characteristics of both the materials has remained same. The different weight percentage of Ni0.5Cu0.5Co2O4 was loaded on the surface of Ni2Cu1-MesoZ, and the resultant materials exhibit similar diffraction patterns to that of Ni0.5Cu0.5Co2O4(30%)/Ni2Cu1-MesoZ (Figure S1, SI). N2-sorption analysis exhibits a type IV isotherm and an H2 hysteresis loop for MesoZ (Figure 1c). A steady increase in the adsorption volume in the range of 0.05 to 0.4 (P/P0) is observed, which is followed by the gradual increase in the adsorbed volume in the range of 0.4 to 0.9 (P/P0). This gradual increase in the adsorption volume is due to the capillary condensation of N2 molecules in the inter-crystalline mesopore void spaces. Mesopore size distribution, determined from BHJ analysis, is in the range of 2-10 nm for MesoZ. Isotherm and hysteresis loop of Ni2Cu1-MesoZ are similar to that of MesoZ but with somewhat reduced adsorbed volume (Figure 1c). These results suggest that porous architecture is retained

during

the

ion-exchange

process.

Though

the

isotherm

for

Ni0.5Cu0.5Co2O4(30%)/Ni2Cu1-MesoZ is almost similar to type IV but its adsorbed volume is significantly reduced than the parent MesoZ (Figure 1c and Table 1). Adsorbed volume (especially the mesopore volume) of Ni0.5Cu0.5Co2O4(30%)/Ni2Cu1-MesoZ is comparatively lower than Ni2Cu1-MesoZ, which suggests that the accessibility of the inter-crystalline mesopores is blocked by the Ni0.5Cu0.5Co2O4 nanocrystals which envelop the external surface of Ni2Cu1-MesoZ resulting in the formation of heterojunction nanocomposite material during the heat treatment process. Surface area (mainly external surface area) and porosity (mainly mesopore volume) determined from N2-sorption analysis are significantly reduced for Ni0.5Cu0.5Co2O4(30%)/Ni2Cu1-MesoZ after the loading of Ni0.5Cu0.5Co2O4 on the surface of Ni2Cu1-MesoZ. Table 1 shows that an increase in the content of Ni0.5Cu0.5Co2O4 over Ni2Cu1MesoZ, leading to the reduction in their textural properties. The contents of Ni and Cu in the resulting nanocomposite materials influenced the electrocatalytic activity. Therefore, the contents of Ni and Cu were determined using microwave plasma atomic emission spectroscopy (MP-AES) for various materials investigated in this study (Table S2, SI). Elemental analysis shows that more amount of Ni2+ is ion-exchanged on MesoZ than Cu2+. Ion-exchange of zeolite depends on the exchange capacity as well as the nature of metal ions.44 Moreover, elemental analysis also shows that almost equivalent amounts of Ni and Cu are present in NiCo2O4/CuCo2O4 (Table S1, SI). Slightly higher amount of Ni is incorporated in Ni0.5Cu0.5Co2O4 when compared to Cu.


Page 7 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


Elemental analysis also confirms that the input and output quantities of Ni0.5Cu0.5Co2O4 loaded on Ni2Cu1-MesoZ in the nanocomposite materials are almost similar (Table S1, SI). The morphology of spinels, zeolite, and nanocomposite materials was determined by field emission scanning electron microscope (FE-SEM). CuCo2O4 and NiCo2O4 exhibit nanorod-like morphology (length (~1 m) and diameter (

NiCuCo2O4 Supported NiâCu Ion-Exchanged ... - ACS Publications

Recommend Documents

NiCuCo2O4 Supported NiâCu Ion-Exchanged ... - ACS Publications