02386nas a2200253 4500008004100000022001400041245008400055210006900139260007100208300001600279490000600295520147900301653002101780653002001801653002001821653001401841653003001855100002501885700002701910700002801937700002701965700002401992856011602016 2015 eng d a1944-824400aCarbon nanohorn-derived graphene nanotubes as a platinum-free fuel cell cathode0 aCarbon nanohornderived graphene nanotubes as a platinumfree fuel a1155 16TH ST, NW, WASHINGTON, DC 20036 USAbAMER CHEMICAL SOCcNOV a24256-242640 v73 a

Current low-temperature fuel cell research mainly focuses on the development of efficient nonprecious electrocatalysts for the reduction of dioxygen molecule due to the reasons like exorbitant cost and scarcity of the current state-of-the-art Pt-based catalysts. As a potential alternative to such costly electrocatalysts, we report here the preparation of an efficient graphene nanotube based oxygen reduction electrocatalyst which has been derived from single walled nanohorns, comprising a thin layer of graphene nanotubes and encapsulated iron oxide nanopartides (FeGNT). FeGNT shows a surface area of 750 m(2)/g, which is the highest ever reported among the metal encapsulated nanotubes. Moreover, the graphene protected iron oxide nanoparticles assist the system to attain efficient distribution of Fe-N-x and quaternary nitrogen based active reaction centers, which provides better activity and stability toward the oxygen reduction reaction (ORR) in acidic as well as alkaline conditions. Single cell performance of a proton exchange membrane fuel cell by using FeGNT as the cathode catalyst delivered a maximum power density of 200 mW cm(-2) with Nafion as the proton exchange membrane at 60 degrees C. The facile synthesis strategy with iron oxide encapsulated graphitic carbon morphology opens up a new horizon of hope toward developing Pt-free fuel cells and metal-air batteries along with its applicability in other energy conversion and storage devices.

10acarbon nanohorns10acarbon nanotube10aelectrocatalyst10afuel cell10aoxygen reduction reaction1 aUnni, SreeKuttan, M.1 aIllathvalappil, Rajith1 aBhange, Siddheshwar, N.1 aPuthenpediakkal, Hasna1 aKurungot, Sreekumar uhttps://library.ncl.res.in/content/carbon-nanohorn-derived-graphene-nanotubes-platinum-free-fuel-cell-cathode-002350nas a2200241 4500008004100000022001400041245013100055210006900186260007100255300001400326490000600340520141500346653003301761653001901794653002001813653002601833653003001859653002401889653001901913100002401932700002401956856012801980 2015 eng d a2155-543500aCu-Pt nanocage with 3-D electrocatalytic surface as an efficient oxygen reduction electrocatalyst for a primary Zn-air battery0 aCuPt nanocage with 3D electrocatalytic surface as an efficient o a1155 16TH ST, NW, WASHINGTON, DC 20036 USAbAMER CHEMICAL SOCcMAR a1445-14520 v53 a

Cu-Pt nanocage (CuPt-NC) intermetallic structures have been prepared by an in situ galvanic displacement reaction. The structures are found to be well organized within the framework demarcated with distinguishing arms, having clear edges and corners with a size of similar to 20 nm. The unique nanocage structure possessing large specific surface area and better structural integrity helps to achieve improved electrochemical oxygen reduction reaction activity and stability in alkaline solution in comparison to the commercially available 20 wt % Pt/C. CuPt-NC shows 50 mV positive onset potential shift with significantly higher limiting current in comparison to Pt/C. Interestingly, CuPt-NC has shown 2.9- and 2.5-fold improved mass activity and specific activity, respectively, for ORR at 0.9 V vs RHE in comparison to Pt/C. Moreover, the stability of CuPt-NC has been tested by an accelerated durability test under alkaline conditions. CuPt-NC has been subsequently utilized as the air electrode in a primary Zn-air battery and is found to possess 1.30- and 1.34-fold improved power density and current density at 1 V, respectively, in comparison to the state-of-the-art Pt/C catalyst. In addition, CuPt-NC has shown several hours of constant discharge stability at 20 mA cm(-2) with a specific capacity of 560 mAh gZn(-1) and energy density of 728 Wh kgZn(-1) in the primary Zn-air battery system.

10a3-D electrocatalytic surface10aCu-Pt nanocage10aelectrocatalyst10agalvanic displacement10aoxygen reduction reaction10asolvothermal method10aZn-air battery1 aDhavale, Vishal, M.1 aKurungot, Sreekumar uhttps://library.ncl.res.in/content/cu-pt-nanocage-3-d-electrocatalytic-surface-efficient-oxygen-reduction-electrocatalyst-002716nas a2200229 4500008004100000022001400041245017200055210006900227260007100296300001600367490000600383520177500389653002002164653001702184653003002201653003402231653002302265100002302288700002402311700002402335856012702359 2015 eng d a1944-824400aSurface-tuned Co3O4 nanoparticles dispersed on nitrogen-doped graphene as an efficient cathode electrocatalyst for mechanical rechargeable zinc-air battery application0 aSurfacetuned Co3O4 nanoparticles dispersed on nitrogendoped grap a1155 16TH ST, NW, WASHINGTON, DC 20036 USAbAMER CHEMICAL SOCcSEP a21138-211490 v73 a

The most vital component of the fuel cells and metal air batteries is the electrocatalyst, which can facilitate the oxygen reduction reaction (ORR) at a significantly reduced overpotential. The present work deals with the development of surface-tuned cobalt oxide (Co3O4) nanoparticles dispersed on nitrogen-doped graphene as a potential ORR electrocatalyst possessing some unique advantages. The thermally reduced nitrogen-doped graphene (NGr) was decorated with three different morphologies of Co3O4 nanoparticles, viz., cubic, blunt edged cubic, and spherical, by using a simple hydrothermal method. We found that the spherical Co3O4 nanoparticle supported NGr catalyst (Co3O4-SP/NGr-24h) has acquired a significant activity makeover to display the ORR activity closely matching with the state-of-the-art Pt supported carbon (PtC) catalyst in alkaline medium. Subsequently, the Co3O4-SP/NGr-24h catalyst has been utilized as the air electrode in a Zn-air battery, which was found to show comparable performance to the system derived from PtC. Co3O4-SP/NGr-24h catalyst has shown several hours of flat discharge profile at the discharge rates of 10, 20, and 50 mA/cm(2) with a specific capacity and energy density of similar to 590 mAh/g(-zn) and,840 Wh/kg(-zn), respectively, in the primary Zn-air battery system. In conjunction, Co3O4-SP/NGr-24h has outperformed as an air electrode in mechanical rechargeable Zn-air battery as well, which has shown consistent flat discharge profile with minimal voltage loss at a discharge rate of 50 mA/cm(2). The present results, thus demonstrate that the proper combination of the tuned morphology of Co3O4 with NGr will be a promising and inexpensive material for efficient and ecofriendly cathodes for Zn-air batteries.

10aelectrocatalyst10amixed facets10aoxygen reduction reaction10arechargeable zinc-air battery10asurface morphology1 aSingh, Santosh, K.1 aDhavale, Vishal, M.1 aKurungot, Sreekumar uhttps://library.ncl.res.in/content/surface-tuned-co3o4-nanoparticles-dispersed-nitrogen-doped-graphene-efficient-cathode-002299nas a2200253 4500008004100000022001400041245014600055210006900201260007500270300001400345490000700359520131800366653002001684653002001704653003001724653002001754653001701774100002901791700002401820700002601844700002001870700002401890856013101914 2016 eng d a1616-301X00aNanoporous graphene enriched with Fe/Co-N active sites as a promising oxygen reduction electrocatalyst for anion exchange membrane fuel cells0 aNanoporous graphene enriched with FeCoN active sites as a promis aPOSTFACH 101161, 69451 WEINHEIM, GERMANYbWILEY-V C H VERLAG GMBHcAPR a2150-21620 v263 a

Here, a simple but efficient way is demonstrated for the preparation of nanoporous graphene enriched with Fe/Co-nitrogen-doped active sites (Fe/Co-NpGr) as a potential electrocatalyst for the electrochemical oxygen reduction reaction (ORR) applications. Once graphene is converted into porous graphene (pGr) by a controlled oxidative etching process, pGr can be converted into a potential electrocatalyst for ORR by utilizing the created edge sites of pGr for doping nitrogen and subsequently to utilize the doped nitrogens to build Fe/Co coordinated centers (Fe/Co-NpGr). The structural information elucidated using both XPS and TOF-SIMS study indicates the presence of coordination of the M-N (M = Fe and Co)-doped carbon active sites. Creation of this bimetallic coordination assisted by the nitrogen locked at the pore openings is found to be helping the system to substantially reduce the overpotential for ORR. A 30 mV difference in the overpotential () with respect to the standard Pt/C catalyst and high retention in half wave potential after 10 000 cycles in ORR can be attained. A single cell of an anion exchange membrane fuel cell (AEMFC) by using Fe/Co-NpGr as the cathode delivers a maximum power density of approximate to 35 mWcm(-2) compared to 60 mWcm(-2) displayed by the Pt-based system.

10aelectrocatalyst10anitrogen doping10aoxygen reduction reaction10aporous grapheme10aquantum dots1 aPalaniselvam, Thangavelu1 aKashyap, Varchaswal1 aBhange, Siddeswar, N.1 aBaek, Jong-Beom1 aKurungot, Sreekumar uhttps://library.ncl.res.in/content/nanoporous-graphene-enriched-feco-n-active-sites-promising-oxygen-reduction-electrocatalyst02503nas a2200289 4500008004100000022001400041245016700055210006900222260000800291300001400299490000600313520146900319653002001788653001401808653002201822653003001844100002501874700002701899700002401926700002401950700001801974700002101992700003002013700002002043700002002063856013002083 2017 eng d a2365-654900aChitosan intercalated metal organic gel as a green precursor of fe entrenched and fe distributed N-doped mesoporous graphitic carbon for oxygen reduction reaction0 aChitosan intercalated metal organic gel as a green precursor of  cSEP a8762-87700 v23 a

Herein, we present Metal-Organic Gel intercalated with chitosan, a `green'' precursor for the synthesis of intrinsic N-doped Fe entrenched (CHI-TMA-Fe-CW) and Fe distributed mesoporous graphitic carbon structures (CHI-TMA-Fe-CW-M1) with appreciable Oxygen Reduction Reaction (ORR) activity in alkaline medium. Modulation of the synthetic protocol as a function of reaction kinetics and gelation time while maintaining identical pyrolysis conditions (900 degrees C, flowing N-2 atmosphere) improves the microstructure, surface area and Fe distribution of the graphitic structures (CHI-TMA-Fe-CW-M1). CHI-TMA-Fe-CW has a Fe entrenched graphitic nanocapsule like morphology while Fe distributed mesoporous graphitic carbon sheets, with a specific surface area value of 565 m(2) g(-1) obtained by modulating the synthesis chemistry in CHI-TMA-Fe-CW-M1. The higher percentage of graphitic N in CHI-TMA-Fe-CW-M1 apparent from the XPS data validate that the modified synthetic method favours creation of more graphitic N sites contributing for better catalytic performance. CHI-TMA-Fe-CW-M1 catalyst exhibited comparable electrocatalytic activity with that of the commercially available Pt/C via an efficient four-electron-dominant ORR pathway with a positive onset potential value of 0.925 V vs RHE. Good durability of CHI-TMA-Fe-CW-M1 after 5000 cycles further confirm the prospects of MOG-chitosan and the feasibility to be used as a potential catalyst for ORR.

10aelectrocatalyst10afuel cell10aMetal-Organic-Gel10aoxygen reduction reaction1 aShijina, Kottarathil1 aIllathvalappil, Rajith1 aKurungot, Sreekumar1 aNair, Balagopal, N.1 aMohamed, Peer1 aYamaguchi, Takeo1 aAnilkumar, Gopinathan, M.1 aHareesh, U., S.1 aSailaja, G., S. uhttps://library.ncl.res.in/content/chitosan-intercalated-metal-organic-gel-green-precursor-fe-entrenched-and-fe-distributed-n02139nas a2200253 4500008004100000022001400041245016900055210006900224260000800293300001400301490000600315520119100321653001901512653003001531653002001561653003201581653002801613100002801641700002501669700001801694700002101712700002401733856012801757 2017 eng d a2196-021600aNitrogen-doped graphene with a three-dimensional architecture assisted by carbon nitride tetrapods as an efficient metal-free electrocatalyst for hydrogen evolution0 aNitrogendoped graphene with a threedimensional architecture assi cOCT a2643-26520 v43 aCurrent polymer membrane-based electrolyzers use Pt as a cathode catalyst for efficient reduction of water. The high cost of Pt-based catalysts forces researchers to develop alternative electrocatalysts. Here, a simple strategy has been proposed to synthesize a metal-free electrocatalyst for the hydrogen evolution reaction (HER) by high-temperature annealing of graphene oxide-coated melamine foam. The prepared catalyst possesses both structural and functional advantages with its three-dimensional (3D) interconnected arms of carbon nitride (CNx) backbone wrapped with nitrogen-doped graphene (N-RGO) sheets (CNx@N-RGO). CNx@N-RGO faces only a 193 mV overpotential to achieve a current density of 10mAcm(-2), which is far superior to the previously reported Pt-free systems. Along with the high exchange current density 34.7 x 10(-6)A cm(-2) and low Tafel slope of 54 mV dec(-1), CNx@N-RGO follows a Volmer-Heyrovsky mechanism for the HER. DFT calculations show that the synergy between CNx and N-RGO facilitates good electrical coupling between the two moieties and provides optimal binding to H+ ions on the catalyst that, in turn, results in efficient reduction of hydrogen ions.10acarbon nitride10aDensity functional theory10aelectrocatalyst10ahydrogen evolution reaction10anitrogen doped graphene1 aGangadharan, Pranav, K.1 aUnni, SreeKuttan, M.1 aKumar, Nandha1 aGhosh, Prasenjit1 aKurungot, Sreekumar uhttps://library.ncl.res.in/content/nitrogen-doped-graphene-three-dimensional-architecture-assisted-carbon-nitride-tetrapods02277nas a2200289 4500008004100000022001400041245014000055210006900195260000800264300001400272490000600286520128800292653002001580653001401600653002601614653003001640653001001670100001801680700002701698700002401725700002401749700001801773700003001791700002101821700002001842856012501862 2018 eng d a2365-654900aMorphological ensembles of N-doped porous carbon derived from ZIF-8/Fe-graphene nanocomposites: processing and electrocatalytic studies0 aMorphological ensembles of Ndoped porous carbon derived from ZIF cAUG a8688-86970 v33 a

Engineering the active site density of porous carbon catalysts for enhanced electrocatalytic activity is the current focus in the quest for economically viable fuel cells. Herein, we synthesise ZIF-8/Fe-graphene composites for the formation of N and Fe co-doped carbon with diverse morphologies ranging from tubes and sheets to frameworks of carbon. A synthetic strategy involving the one pot synthesis of ZIF-8 based composites is accomplished by the reaction of 2-methylimidazole with mixed Zn/Fe salt solution containing graphene dispersions. The high temperature heat treatment of this precursor mix yielded micro-meso porous architectures of N, Fe co-doped carbon with dispersions of Fe/Fe3C. An onset potential value of 0.95 V and a half-wave potential of 0.82 V coupled with excellent durability and stability in alkaline medium indicated improved electrocatalytic performances over its commercial Pt/C counterpart. The appreciable electrocatalytic properties of the synthesized carbon are attributed to its morphological diversity, hybrid structure, high N doping and its heteroporous characteristics. The dispersed Fe/Fe3C and FeNx sites facilitated enhanced oxygen adsorption and the graphene inclusions in the composite provided retention of high nitrogen contents.

10aelectrocatalyst10afuel cell10aN- Fe co-doped carbon10aoxygen reduction reaction10aZIF-81 aThomas, Minju1 aIllathvalappil, Rajith1 aKurungot, Sreekumar1 aNair, Balagopal, N.1 aMohamed, Peer1 aAnilkumar, Gopinathan, M.1 aYamaguchi, Takeo1 aHareesh, U., S. uhttps://library.ncl.res.in/content/morphological-ensembles-n-doped-porous-carbon-derived-zif-8fe-graphene-nanocomposites02872nas a2200253 4500008004100000022001400041245010000055210006900155260000800224300001400232490000600246520202700252653002002279653002002299653001402319653003002333653001602363100002802379700001502407700001902422700002302441700002402464856013002488 2020 eng d a2574-097000aFeNx/FeSx-anchored carbon sheet-carbon nanotube composite electrocatalysts for oxygen reduction0 aFeNxFeSxanchored carbon sheetcarbon nanotube composite electroca cMAR a2234-22450 v33 a

Even though various Pt-free electrocatalysts for oxygen reduction reaction (ORR) have been introduced, many of them are found to be active only in alkaline conditions. Considering Nafion, phosphoric acid-doped polybenzimidazole (PBI), and so on as the prominent ionomer membranes, used in the commercially available polymer electrolyte membrane fuel cells (PEMFCs), it becomes important that any development on the Pt-free catalysts should ensure the better ORR performance under acidic conditions. The present work effectively tackles this issue, where an ORR-based catalyst could be prepared with simultaneous incorporation of both Fe-N and Fe-S active sites on in situ generated carbon sheets which are spatially separated by the carbon nanotube (CNT) network. This catalyst shows ability to perform under both acidic and basic conditions. This has been achieved by growing a polyethylenedioxythiophene polymer network in the presence of CNT and melamine followed by its pyrolysis under an inert atmosphere. The catalyst formed at 900 degrees C (PMCNT-900) displays 0.94 V onset potential for ORR under acidic electrolyte conditions, which corresponds to 60 mV overpotential compared to its 40 wt % Pt/C counterpart. Interestingly, in single cell demonstration of Nafion-based PEMFC with PMCNT-900 as the cathode catalyst, the system delivered a maximum power density (PD) of 500 and 275 mW/cm(2) at 60 degrees C under H-2-O-2 and H-2-air feed conditions, respectively. On the other hand, in a single cell test in the anion exchange membrane fuel cell (AEMFC) mode, a maximum power density of 65 mW/cm(2) at 50 degrees C could be achieved with the same cathode catalyst, which is a comparable value obtained while employing Pt/C as the cathode. These results, thus, infer to the efficiency of the catalyst to facilitate ORR under the extreme pH conditions, and particularly its performance under acidic condition reveals its prospect as a potential Pt-free electrocatalyst to serve in the Nafion-based systems.

10acarbon nanotube10aelectrocatalyst10afuel cell10aoxygen reduction reaction10aPt-free ORR1 aBhange, Siddheshwar, N.1 aSoni, Roby1 aSingla, Gourav1 aAjithkumar, T., G.1 aKurungot, Sreekumar uhttps://library.ncl.res.in/content/fenxfesx-anchored-carbon-sheet-carbon-nanotube-composite-electrocatalysts-oxygen-reduction02844nas a2200241 4500008004100000022001400041245017400055210006900229260000800298300001400306490000600320520196200326653001602288653002002304653001402324653003002338653001902368100001802387700002802405700001502433700002402448856013002472 2020 eng d a2574-096200aWO3 nanorods bearing interconnected Pt nanoparticle units as an activity-modulated and corrosion-resistant carbon-free system for polymer electrolyte membrane fuel cells0 aWO3 nanorods bearing interconnected Pt nanoparticle units as an  cFEB a1908-19210 v33 a

Commercial platinum-supported carbon (Pt/C) catalyst is the most widely used oxygen reduction reaction (ORR) electrocatalyst in polymer electrolyte membrane fuel cells (PEMFCs). However, carbon oxidation in Pt/C during the operation of PEMFCs poses serious issues, particularly in meeting long-term durability of the cells. Although carbon-free Pt-based catalysts are considered to be the best alternatives, the single-cell performances reported for many such systems are found to be inferior to that of the carbon-based systems. As a practical way to realize a carbon-free electrocatalyst, we have developed a system by dispersing an interconnected Pt nanoparticle network on the nanorods of tungsten oxide (WO3). Uniform dispersion of the WO3 nanorods by fine and more or less interconnected Pt nanoparticles (20 wt %) is a key feature of the electrocatalyst. This has helped the system to achieve an intrinsic ORR characteristics which is very similar to that of Pt/C, as reflected from the comparative analysis of the onset potential, half-wave potential, limiting current density, and the number of electrons transferred in the ORR process. Pt/WO3 also shows better stability under start-stop accelerated potential cycling after 10 000 cycles, compared to Pt/C. The relative decrement in the electrochemically active surface area (ECSA) for Pt/WO3 nanorods was negligible, compared to the similar to 26% decrement registered by Pt/C under the identical testing conditions. Finally, a system-level validation in a single-cell model of PEMFC by fabricating a membrane electrode assembly (MEA) with Pt/WO3 as both the anode and cathode catalyst delivered comparable output power density as that of a similar system fabricated by using Pt/C. ECSA comparison in MEA shows the potential use of Pt/WO3-400 as the catalyst for the fuel cells, since it is exhibiting an ECSA value that is 3.4 greater than that of Pt/C at a Pt loading of 0.5 mg cm(-2).

10aCarbon-free10aelectrocatalyst10afuel cell10aoxygen reduction reaction10atungsten oxide1 aKumar, Sachin1 aBhange, Siddheshwar, N.1 aSoni, Roby1 aKurungot, Sreekumar uhttps://library.ncl.res.in/content/wo3-nanorods-bearing-interconnected-pt-nanoparticle-units-activity-modulated-and-corrosion02706nas a2200265 4500008004100000022001400041245013400055210006900189260000900258300001400267490000700281520178300288653001802071653002002089653001402109653002102123653001702144653002002161653002202181653003002203100002802233700002402261700002402285856013102309 2021 eng d a1944-824400aToward pH independent oxygen reduction reaction by polydopamine derived 3D interconnected, iron carbide embedded graphitic carbon0 aToward pH independent oxygen reduction reaction by polydopamine  cFEB  a8147-81580 v133 a

Recent advancements on the development of nonprecious electrocatalysts with iron (Fe) incorporated active centers have generated confidence on realizing cost-effective proton exchange membrane fuel cells (PEMFCs). However, most of these catalysts that emerged as a substitution for the platinum supported on carbon (Pt/C) catalysts in oxygen reduction reaction (ORR) are active under basic conditions, and their feasibility in PEMFCs remains as a challenge. In this scenario, this work reports the synthesis of a Pt-free oxygen reduction electrocatalyst prepared by the annealing of polydopamine grown melamine foam. The prepared catalyst has a three-dimensional (3D) interconnected bilayer network structure possessing the carbon nitride backbone wrapped by graphitic carbon layer bearing iron carbides and nitrides as the active centers (3DFePDC). Interestingly, the 3D-FePDC catalyst displayed an ORR activity both under acidic and basic conditions. Whereas the ORR performance of 3D-FePDC closely matches that of the commercial Pt/C in the basic medium, it displays only a low overpotential value of 60 mV under acidic conditions compared to its Pt counterpart. The kinetics of ORR on 3DFePDC is found to be similar to the four-electron (4e) reduction pathway displayed by Pt/C. Testing of a PEMFC in a single cell mode by using 3D-FePDC as the cathode catalyst and Nafion membrane delivered a maximum power density of 278 mW cm(-2), which is a promising value expected from a system based on the nonprecious metal cathode. Ultimately, as a cost-effective catalyst that can effectively perform irrespective of the pH conditions, 3D-FePDC offers significant prospects in the areas like fuel cells and metal-air batteries which work in acidic and/or basic conditions.

10aacidic medium10aelectrocatalyst10afuel cell10agraphitic carbon10aIron carbide10anitrogen doping10anonprecious metal10aoxygen reduction reaction1 aGangadharan, Pranav, K.1 aPandikassala, Ajmal1 aKurungot, Sreekumar uhttps://library.ncl.res.in/content/toward-ph-independent-oxygen-reduction-reaction-polydopamine-derived-3d-interconnected-iron02589nas a2200325 4500008004100000022001400041245014000055210006900195260000800264490000700272520142200279653002001701653001901721653002801740653002801768653003001796653003901826653001601865653001801881653005001899100002201949700002401971700002701995700002402022700001802046700002602064700001802090700002402108856013102132 2025 eng d a1613-681000aHot injection assisted electronically modulated twin and grain boundary rich sub-2 nm pt3co alloy resistant to phosphate ion for PEMFCs0 aHot injection assisted electronically modulated twin and grain b cMAY0 v213 a

Modulation of the electronic d-band center, structural defects (line defects), and particle size of Pt3Co alloy electrocatalyst have huge significance in elevating its electrochemical oxygen reduction reaction activity. Deviating from traditional high-temperature strategies, the current work focuses on ripening these benefits by implying a simple economically viable hot-injection-assisted modified polyol process. A conclusive control over decrementing particle size starting from 2.7 to 1.3 nm, an increasing degree of strain (twin boundary), and shifting of the d-band center away from the Fermi level are obtained via varying the temperature to which the solution is injected. The catalyst prepared via the injection at 200 degrees C (Pt3Co(1.3 t,g-b)/fVC-200) has delivered an electrochemical surface area of 84 m(2) g(Pt)(-1) with the onset and half-wave potentials of 0.980 and 0.858 V, respectively, versus RHE and a limiting current of -6.0 mA cm(-2) with stability till 20k cycles. In the high-temperature proton exchange membrane fuel cell Pt3Co(1.3 t,g-b)/fVC-200-based cell has outperformed Pt/C rendering 600 mWcm(-2) under H-2-Air compared to 529 mWcm(-2) of Pt/C with 20% lower Pt loading and double the stability due to enhanced resistance toward phosphoric acid for accelerated voltage cycling. A similar enhancement is seen while employing the catalyst for low-temperature fuel cells.

10aelectrocatalyst10agrain boundary10ahot injection synthesis10amodified polyol process10aoxygen reduction reaction10aproton exchange membrane fuel cell10aPt3Co alloy10atwin boundary10avalance band X-ray photoelectron spectroscopy1 aSingh, Mayank, U.1 aJadhav, Swapnil, D.1 aShivankar, Bhavana, R.1 aPandikassala, Ajmal1 aKumar, Yogesh1 aKrishnamurty, Sailaja1 aVinod, C., P.1 aKurungot, Sreekumar uhttps://library.ncl.res.in/content/hot-injection-assisted-electronically-modulated-twin-and-grain-boundary-rich-sub-2-nm-pt3co