ORCID Profile
0000-0003-1852-0429
Current Organisation
University of Melbourne
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Electrochemistry | Functional Materials | Nanotechnology not elsewhere classified | Materials Engineering
Hydrogen Production from Renewable Energy | Expanding Knowledge in the Chemical Sciences |
Publisher: Elsevier BV
Date: 12-2022
Publisher: Royal Society of Chemistry (RSC)
Date: 2016
DOI: 10.1039/C6TA01655C
Abstract: A three-dimensional hybrid of carbon nanosheets and nanotubes prepared via a recyclable NaCl-assisted pyrolysis of small molecules exhibits high activity for the ORR.
Publisher: Elsevier BV
Date: 03-2018
Publisher: American Chemical Society (ACS)
Date: 02-2017
Abstract: Developing highly efficient and stable non-Pt electrocatalysts for the oxygen reduction reaction (ORR) to replace the state-of-the-art noble metal is essential for commercialization of fuel cells. Fe-N-C-based electrocatalysts are considered as a promising alternative to commercial Pt/C. An efficient electrocatalyst commonly requires large density of active site, high surface area, and desirable porosity, especially multimodal porosity with both large pores for efficient mass transfer and small pores for exposing as many active sites as possible. Herein, a lamellar metal organic framework (MOF) was developed as a precursor to directly achieve such a highly active Fe-N-C electrocatalyst with high surface area and desirable bimodal porosity. The mesopores arising from the special lamellar morphology of MOF benefits efficient mass transfer, and the nanopores resulting from pyrolysis of the MOF makes the majority of active sites accessible to electrolyte and thus effective for ORR. Uniform distribution of active elements N, C, and Fe at the molecular level in MOF precursor ensures abundant well-dispersed highly active sites in the catalyst. As a result, the catalyst exhibited superior ORR electrocatalytic activity and stability to commercial Pt/C. This strategy, using rarely reported lamellar MOF to prepare ORR catalysts with the merits mentioned, could inspire the exploration of a wide range of electrocatalysts from lamellar MOF precursors for various applications.
Publisher: Royal Society of Chemistry (RSC)
Date: 2018
DOI: 10.1039/C8CC02500B
Abstract: A facile and scalable solid-state synthesis strategy is developed to produce hierarchical coralline-like nanostructured electrocatalysts with cobalt nanoparticles and Co–N X sites for efficient oxygen reduction.
Publisher: Elsevier BV
Date: 10-2016
Publisher: American Chemical Society (ACS)
Date: 22-05-2015
Abstract: The development of low-cost electrocatalysts with comparable activity for oxygen reduction reaction (ORR) to substitute platinum-based catalysts is imperative but still challenging for the commercialization of fuel cells. Herein, we reported a strategy to effectively confine iron carbide nanocrystals in N-doped carbon coated on carbon nanotubes (CNx@CNT), which prevented the agglomeration of iron carbide during pyrolysis and thus provided the sufficient highly active catalytic sites. Together with the benefit from three-dimensional conductive network of CNT-based core-shell structure for fast electron transfer and rapid mass transfer, the developed nanocatalyst exhibited the significantly enhanced electrocatalytic activity for ORR, as well as high durability and methanol tolerance. Moreover, it was interestingly found that the types of the confined iron compounds appreciably affected the performance of the catalysts, and Fe3C might be most effective on improving ORR activity in this case.
Publisher: Springer Science and Business Media LLC
Date: 04-05-2022
DOI: 10.1038/S41467-022-30155-4
Abstract: Platinum is the most efficient catalyst for hydrogen evolution reaction in acidic conditions, but its widespread use has been impeded by scarcity and high cost. Herein, Pt atomic clusters (Pt ACs) containing Pt-O-Pt units were prepared using Co/N co-doped carbon (CoNC) as support. Pt ACs are anchored to single Co atoms on CoNC by forming strong interactions. Pt-ACs/CoNC exhibits only 24 mV overpotential at 10 mA cm −2 and a high mass activity of 28.6 A mg −1 at 50 mV, which is more than 6 times higher than commercial Pt/C with any Pt loadings. Spectroscopic measurements and computational modeling reveal the enhanced hydrogen generation activity attributes to the charge redistribution between Pt and O atoms in Pt-O-Pt units, making Pt atoms the main active sites and O linkers the assistants, thus optimizing the proton adsorption and hydrogen desorption. This work opens an avenue to fabricate noble-metal-based ACs stabilized by single-atom catalysts with desired properties for electrocatalysis.
Publisher: Royal Society of Chemistry (RSC)
Date: 2017
DOI: 10.1039/C7TA01859B
Abstract: PtCu nanodendrites with tunable sizes, branches, and composition are rapidly and cost-effectively prepared for efficient oxygen reduction and methanol oxidation.
Publisher: American Chemical Society (ACS)
Date: 14-09-2016
Abstract: Well-defined pomegranate-like N,P-doped Mo2C@C nanospheres were prepared by simply using phosphomolybdic acid (PMo12) to initiate the polymerization of polypyrrole (PPy) and as a single source for Mo and P to produce N,P-doped Mo2C nanocrystals. The existence of PMo12 at the molecular scale in the polymer network allows the formation of pomegranate-like Mo2C@C nanospheres with a porous carbon shell as peel and Mo2C nanocrystals well-dispersed in the N-doped carbon matrix as seeds. This nanostructure provides several favorable features for hydrogen evolution application: (1) the conductive carbon shell and matrix effectively prevent the aggregation of Mo2C nanocrystals and facilitate electron transportation (2) the uniform N,P-doping in the carbon shell/matrix and plenty of Mo2C nanocrystals provide abundant catalytically highly active sites and (3) nanoporous structure allows the effective exposure of active sites and mass transfer. Moreover, the uniform distribution of P and Mo from the single source of PMo12 and N from PPy in the polymeric PPy-PMo12 precursor guarantees the uniform N- and P-co-doping in both the graphitic carbon matrix and Mo2C nanocrystals, which contributes to the enhancement of electrocatalytic performance. As a result, the pomegranate-like Mo2C@C nanospheres exhibit extraordinary electrocatalytic activity for the hydrogen evolution reaction (HER) in terms of an extremely low overpotential of 47 mV at 10 mA cm(-2) in 1 M KOH, which is one of the best Mo-based HER catalysts. The strategy for preparing such nanostructures may open up opportunities for exploring low-cost high-performance electrocatalysts for various applications.
Publisher: American Chemical Society (ACS)
Date: 06-04-2015
Publisher: Royal Society of Chemistry (RSC)
Date: 2014
DOI: 10.1039/C4TA01780C
Publisher: Royal Society of Chemistry (RSC)
Date: 2015
DOI: 10.1039/C5CC05211D
Abstract: Urchin-like micro/nano heterostructure Au@CdS/WO 3 exhibited a high H 2 evolution rate as an all-solid Z-scheme visible-light driven photocatalyst.
Publisher: Royal Society of Chemistry (RSC)
Date: 2020
DOI: 10.1039/D0TA01437K
Abstract: An effective strategy was demonstrated to develop a highly durable catalyst prototype that combines superfine Pt-based intermetallic nanoparticles with mesoporous carbon.
Publisher: Elsevier BV
Date: 05-2019
Publisher: Royal Society of Chemistry (RSC)
Date: 2019
DOI: 10.1039/C9TA07882G
Abstract: A metal sulfide and metal carbonate hydroxide heterostructure featuring a unique “nanoparticle-in-nanosheet” structure with abundant accessible hetero-interfaces is developed for efficient and robust water oxidation.
Publisher: American Chemical Society (ACS)
Date: 04-03-2016
DOI: 10.1021/JACS.6B00757
Abstract: Understanding the origin of high activity of Fe-N-C electrocatalysts in oxygen reduction reaction (ORR) is critical but still challenging for developing efficient sustainable nonprecious metal catalysts in fuel cells and metal-air batteries. Herein, we developed a new highly active Fe-N-C ORR catalyst containing Fe-N(x) coordination sites and Fe/Fe3C nanocrystals (Fe@C-FeNC), and revealed the origin of its activity by intensively investigating the composition and the structure of the catalyst and their correlations with the electrochemical performance. The detailed analyses unambiguously confirmed the coexistence of Fe/Fe3C nanocrystals and Fe-N(x) in the best catalyst. A series of designed experiments disclosed that (1) N-doped carbon substrate, Fe/Fe3C nanocrystals or Fe-N(x) themselves did not deliver the high activity (2) the catalysts with both Fe/Fe3C nanocrystals and Fe-N(x) exhibited the high activity (3) the higher content of Fe-N(x) gave the higher activity (4) the removal of Fe/Fe3C nanocrystals severely degraded the activity (5) the blocking of Fe-N(x) downgraded the activity and the recovery of the blocked Fe-N(x) recovered the activity. These facts supported that the high ORR activity of the Fe@C-FeNC electrocatalysts should be ascribed to that Fe/Fe3C nanocrystals boost the activity of Fe-N(x). The coexistence of high content of Fe-N(x) and sufficient metallic iron nanoparticles is essential for the high ORR activity. DFT calculation corroborated this conclusion by indicating that the interaction between metallic iron and Fe-N4 coordination structure favored the adsorption of oxygen molecule. These new findings open an avenue for the rational design and bottom-up synthesis of low-cost highly active ORR electrocatalysts.
Publisher: American Chemical Society (ACS)
Date: 08-07-2019
Publisher: Wiley
Date: 19-07-2019
Publisher: American Chemical Society (ACS)
Date: 18-08-2017
Abstract: Metal-nitrogen coordination sites, M-N
Publisher: American Chemical Society (ACS)
Date: 04-2019
DOI: 10.1021/JACS.9B01214
Abstract: Ni or Co is commonly required in efficient electrocatalysts for oxygen evolution reaction (OER). Although Fe is much more abundant and cheaper, full-Fe or Fe-rich catalysts suffer from insufficient activity. Herein, we discover that Se-doping can drastically promote OER on FeOOH and develop a facile on-site electrochemical activation strategy for achieving such a Se-doped FeOOH electrode via an FeSe precatalyst. Theoretical analysis and systematic experiments prove that Se-doping enables FeOOH as an efficient and low-cost OER electrocatalyst. By optimizing the electrode structure, an industrial-level OER current output of 500 mA cm
Publisher: American Chemical Society (ACS)
Date: 28-09-2018
Abstract: Doping unary transition-metal phosphides (TMPs) by secondary metal is a powerful method to improve their catalytic activity for electrochemical oxygen evolution reaction (OER). However, the composition-activity relationship of such doping has not been systematically investigated yet because of the challenge in constructing bimetal TMPs with continuously variable composition while keeping homogenous elemental distribution. Herein, we develop a strategy of using bimetal Prussian blue analogues with homogenous elemental distribution at molecular scale as an ideal platform to achieve bimetal cobalt-iron phosphides (Co
Publisher: American Chemical Society (ACS)
Date: 02-10-2017
Abstract: Amorphous materials have been widely researched in heterogeneous catalysis and for next-generation batteries. However, the well-defined production of high-quality (e.g., monodisperse and high surface area) amorphous alloy nanomaterials has rarely been reported. In this work, we investigated the correlations among the composition, morphology, and catalysis of various Pd-M-P nanoparticles (NPs) (M = Cu or Ni), which indicated that less Cu (≤20 atom %) was necessary for the formation of an amorphous morphology. The amorphous Pd-Cu-Ni-P NPs were fabricated with a controllable size and characterized carefully, which show excellent selective catalysis in the semihydrogenation of alkynes, hydrogenation of quinoline, and oxidation of primary alcohols. The uniqueness of the catalytic performance was confirmed by control experiments with monometallic Pd, amorphous Pd-Ni-P NPs, crystalline Pd-Cu-P NPs, and a crystalline counterpart of Pd-Cu-Ni-P catalyst. The catalytic selectivity likely arose from improved Pd-M (M = Cu or Ni) synergistic effects in the amorphous phase and the electron deficiency of Pd. The model reactions proceeded under H
Publisher: American Chemical Society (ACS)
Date: 15-08-2018
DOI: 10.1021/JACS.8B05949
Abstract: Despite the recent surge of interest in inorganic lead halide perovskite nanocrystals, there are still significant gaps in their stability disturbance and the understanding of their destabilization, assembly, and growth processes. Here, we discover that polar solvent molecules can induce the lattice distortion of ligand-stabilized cubic CsPbI
Publisher: Wiley
Date: 03-09-2021
Abstract: Single‐atom catalysts (SACs) have been at the frontier of research field in catalysis owing to the maximized atomic utilization, unique structures and properties. The atomically dispersed and catalytically active metal atoms are necessarily anchored by surrounding atoms. As such, the structure and composition of anchoring sites significantly influence the catalytic performance of SACs even with the same metal element. Significant progress has been made to understand structure–activity relationships at an atomic level, but in‐depth understanding in precisely designing highly efficient SACs for the targeted reactions is still required. In this review, various anchoring sites in SACs are summarized and classified into five different types (doped heteroatoms, defect sites, surface atoms, metal sites, and cavity sites). Then, their impacts on catalytic performance are elucidated for electrochemical reactions based on their distance from the metal center (first coordination shell and beyond). Further, SACs anchored on two typical types of hosts, carbon‐ and metal‐based materials, are highlighted, and the effects of anchoring points on achieving the desirable atomic structure, catalytic performance, and reaction pathways are elaborated. At last, insights and outlook to the SAC field based on current achievements and challenges are presented.
Publisher: Royal Society of Chemistry (RSC)
Date: 2019
DOI: 10.1039/C9CC01235D
Abstract: An NiS 2 nanodotted carnation-like CoS 2 bifunctional electrocatalyst is demonstrated with enhanced electrochemical performances for the OER, the HER, and overall water splitting.
Publisher: American Chemical Society (ACS)
Date: 13-06-2017
DOI: 10.1021/JACS.7B03507
Abstract: Developing bifunctional efficient and durable non-noble electrocatalysts for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is highly desirable and challenging for overall water splitting. Herein, Co-Mn carbonate hydroxide (CoMnCH) nanosheet arrays with controllable morphology and composition were developed on nickel foam (NF) as such a bifunctional electrocatalyst. It is discovered that Mn doping in CoCH can simultaneously modulate the nanosheet morphology to significantly increase the electrochemical active surface area for exposing more accessible active sites and tune the electronic structure of Co center to effectively boost its intrinsic activity. As a result, the optimized Co
Publisher: Royal Society of Chemistry (RSC)
Date: 2013
DOI: 10.1039/C3TA10298J
Publisher: The Chemical Society of Japan
Date: 05-02-2019
DOI: 10.1246/CL.180836
Publisher: Wiley
Date: 06-02-2020
Publisher: Royal Society of Chemistry (RSC)
Date: 2019
DOI: 10.1039/C9TA05937G
Abstract: Three-dimensional porous carbon sheets with abundant micropores and macropores are used to uniformly disperse SnO 2 nanoparticles with high loading, and the obtained SnO 2 /PC exhibits efficient formate production from electrochemical CO 2 reduction.
Publisher: American Chemical Society (ACS)
Date: 20-03-2020
DOI: 10.1021/JACS.0C01349
Publisher: Wiley
Date: 11-10-2018
Publisher: Elsevier BV
Date: 10-2016
Publisher: Springer Science and Business Media LLC
Date: 14-10-2022
Publisher: Royal Society of Chemistry (RSC)
Date: 2015
DOI: 10.1039/C5TA05793K
Abstract: Amorphous MoS 2 nanosheet arrays on carbon cloth were directly prepared via a highly reproducible PVD, which exhibited superior catalytic activity and durability for the HER.
Publisher: Wiley
Date: 18-04-2017
Publisher: Springer Science and Business Media LLC
Date: 15-01-2020
Publisher: Royal Society of Chemistry (RSC)
Date: 2018
DOI: 10.1039/C8RA03650K
Abstract: The Ni-CAT-derived porous carbon materials at 800 °C remain regular with a rod-like morphology and exhibit enhanced capacitive performance.
Publisher: Elsevier BV
Date: 08-2019
Publisher: Elsevier BV
Date: 11-2019
Publisher: Royal Society of Chemistry (RSC)
Date: 2014
DOI: 10.1039/C3NR05352K
Abstract: Development of a simple, reproducible and cost-effective protocol for mass production of non-precious-metal electrocatalysts for oxygen reduction reaction (ORR) is still challenging but highly desirable for their practical applications in industry. Herein, we developed a facile and scalable method to directly produce graphene (G) supported CoFe-LDHs and successfully used them as a precursor for mass production of Co/CoO/CoFe2O4/G as a low-cost and Pt-free efficient electrocatalyst, which exhibits comparable electrocatalytic activity and much better durability for ORR in comparison with commercial Pt/C catalysts. The result may provide a way for cost-effective production of ORR electrocatalysts on a large scale for practical applications.
Publisher: American Chemical Society (ACS)
Date: 12-10-2017
Abstract: Nitrogen (N)-doped carbons combined with transition-metal nanoparticles are attractive as alternatives to the state-of-the-art precious metal catalysts for hydrogen evolution reaction (HER). Herein, we demonstrate a strategy for fabricating three-dimensional (3D) Cu-encased N-doped carbon nanotube arrays which are directly grown on Cu foam (Cu@NC NT/CF) as a new efficient HER electrocatalyst. Cu nanoparticles are encased here instead of common transition metals (Fe, Co, or Ni) for pursuing a well-controllable morphology and an excellent activity by taking advantage of its more stable nature at high temperature and in acidic or alkaline electrolyte. It is discovered that metallic Cu exhibits strong electronic modulation on N-doped carbon to boost its electrocatalytic activity for HER. Such a nanostructure not only offers plenty of accessible highly active sites but also provides a 3D conductive open network for fast electron/mass transfer and facilitates gas escape for prompt mass exchange. As a result, the Cu@NC NT/CF electrode exhibits superior HER performance and durability, outperforming most of the reported M@NC materials. Furthermore, the etching experiments together with X-ray photoelectron spectroscopy (XPS) analysis reveal that the electronic modulation from encased Cu significantly enhances the HER activity of N-doped carbon. These findings open up opportunities for exploring other Cu-based nanomaterials as efficient electrocatalysts and understanding their catalytic processes.
Publisher: American Chemical Society (ACS)
Date: 28-05-2020
Publisher: Royal Society of Chemistry (RSC)
Date: 2014
DOI: 10.1039/C4CP00757C
Abstract: Tuning the composition of N-doped graphene–carbon nanotube composites can boost their electrocatalytic performance for the oxygen reduction reaction.
Publisher: Wiley
Date: 22-11-2017
Publisher: Wiley
Date: 23-09-2022
Abstract: The recent emergence of electrically conductive nanoporous membranes based on graphene and other 2D materials opens up new opportunities to revisit some longstanding nanoconfined ion transport problems under electrification. This work probes the ionic resistance in electrified multilayered graphene membranes with electrochemical impedance spectroscopy. This study demonstrates that the combination of additive‐free feature and tunable slit pore sizes in the sub‐10 nm range in graphene‐based membranes has made it possible to deconvolute the different ionic processes from the impedance obtained and examine the exclusive influence of pore size on the ionic resistance in a quantitative manner. The trends revealed for the ionic resistance at the pore entrance and inside the pores under severe nanoconfinement ( nm) are found to be generally consistent with the microscale theoretical simulations previously reported. It also allows a quantitative analysis of the relative effects of the external polarization potential and ion identity under nanoconfinement. The results suggest that the classic electrochemical impedance spectroscopy technique, when applied to appropriate nanoporous electrode materials, can provide rich information about nanoconfined ion transport phenomena under electrification for fundamental understanding and application development.
Publisher: Royal Society of Chemistry (RSC)
Date: 2018
DOI: 10.1039/C7CC08149A
Abstract: Inspired by metabolic processes in biological systems, animal blood as a biowaste rich in biological enzymes with molecular Fe–N centers was successfully explored to produce an efficient electrocatalyst with single atomic Fe–N–C active sites for oxygen reduction reaction.
Publisher: American Chemical Society (ACS)
Date: 05-01-2021
Publisher: American Chemical Society (ACS)
Date: 18-12-2013
DOI: 10.1021/NL404251P
Abstract: Quantum-dot-sensitized solar cell (QDSSC) has been considered as an alternative to new generation photovoltaics, but it still presents very low power conversion efficiency. Besides the continuous effort on improving photoanodes and electrolytes, the focused investigation on charge transfer at interfaces and the rational design for counter electrodes (CEs) are recently receiving much attention. Herein, core-shell nanowire arrays with tin-doped indium oxide (ITO) nanowire core and Cu2S nanocrystal shell (ITO@Cu2S) were dedicatedly designed and fabricated as new efficient CEs for QDSSCs in order to improve charge collection and transport and to avoid the intrinsic issue of copper dissolution in popular and most efficient Cu/Cu2S CEs. The high-quality tunnel junctions formed between n-type ITO nanowires and p-type Cu2S nanocrystals led to the considerable decrease in sheet resistance and charge transfer resistance and thus facilitated the electron transport during the operation of QDSSCs. The three-dimensional structure of nanowire arrays provided high surface area for more active catalytic sites and easy accessibility for an electrolyte. As a result, the power conversion efficiency of QDSSCs with the designed ITO@Cu2S CEs increased by 84.5 and 33.5% compared to that with planar Au and Cu2S CEs, respectively.
Publisher: Wiley
Date: 24-04-2020
Publisher: Royal Society of Chemistry (RSC)
Date: 2020
DOI: 10.1039/D0TA03895D
Abstract: The importance of charge diffusion in electrocatalysts is shown by regulating the thickness of CoFe hydroxide nanosheets on graphene. The few-layer nanosheets allow effective charge diffusion, enabling a 2000 mA cm −2 output at only 1.507 V cost in near-industrial conditions.
Publisher: American Chemical Society (ACS)
Date: 07-06-2016
Abstract: Semiconductor-based photocatalytic H2 generation as a direct approach of converting solar energy to fuel is attractive for tackling the global energy and environmental issues but still suffers from low efficiency. Here, we report a MoS2/CdS nanohybrid as a noble-metal-free efficient visible-light driven photocatalyst, which has the unique nanosheets-on-nanorod heterostructure with partially crystalline MoS2 nanosheets intimately but discretely growing on single-crystalline CdS nanorod. This heterostructure not only facilitates the charge separation and transfer owing to the formed heterojunction, shorter radial transfer path, and fewer defects in single-crystalline nanorod, thus effectively reducing the charge recombination, but also provides plenty of active sites for hydrogen evolution reaction due to partially crystalline structure of MoS2 as well as enough room for hole extraction. As a result, the MoS2/CdS nanosheets-on-nanorod exhibits a state-of-the-art H2 evolution rate of 49.80 mmol g(-1) h(-1) and an apparent quantum yield of 41.37% at 420 nm, which is the advanced performance among all MoS2/CdS composites and CdS/noble metal photocatalysts. These findings will open opportunities for developing low-cost efficient photocatalysts for water splitting.
Publisher: Wiley
Date: 04-05-2017
Abstract: The exploration of new efficient OER electrocatalysts based on nonprecious metals and the understanding of the relationship between activity and structure of electrocatalysts are important to advance electrochemical water oxidation. Herein, we developed an efficient OER electrocatalyst with nickel boride (Ni
Publisher: American Chemical Society (ACS)
Date: 27-08-2014
DOI: 10.1021/AM504057Y
Abstract: Among the issues that restrict the power conversion efficiency (PCE) of quantum-dot-sensitized solar cells (QDSSCs), insufficient catalytic activity and stability of counter electrodes (CEs) are critical but challenging ones. The state-of-the-art Cu/Cu2S CEs still suffer from mechanical instability and uncertainty due to the reaction of copper and electrolyte. Herein, ITO@Cu2S core-shell nanowire arrays were developed to fabricate CEs for QDSSCs, which have no such issues in Cu/Cu2S CEs. These nanowire arrays exhibited small charge transfer resistance and sheet resistance, and provided more active catalytic sites and easy accessibility for electrolyte due to the three-dimensional structure upon use as CEs. More interestingly, it was found that the interface of ITO/Cu2S significantly affected the performance of ITO@Cu2S nanowire array CEs. By varying synthetic methods, a series of ITO@Cu2S nanowire arrays were prepared to investigate the influence of ITO/Cu2S interface on their performance. The results showed that ITO@Cu2S nanowire array CEs with a continuous Cu2S nanocrystal shell fabricated via an improved cation exchange route exhibited excellent and thickness-dependent performance. The PCE of corresponding QDSSCs increased by 11.6 and 16.5% compared to that with the discrete Cu2S nanocrystal and the classic Cu/Cu2S CE, respectively, indicating its promising potential as a new type of CE for QDSSCs.
Publisher: Royal Society of Chemistry (RSC)
Date: 2020
DOI: 10.1039/D0CC01024C
Abstract: Self-standing Fe-Co 3 O 4 @CC bifunctional electrocatalysts enabled high-performance Zn–air batteries with a power density of 268.6 mW cm −2 and superior cycling stability.
Publisher: Springer Science and Business Media LLC
Date: 04-09-2018
Publisher: Royal Society of Chemistry (RSC)
Date: 2019
DOI: 10.1039/C8TA12269E
Abstract: Fe/P dual doping synergistically improves the activity and durability of CoS 2 polycrystalline nanowire arrays towards efficient hydrogen production.
Publisher: Springer Science and Business Media LLC
Date: 19-03-2018
Publisher: Elsevier BV
Date: 08-2021
Publisher: American Chemical Society (ACS)
Date: 11-2020
Start Date: 01-2022
End Date: 01-2025
Amount: $433,000.00
Funder: Australian Research Council
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