E02-JEM ARM 300CF
I22-Small angle scattering & Diffraction
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Diamond Proposal Number(s):
[14925, 10330, 16964]
Abstract: Fuel cells are a key new green technology that have applications in both transport and portable power generation. Carbon supported platinum (Pt) is used as an anode and cathode electrocatalyst in low-temperature fuel cells fuelled with hydrogen or low molecular weight alcohols. The cost of Pt and the limited world supply are significant barriers to the widespread use of these types of fuel cells. Compara-tively palladium has a three times higher abundance in the Earth’s crust. Here a facile, low temperature and scalable synthetic route to-wards 3D nanostructured palladium (Pd) employing electrochemical templating from inverse lyotropic lipid phases is presented. The obtained single diamond morphology Pd nanostructures exhibited excellent catalytic activity and stability towards methanol, ethanol and glycerol oxidation compared to commercial Pd black and the nanostructure was verified by small-angle X-ray scattering (SAXS), scanning tunneling electron microscopy (STEM) as well as by cyclic voltammetry (CV).
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Oct 2018
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E02-JEM ARM 300CF
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Lele
Peng
,
Ziyang
Wei
,
Chengzhang
Wan
,
Jing
Lin
,
Zhuo
Chen
,
Dan
Zhu
,
Daniel
Baumann
,
Haotian
Liu
,
Christopher S.
Allen
,
Xiang
Xu
,
Angus I.
Kirkland
,
Imran
Shakir
,
Zeyad
Almutairi
,
Sarah
Tolbert
,
Bruce
Dunn
,
Yu
Huang
,
Philippe
Sautet
,
Xiangfeng
Duan
Diamond Proposal Number(s):
[23956]
Abstract: The fundamental kinetics of the electrocatalytic sulfur reduction reaction (SRR), a complex 16-electron conversion process in lithium–sulfur batteries, is so far insufficiently explored. Here, by directly profiling the activation energies in the multistep SRR, we reveal that the initial reduction of sulfur to the soluble polysulfides is relatively easy owing to the low activation energy, whereas the subsequent conversion of the polysulfides into the insoluble Li2S2/Li2S has a much higher activation energy, contributing to the accumulation of polysulfides and exacerbating the polysulfide shuttling effect. We use heteroatom-doped graphene as a model system to explore electrocatalytic SRR. We show that nitrogen and sulfur dual-doped graphene considerably reduces the activation energy to improve SRR kinetics. Density functional calculations confirm that the doping tunes the p-band centre of the active carbons for an optimal adsorption strength of intermediates and electroactivity. This study establishes electrocatalysis as a promising pathway to tackle the fundamental challenges facing lithium–sulfur batteries.
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Sep 2020
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E02-JEM ARM 300CF
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Zupeng
Chen
,
Evgeniya
Vorobyeva
,
Sharon
Mitchell
,
Edvin
Fako
,
Manuel A.
Ortuño
,
Núria
López
,
Sean M.
Collins
,
Paul A.
Midgley
,
Sylvia
Richard
,
Gianvito
Vilé
,
Javier
Pérez-ramírez
Diamond Proposal Number(s):
[16967]
Abstract: Palladium-catalysed cross-coupling reactions, central tools in fine-chemical synthesis, predominantly employ soluble metal complexes despite recognized challenges with product purification and catalyst reusability. Attempts to tether these homogeneous catalysts on insoluble carriers have been thwarted by suboptimal stability, which leads to a progressively worsening performance due to metal leaching or clustering4. The alternative application of supported Pd nanoparticles has faced limitations because of insufficient activity under the mild conditions required to avoid thermal degradation of the substrates or products. Single-atom heterogeneous catalysts lie at the frontier. Here, we show that the Pd atoms anchored on exfoliated graphitic carbon nitride (Pd-ECN) capture the advantages of both worlds, as they comprise a solid catalyst that matches the high chemoselectivity and broad functional group tolerance of state-of-the-art homogeneous catalysts for Suzuki couplings, and also demonstrate a robust stability in flow. The adaptive coordination environment within the macroheterocycles of ECN facilitates each catalytic step. The findings illustrate the exciting opportunities presented by nanostructuring single atoms in solid hosts for catalytic processes that remain difficult to heterogenize.
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Jun 2018
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E02-JEM ARM 300CF
I15-1-X-ray Pair Distribution Function (XPDF)
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Shichun
Li
,
Shuwen
Yu
,
Sean M.
Collins
,
Duncan N.
Johnstone
,
Christopher W.
Ashling
,
Adam F.
Sapnik
,
Philip A.
Chater
,
Dean S.
Keeble
,
Lauren N.
Mchugh
,
Paul A.
Midgley
,
David A.
Keen
,
Thomas D.
Bennett
Diamond Proposal Number(s):
[20038, 22632, 21979]
Open Access
Abstract: Metal–organic framework crystal–glass composite (MOF CGC) materials consist of a crystalline MOF embedded within a MOF–glass matrix. In this work, a new synthetic route to these materials is demonstrated through the preparation of two ZIF-62 glass-based CGCs, one with crystalline ZIF-67 and the other with crystalline UiO-66. Previous attempts to form these CGCs failed due to the high processing temperatures involved in heating above the melting point of ZIF-62. Annealing of the ZIF-62 glass above the glass transition with each MOF however leads to stable CGC formation at lower temperatures. The reduction in processing temperatures will enable the formation of a greatly expanded range of MOF CGCs.
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Sep 2020
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E02-JEM ARM 300CF
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Diamond Proposal Number(s):
[16972]
Abstract: The geometric and chromatic aberration coefficients of the probe-forming system in an aberration corrected transmission electron microscope have been measured using a Ronchigram recorded from monolayer graphene. The geometric deformations within individual local angular sub-regions of the Ronchigram were analysed using an auto-correlation function and the aberration coefficients for the probe forming lens were calculated. This approach only requires the acquisition of a single Ronchigram allowing rapid measurement of the aberration coefficients. Moreover, the measurement precision for defocus and two-fold astigmatism is improved over that which can be achieved from analysis of Ronchigrams recorded from amorphous films. This technique can also be applied to aberration corrected STEM imaging of any hexagonal two-dimensional material.
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Nov 2017
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E02-JEM ARM 300CF
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Open Access
Abstract: The influence of residual three-fold astigmatism on high-resolution STEM imaging of graphene has been investigated. The aberration was measured by the segmented Ronchigram auto-correlation function method using the graphene lattice. In the presence of residual threefold astigmatism the graphene lattice showed a lower three-fold rotational symmetry where three C atoms in the six membered ring had a higher intensity.
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Sep 2017
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B18-Core EXAFS
E01-JEM ARM 200CF
E02-JEM ARM 300CF
I11-High Resolution Powder Diffraction
I20-Scanning-X-ray spectroscopy (XAS/XES)
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Liqun
Kang
,
Bolun
Wang
,
Qiming
Bing
,
Michal
Zalibera
,
Robert
Büchel
,
Ruoyu
Xu
,
Qiming
Wang
,
Yiyun
Liu
,
Diego
Gianolio
,
Chiu C.
Tang
,
Emma K.
Gibson
,
Mohsen
Danaie
,
Christopher
Allen
,
Ke
Wu
,
Sushila
Marlow
,
Ling-dong
Sun
,
Qian
He
,
Shaoliang
Guan
,
Anton
Savitsky
,
Juan J.
Velasco-vélez
,
June
Callison
,
Christopher W. M.
Kay
,
Sotiris E.
Pratsinis
,
Wolfgang
Lubitz
,
Jing-yao
Liu
,
Feng Ryan
Wang
Diamond Proposal Number(s):
[15151, 15763, 16966, 17377, 19072, 19246, 20939, 17559, 24285, 19318, 19850]
Open Access
Abstract: Supported atomic metal sites have discrete molecular orbitals. Precise control over the energies of these sites is key to achieving novel reaction pathways with superior selectivity. Here, we achieve selective oxygen (O2) activation by utilising a framework of cerium (Ce) cations to reduce the energy of 3d orbitals of isolated copper (Cu) sites. Operando X-ray absorption spectroscopy, electron paramagnetic resonance and density-functional theory simulations are used to demonstrate that a [Cu(I)O2]3− site selectively adsorbs molecular O2, forming a rarely reported electrophilic η2-O2 species at 298 K. Assisted by neighbouring Ce(III) cations, η2-O2 is finally reduced to two O2−, that create two Cu–O–Ce oxo-bridges at 453 K. The isolated Cu(I)/(II) sites are ten times more active in CO oxidation than CuO clusters, showing a turnover frequency of 0.028 ± 0.003 s−1 at 373 K and 0.01 bar PCO. The unique electronic structure of [Cu(I)O2]3− site suggests its potential in selective oxidation.
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Aug 2020
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E02-JEM ARM 300CF
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Diamond Proposal Number(s):
[19045]
Abstract: A brittle material under loading fails by the nucleation and propagation of a sharp crack. In monatomic crystals, such as silicon, the lattice geometries front to the crack-tip changes the way of propagation even with the same cleavage surface. In general, however, crystals have multiple kinds of atoms and how the deformation of each atom affects the failure is still elusive. Here, we show that local atomic distortions from the different types of atoms causes a propagation anisotropy in suspended WS2 monolayers by combining annular dark-field scanning transmission electron microscopy and empirical molecular dynamics that are validated by first-principles calculations. Conventional conditions for brittle failure such as surface energy, elasticity, and crack geometry cannot account for this anisotropy. Further simulations predict the enhancement of the strengths and fracture toughness of the materials by designing void shapes and edge structures.
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May 2019
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E02-JEM ARM 300CF
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Diamond Proposal Number(s):
[16854]
Abstract: We have studied atomic level interactions between single Pt atoms and the surface of monolayer MoS2 using aberration-corrected annular dark field scanning transmission electron microscopy at an accelerating voltage of 60 kV. Strong contrast from single Pt atoms on the atomically resolved monolayer MoS2 lattice enables their exact position to be determined with respect to the MoS2 lattice, revealing stable binding sites. In regions of MoS2 free from surface contamination, the Pt atoms are localized in S vacancy sites and exhibit dynamic hopping to nearby vacancy sites driven by the energy supplied by the electron beam. However, in areas of MoS2 contaminated with carbon surface layers, the Pt atoms appear at various positions with respect to the underlying MoS2 lattice, including on top of Mo and in off-axis positions. These variations are due to the Pt bonding with the surrounding amorphous carbon layer, which disrupts the intrinsic Pt–MoS2 interactions, leading to more varied positions. Density functional theory (DFT) calculations reveal that Pt atoms on the surface of MoS2 have a small barrier for migration and are stabilized when bound to either a single or double sulfur vacancies. DFT calculations have been used to understand how the catalytic activity of the MoS2 basal plane for hydrogen evolution reaction is influenced by Pt dopants by variation of the hydrogen adsorption free energy. This strong dependence of catalytic effect on interfacial configurations is shown to be common for a series of dopants, which may provide a means to create and optimize reaction centers.
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Mar 2017
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E02-JEM ARM 300CF
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Alex W.
Robertson
,
Yung-chang
Lin
,
Shanshan
Wang
,
Hidetaka
Sawada
,
Christopher S.
Allen
,
Qu
Chen
,
Sungwoo
Lee
,
Gun-do
Lee
,
Joohee
Lee
,
Seungwu
Han
,
Euijoon
Yoon
,
Angus I.
Kirkland
,
Heeyeon
Kim
,
Kazu
Suenaga
,
Jamie H.
Warner
Abstract: Dopants in two-dimensional dichalcogenides have a significant role in affecting electronic, mechanical, and interfacial properties. Controllable doping is desired for the intentional modification of such properties to enhance performance; however, unwanted defects and impurity dopants also have a detrimental impact, as often found for chemical vapor deposition (CVD) grown films. The reliable identification, and subsequent characterization, of dopants is therefore of significant importance. Here, we show that Cr and V impurity atoms are found in CVD grown MoS2 monolayer 2D crystals as single atom substitutional dopants in place of Mo. We attribute these impurities to trace elements present in the MoO3 CVD precursor. Simultaneous annular dark field scanning transmission electron microscopy (ADF-STEM) and electron energy loss spectroscopy (EELS) is used to map the location of metal atom substitutions of Cr and V in MoS2 monolayers with single atom precision. The Cr and V are stable under electron irradiation at 60 to 80 kV, when incorporated into line defects, and when heated to elevated temperatures. The combined ADF-STEM and EELS differentiates these Cr and V dopants from other similar contrast defect structures, such as 2S self-interstitials at the Mo site, preventing misidentification. Density functional theory calculations reveal that the presence of Cr or V causes changes to the density of states, indicating doping of the MoS2 material. These transferred impurities could help explain the presence of trapped charges in CVD prepared MoS2.
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Nov 2016
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