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1 ing Fe and Ni particles supported on silicon carbide.
2 w and measure stable crack growth in silicon carbide.
3 erfaces of few-nm thick germanium on silicon carbide.
4 cal SAM chemistry for generating the central carbide.
5 tural instability and amorphization of boron carbide.
6 tial similar to or exceeding that of silicon carbide.
7 hyl transfer and conversion to an iron-bound carbide.
8 ilicon and carbon faces of hexagonal silicon carbide.
9 table than a mixture of SiO2, C, and silicon carbide.
10 n epitaxial graphene on silicon-face silicon carbide.
11 uctors such as transition-metal nitrides and carbides.
12 antum dots and defects in diamond or silicon carbide(6-10), have emerged as promising candidates for
13       ZrC(1-x) (sub-stoichiometric zirconium carbide), a group IV transition metal carbide, is being
14 aman spectra of 2D alpha-Mo(2) C (molybdenum carbide), a promising member in MXene family, is conduct
15 ase synthesis route to phase-pure molybdenum carbide (alpha-MoC(1-x)) nanoparticles (NPs) in a contin
16 Pt) atomically dispersed on alpha-molybdenum carbide (alpha-MoC) enables low-temperature (150-190 deg
17 d layered gold (Au) clusters on a molybdenum carbide (alpha-MoC) substrate to create an interfacial c
18           The Mossbauer spectroscopy of iron carbides (alpha-Fe, gamma'-FeC, eta-Fe2C, zeta-Fe2C, chi
19 reaction of molybdenum with the SWNT to form carbide, also exhibited no Schottky barrier.
20              The electronic structures of Mo carbide and carbyne species were investigated quantum me
21                                      Silicon carbide and gallium nitride, two leading wide band gap s
22 s) which are observed in both the molybdenum carbide and nitride samples.
23            Reduction of Mo(IV) CO adducts of carbide and silylcarbyne species allowed for the spectro
24 ace reconstruction of single-crystal silicon carbide and study this process by high-resolution transm
25 tance and influence of both the interstitial carbide and the identity of the heteroatom on the electr
26  to the weak Mo C bonds in this interstitial carbide and the low formation energy of the carbon chain
27 s ratio governs the chemical behavior of the carbide and the properties of the admetal, up to the poi
28   While the fabrication of bulk high-entropy carbides and borides is well established, high-entropy n
29 in the deep Earth, involving Fe-C phases (Fe carbides and C dissolved in Fe-Ni metal).
30 s a basis for exploring a large family of 2D carbides and carbonitrides in electrochemical energy sto
31  two-dimensional (2D) early transition metal carbides and carbonitrides, called MXenes, was discovere
32 emonstrate the freestanding transition-metal carbides and graphene oxide hybrid membranes as high-per
33                          2D transition metal carbides and nitrides (MXenes), a class of emerging nano
34                             Transition metal carbides and nitrides (MXenes), a family of two-dimensio
35 , boron nitrides along with transition metal carbides and nitrides (MXenes).
36                   Two-dimensional (2D) metal carbides and nitrides, called MXenes, have attracted gre
37           MXenes, two-dimensional (2D) metal carbides and nitrides, have attracted attention for appl
38     The family of two-dimensional (2D) metal carbides and nitrides, known as MXenes, are among the mo
39                        Two-dimensional metal carbides and nitrides, known as MXenes, combine metallic
40                          2D transition-metal carbides and nitrides, known as MXenes, have displayed p
41                          2D transition metal carbides and nitrides, named MXenes, are attracting incr
42 ess presents an approach for construction of carbides and their subsequent applications.
43 activity among all four phases of molybdenum carbide, and is exceedingly stable in acidic solution.
44 als such as hexagonal boron nitride, silicon carbide, and others.
45           The identification of an analogous carbide, and thus an atomically homologous active site i
46 ivation on monofunctional catalysts (metals, carbides, and oxides) is challenging due to activity con
47 engths and show that the icosahedra in boron carbide are not as stable as anticipated.
48  and the stacking faults of the primary M7C3 carbide are observed by scanning electron microscopy (SE
49                     Point defects in silicon carbide are rapidly becoming a platform of great interes
50 ene nanoribbons epitaxially grown on silicon carbide are single-channel room-temperature ballistic co
51            Bulk polycrystalline high-entropy carbides are a newly developed group of materials that i
52 and potential catalytic applications of iron carbides are also summarized.
53                            Some primary M7C3 carbides are formed by layers of shell or/and consist of
54  precursor-free methods to prepare ultrathin carbides are lacking.
55                                   Novel iron carbides are particularly promising catalytic materials
56 ransition metal oxides, dichalcogenides, and carbides, are presented.
57 unattributed point defect centers in silicon carbide as a near-stacking fault axial divacancy and sho
58 nts for promoting methylidene formation from carbide as energetically viable relative to the heteroly
59  12 times better than conventional zirconium carbide at 2,500 degrees C).
60 we systematically explore all stable calcium carbides at pressures from ambient to 100 GPa using vari
61 on of slip systems in mono- and high-entropy carbides at room temperature.
62 s of S-adenosyl methionine (SAM) to insert a carbide atom and fuse two substrate [Fe-S] clusters form
63   In this study, we labeled the interstitial carbide atom with (14)C and (13)C isotopes and traced th
64 forcing and enhancing the wear resistance of carbide based materials.
65 n the surfaces and in the interiors of boron carbide based nanowires.
66       Herein, a highly durable and efficient carbide-based bifunctional catalyst consisting of iron-m
67                           The discovery of a carbide-based surface able to activate methane at low te
68 ed from a cobalt-substituted bulk molybdenum carbide (beta-Mo(2)C:Co) through a two-step synthesis: f
69      A versatile method for achieving atomic carbide-bonded graphene networks on both metallic and no
70 ition on substrates and in situ formation of carbide bonds.
71 mpounds and applied to samples such as boron carbide, boric acid, carborane, and borosilicate glass.
72 extended to other metals to synthesize metal carbide, boride, and nitride coatings.
73 f making scalable ultrathin transition metal-carbide/boride/nitride using immiscibility of two metals
74 metal and main-group-element surface alloys: carbides, borides, and nitrides, which feature high stab
75 oscopy confirmed the formation of transition carbides by auto-tempering as well as the presence of re
76 theoretical calculations show that Fe and Si carbides can be significantly depleted in (13)C relative
77                             The formation of carbides can significantly modify the physical and chemi
78       Our results show that the interstitial carbide cannot be exchanged upon turnover, nor can it be
79                            Treatment of iron carbide carbonyl clusters [Fe(n) (mu(n) -C)(CO)(m) ](x)
80 anic product release, as evidenced by direct carbide carbonylation experiments.
81 achieved over a high-surface-area molybdenum carbide catalyst prepared by a temperature-programmed re
82         Additive-free films of this titanium carbide 'clay' have volumetric capacitances of up to 900
83 d U(2)C(2) is the first example of a uranium carbide cluster featuring two U centers bridged by a C=C
84        A non-isolated pentagon rule metallic carbide clusterfullerene containing a heptagonal ring, S
85 e classes of EMFs with nitride, sulfide, and carbide clusters and different metal atoms (Sc, Y, Ti).
86 veloping syntheses of biomimetic iron-sulfur-carbide clusters like FeMoco.
87 rication of vertically aligned CNS and metal carbide@CNS composites via a facile salt templating indu
88 e resulting vertically aligned CNS and metal carbide@CNS structures possess ultrathin walls, good ele
89 olimus-eluting DP-DES, or thin-strut silicon-carbide-coated BMS in 8 European centers.
90                                     Tungsten carbide cobalt (WC-Co) matrix nanocomposites reinforced
91 ents with enhanced properties over the metal carbides commonly used in cutting, drilling, and wear-re
92 nded to provide the first ever thiolato-iron-carbide complex: an analogous reaction with toluylsulfen
93 ynthesis of other micro/nanostructured metal carbides/composites from metal oxides/carbon precursors.
94 an be considered to be a novel form of boron carbide consisting of boron doped, distorted multiwalled
95 ction (EBSD) maps show that the primary M7C3 carbide consists of multiple parts.
96                                  Though some carbide-containing iron clusters are known, none yet hav
97 lybdenum-dependent nitrogenase is the unique carbide-containing iron-sulfur cluster called the iron-m
98                         The semi-molten M7C3 carbide contains unmelted shell and several small-scale
99 cally have martensitic microstructures, high carbide contents, and various coatings to exhibit high h
100 al matrix with in-situ formation of chromium carbide (Cr7C3) at the CNT/copper (Cu) interface.
101 on process by transferring oxide crystals to carbide crystals, leading to the surface enrichment of a
102 micro-supercapacitors with embedded titanium carbide current collectors, fully compatible with curren
103 ry of crystallographic planes in these boron carbide datasets substantiates that crystallinity is mai
104              Novel nanostructured sulfur (S)-carbide derived carbon (CDC) composites with ordered mes
105 ition of proton and hydride to a terminal Mo carbide derived from CO.
106  were used to characterize ion adsorption in carbide-derived carbon (CDC) with two different average
107 ping on hydrophobicity of nanoporous silicon carbide-derived carbon (SiCDC), and investigate the unde
108  process for manufacturing strongly adhering carbide-derived carbon films and interdigitated micro-su
109      The result is a predominantly amorphous carbide-derived carbon, with a narrow distribution of mi
110 with electrodes composed of porous nanosized carbide-derived carbons (CDCs) and nonporous onion-like
111 tive catenation involves C-C coupling from a carbide-derived surface methylidene.
112  fracture energy for a bi-crystal of silicon carbide, diffusion bonded with a thin glassy layer.To im
113  structures, the observation of a H(2) MC(+) carbide dihydride structure implies that it is imperativ
114 ce of vibrational bands of a H(2) Ta(4) C(+) carbide dihydride structure over those indicative for a
115  the ground-state electron spin of a silicon carbide divacancy defect.
116                Joining the intermetallic and carbide domains together then provides substantial relie
117 (in the first 15 h) of the high-surface-area carbide during the reaction was ascribed to considerable
118 d atom probe tomography experiments on boron carbide elucidate an approach for characterizing the ato
119  a strategy to produce highly dispersed iron carbides embedded in a matrix of porous carbon.
120 d with an approximately 1,455-kelvin silicon carbide emitter.
121                                 For tungsten carbide - epoxy crystals we identify all angle all mode
122 ther nuclear fuel materials (e.g., nitrides, carbides, etc.) in the form of pellets, powders, and mic
123 ional catalyst consisting of iron-molybdenum carbide (Fe3 Mo3 C) and IrMn nanoalloys is demonstratred
124 perimental data up to core pressures on iron carbide Fe7C3, a candidate component of the inner core,
125 used in combination with an uncoated silicon carbide filter and report effects on emissions of polych
126 ween K1 and K2 and concurrently facilitating carbide formation via deprotonation of the initial carbo
127 -O cleavage as rate-determining steps toward carbide formation.
128  the initial growth period, the primary M7C3 carbide forms protrusion parallel to {} crystal planes.
129 t the synthesis and crystal structure of the carbide Gd(13)Fe(10)C(13).
130 y exposure ages of 40 large presolar silicon carbide grains extracted from the Murchison CM2 meteorit
131                                   Molybdenum carbide has been proposed as a possible alternative to p
132 ally been elucidated, and the discovery of a carbide has generated new questions and targets for coor
133               The unusual structure of these carbides has attracted much attention: C assumes a tetra
134  metallic ruthenium and a shell of ruthenium carbide have been synthesized by a mild and easy hydroth
135                      Spin defects in silicon carbide have the advantage of exceptional electron spin
136     New two-dimensional niobium and vanadium carbides have been synthesized by selective etching, at
137 d to image key features such as microcracks, carbides, heat affected zone, and dendrites in a laser a
138 nt discovery of chemically ordered hexagonal carbides, i-MAX phases, we perform an extensive first-pr
139 -plasma sintered (Hf-Ta-Zr-Nb)C high-entropy carbide in a specific orientation during micropillar com
140            It is found that the primary M7C3 carbide in hypereutectic Fe-Cr-C alloy is irregular poly
141 ggests an essential role of the interstitial carbide in maintaining the stability while permitting a
142 rvations point to a role of the interstitial carbide in stabilizing the cofactor structure, although
143     As for our identification of the central carbide in the Fe-Mo cofactor, we employed Fe Kbeta vale
144 provided for the presence of an interstitial carbide in the Fe-V cofactor of Azotobacter vinelandii v
145 searched since the discovery of interstitial carbide in the FeMo cofactor of Mo-dependent nitrogenase
146 he incorporation of finely dispersed V-Mo-Nb carbides in a ferrite matrix.
147 d on the unique catalytic activities of iron carbides in CO(x) hydrogenation and HER and the correlat
148        The latter is produced by placing the carbides in HF, HCl or NaCl solutions and applying anodi
149 stic insights into the radical SAM-dependent carbide insertion concomitant with cofactor core formati
150 ters (designated K1 and K2) concomitant with carbide insertion into an [Fe(8)S(9)C] cofactor core (de
151                    Previously, we proposed a carbide insertion pathway involving methyltransfer from
152 n, thereby refining the initial steps of the carbide insertion pathway.
153                                              Carbide insertion plays a pivotal role in the biosynthes
154 tains unmelted shell and several small-scale carbides inside, which further proves that the primary M
155 gregation of Mn-Si (intermetallic) and Mn-C (carbide) interactions in these structures can be underst
156 nduced transformation of diamond and silicon carbide into graphene suffers from metal contamination a
157 rected towards converting silicon or silicon carbide into other chemicals.
158 yl-L-methionine (SAM)-dependent insertion of carbide into the M cluster, the cofactor of the molybden
159 adical-based incorporation of methyl-derived carbide into the M cluster.
160 an essential role, concomitantly inserting a carbide ion and coupling two [Fe(4)S(4)] clusters to for
161                                          The carbide is a substitutional solid solution of Zr-Ti cont
162                           Supported tungsten carbide is an efficient and vital nanomaterial for the d
163                                         This carbide is chemically stable in alkaline media and over
164                      Cradle-to-gate, silicon carbide is estimated to require more than twice the ener
165 ered in this work, graphene grown on silicon carbide is found to be the most promising substrate for
166 ly charged silicon-vacancy centre in silicon carbide is immune to both drawbacks.
167 , which further proves that the primary M7C3 carbide is not an overall block.
168 ved that the coalescence of the primary M7C3 carbides is ascribed to the growing condition of the pro
169 conium carbide), a group IV transition metal carbide, is being considered for various high temperatur
170 dulation of ripples on both graphene-silicon carbide junctions.
171  blocks, cured and sectioned with a tungsten carbide knife to obtain mineralized bone sections for dy
172 operties of two-dimensional transition metal carbides known as MXenes.
173                          2D transition metal carbides, known as MXenes, are transparent when the samp
174 ansion compared with the unstrained titanium carbide lattice.
175                 MXenes combine 2D conductive carbide layers with a hydrophilic, primarily hydroxyl-te
176  results show that the presence of carbon or carbide-like species at the interface between the Ni clu
177         The laser-sculptured polycrystalline carbides (macroporous, ~10-20 nm wall thickness, ~10 nm
178 e ammonia nitridation of a parent core-shell carbide material (Pt/TiWC).
179  This work highlights the potential of using carbide materials to reduce the costs of hydrogen produc
180 ore metastable synthesis of boron-rich boron-carbide materials.
181 mma-UMo matrix, and across interfaces (e.g., carbide/matrix, grain boundary).
182                       Consequently, tungsten carbide may be a promising catalyst in self-hydrating cr
183 e for this top-down mechanism based on metal carbide metallofullerenes M2C2@C1(51383)-C84 (M = Y, Gd)
184 demonstrate high-frequency multimode silicon carbide microdisk resonators and spatial mapping of the
185 nd characterization of two new intermetallic carbides: Mn16SiC4 (mC42) and Mn17Si2C4 (mP46).
186 o oxide species agglomerate and convert into carbided Mo nanoparticles.
187                                   Molybdenum carbide (Mo(2) C), a class of unterminated MXene, is end
188 ungsten carbide (WC) and molybdenum tungsten carbide (Mo(x)W(1-x)C) nanoparticles are highly active a
189 NC that is composed of ultrasmall molybdenum carbide (Mo2 C) nanoparticles embedded within nitrogen-r
190 g the non-precious metal material molybdenum carbide (Mo2C) as an active and selective catalyst for C
191 rect pattern method to manufacture ultrathin carbides (MoC(x), WC(x), and CoC(x)) on versatile substr
192 ganic sulfides or thiolate with interstitial carbide motifs, are reported.
193 ch improves the rate performance of titanium carbide MXene (Ti(3) C(2) T(x,) T(x) refers to -F, =O, -
194                                     Titanium carbide MXene (Ti3 C2 Tx ), in particular, has shown sig
195 foliated two-dimensional (2D) Ti3C2 titanium carbide (MXene) nanosheets.
196 es, conducting polymers, 2D transition metal carbides (MXene), and other transition metal dichalcogen
197 ps also control superconductivity of niobium carbide MXenes.
198             Two-dimensional transition metal carbides (MXenes) have attracted a great interest of the
199                          2D transition metal carbides (MXenes) have been recently introduced as high-
200 l groups in two-dimensional transition-metal carbides (MXenes) open up a previously unexplored design
201 nides, and more recently 2D transition metal carbides (MXenes).
202 w that a dense uniform dispersion of silicon carbide nanoparticles (14 per cent by volume) in magnesi
203 enzene hydrogenation reactions on molybdenum carbide nanoparticles (MCNPs) in the process of in situ
204        High-temperature oxidation of silicon-carbide nanoparticles (nSiC) underlies a wide range of t
205 lex, the zinc prevents the formation of iron carbide nanoparticles and the SiO(2) template promotes t
206 s been developed for the preparation of iron carbide nanoparticles and their nanocomposites.
207 d to produce well-dispersed transition metal carbide nanoparticles as additives to enhance the perfor
208 trated the self-assembly of transition metal carbide nanoparticles coated with atomically thin noble
209 e report a novel anode electrocatalyst, iron carbide nanoparticles dispersed in porous graphitized ca
210 nowires can be alleviated by adding tungsten carbide nanoparticles to the metal core to arrive at wir
211 ons confirm the unique configuration of iron carbide nanoparticles with porous graphitized carbon.
212 lasses, polymers, metal nanoparticles, metal carbide nanoparticles, and carbon materials.
213 d to produce well-dispersed transition metal carbide nanoparticles.
214                                     Tungsten carbide nanorods (WC NRs) are demonstrated for the first
215                                      Silicon carbide nanowires (SiC NWs) have attracted intensive att
216 the amorphization of nanocrystalline silicon carbide (nc-SiC) by point defect accumulation.
217 re, the sculptured microstructures endow the carbide network with enhanced visible light absorption,
218                           Ultrathin tantalum carbide, nitride, and boride are grown using chemical va
219 ass of two-dimensional (2D) transition metal carbides, nitrides and carbonitrides that have shown pro
220                          2D transition metal carbides, nitrides, and carbonitides called MXenes have
221                         Two-dimensional (2D) carbides, nitrides, and carbonitrides known as MXenes ar
222 d of a few atomic layers of transition metal carbides, nitrides, or carbonitrides.
223             Two-dimensional transition metal carbides/nitrides, known as MXenes, have been recently r
224 tic method could be a versatile route toward carbide NPs of varying size, composition, and phase, on
225                                      Surface carbides of cobalt and nickel are exceptionally stable,
226          The microdisks are made in a 500-nm-carbide on 500-nm-oxide thin-film technology that facili
227  the impact of the metal/carbon ratio in the carbide on the performance of the catalysts.
228 ipation limits in 4H monocrystalline silicon carbide-on-insulator (4H-SiCOI) mechanical resonators fa
229 erein, we show that two-dimensional titanium carbide or carbonitride nanosheets, known as MXenes, can
230 alized two-dimensional (2D) transition-metal carbides or MXenes: Sc2C, Ti2C, Ti3C2, V2C, Cr2C, and Nb
231                    The influence of the iron carbide particle size of promoted and unpromoted carbon
232      These results demonstrate that the iron carbide particle size plays a crucial role in the design
233 ing an optimal dispersion of the active iron carbide phase when a metal organic framework is used as
234 ap enrichment in various morphologies of a U carbide phase, the adjacent gamma-UMo matrix, and across
235 ns of the surface energy of the same silicon carbide plane.
236 eport the directional amorphization in boron carbide polycrystals.
237 d on group IV-V transition metal borides and carbides possess melting points above 3000 degrees C, ar
238 ticle inclusions representative of oxide and carbide precipitates.
239 ated forms; hexagonal boron nitride; silicon carbide), rare earth, semimetals, transition metal chalc
240 ity can be associated with surface ruthenium carbide (RuC) species, which enable CO(2) activation and
241 al X-ray diffraction revealed that it is the carbide Sc2C2@C(2v)(9)-C86 with a planar, twisted Sc2C2
242 extending and revolving protrusion forms the carbide shell.
243 noparticles supported on graphite-rich boron carbide show a 50-100% increase in activity in acidic me
244 ium disilicide (U(3)Si(2)) fuel with silicon carbide (SiC) composite cladding is being considered as
245                                      Silicon carbide (SiC) exhibits excellent material properties att
246                           Defects in silicon carbide (SiC) have emerged as a favorable platform for o
247                                      Silicon carbide (SiC) is a fascinating wide-band gap semiconduct
248 ed as sludge waste consisting of Si, silicon carbide (SiC) particles and metal impurities from the fr
249 e field-effect transistors (GFET) on silicon carbide (SiC) substrates by scanning a focused laser bea
250       Lattice distortions (LD) in 4H-silicon carbide (SiC) wafers were quantified using synchrotron X
251 measurement of the surface energy of silicon carbide single crystals.
252 bar increased 6-8-fold when the average iron carbide size decreased from 7 to 2 nm, while methane and
253 c amine system could be regenerated by using carbide slag as the regeneration agent and could still s
254  the inner layers of the material, ruthenium carbide species being located on the upper surface layer
255 raphene, monolayer graphene grown on silicon carbide substrate).
256 illars etched into a semi-insulating silicon carbide substrate.
257 single crystalline graphene grown on silicon carbide substrates to flexible polycarbonate track etche
258 ounts of precious metals on transition metal carbide substrates.
259 discuss opportunities for future research on carbide-supported metal surfaces.
260  irradiation triggers melting of the silicon carbide surface, resulting in a phase separation into a
261 that the metal ML-supported transition metal carbide surfaces exhibit HER activity that is consistent
262 table crystal structures in boron-rich boron-carbide system and provides a pathway for large-area syn
263 different chemistry takes place on our metal/carbide system.
264 and muB with a slope of 12.81 T/muB for iron carbide systems and that the proportionality constant ma
265             Two-dimensional transition metal carbides (termed MXenes) are a new family of compounds g
266 re significantly more endergonic on tungsten carbide than on platinum.
267 rt with carbon-both through the interstitial carbide that resides in the central cavity of its cofact
268                        Herein, a 2D titanium carbide (Ti(3) C(2) ) MXene film with transparent conduc
269 strate two types of two-dimensional titanium carbide (Ti(3)C(2)T(x)) MXene inks, aqueous and organic
270 re, the metal atoms from the ternary layered carbides, Ti3 AlC2 , Ti2 AlC and Ti3 SiC2 (MAX phases).
271 by etching aluminium from titanium aluminium carbide (Ti3AlC2, a 'MAX' phase) in concentrated hydrofl
272  electrodes made of two-dimensional titanium carbide (Ti3C2, a member of the 'MXene' family), produce
273 rial properties of micrometer-thick titanium carbide (Ti3C2Tx) MXene membranes prepared by filtration
274 is of an ultra-high-temperature high-entropy carbide, (TiNbTaZrHf)C, via a facile electrochemical pro
275 water and C1 molecules over transition metal carbide (TMC) and metal-modified TMC surfaces and thin f
276 supported on cost-effective transition-metal carbides (TMCs) are studied to reduce the Pd usage and t
277                             Transition-metal carbides (TMCs) exhibit catalytic activities similar to
278                             Transition metal carbides (TMCs) have demonstrated outstanding potential
279 ow to exploit long-cell polytypes of silicon carbide to achieve strong coupling between transverse ph
280 single layer and bilayer graphene on silicon carbide to investigate lateral electronic structure vari
281 riuranium pentasilicide (U(3)Si(5)), uranium carbide (UC), U(20)Si(16)C(3), and uranium silicide (USi
282    We demonstrate that the amorphous silicon carbide ultramicroelectrode arrays (a-SiC UMEAs) provide
283 cific surface area due to nitridation of the carbide under the reaction conditions.
284 e in-suit growth process of the primary M7C3 carbide was observed by confocal laser microscope (CLM).
285                    Carbon-supported tungsten carbide (WC) and molybdenum tungsten carbide (Mo(x)W(1-x
286 e different metallic nanoparticles, tungsten carbide (WC), silver (Ag) and copper (Cu), in combinatio
287 ise a range of compositions, including metal carbides (WC), sulfides (MoS2 ), phosphides (Ni5 P4 , Co
288                       Results indicate the U carbides were formed during casting, rather than retaine
289 ining largely debris of silicon, and silicon carbide, which is a common cutting material on the slici
290 nt pathway was revealed for the insertion of carbide, which signifies a novel biosynthetic route to c
291 deposition (CVD) or via reduction of silicon carbide, which unfortunately relies on the ability to fo
292 -photon absorption (TPA) occuring in silicon carbide with either cubic or wurtzite structure.
293  we fabricate 1D nanobeam PCCs in 4H-silicon carbide with embedded silicon vacancy centers.
294                       In this work, tungsten carbide with tube-like nanostructures (WC NTs) supported
295                   Ultrathin transition metal carbides with high capacity, high surface area, and high
296 rapping of hydrogen within the core of these carbides with quantitative composition profiles.
297 he metallic conductivity of transition metal carbides with the hydrophilic nature of their hydroxyl o
298 sional graphitic carbon nitride and titanium carbide (with MXene phase) nanosheets, display outstandi
299               Here we design and fabricate a carbide (Zr0.8Ti0.2C0.74B0.26) coating by reactive melt
300 ced thermomechanical properties of zirconium carbide (ZrC(x)) with sample purity and stoichiometry ar

 
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