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1 fundamental questions in the field of CO(2) electroreduction.
2 important role for M-OH species in peroxide electroreduction.
3 ogel from a noncatalyst to catalyst for H2O2 electroreduction.
4 oenvironments for high-rate, selective CO(2) electroreduction.
5 y at high current densities during the CO(2) electroreduction.
6 exposure of porphyrin active sites for CO(2) electroreduction.
7 to study multi-metallic catalysts for CO(2) electroreduction.
8 n the complex dynamic mechanism of the CO(2) electroreduction.
9 tics and unfavorable thermodynamics of CO(2) electroreduction.
10 ormation with >80% Faradaic efficiency in NO electroreduction.
11 lie the unique reactivity of Cu toward CO(2) electroreduction.
12 , thus lowering the energy barriers of CO(2) electroreduction.
13 olecular catalysts in carbon dioxide (CO(2)) electroreduction.
14 of a bimetallic copper-gold system for CO(2) electroreduction.
15 hance the activity of copper catalyzed CO(2) electroreduction.
16 efficient electrosynthesis of acetate via CO electroreduction.
17 anocatalysts (Au and Pd) for efficient CO(2) electroreduction.
18 the influence of gaseous impurities in CO(2) electroreduction.
19 atalytic hydrogenation (ECH) and (ii) direct electroreduction.
20 rastically decrease the overpotential of CO2 electroreduction.
21 zed monolayer (SOM) obtained using diazonium electroreduction.
22 surface chemistry necessary for efficient CO electroreduction.
23 sed ionic liquids have led to enhanced CO(2) electroreduction activity due to cation effects at the c
26 ying lower overpotentials for carbon dioxide electroreduction and record selectivity towards ethylene
27 electroreduced films using a newly developed electroreduction approach, (2) SAM formation on freshly
28 y and efficiency of Cu-catalyzed CO(2) or CO electroreduction are known to be sensitive to the electr
30 electrochemical instrumentation that enables electroreduction as a surrogate for charge neutralizatio
34 cations on the overall performance of CO(2) electroreduction by facilitating CO(2) adsorption while
35 ction (at ~$190 per ton) can be achieved via electroreduction by meeting practical targets for curren
37 mising approach for designing carbon dioxide electroreduction catalysts to enable one-pot reduction o
40 wn promising catalytic performance for CO(2) electroreduction (CO(2) R) to CO; this activity has ofte
43 CO partial pressures were measured for CO(2) electroreduction (CO(2)R) on Au under mass-transfer-cont
45 Studies focused on the mechanism of CO(2) electroreduction (CO(2)RR) aim to open up opportunities
49 3) electrolytes with CO(2)(aq) > ~1 M, CO(2) electroreduction (CO(2)RR) to formate reached >98% Farad
50 the most promising metal catalyst for CO(2) electroreduction (CO(2)RR) to multi-carbon products, yet
54 The dynamic restructuring of Cu surfaces in electroreduction conditions is of fundamental interest i
55 ring under coverage of CO and H in realistic electroreduction conditions, by combining grand canonica
56 mistic insight into surface restructuring in electroreduction conditions, which is required for the u
57 ndings will benefit researchers in designing electroreduction conversions of CO(2) to multicarbon C(2
59 the urate electrooxidation current to the O2 electroreduction current is reduced from 1:3 to 1:100 fo
62 to the design of Cu nanocatalysts for CO(2) electroreduction due to their dynamic nature under bias.
63 rgeable metal and metal-ion batteries, where electroreduction during charging often occurs beyond ele
64 in dictating the mechanistic landscape of CO electroreduction, exposing new strategies for tuning pro
66 of any intervening surface oxides and a low electroreduction flux are necessary to avoid polycrystal
67 sively prepared on a multigram scale by mild electroreduction from the corresponding C(sp(2)) electro
68 induced by the KOH electrolyte during pulsed electroreduction greatly enriched the Cu(delta+)O/Zn(del
69 organic frameworks as the catalyst for CO(2) electroreduction has been challenging due to issues such
70 reaction (HER) fundamentally limits aluminum electroreduction in aqueous electrolytes by dominating i
74 important to CO(2) capture, storage, photo-/electroreduction in the fight against global warming and
76 lectrochemical sensors for hydrogen peroxide electroreduction integrated with printed electrochromic
81 lvent-free method, to regulate transport and electroreduction kinetics at Li-metal anodes, achieving
82 ion of the NHC with (13)CO(2) and subsequent electroreduction led to (13)C-labeled formate, supportin
85 efficiency of this method is credited to the electroreduction-mediated turnover of the nickel catalys
86 c supported Cu electrocatalyst with a pulsed electroreduction method to achieve enhanced performance
88 icroenvironment that is created during CO(2) electroreduction near the surface of heterogeneous Cu el
89 the four-electron electroreduction of oxygen electroreduction occurs via a series pathway on the Bi-m
90 ndings, we have proposed a mechanism for the electroreduction of 1, which has been further corroborat
95 t most importantly also allow stereospecific electroreduction of a prochiral compound, with very sign
96 Here, we for the first time report selective electroreduction of a series of oximes to their correspo
97 to produce ethylamine selectively through an electroreduction of acetonitrile at ambient temperature
100 (c-GaAs) has been prepared directly through electroreduction of As(2)O(3) dissolved in an alkaline a
103 context of carbon reutilization, the direct electroreduction of captured CO(2) (c-CO(2)RR) appears a
104 y demands of the world continue to grow, the electroreduction of captured CO(2) (c-CO(2)RR) is an app
113 ve been demonstrated to be selective for the electroreduction of carbon dioxide to carbon monoxide.
115 ing that the bismuth electrode catalyzed the electroreduction of chloroacetamides, alpha-halocarbonyl
117 a minor product and key intermediate in the electroreduction of CO to ethanol on OD-Cu electrodes.
122 e that both isomeric precatalysts facilitate electroreduction of CO(2) to CO in 95/5 MeCN/H(2)O with
123 ic F-CTF-1 exhibits good capability to boost electroreduction of CO(2) to CO, with faradaic efficienc
125 lopment of efficient catalysts for selective electroreduction of CO(2) to high-value products is esse
128 nterest as a new generation of catalysts for electroreduction of CO(2), but these structures have lim
129 to form carbon-heteroatom bonds through the electroreduction of CO, expanding the scope of products
130 tivity for a single product are essential if electroreduction of CO2 is to become a viable route to t
135 rption spectroscopy unambiguously probes the electroreduction of Cu@Cu(2)O to fully metallic Cu nanog
137 corrole (Me(4)Ph(5)Cor)Co also catalyzes the electroreduction of dioxygen at E(1/2) = 0.38 V with the
140 and that the degradation rate from parasitic electroreduction of electrolyte components is about an o
145 alytic activity of Fe3O4 nanodots toward the electroreduction of H2O2 was described by cyclic voltamm
146 displays high performance catalysis towards electroreduction of H2O2 with a high sensitivity of 1.5A
147 s exhibit remarkably high activities for the electroreduction of molecular oxygen (oxygen reduction r
148 g studies with (15)N(2) confirmed the direct electroreduction of N(2), while kinetic analyses undersc
150 To asses the limits of the method, both the electroreduction of nitrate and UPD of lead monolayer on
151 ally deposited (UPD) lead layer inhibits the electroreduction of nitrate on a bare Cu(111) electrode.
152 on of nitrate to the anodically charged GAC, electroreduction of nitrate to ammonium, and the oxidati
153 duction, which is caused by the preferential electroreduction of nitrogen oxides over carbon dioxide.
154 catalytic base layer into a catalyst for the electroreduction of O(2) to water at +0.12 V (vs Ag/AgCl
157 ow for the first time that the four-electron electroreduction of oxygen electroreduction occurs via a
161 in the interplay of the chemistries for the electroreduction of protons, free CO(2), and captured CO
162 ew strategy for silyl radical generation via electroreduction of readily available chlorosilanes.
165 hat as-synthesized Cu@Cu(2)O NWs experienced electroreduction of surface Cu(2)O to disordered (spongy
167 s as a key reductive mediator to mediate the electroreduction of the Cr(III)/chiral ligand complex.
172 n prolonged exposure to the electrolyte, and electroreduction of water are well-studied but remain un
174 nnot sustain the interfacial pH during CO(2) electroreduction on copper electrodes at relatively low
175 ying this design strategy, we achieved CO(2) electroreduction on copper in 7 M potassium hydroxide el
176 ed understanding of the initial steps of CO2 electroreduction on copper surfaces, the best current ca
178 transfer-proton transfer mechanism for CO(2) electroreduction on PCN-222(Fe) electrodes, which follow
179 mine electrooxidation/reduction, and nitrite electroreduction on Pt have also been studied to enhance
181 rticle size effects during the catalytic CO2 electroreduction on size-controlled Cu nanoparticles (NP
182 on the initial atomic level events for CO(2) electroreduction on the metal catalysts to provide the b
183 ioxide, and nitrous oxide, on carbon dioxide electroreduction on three model electrocatalysts (i.e.,
184 These interfacial effects promote CO(2) electroreduction, particularly under diffusion-limited c
188 (111) alloy surface, of interest for nitrate electroreduction processes, where high adsorbate coverag
189 C)(2)], HKUST-1), the Cu-Pd MOF shifts CO(2) electroreduction products from diverse chemical species
190 y, we have taken advantage of a pulsed CO(2) electroreduction reaction (CO(2)RR) approach to tune the
192 , BIF-29(Cu), to enable coupling between the electroreduction reaction of CO(2) (CO(2)RR) with NO(3)(
195 ve sites for NH(3) synthesis through nitrate electroreduction reaction, but still face significant ch
199 to enhance rates and selectivities of (photo)electroreduction reactions could be a crucial component
203 urthermore, the partial pressure study of NO electroreduction revealed that a high NO coverage facili
204 irms the presence of free radicals during AN electroreduction, suggesting that coupling of PN radical
205 We showcase NiCoFeP in a membrane-free CO2 electroreduction system that achieves a 1.99 V cell volt
209 ealed optimal turnover frequencies for CO(2) electroreduction to CO at 1 wt.% catalyst loading, beyon
210 metal coordination compounds catalyze CO(2) electroreduction to CO, but cobalt phthalocyanine hybrid
213 nteractions to tune the selectivity of CO(2) electroreduction to ethanol, bringing it closer to pract
217 yst, for the first time O(2) -tolerant CO(2) electroreduction to liquid products is realized, generat
219 ign for highly selective catalysts for CO(2) electroreduction to multicarbon (C(2+)) fuels is pressin
220 e electrode potential and can be released by electroreduction to Pu(III), whereas other actinides (e.
222 ing the kinetics and selectivity of CO(2)/CO electroreduction to valuable multi-carbon products is a
223 improving the conversion efficiency of CO(2) electroreduction toward value-added chemicals and fuels
224 ighly active toward nitrite and nitric oxide electroreduction under various pH values with ammonia as
225 pointed different approach of 5f metal ions electroreduction unlike 4p metal ions such as As(III).
226 atalytic activity and selectivity during CO2 electroreduction were analyzed and compared to a bulk Cu
227 e Faradaic efficiency loss in carbon dioxide electroreduction, which is caused by the preferential el
228 ed onto the bottom electrode using diazonium electroreduction, which yields a stable and robust gold-
229 on the junction base electrode by diazonium electroreduction, while the counter electrode was direct
231 f size-selected gold nanoparticles for CO(2) electroreduction with sizes ranging from 1.5 to 6.5 nm.
232 critical surface chemistry insights in CO(2) electroreduction with sub-electronvolt energy resolution