Materials Today, Journal Year: 2024, Volume and Issue: 73, P. 208 - 259
Published: Feb. 7, 2024
Language: Английский
Materials Today, Journal Year: 2024, Volume and Issue: 73, P. 208 - 259
Published: Feb. 7, 2024
Language: Английский
Angewandte Chemie International Edition, Journal Year: 2023, Volume and Issue: 62(13)
Published: Feb. 3, 2023
We demonstrate the great feasibility of MBenes as a new class tandem catalysts for electrocatalytic nitrate reduction to ammonia (NO3 RR). As proof concept, FeB2 is first employed model MBene catalyst NO3 RR, showing maximum NH3 -Faradaic efficiency 96.8 % with corresponding yield 25.5 mg h-1 cm-2 at -0.6 V vs. RHE. Mechanistic studies reveal that exceptional RR activity arises from catalysis mechanism, is, B sites activate NO3- form intermediates, while Fe dissociate H2 O and increase *H supply on promote intermediate hydrogenation enhance -to-NH3 conversion.
Language: Английский
Citations
292Chem, Journal Year: 2023, Volume and Issue: 9(7), P. 1768 - 1827
Published: June 21, 2023
Language: Английский
Citations
270Advanced Materials, Journal Year: 2023, Volume and Issue: 36(17)
Published: June 9, 2023
Natural nitrogen cycle has been severely disrupted by anthropogenic activities. The overuse of N-containing fertilizers induces the increase nitrate level in surface and ground waters, substantial emission oxides causes heavy air pollution. Nitrogen gas, as main component air, used for mass ammonia production over a century, providing enough nutrition agriculture to support world population increase. In last decade, researchers have made great efforts develop processes under ambient conditions combat intensive energy consumption high carbon associated with Haber-Bosch process. Among different techniques, electrochemical reduction reaction (NO
Language: Английский
Citations
214Advanced Materials, Journal Year: 2024, Volume and Issue: 36(16)
Published: Jan. 11, 2024
The excessive enrichment of nitrate in the environment can be converted into ammonia (NH
Language: Английский
Citations
157Advanced Functional Materials, Journal Year: 2023, Volume and Issue: 33(13)
Published: Jan. 18, 2023
Abstract Electrochemical reduction of nitrate to ammonia (NO 3 RR) has been recognized as an appealing approach realize both sustainable NH production and waste removal. Herein, from the perspective Lewis acid‐base interaction, a single‐atom Fe‐doped V 2 O 5 (Fe‐V ) catalyst enriched is designed with acid sites, which present maximum ‐Faradaic efficiency 97.1% corresponding yield 12.5 mg h −1 cm −2 at –0.7 versus RHE. Mechanistic studies based on theoretical calculations operando spectroscopic characterizations identify creation Fe‐V pairs , can synergetically activate NO − promote hydrogenation energetics, restrain hydrogen evolution, leading enhanced RR activity selectivity.
Language: Английский
Citations
144Nano Research, Journal Year: 2023, Volume and Issue: 16(7), P. 8737 - 8742
Published: March 8, 2023
Language: Английский
Citations
119ACS Energy Letters, Journal Year: 2023, Volume and Issue: 8(3), P. 1281 - 1288
Published: Feb. 3, 2023
Electrocatalytic NO reduction to NH3 (NORR) offers a prospective approach attain both harmful removal and efficient electrosynthesis. Main-group p-block metals are promising NORR candidates but still lack adequate exploration. Herein, Sb single atoms confined in amorphous MoO3 (Sb1/a-MoO3) designed as an catalyst, exhibiting the highest yield rate of 273.5 μmol h–1 cm–2 NO-to-NH3 Faradaic efficiency 91.7% at −0.6 V vs RHE. In situ spectroscopic characterizations theoretical computations reason that outstanding performance Sb1/a-MoO3 arises from isolated Sb1 sites, which can optimize adsorption *NO/*NHO lower reaction energy barriers simultaneously exhibit higher affinity than H2O/H species. Moreover, our strategy be extended prepare Bi1/a-MoO3, showing high property, demonstrating immense potential metal single-atom catalysts toward high-performing electrocatalysis.
Language: Английский
Citations
116Nano Letters, Journal Year: 2023, Volume and Issue: 23(5), P. 1735 - 1742
Published: Feb. 14, 2023
We design single-atom W confined in MoO3-x amorphous nanosheets (W1/MoO3-x) comprising W1-O5 motifs as a highly active and durable NORR catalyst. Theoretical operando spectroscopic investigations reveal the dual functions of to (1) facilitate activation protonation NO molecules (2) promote H2O dissociation while suppressing *H dimerization increase proton supply, eventually resulting self-tandem mechanism W1/MoO3-x greatly accelerate energetics NO-to-NH3 pathway. As result, exhibits highest NH3-Faradaic efficiency 91.2% NH3 yield rate 308.6 μmol h-1 cm-2, surpassing that most previously reported catalysts.
Language: Английский
Citations
96Journal of the American Chemical Society, Journal Year: 2023, Volume and Issue: 146(1), P. 668 - 676
Published: Dec. 28, 2023
Electrochemical synthesis of ammonia via the nitrate reduction reaction (NO3RR) has been intensively researched as an alternative to traditional Haber–Bosch process. Most research focuses on low concentration range representative level in wastewater, leaving high range, which exists nuclear and fertilizer wastes, unexplored. The use a concentrated electrolyte (≥1 M) for higher rate production is hampered by poor hydrogen transfer kinetics. Herein, we demonstrate that cocatalytic system Ru/Cu2O catalyst enables NO3RR at 10.0 A 1 M 16 cm2 flow electrolyzer, with 100% faradaic efficiency toward ammonia. Detailed mechanistic studies deuterium labeling operando Fourier transform infrared (FTIR) spectroscopy allow us probe intermediate species Ru/Cu2O. Ab initio molecular dynamics (AIMD) simulations reveal adsorbed hydroxide Ru nanoparticles increases density hydrogen-bonded water network near Cu2O surface, promotes rate. Our work highlights importance engineering synergistic interactions cocatalysts addressing kinetic bottleneck electrosynthesis.
Language: Английский
Citations
89Angewandte Chemie International Edition, Journal Year: 2023, Volume and Issue: 62(19)
Published: March 13, 2023
Abstract The electrochemical NO 3 − reduction and its coupling with CO 2 can provide novel clean routes to synthesize NH urea, respectively. However, their practical application is still impeded by the lack of efficient catalysts desirable Faradaic efficiency (FE) yield rate. Herein, we report synthesis molybdenum oxide nanoclusters anchored on carbon black (MoO x /C) as electrocatalyst. It affords an outstanding FE 98.14 % rate 91.63 mg h −1 cat. in reduction. Besides, highest 27.7 a maximum urea 1431.5 μg toward also achieved. formation electron‐rich MoO highly unsaturated metal sites /C heterostructure beneficial for enhanced catalytic performance. Studies mechanism reveal that stabilization *NO *CO NOOH intermediates are critical synthesis,
Language: Английский
Citations
76