p-d hybridized In-Co dual sites promote nitrite electroreduction to ammonia at high current density DOI
Nana Zhang,

Yuying Wan,

Kai Chen

и другие.

Nano Energy, Год журнала: 2024, Номер 125, С. 109594 - 109594

Опубликована: Апрель 6, 2024

Язык: Английский

Sustainable Ammonia Electrosynthesis from Nitrate Wastewater Coupled to Electrocatalytic Upcycling of Polyethylene Terephthalate Plastic Waste DOI

Tianlun Ren,

Zuan Yu,

Hongjie Yu

и другие.

ACS Nano, Год журнала: 2023, Номер 17(13), С. 12422 - 12432

Опубликована: Июнь 26, 2023

Integrating the nitrate reduction reaction (NO3RR) with polyethylene terephthalate (PET) hydrolysate oxidation to construct nitrate/PET coelectrolysis system holds a great promise of realizing simultaneous upcycling wastewater and PET plastic waste, which, however, is still an almost untouched research area. Herein, we develop ultralow content Ru-incorporated Co-based metal-organic frameworks as bifunctional precatalyst, which can be in situ reconstructed Ru-Co(OH)2 at cathode Ru-CoOOH anode under electrocatalytic environments, function real active catalysts for NO3RR oxidation, respectively. With two-electrode system, current density 50 mA cm-2 achieved cell voltage only 1.53 V, production ammonia formate lower energy consumption. This study provides concept construction systems waste.

Язык: Английский

Процитировано

78

Crystal Phase Engineering of Ultrathin Alloy Nanostructures for Highly Efficient Electroreduction of Nitrate to Ammonia DOI Creative Commons
Yunhao Wang,

Fengkun Hao,

Mingzi Sun

и другие.

Advanced Materials, Год журнала: 2024, Номер 36(14)

Опубликована: Янв. 26, 2024

Abstract Electrocatalytic nitrate reduction reaction (NO 3 RR) toward ammonia synthesis is recognized as a sustainable strategy to balance the global nitrogen cycle. However, it still remains great challenge achieve highly efficient production due complex proton‐coupled electron transfer process in NO RR. Here, controlled of RuMo alloy nanoflowers (NFs) with unconventional face‐centered cubic (fcc) phase and hexagonal close‐packed/fcc heterophase for RR reported. Significantly, fcc NFs demonstrate high Faradaic efficiency 95.2% large yield rate 32.7 mg h −1 cat at 0 −0.1 V (vs reversible hydrogen electrode), respectively. In situ characterizations theoretical calculations have unraveled that possess highest d‐band center superior electroactivity, which originates from strong Ru─Mo interactions intrinsic activity phase. The optimal electronic structures supply adsorption key intermediates suppression competitive evolution, further determines remarkable performance. successful demonstration high‐performance zinc‐nitrate batteries suggests their substantial application potential electrochemical energy systems.

Язык: Английский

Процитировано

78

Optimizing Intermediate Adsorption via Heteroatom Ensemble Effect over RuFe Bimetallic Alloy for Enhanced Nitrate Electroreduction to Ammonia DOI
Xinying Zhao, Yuzhuo Jiang, Mengfan Wang

и другие.

Advanced Energy Materials, Год журнала: 2023, Номер 13(31)

Опубликована: Июнь 30, 2023

Abstract The electrochemical nitrate reduction reaction (NO 3 RR) is a promising approach for removal and NH synthesis at ambient conditions. As complex eight‐electron/nine‐proton transfer process, its performance relies heavily on the adsorption ability of intermediates catalyst surface, which determined by geometric electronic configurations active sites. In this work, heteroatom ensemble effect deliberately triggered over RuFe bimetallic alloy to optimize intermediate NO RR. A record‐high yield rate 118.8 mg h −1 high Faradaic efficiency 92.2% are achieved −1.4 V vs reversible hydrogen electrode, ranking top state‐of‐the‐art. Experimental computational results reveal that characteristics induced play crucial roles. Both Ru Fe display continuous state throughout Fermi level, suggesting electron density benefits whole result, facilitated − , efficient stabilization key intermediates, as well timely desorption simultaneously achieved, thus significantly promoting direct .

Язык: Английский

Процитировано

76

H* Species Regulation by Mn‐Co(OH)2 for Efficient Nitrate Electro‐reduction in Neutral Solution DOI

Shaozhen Liang,

Teng Xue, Heng Xu

и другие.

Angewandte Chemie International Edition, Год журнала: 2024, Номер 63(11)

Опубликована: Янв. 23, 2024

Abstract During the electrocatalytic NO 3 − reduction reaction (NO RR) under neutral condition, activation of H 2 O to generate H* and inhibition inter‐H* species binding, are critically important but remain challenging for suppressing non‐desirable hydrogen evolution (HER). Here, a Mn‐doped Co(OH) (named as Mn‐Co(OH) ) has been synthesized by in situ reconstruction electrolyte, which is able dissociate molecules inhibits binding between each other owing increased interatomic spacing Mn‐doping. The electrocatalyst offers faradaic efficiency (FE) high 98.9±1.7% at −0.6 V vs. reversible electrode (RHE) an energy (EE) 49.90±1.03% NH production RR, among highest recently reported state‐of‐the‐art catalysts electrolyte. Moreover, negligible degradation −200 mA cm −2 found least 500 h, longest catalytic durations ever reported. This work paves novel approach design synthesis efficient RR electrocatalysts.

Язык: Английский

Процитировано

68

Tandem Electrocatalytic Nitrate Reduction to Ammonia on MBenes DOI
Guike Zhang, Xiaotian Li, Kai Chen

и другие.

Angewandte Chemie, Год журнала: 2023, Номер 135(13)

Опубликована: Фев. 3, 2023

Abstract We demonstrate the great feasibility of MBenes as a new class tandem catalysts for electrocatalytic nitrate reduction to ammonia (NO 3 RR). As proof concept, FeB 2 is first employed model MBene catalyst NO RR, showing maximum NH ‐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 − form intermediates, while Fe dissociate H O and increase *H supply on promote intermediate hydrogenation enhance ‐to‐NH conversion.

Язык: Английский

Процитировано

67

Atomically dispersed Cu coordinated Rh metallene arrays for simultaneously electrochemical aniline synthesis and biomass upgrading DOI Creative Commons

Qiqi Mao,

Mu Xu,

Wenxin Wang

и другие.

Nature Communications, Год журнала: 2023, Номер 14(1)

Опубликована: Сен. 14, 2023

Organic electrocatalytic conversion is an essential pathway for the green of low-cost organic compounds to high-value chemicals, which urgently demands development efficient electrocatalysts. Here, we report a Cu single-atom dispersed Rh metallene arrays on foam cathodic nitrobenzene electroreduction reaction and anodic methanol oxidation reaction. In coupled system, Cusingle-atom-Rh requires only low voltages 1.18 V reach current densities 100 mA cm-2 generating aniline formate, with up ~100% conversion/ selectivity over ~90% formate Faraday efficiency, achieving synthesis chemicals. Density functional theory calculations reveal electron effect between host catalytic mechanism. The synergistic H*-spillover can improve process reduce energy barrier process, thus enhancing activity target product selectivity.

Язык: Английский

Процитировано

62

Tandem Electrocatalytic Reduction of Nitrite to Ammonia on Rhodium–Copper Single Atom Alloys DOI

Jiaqi Xiang,

Chaofan Qiang,

Shiyao Shang

и другие.

Advanced Functional Materials, Год журнала: 2024, Номер 34(36)

Опубликована: Апрель 23, 2024

Abstract Electrocatalytic reduction of NO 2 − to NH 3 (NO RR) presents a fascinating approach for simultaneously migrating pollutants and producing valuable . In this study, single‐atom Rh‐alloyed copper (CuRh 1 ) is explored as highly active selective catalyst toward the RR. Combined theoretical calculations in situ FTIR/EPR spectroscopic experiments uncover synergistic effect Rh Cu promote RR energetics CuRh through tandem catalysis pathway, which activates preliminary adsorption hydrogenation → *NO *NOOH *NO), while generated on then transferred substrate promotes rate‐determining step *NHO synthesis. As result, equipped flow cell an unprecedented yield rate 2191.6 µmol h −1 cm −2 ‐Faradaic efficiency 98.9% at high current density 322.5 mA , well long‐term stability 100 electrolysis.

Язык: Английский

Процитировано

62

Main-group indium single-atom catalysts for electrocatalytic NO reduction to NH3 DOI
Kai Chen, Nana Zhang, Fuzhou Wang

и другие.

Journal of Materials Chemistry A, Год журнала: 2023, Номер 11(13), С. 6814 - 6819

Опубликована: Янв. 1, 2023

In single atoms confined in amorphous MoO 3 (In 1 /a-MoO ) are reported to be an efficient catalyst for NO electroreduction NH , attributed the ability of single-site inhibit hydrogen evolution and optimize NO-to-NH hydrogenation energetics.

Язык: Английский

Процитировано

58

Strategies and applications of electrocatalytic nitrate reduction towards ammonia DOI
Huijie Zhang,

K. Fang,

Jian Yang

и другие.

Coordination Chemistry Reviews, Год журнала: 2024, Номер 506, С. 215723 - 215723

Опубликована: Фев. 26, 2024

Язык: Английский

Процитировано

53

Electrochemical NO3 Reduction Catalyzed by Atomically Precise Ag30Pd4 Bimetallic Nanocluster: Synergistic Catalysis or Tandem Catalysis? DOI
Lubing Qin, Fang Sun,

Zhiheng Gong

и другие.

ACS Nano, Год журнала: 2023, Номер 17(13), С. 12747 - 12758

Опубликована: Июнь 28, 2023

Electrochemically converting NO3- compounds into ammonia represents a sustainable route to remove industrial pollutants in wastewater and produce valuable chemicals. Bimetallic nanomaterials usually exhibit better catalytic performance than the monometallic counterparts, yet unveiling reaction mechanism is extremely challenging. Herein, we report an atomically precise [Ag30Pd4 (C6H9)26](BPh4)2 (Ag30Pd4) nanocluster as model catalyst toward electrochemical reduction (eNO3-RR) elucidate different role of Ag Pd site unveil comprehensive mechanism. Ag30Pd4 homoleptic alkynyl-protected superatom with 2 free electrons, it has metal core where 4 atoms are located at subcenter core. Furthermore, exhibits excellent eNO3-RR robust stability for prolonged operation, can achieve highest Faradaic efficiency NH3 over 90%. In situ Fourier-transform infrared study revealed that plays more critical NO2-, while makes major contribution catalyze NO2- NH3. The bimetallic adopts tandem rather synergistic effect eNO3-RR. Such finding was further confirmed by density functional theory calculations, they disclosed most preferable binding NO3-, which then binds water molecule release NO2-. Subsequently, transfer vicinal exposed promote formation.

Язык: Английский

Процитировано

51