Boosting electrocatalytic ammonia synthesis from nitrate by asymmetric chemical potential activated interfacial electric fields.

J Colloid Interface Sci

Center of Materials Science and Optoelectronics Engineering, Chinese Academy of Sciences, Beijing 100049, PR China; CAS Key Laboratory of Green Process and Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, PR China; Key Laboratory of Green and High-value Uti

Published: December 2024


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

The electrocatalytic nitrate reduction reaction (NO RR) has immense potential to alleviate the problem of groundwater pollution and may also become a key route for the environmentally benign production of ammonia (NH) products. Here, the unique effects of interfacial electric fields arising from asymmetric chemical potentials and local defects were integrated into the binary BiS-BiO sublattices for enhancing electrocatalytic nitrate reduction reactions. The obtained binary system showed a superior Faraday efficiency (FE) for ammonia production of 94 % and an NH yield rate of 89.83 mg gh at -0.4 V vs. RHE. Systematic experimental and computational results confirmed that the concerted interplay between interfacial electric fields and local defects not only promoted the accumulation and adsorption of NO, but also contributed to the destabilization of *NO and the subsequent deoxygenation hydrogenation reaction. This work will stimulate future designs of heterostructured catalysts for efficient electrocatalytic nitrate reduction reactions.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jcis.2024.07.164DOI Listing

Publication Analysis

Top Keywords

interfacial electric
12
electric fields
12
electrocatalytic nitrate
12
nitrate reduction
12
asymmetric chemical
8
local defects
8
reduction reactions
8
boosting electrocatalytic
4
electrocatalytic ammonia
4
ammonia synthesis
4

Similar Publications

The poor foaming of egg yolks has long plagued the food industry. In this study, four egg yolk spheres (EYS) were prepared via acid- and alkaline pH-shift methods, and the main factors affecting the variation in their foaming capacity were determined. The tertiary structure of EYS under hydrogen bonding and electrostatic interactions unfolded in acidic shifts, exposing many functional groups, and refolded in basic shifts and exposed hydrophobic side chains.

View Article and Find Full Text PDF

On-liquid surface synthesis of diyne-linked two-dimensional polymer crystals.

Nat Commun

September 2025

Center for Advancing Electronics Dresden & Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, Dresden, Germany.

The synthesis of thin crystalline two-dimensional polymers (2DPs) typically relies on reversible dynamic covalent reactions. While substantial progress has been made in solution-based and interfacial syntheses, achieving 2DPs through irreversible carbon-carbon coupling reactions remains a formidable challenge. Herein, we present an on-liquid surface (a mixture of N,N-dimethylacetamide and water, DMAc-HO) synthesis method for constructing diyne-linked 2DP (DY2DP) crystals via Glaser coupling, assisted by a perfluoro-surfactant (PFS) monolayer.

View Article and Find Full Text PDF

Lanthanum-Induced Gradient Fields in Asymmetric Heterointerface Catalysts for Enhanced Oxygen Electrocatalysis.

Adv Mater

September 2025

KU-KIST Graduate School of Converging Science and Technology, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul, 02841, Republic of Korea.

Metal-nitrogen-carbon (M-N-C) catalysts display considerable potential as cost-effective alternatives to noble metals in oxygen electrocatalysis. However, uncontrolled atomic migration and random structural rearrangement during pyrolysis often lead to disordered coordination environments and sparse active sites, fundamentally limiting their intrinsic catalytic activities and long-term durability. Herein, a novel strategy is reported for use in directionally regulating atomic migration pathways via the incorporation of a foreign metal (La).

View Article and Find Full Text PDF

Cation Dehydration by Surface-Grafted Phenyl Groups for Enhanced C Production in Cu-Catalyzed Electrochemical CO Reduction.

J Am Chem Soc

September 2025

Laboratory of Inorganic Synthesis and Catalysis (LSCI), Institute of Chemical Sciences and Engineering, École Polytechnique Fédéralede Lausanne (EPFL), Lausanne 1015, Switzerland.

The challenge to produce multicarbon (C) products in high current densities in the electrochemical reduction of carbon dioxide (CORR) has motivated intense research. However, the ability of solvated cations to tune and activate water for C production in the CORR has been overlooked. In this study, we report the incorporation of a covalently grown layer of functionalized phenyl groups on the Cu surface that leads to a 7-fold increase in ethylene production (to -530 mA cm) and a 6-fold increase in C products (to -760 mA cm).

View Article and Find Full Text PDF

Cycloaliphatic epoxy resin (CEP) is a promising candidate for rigid housings in high-voltage composite insulators due to its superior hardness, water resistance, and interfacial adhesion compared with conventional high-temperature vulcanized silicone rubber (HTV-SR). However, the long-term insulation degradation mechanisms of CEP under corona discharge are still not fully understood. In this study, CEP, HTV-SR, and glass fiber-reinforced epoxy (GFRP) were subjected to AC corona aging using a multi-needle plate electrode.

View Article and Find Full Text PDF