Industrial wastewater rich in nitrite and anthropogenic CO2 emissions are typically treated as separate waste streams, requiring energy‐intensive management. Here we report an electrochemical strategy that couples nitrite and carbon dioxide to synthesize urea, enabling simultaneous pollution mitigation and resource recovery. An erbium‐doped copper nanocatalyst is developed to promote selective C─N coupling, delivering a urea yield of 510.29 mg h−1 gcat−1 with a Faradaic efficiency of 34.04%. At the same time, higher removal rate of nitrite can be achieved and sustained performance over repeated cycles. The mechanism reveals that Er doping can adjust the adsorption behavior of intermediate substances at Cu interface, make the upward shift of the d‐band center of Cu, enhance the adsorption of *CO2 and *NH2 at the active site of Cu, reduce the energy barrier formed of the C─N coupling step *CO2NH2, and reduce the energy barrier of thermodynamically limiting step *COOHNH2 formation, and promote the synthesis of urea. Beyond catalytic performance, the resulting electrolyte can be directly reused for irrigation, where it enhances early‐stage growth of crops, demonstrating a closed‐loop integration of carbon and nitrogen utilization. This work establishes a proof‐of‐concept for transforming coupled waste streams into value‐added chemicals while linking electrochemical conversion with agricultural application. The approach provides a scalable pathway toward circular carbon‐nitrogen management and sustainable environmental remediation.
The electrocatalytic co-reduction of CO2 and nitrate to urea offers a sustainable route for carbon fixation, nitrogen waste recycling, and high-value chemical production. However, the rational design of efficient electrocatalysts with synergistic activation capability toward both reactants and the ability to suppress s...
The sustainable management of trace emerging contaminants (ECs) is essential for safeguarding water resources and achieving global carbon-neutrality targets. To address the bottleneck of high energy-consumption and carbon emission caused by the non-selective oxidation of complex organics in conventional advanced oxidat...
Metal–organic frameworks (MOF) and conventional bioadsorbents, such as UiO‐66‐NH
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and poplar cellulose fibers (PCF), often suffer inefficient charge separation, limited uranium binding affinity, and severe biofouling, restricting their performance in seawater. Here, we report a cellulose‐based aerogel catalyst i...
The increasing discharge of ammonium‐rich wastewater has become a critical challenge for aquatic ecosystems and sustainable nitrogen management, creating an urgent need for efficient NH4+ removal and recovery technologies. Among emerging electrochemical approaches, capacitive deionization (CDI) is attractive because of...
He Liu, Yu-Xin Zhang, Su-Wan Yang et al.· Advanced Functional Material...· 0 citations
Recovering ammonium from wastewater is a promising strategy to mitigate nitrogen pollution and close the anthropogenic nitrogen cycle. Electrosorption offers a green recovery route but suffers from low selectivity and capacity in complex aqueous matrices. Herein, we report a phosphate-functionalized WO3 (PWO)-based Far...
R. Wei, Peng Xu, Yan-Biao Liu et al.· Environmental Science and Te...· 0 citations
Odor pollution caused by low-concentration volatile organic sulfur compounds (VOSCs) pose a persistent challenge in air quality management, and their complex interactions with co-existing air pollutants or oxidation products during photocatalytic process remained underexplored. In this work, SO42-, a common particulate...
Qian Li, Hong-Wei Xu, Da Li et al.· Journal of Hazardous Materia...· 0 citations
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