The overuse of nitrate has led to the accumulation in natural water, being a globe issue in environment and human health. Electrochemical NO3- reduction reaction (eNO3RR) to ammonia occurs under ambient condition with low energy consumption and the yield of value-added product, being promising for NO3- removal. Cu(I)-based eNO3RR catalysts suffer from unavoidable oxidation reconstruction to Cu(II), reducing the performance of NO3- removal. In this work, we demonstrate charge compensation strategy to resist oxidation reconstruction of Cu(I)-based eNO3RR catalysts by introducing self-recycled electron donor. Taking Ti(III)-modified Cu2O/Cu as the proof-of-concept model, electron donor Ti(III) can donate electron to Cu(II) to regenerate Cu(I), meanwhile the expended Ti(III) can be recycled from the generated Ti(IV) via intervalence charge transfer (IVCT). Benefiting from those, Ti-Cu2O/Cu-10 exhibits significantly improved activity and durability for NO3- removal compared to Cu2O/Cu. The percentage of NO3- removal keeps at ∼95.0 % with the initial concentration of 60 mg•L-1 NO3--N at -0.9 V vs. RHE in 15 consecutive cycling tests (corresponding to 30 h). This work presents a feasible strategy to resist oxidation reconstruction of Cu(I)-based eNO3RR catalysts, making NO3- removal more effective, more durable, and more sustainable.
Keywords: Charge compensation; Cu-based electrocatalyst; NO(3)RR; Oxidation reconstruction; Self-recycled electron donor.
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