Direct ammonia and dihydroxyacetone production in an unbiased photoelectrochemical cell
Xiaotian Guo,
Rui-Ting Gao (),
Shijie Ren,
Nhat Truong Nguyen,
Haojie Chen,
Limin Wu () and
Lei Wang ()
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Xiaotian Guo: Inner Mongolia University
Rui-Ting Gao: Inner Mongolia University
Shijie Ren: Inner Mongolia University
Nhat Truong Nguyen: Concordia University
Haojie Chen: Inner Mongolia University
Limin Wu: Inner Mongolia University
Lei Wang: Inner Mongolia University
Nature Communications, 2025, vol. 16, issue 1, 1-12
Abstract:
Abstract Photoelectrochemical production of ammonia usually suffers from a low solar-to-ammonia efficiency and a high overpotential, which influences the bias-free operation of sustainable photoelectrochemistry. Herein, we realize solar-driven ammonia production from waste nitrate by constructing copper-osmium catalysts deposited on the Sb2(S,Se)3 semiconductor, enabling optimized photo-carrier transport pathways and a beneficial co-adsorption configuration of *NO3-H2O moieties. The photocathode reaches a photocurrent density of 5.6 mA cm−2 at 0 VRHE with a low onset potential of 0.86 VRHE and a Faradaic efficiency of 96.98% at 0.6 VRHE under AM 1.5 G illumination. We further employ glycerol oxidation reaction on ruthenium doped bismuth oxide catalyst decorated on titanium oxide photoanode, requiring an onset potential of 0.3 VRHE to enable bias-free operation. The unbiased photoelectrochemical system shows Faradaic efficiencies of over 97% for ammonia products and above 77% for glycerol oxidation product under AM 1.5 G illumination. The large-sized photoelectrodes maintain a stability for 24 h without noticeable degradation. Our works indicate that unassisted and stable PEC ammonia production is feasible with in situ glycerol valorization using the photoanode and photocathode.
Date: 2025
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DOI: 10.1038/s41467-025-61080-x
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