TY - JOUR
T1 - Plasmon-Assisted Ammonia Electrosynthesis
AU - Contreras, Enrique
AU - Nixon, Rachel
AU - Litts, Chloe
AU - Zhang, Wenxin
AU - Alcorn, Francis M.
AU - Jain, Prashant K.
N1 - This material is based on the work supported by the National Science Foundation under grant no. NSF CHE-1455011. W.Z. was supported by a Strategic Research Initiative (P.K.J.) of the UIUC Grainger College of Engineering. F.A. was supported by a Future Interdisciplinary Research Explorations (FIRE) award (P.K.J.) from the UIUC College of Agricultural, Consumer, and Environmental Sciences. Portions of this work were conducted at the Materials Research Laboratory and the School of Chemical Sciences NMR Laboratory at UIUC.
PY - 2022/6/22
Y1 - 2022/6/22
N2 - Ammonia is a promising liquid-phase carrier for the storage, transport, and deployment of carbon-free energy. However, the realization of an ammonia economy is predicated on the availability of green methods for the production of ammonia powered by electricity from renewable sources or by solar energy. Here, we demonstrate the synthesis of ammonium from nitrate powered by a synergistic combination of electricity and light. We use an electrocatalyst composed of gold nanoparticles, which have dual attributes of electrochemical nitrate reduction activity and visible-light-harvesting ability due to their localized surface plasmon resonances. Plasmonic excitation of the electrocatalyst induces ammonium synthesis with up to a 15× boost in activity relative to conventional electrocatalysis. We devise a strategy to account for the effect of photothermal heating of the electrode surface, which allows the observed enhancement to be attributed to non-thermal effects such as energetic carriers and charged interfaces induced by plasmonic excitation. The synergy between electrochemical activation and plasmonic activation is the most optimal at a potential close to the onset of nitrate reduction. Plasmon-assisted electrochemistry presents an opportunity for conventional limits of electrocatalytic conversion to be surpassed due to non-equilibrium conditions generated by plasmonic excitation.
AB - Ammonia is a promising liquid-phase carrier for the storage, transport, and deployment of carbon-free energy. However, the realization of an ammonia economy is predicated on the availability of green methods for the production of ammonia powered by electricity from renewable sources or by solar energy. Here, we demonstrate the synthesis of ammonium from nitrate powered by a synergistic combination of electricity and light. We use an electrocatalyst composed of gold nanoparticles, which have dual attributes of electrochemical nitrate reduction activity and visible-light-harvesting ability due to their localized surface plasmon resonances. Plasmonic excitation of the electrocatalyst induces ammonium synthesis with up to a 15× boost in activity relative to conventional electrocatalysis. We devise a strategy to account for the effect of photothermal heating of the electrode surface, which allows the observed enhancement to be attributed to non-thermal effects such as energetic carriers and charged interfaces induced by plasmonic excitation. The synergy between electrochemical activation and plasmonic activation is the most optimal at a potential close to the onset of nitrate reduction. Plasmon-assisted electrochemistry presents an opportunity for conventional limits of electrocatalytic conversion to be surpassed due to non-equilibrium conditions generated by plasmonic excitation.
UR - https://www.scopus.com/pages/publications/85132454670
UR - https://www.scopus.com/pages/publications/85132454670#tab=citedBy
U2 - 10.1021/jacs.2c01272
DO - 10.1021/jacs.2c01272
M3 - Article
C2 - 35671395
AN - SCOPUS:85132454670
SN - 0002-7863
VL - 144
SP - 10743
EP - 10751
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 24
ER -