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Static Organic p-n Junctions in Photoelectrodes for Solar Ammonia Production with 86 % Internal Quantum Efficiency.
Fang, Yanjie; Li, Mengjie; Gao, Yifan; Wen, Yingke; Shan, Bing.
Afiliação
  • Fang Y; Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
  • Li M; Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
  • Gao Y; Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
  • Wen Y; Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
  • Shan B; Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
Angew Chem Int Ed Engl ; : e202415729, 2024 Sep 18.
Article em En | MEDLINE | ID: mdl-39294096
ABSTRACT
For photoelectrocatalytic cells, a limitation exists in finding appropriate photoelectrode configurations that couple efficient extraction of high-energy electrons from absorbed photons and selective catalysis. Here we report an organic p-n junction approach to fabricate molecular photoelectrodes for conversion of solar energy and nitrate into valuable ammonia product. Solar irradiation of the photoelectrode generates charge-separated states with electrons and holes spatially separated at the n-type and p-type components, as revealed by surface photovoltage mapping, at a quantum yield of 90 %. The high-flux photogenerated electrons are rapidly transferred to the catalyst for solar ammonia production from nitrate reduction at an external quantum efficiency (EQE) and an internal quantum efficiency (IQE) of 57 % and 86 %, respectively. Time-resolved spectroscopic studies reveal that the large IQE originates from the combined high efficiencies for photoelectron generation, catalyst activation and dark catalysis. In a flow-cell setup coupled with a silicon solar cell, the photoelectrode without bias generates photocurrent of 57 mA cm-2 and ammonia at an EQE of 52 %.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article