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Interfacial Accumulation and Stability Enhancement Effects Triggered by Built-in Electric Field of SnO 2 /LaOCl Nanofibers Boost Carbon Dioxide Electroreduction
Constructing a built-in interfacial electric field (BIEF) is an effective approach to enhance the electrocatalysts performance, but it has been rarely demonstrated for electrochemical carbon dioxide reduction reaction (CO RR) to date. Herein, for the first time, SnO /LaOCl nanofibers (NFs) with BIEF...
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Published in: | Small (Weinheim an der Bergstrasse, Germany) Germany), 2024-10, Vol.20 (40), p.e2402654 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Constructing a built-in interfacial electric field (BIEF) is an effective approach to enhance the electrocatalysts performance, but it has been rarely demonstrated for electrochemical carbon dioxide reduction reaction (CO
RR) to date. Herein, for the first time, SnO
/LaOCl nanofibers (NFs) with BIEF is created by electrospinning, exhibiting a high Faradaic efficiency (FE) of 100% C
product (CO and HCOOH) at -0.9--1.1 V versus reversible hydrogen electrode (RHE) and a maximum FE
of 90.1% at -1.2 V
in H-cell, superior to the commercial SnO
nanoparticles (NPs) and LaOCl NFs. SnO
/LaOCl NFs also exhibit outstanding stability, maintaining negligible activity degradation even after 10 h of electrolysis. Moreover, their current density and FE
are almost 400 mA cm
at -2.31 V and 83.4% in flow-cell. The satisfactory CO
RR performance of SnO
/LaOCl NFs with BIEF can be ascribed to tight interface of coupling SnO
NPs and LaOCl NFs, which can induce charge redistribution, rich active sites, enhanced CO
adsorption, as well as optimized Gibbs free energy of *OCHO. The work reveals that the BIEF will trigger interfacial accumulation and stability enhancement effects in promoting CO
RR activity and stability of SnO
-based materials, providing a novel approach to develop stable and efficient CO
RR electrocatalysts. |
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ISSN: | 1613-6810 1613-6829 |
DOI: | 10.1002/smll.202402654 |