Cooperative interaction between Cu and sulfur vacancies in SnS2 nanoflowers for highly efficient nitrate electroreduction to ammonia. Issue 4 (10th January 2023)
- Record Type:
- Journal Article
- Title:
- Cooperative interaction between Cu and sulfur vacancies in SnS2 nanoflowers for highly efficient nitrate electroreduction to ammonia. Issue 4 (10th January 2023)
- Main Title:
- Cooperative interaction between Cu and sulfur vacancies in SnS2 nanoflowers for highly efficient nitrate electroreduction to ammonia
- Authors:
- Li, Heen
Xu, Xiaoyue
Lin, Xiaohu
Chen, Shuheng
He, Maoyue
Peng, Fei
Gao, Faming - Abstract:
- Abstract : In this work, co-introduced Cu and sulfur vacancies cooperate to improve the NO3 RR performance of pristine–SnS2 . Cu-doped SnS2 with abundant sulfur vacancies (Cu-SnS2− x ) achieves a superior NH3 yield of 0.63 mmol h −1 mgcat −1 and faradaic efficiency of 93.8% at −0.7 V vs. RHE. Abstract : Achieving high efficiency in nitrate (NO3 − ) to ammonia (NH3 ) electrocatalysis requires the exploration of advanced electrocatalysts with a well-designed composition. In this work, a facile one-step hydrothermal method was applied for the construction of novel Cu doped SnS2 nanoflowers with rich sulfur vacancies (Cu-SnS2− x ). Two-dimensional Cu-SnS2− x nanosheet arrays could increase the exposure of catalytically active metal centers due to the Cu doping strategy and the generated sulfur vacancies are able to synergistically improve the electrocatalytic activity over the metal active centers. Benefiting from the cooperative interaction between Cu and S, Cu-SnS2− x nanoflowers achieved excellent performance for nitrate reduction to ammonia with a superior NH3 yield (0.63 mmol h −1 mgcat −1 ) and faradaic efficiency (93.8%) at −0.7 V ( vs. RHE), which are almost twice those of pristine SnS2 . 15 N isotope labeling experiments further verify that the source of the produced ammonia is Cu-SnS2− x . DFT calculations demonstrated that sulfur vacancies cause free electron transfer to Sn, which enhances the adsorption capacity and the Cu can further regulate the electronAbstract : In this work, co-introduced Cu and sulfur vacancies cooperate to improve the NO3 RR performance of pristine–SnS2 . Cu-doped SnS2 with abundant sulfur vacancies (Cu-SnS2− x ) achieves a superior NH3 yield of 0.63 mmol h −1 mgcat −1 and faradaic efficiency of 93.8% at −0.7 V vs. RHE. Abstract : Achieving high efficiency in nitrate (NO3 − ) to ammonia (NH3 ) electrocatalysis requires the exploration of advanced electrocatalysts with a well-designed composition. In this work, a facile one-step hydrothermal method was applied for the construction of novel Cu doped SnS2 nanoflowers with rich sulfur vacancies (Cu-SnS2− x ). Two-dimensional Cu-SnS2− x nanosheet arrays could increase the exposure of catalytically active metal centers due to the Cu doping strategy and the generated sulfur vacancies are able to synergistically improve the electrocatalytic activity over the metal active centers. Benefiting from the cooperative interaction between Cu and S, Cu-SnS2− x nanoflowers achieved excellent performance for nitrate reduction to ammonia with a superior NH3 yield (0.63 mmol h −1 mgcat −1 ) and faradaic efficiency (93.8%) at −0.7 V ( vs. RHE), which are almost twice those of pristine SnS2 . 15 N isotope labeling experiments further verify that the source of the produced ammonia is Cu-SnS2− x . DFT calculations demonstrated that sulfur vacancies cause free electron transfer to Sn, which enhances the adsorption capacity and the Cu can further regulate the electron distribution and stabilization intermediates, leading to a high ammonia yield and faradaic efficiency. The present study opens new avenues for the rational construction of efficient electrocatalysts for the synthesis of ammonia from nitrate. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 11:Issue 4(2023)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 11:Issue 4(2023)
- Issue Display:
- Volume 11, Issue 4 (2023)
- Year:
- 2023
- Volume:
- 11
- Issue:
- 4
- Issue Sort Value:
- 2023-0011-0004-0000
- Page Start:
- 2014
- Page End:
- 2022
- Publication Date:
- 2023-01-10
- Subjects:
- Materials -- Research -- Periodicals
Chemistry, Analytic -- Periodicals
Environmental sciences -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/ta ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2ta08095h ↗
- Languages:
- English
- ISSNs:
- 2050-7488
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205100
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 26011.xml