TY - JOUR
T1 - Exploring Bi2Te3 Nanoplates as Versatile Catalysts for Electrochemical Reduction of Small Molecules
AU - Zhang, Nan
AU - Zheng, Fangfang
AU - Huang, Bolong
AU - Ji, Yujin
AU - Shao, Qi
AU - Li, Youyong
AU - Xiao, Xiangheng
AU - Huang, Xiaoqing
N1 - Funding Information:
N.Z., F.Z., and B.H. contributed equally to this work. This work was financially supported by the Ministry of Science and Technology (2016YFA0204100, 2017YFA0208200), the National Natural Science Foundation of China (21571135), Young Thousand Talented Program, Natural Science Foundation of Jiangsu Higher Education Institutions (17KJB150032), the project of scientific and technologic infrastructure of Suzhou (SZS201708), the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), and the start-up supports from Soochow University.
Publisher Copyright:
© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2020/6/1
Y1 - 2020/6/1
N2 - The electroreduction of small molecules to high value-added chemicals is considered as a promising way toward the capture and utilization of atmospheric small molecules. Discovering cheap and efficient electrocatalysts with simultaneously high activity, selectivity, durability, and even universality is desirable yet challenging. Herein, it is demonstrated that Bi2Te3 nanoplates (NPs), cheap and noble-metal-free electrocatalysts, can be adopted as highly universal and robust electrocatalysts, which can efficiently reduce small molecules (O2, CO2, and N2) into targeted products simultaneously. They can achieve excellent activity, selectivity and durability for the oxygen reduction reaction with almost 100% H2O2 selectivity, the CO2 reduction reaction with up to 90% Faradaic efficiency (FE) of HCOOH, and the nitrogen reduction reaction with 7.9% FE of NH3. After electrochemical activation, an obvious Te dissolution happens on the Bi2Te3 NPs, creating lots of Te vacancies in the activated Bi2Te3 NPs. Theoretical calculations reveal that the Te vacancies can modulate the electronic structures of Bi and Te. Such a highly electroactive surface with a strong preference in supplying electrons for the universal reduction reactions improves the electrocatalytic performance of Bi2Te3. The work demonstrates a new class of cheap and versatile catalysts for the electrochemical reduction of small molecules with potential practical applications.
AB - The electroreduction of small molecules to high value-added chemicals is considered as a promising way toward the capture and utilization of atmospheric small molecules. Discovering cheap and efficient electrocatalysts with simultaneously high activity, selectivity, durability, and even universality is desirable yet challenging. Herein, it is demonstrated that Bi2Te3 nanoplates (NPs), cheap and noble-metal-free electrocatalysts, can be adopted as highly universal and robust electrocatalysts, which can efficiently reduce small molecules (O2, CO2, and N2) into targeted products simultaneously. They can achieve excellent activity, selectivity and durability for the oxygen reduction reaction with almost 100% H2O2 selectivity, the CO2 reduction reaction with up to 90% Faradaic efficiency (FE) of HCOOH, and the nitrogen reduction reaction with 7.9% FE of NH3. After electrochemical activation, an obvious Te dissolution happens on the Bi2Te3 NPs, creating lots of Te vacancies in the activated Bi2Te3 NPs. Theoretical calculations reveal that the Te vacancies can modulate the electronic structures of Bi and Te. Such a highly electroactive surface with a strong preference in supplying electrons for the universal reduction reactions improves the electrocatalytic performance of Bi2Te3. The work demonstrates a new class of cheap and versatile catalysts for the electrochemical reduction of small molecules with potential practical applications.
KW - Bi Te nanoplates
KW - carbon dioxide reduction reaction
KW - electrocatalysts
KW - nitrogen reduction reaction
KW - oxygen reduction reaction
UR - http://www.scopus.com/inward/record.url?scp=85083843418&partnerID=8YFLogxK
U2 - 10.1002/adma.201906477
DO - 10.1002/adma.201906477
M3 - Journal article
AN - SCOPUS:85083843418
SN - 0935-9648
VL - 32
JO - Advanced Materials
JF - Advanced Materials
IS - 22
M1 - 1906477
ER -