scholarly journals Microenvironment modulation of single-atom catalysts and their roles in electrochemical energy conversion

2020 ◽  
Vol 6 (39) ◽  
pp. eabb6833 ◽  
Author(s):  
Xuning Li ◽  
Linghui Liu ◽  
Xinyi Ren ◽  
Jiajian Gao ◽  
Yanqiang Huang ◽  
...  

Single-atom catalysts (SACs) have become the most attractive frontier research field in heterogeneous catalysis. Since the atomically dispersed metal atoms are commonly stabilized by ionic/covalent interactions with neighboring atoms, the geometric and electronic structures of SACs depend greatly on their microenvironment, which, in turn, determine the performances in catalytic processes. In this review, we will focus on the recently developed strategies of SAC synthesis, with attention on the microenvironment modulation of single-atom active sites of SACs. Furthermore, experimental and computational advances in understanding such microenvironment in association to the catalytic activity and mechanisms are summarized and exemplified in the electrochemical applications, including the water electrolysis and O2/CO2/N2 reduction reactions. Last, by highlighting the prospects and challenges for microenvironment engineering of SACs, we wish to shed some light on the further development of SACs for electrochemical energy conversion.

JACS Au ◽  
2021 ◽  
Author(s):  
Florian D. Speck ◽  
Jae Hyung Kim ◽  
Geunsu Bae ◽  
Sang Hoon Joo ◽  
Karl J. J. Mayrhofer ◽  
...  

2021 ◽  
pp. 2102801
Author(s):  
Yufei Zhao ◽  
Wen‐Jie Jiang ◽  
Jinqiang Zhang ◽  
Emma C. Lovell ◽  
Rose Amal ◽  
...  

Author(s):  
Regina Kluge ◽  
Richard W. Haid ◽  
Ifan Stephens ◽  
Federico Calle-Vallejo ◽  
Aliaksandr Bandarenka

Carbon is ubiquitous as an electrode material in electrochemical energy conversion devices. If used as support material, the evolution of H2 is undesired on carbon. However, recently carbon-based materials are...


2021 ◽  
Vol 13 (1) ◽  
Author(s):  
Xin Wu ◽  
Huabin Zhang ◽  
Shouwei Zuo ◽  
Juncai Dong ◽  
Yang Li ◽  
...  

AbstractReducing the dimensions of metallic nanoparticles to isolated, single atom has attracted considerable attention in heterogeneous catalysis, because it significantly improves atomic utilization and often leads to distinct catalytic performance. Through extensive research, it has been recognized that the local coordination environment of single atoms has an important influence on their electronic structures and catalytic behaviors. In this review, we summarize a series of representative systems of single-atom catalysts, discussing their preparation, characterization, and structure–property relationship, with an emphasis on the correlation between the coordination spheres of isolated reactive centers and their intrinsic catalytic activities. We also share our perspectives on the current challenges and future research promises in the development of single-atom catalysis. With this article, we aim to highlight the possibility of finely tuning the catalytic performances by engineering the coordination spheres of single-atom sites and provide new insights into the further development for this emerging research field.


2021 ◽  
Vol 7 (13) ◽  
pp. eabf3989
Author(s):  
Jiong Wang ◽  
Shuo Dou ◽  
Xin Wang

Heterogeneous molecular catalysts based on transition metal complexes have received increasing attention for their potential application in electrochemical energy conversion. The structural tuning of first and second coordination spheres of complexes provides versatile strategies for optimizing the activities of heterogeneous molecular catalysts and appropriate model systems for investigating the mechanism of structural variations on the activity. In this review, we first discuss the variation of first spheres by tuning ligated atoms; afterward, the structural tuning of second spheres by appending adjacent metal centers, pendant groups, electron withdrawing/donating, and conjugating moieties on the ligands is elaborated. Overall, these structural tuning resulted in different impacts on the geometric and electronic configurations of complexes, and the improved activity is achieved through tuning the stability of chemisorbed reactants and the redox behaviors of immobilized complexes.


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