Achieving electronic structure reconfiguration in metallic carbides for robust electrochemical water splitting

2020 ◽  
Vol 8 (5) ◽  
pp. 2453-2462 ◽  
Author(s):  
Lulu Qiao ◽  
Anquan Zhu ◽  
Weixuan Zeng ◽  
Rui Dong ◽  
Pengfei Tan ◽  
...  

The electronic structure modification of metallic carbide is achieved by introducing dual-source transition metallic copper and cobalt atoms, thus contributing abundant active sites to afford decent water splitting performances.

2020 ◽  
Vol 10 (18) ◽  
pp. 6266-6273
Author(s):  
Yalan Zhang ◽  
Zebin Yu ◽  
Ronghua Jiang ◽  
Jung Huang ◽  
Yanping Hou ◽  
...  

Excellent electrochemical water splitting with remarkable durability can provide a solution to satisfy the increasing global energy demand in which the electrode materials play an important role.


Nanoscale ◽  
2021 ◽  
Author(s):  
Haibin Ma ◽  
ChangNing SUN ◽  
Zhili Wang ◽  
Qing Jiang

It is of great importance to develop efficient and low-cost oxygen evolution reaction (OER) electrocatalysts for electrochemical water splitting. Herein, S doped NiCoVOx nanosheets grown on Ni-Foam (S-NiCoVOx/NF) with modified...


Author(s):  
Cheng Wang ◽  
Hongyuan Shang ◽  
Hui Xu ◽  
Yukou Du

Non-noble-metal nanoboxes with abundant surface active sites, facilitated electron/mass transport, favorable synergistic effects and electronic effects, serving as promising candidate materials for boosting electrochemical water splitting.


Materials ◽  
2020 ◽  
Vol 13 (14) ◽  
pp. 3119
Author(s):  
Aniruddha Kundu ◽  
Akhmad Irhas Robby ◽  
Arnab Shit ◽  
Hyeong Jun Jo ◽  
Sung Young Park

Electrochemical water splitting is known as a potential approach for sustainable energy conversion; it produces H2 fuel by utilizing transition metal-based catalysts. We report a facile synthesis of FeCo2O4@carbon dots (CDs) nanoflowers supported on nickel foam through a hydrothermal technique in the absence of organic solvents and an inert environment. The synthesized material with a judicious choice of CDs shows superior performance in hydrogen and oxygen evolution reactions (HER and OER) compared to the FeCo2O4 electrode alone in alkaline media. For HER, the overpotential of 205 mV was able to produce current densities of up to 10 mA cm−2, whereas an overpotential of 393 mV was needed to obtain a current density of up to 50 mA cm−2 for OER. The synergistic effect between CDs and FeCo2O4 accounts for the excellent electrocatalytic activity, since CDs offer exposed active sites and subsequently promote the electrochemical reaction by enhancing the electron transfer processes. Hence, this procedure offers an effective approach for constructing metal oxide-integrated CDs as a catalytic support system to improve the performance of electrochemical water splitting.


Materials ◽  
2021 ◽  
Vol 14 (6) ◽  
pp. 1473
Author(s):  
Changhao Zhao ◽  
Fen Wei ◽  
Haolin Lv ◽  
Dengke Zhao ◽  
Nan Wang ◽  
...  

It remains an urgent demand and challenging task to design and fabricate efficient, stable, and inexpensive catalysts toward sustainable electrochemical water splitting for hydrogen production. Herein, we explored the use of Fe(III) ion-assisted aniline polymerization strategy to embed bimetallic CoFeP nanospheres into the nitrogen-doped porous carbon framework (referred CoFeP-NC). The as-prepared CoFeP-NC possesses excellent hydrogen evolution reaction (HER) performance with the small overpotential (η10) of 81 mV and 173 mV generated at a current density of 10 mA cm−2 in acidic and alkaline media, respectively. Additionally, it can also efficiently catalyze water oxidation (OER), which shows an ideal overpotential (η10) of 283 mV in alkaline electrolyte (pH = 14). The remarkable catalytic property of CoFeP-NC mainly stems from the strong synergetic effects of CoFeP nanospheres and carbon network. On the one hand, the interaction between the two can make better contact between the electrolyte and the catalyst, thereby providing a large number of available active sites. On the other hand, it can also form a network to offer better durability and electrical conductivity (8.64 × 10−1 S cm−1). This work demonstrates an efficient method to fabricate non-noble electrocatalyst towards overall water splitting, with great application prospect.


2022 ◽  
Vol 9 ◽  
Author(s):  
Jiabiao Yan ◽  
Mingkun Xia ◽  
Chenguang Zhu ◽  
Dawei Chen ◽  
Fanglin Du

Perovskite oxides have been established as a promising kind of catalyst for alkaline oxygen evolution reactions (OER), because of their regulated non-precious metal components. However, the surface lattice is amorphous during the reaction, which gradually decreases the intrinsic activity and stability of catalysts. Herein, the precisely control tungsten atoms substituted perovskite oxides (Pr0.5Ba0.5Co1-xWxO3-δ) nanowires were developed by electrostatic spinning. The activity and Tafel slope were both dependent on the W content in a volcano-like fashion, and the optimized Pr0.5Ba0.5Co0.8W0.2O3-δ exhibits both excellent activity and superior stability compared with other reported perovskite oxides. Due to the outermost vacant orbitals of W6+, the electronic structure of cobalt sites could be efficiently optimized. Meanwhile, the stronger W-O bond could also significantly improve the stability of latticed oxide atoms to impede the generation of surface amorphous layers, which shows good application value in alkaline water splitting.


2021 ◽  
Vol 23 (15) ◽  
pp. 9539-9552
Author(s):  
Afsaneh Zareie-Darmian ◽  
Hossein Farsi ◽  
Alireza Farrokhi ◽  
Reza Sarhaddi ◽  
Zhihai Li

In this paper, we demonstrate a combined theoretical and experimental study on the electronic structure, and the optical and electrochemical properties of β-Ag2MoO4 and Ag2O as significant Ag-containing compounds.


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