An amorphous cobalt–cobalt oxide/cobalt selenide composite film has been fabricated directly on a 3D macro-porous Ni foam substrate by a facile electrodeposition method, which can be an efficient and cheap bifunctional electrocatalyst for both the OER and HER and offer potential applications in the field of full water splitting.

Developing cost‐effective and high‐performance catalysts for oxygen evolution reaction (OER) is essential to improve the efficiency of electrochemical conversion devices. Unfortunately, current studies greatly depend on empirical exploration and ignore the inherent relationship between electronic structure and catalytic activity, which impedes the rational design of high‐efficiency OER catalysts. Herein, a series of bimetallic Ni‐based metal‐organic frameworks (Ni‐M‐MOFs, M = Fe, Co, Cu, Mn, and Zn) with well‐defined morphology and active sites are selected as the ideal platform to explore the electronic‐structure/catalytic‐activity relationship. By integrating density‐functional theory calculations and experimental measurements, a volcano‐shaped relationship between electronic properties (d‐band center and eg filling) and OER activity is demonstrated, in which the NiFe‐MOF with the optimized energy level and electronic structure situated closer to the volcano summit. It delivers ultra‐low overpotentials of 215 and 297 mV for 10 and 500 mA cm−2, respectively. The identified electronic‐structure/catalytic activity relationship is found to be universal for other Ni‐based MOF catalysts (e.g., Ni‐M‐BDC‐NH2, Ni‐M‐BTC, Ni‐M‐NDC, Ni‐M‐DOBDC, and Ni‐M‐PYDC). This work widens the applicability of d band center and eg filling descriptors to activity prediction of MOF‐based electrocatalysts, providing an insightful perspective to design highly efficient OER catalysts.

A promising Ca doping approach was reported to improve the durability and electrocatalytic OER activity of the perovskite PrBaCoO (PBC). Compared to the pristine PBC, the electrocatalytic activity of Ca-doped PrBaCaCoO perovskite was increased by ca. 90%. More importantly, its durability was significantly enhanced after doping with calcium.

This review article deals with the challenge to identify catalyst materials from literature studies for the ammonia decomposition reaction with potential for application in large-scale industrial processes. On the one hand, the requirements on the catalyst are quite demanding. Of central importance are the conditions for the primary reaction that have to be met by the catalyst. Likewise, the catalytic performance, i.e., an ideally quantitative conversion, and a high lifetime are critical as well as the consideration of requirements on the product properties in terms of pressure or by-products for potential follow-up processes, in this case synthesis gas applications. On the other hand, the evaluation of the multitude of literature studies poses difficulties due to significant varieties in catalytic testing protocols.