Daqin Guan, Hengyue Xu, Qingwen Zhang, Yu‐Cheng Huang, Chenliang Shi, Yu‐Chung Chang, Xiaomin Xu, Jiayi Tang, Yuxing Gu, Chih‐Wen Pao, Shu‐Chih Haw, Jin‐Ming Chen, Zhiwei Hu, Meng Ni, Zongping Shao

Identifying a Universal Activity Descriptor and a Unifying Mechanism Concept on Perovskite Oxides for Green Hydrogen Production

  • Mechanical Engineering
  • Mechanics of Materials
  • General Materials Science
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AbstractProducing indispensable hydrogen and oxygen for social development via water electrolysis shows more prospects than other technologies. Although electrocatalysts have been explored for centuries, a universal activity descriptor for both hydrogen‐evolution reaction (HER) and oxygen‐evolution reaction (OER) is not yet developed. Moreover, a unifying concept is not yet established to simultaneously understand HER/OER mechanisms. Here, the relationships between HER/OER activities in three common electrolytes and over ten representative material properties on 12 3d‐metal‐based model oxides are rationally bridged through statistical methodologies. The orbital charge‐transfer energy (Δ) can serve as an ideal universal descriptor, where a neither too large nor too small Δ (≈1 eV) with optimal electron‐cloud density around Fermi level affords the best activities, fulfilling Sabatier's principle. Systematic experiments and computations unravel that pristine oxide with Δ ≈ 1 eV possesses metal‐like high‐valence configurations and active lattice‐oxygen sites to help adsorb key protons in HER and induce lattice‐oxygen participation in the OER, respectively. After reactions, partially generated metals in the HER and high‐valence hydroxides in the OER dominate proton adsorption and couple with pristine lattice‐oxygen activation, respectively. These can be successfully rationalized by the unifying orbital charge‐transfer theory. This work provides the foundation of rational material design and mechanism understanding for many potential applications.

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