Developing efficient and low‐cost replacements for precious metals as electrocatalysts active in electrochemical reactions—the oxygen evolution reaction (OER), hydrogen evolution reaction (HER), and oxygen reduction reaction (ORR)—is a top priority in renewable energy technology. In this work a highly active and very stable trifunctional electrocatalyst composed of Co2P embedded in Co, N, and P multi‐doped carbon has been synthesized using zeolitic imidazolate frameworks as precursors. The synergistic effects between Co2P and the multi‐heteroatom‐doped carbon substrates afford materials having electrocatalytic activities for HER, OER, and ORR, which are comparable—or even superior to—those of commercial RuO2 or Pt/C catalysts. Density functional theory calculations show that Co2P has a higher density of states at the Fermi level than ConP (0 < n < 2), which promotes electron transfer and intermediates adsorption in the catalytic process. Zinc–air batteries and water splitting devices assembled using the materials as electrode electrocatalysts show good performance and outstanding stability. This work represents a breakthrough in improving the catalytic performance of non‐precious metal electrocatalysts for OER, HER, and ORR, and opens new avenues for clean energy generation.

This review provides a timely and comprehensive overview of the recent progresses in the synthesis and application of phthalocyanine-based heterogeneous electrocatalysts, as well as the structure/composition–catalytic activity relationship, and future prospects.

Two‐dimensional conjugated aromatic networks (CAN) with ultra‐thin conjugated layers (ca. 3.5 nm) and high single‐metal‐atom‐site density (mass content of 10.7 wt %, and 0.73 metal atoms per nm2) are prepared via a facile pyrolysis‐free route involving a one‐step ball milling of the solid‐phase‐synthesized polyphthalocyanine. These materials display outstanding oxygen reduction reaction (ORR) mass activity of 47 mA mgcat.−1 represents 1.3‐ and 6.4‐fold enhancements compared to Pt and Pt/C in benchmark Pt/C, respectively. Moreover, the primary Zn‐air batteries constructed with CAN as an air electrode demonstrate a mass/volume power density of 880 W gcat.−1/615 W cmcat.−3 and stable long‐term operation for 100 h. This strategy offers a new way to design high‐performance electrocatalysts with atomic precision for use in other energy‐storage and conversion applications.

Although carbon is the second most abundant element in the biosphere, a large proportion of the available carbon resources in biomass from agriculture, stock farming, ocean fisheries, and other human activities is currently wasted. The use of sustainable carbonaceous materials as an alternative to precious metals in electrocatalysis is a promising pathway for transforming sustainable biomass resources into sustainable energy‐conversion systems. The development of rational syntheses of metal‐free carbonaceous catalysts derived from sustainable biomass has therefore become a topic of significant interest in materials chemistry. However, great efforts are still required to develop methods that are low cost, scalable, and environmentally friendly and which afford carbonaceous materials having an electrocatalytic performance comparable to, or even better than, existing precious metal catalysts. Herein, recent achievements in developing metal‐free carbonaceous catalysts based on biomass are reviewed and discussed and the critical issues which still need to be addressed are highlighted. The focus is on representative synthesis and optimization strategies applicable to different kinds of biomass, as well as studies of the physicochemical structure and electrochemical performance of the resulting metal‐free carbonaceous catalysts. Finally, some guidelines for the future development of this important area are provided.

A facile approach is reported to prepare a series of transition-metal phthalocyanines supported on graphitized carbon black (TMPc/GCB, TM: Fe, Co, Ni and Cu) as oxygen reduction reaction electrocatalysts,viaπ–π interaction self-assembly.