# Efficient electroreduction of CO2 to C1 and C2 products using atomically dispersed boron N–C@graphite catalysts

## TL;DR

This paper introduces a new metal-free catalyst that efficiently converts CO2 into useful products like CO and acetate using boron and nitrogen-doped graphite.

## Contribution

The study introduces a scalable method to create B,N-co-doped carbon catalysts from a molecular precursor for CO2 reduction.

## Key findings

- Catalysts pyrolyzed at 800°C favor formate and acetate production, while those at 1000°C show higher CO selectivity.
- B–N synergy stabilizes CO2 intermediates and enables C–C coupling, improving CO2RR performance.
- The catalysts show long-term stability and high current densities in zero-gap electrolyzers.

## Abstract

Atomically precise control of active sites is essential for advancing metal-free electrocatalysts for the CO2 reduction reaction (CO2RR). We report boron- and nitrogen-co-doped graphite (boron–N–C@graphite) derived from chloro-boron subphthalocyanine (Cl-B-SubPc), an aromatic macrocyclic precursor that directs simultaneous incorporation of B and N into conductive carbon frameworks. X-Ray photoelectron spectroscopy reveals the formation of B–C and B–N motifs alongside pyridinic and graphitic N, generating electron-deficient centers that modulate intermediate binding energies. The resulting catalysts display pronounced structure–activity correlations: pyrolysis at 800 °C favors formate and acetate formation, whereas 1000 °C yields a more graphitic catalyst with enhanced CO selectivity (faradaic efficiency up to 26.9%). Mechanistic analysis indicates that the B–N synergy stabilizes *CO2-intermediates, suppresses hydrogen evolution, and enables C–C coupling. Both catalysts exhibit long-term stability (>180 h), and in zero-gap electrolyzers deliver industrially relevant current densities (150 mA cm−2) with CO faradaic efficiencies of 79.0% and 87.4%, respectively. These findings establish B,N-co-doped carbons from molecular precursors as a versatile platform for elucidating active-site chemistry and for guiding the rational design of sustainable, high-performance CO2RR catalysts.

Boron NC@graphite catalysts function as efficient, noble-metal-free electrocatalysts for CO2 conversion to CO and C1/C2 products. Boron subphthalocyanines represent a new, scalable class of molecular electrocatalysts.