Harmonized Physical and Electrochemical Process Design for Densely Dispersed Cu Catalysts on Cu<sub>2</sub>O Absorbers for Efficient Photoelectrochemical CO<sub>2</sub> Reduction Reaction
Dong Su Kim, Shin Young Oh, Hak Hyeon Lee, Hyung Koun Cho
Abstract
Abstract The photoelectrochemical CO 2 reduction reaction (photo‐CO 2 RR) is a promising technology to convert CO 2 into high‐value‐added carbon‐based chemicals using a relatively low voltage, which can economically solve the problem of CO 2 emissions. Nevertheless, unlike the conventional electrochemical CO 2 RR approach, photo‐CO 2 RR technology is in its initial development stage. Particularly, when sunlight is applied to photoelectrodes for photo‐CO 2 RR, severe photocorrosion is unavoidable, resulting in the deterioration of fundamental functions including device long‐term stability and conversion performance. This study proposes an innovative two‐step catalyst formation strategy to enable the efficient photo‐CO 2 RR with Cu catalysts prepared using intrinsic photocorrosion of the Cu 2 O absorption layer. This approach is based on the harmonized process design of the i) growth of physically generated Cu nanoparticles and ii) construction of improved photoelectrochemical Cu cluster catalysts. The vacuum‐evaporated Cu seeds are designed to induce an evenly dispersed electrical path on Cu 2 O, and the selectively concentrated electrical field from the Cu seeds provides preferential sites for metallic Cu catalysts in subsequent photoelectrochemical reduction. This harmonized combination process of Cu catalysts on Cu 2 O demonstrates a synergistic performance of −1.2 mA cm −2 at 0 V RHE with suppression of photocorrosion and produces ≈95% CO product gas (0.4 V RHE ).