Ziwei Guo, Chunhui Zhang, Yuejing Zhao, Shihao Guo, Nana Han, Nan Wu, A. Colin, Yuzhen Ning, Kesong Liu, Cunming Yu, Liping Jiang
ABSTRACT The effect of mass transfer on hydrogen evolution reaction (HER) is significantly underestimated under high‐current‐density conditions. Here, we designed a quasi‐chimney electrode by integrating 3D superaerophilic microchannels with superaerophobic Pt catalysts to elucidate the influence of mass transfer on HER. Upon encountering superaerophilic channels, hydrogen (H 2 ) bubbles generated on Pt catalysts experience Laplace pressure polarization at the bubble/channel interface, which drives both surface and internal bubbles from the superaerophobic catalytic sites into the superaerophilic network, functioning as a micro‐chimney for efficient bubble transport. In addition, the superaerophilic channels shorten the diffusion path of dissolved H 2 to the air/water interface, thereby reducing the dissolved H 2 concentration. This mass‐transfer enhancement yields an exceptional HER performance (a record‐low overpotential of about −30 mV at −100 mA cm −2 , and a high current density of −2.93 A cm −2 at −0.3 V vs RHE in H 2 SO 4 (0.5 M) along with remarkable durability, confirmed by <5% activity decay at −1000 and −2000 mA cm −2 for 160 h. The proposed quasi‐chimney design, which is also applicable to various catalysts, results in an 8‐ and 14‐times increase in current density for Cu–Co and Cu–Mo catalysts, at an overpotential of −500 mV compared with their superaerophobic electrode structures.