TY - JOUR
T1 - pH-Universal Decoupled Water Electrolysis Enabled by Electrocatalytic Hydrogen Gas Capacitive Chemistry
AU - Zhu, Zhengxin
AU - Jiang, Taoli
AU - Sun, Jifei
AU - Liu, Zaichun
AU - Xie, Zehui
AU - Liu, Shuang
AU - Meng, Yahan
AU - Peng, Qia
AU - Wang, Weiping
AU - Zhang, Kai
AU - Liu, Hongxu
AU - Yuan, Yuan
AU - Li, Ke
AU - Chen, Wei
N1 - Publisher Copyright:
© 2023 The Authors. Published by American Chemical Society.
PY - 2023/2/27
Y1 - 2023/2/27
N2 - In conventional water electrolysis (CWE), the H2 and O2 evolution reactions (HER/OER) are tightly coupled, making the generated H2 and O2 difficult to separate, thus resulting in complex separation technology and potential safety issues. Previous efforts on the design of decoupled water electrolysis mainly concentrated on multi-electrode or multi-cell configurations; however, these strategies have the limitation of involving complicated operations. Here, we propose and demonstrate a pH-universal, two-electrode capacitive decoupled water electrolyzer (referred to as all-pH-CDWE) in a single-cell configuration by utilizing a low-cost capacitive electrode and a bifunctional HER/OER electrode to separate H2 and O2 generation for decoupling water electrolysis. In the all-pH-CDWE, high-purity H2 and O2 generation alternately occur at the electrocatalytic gas electrode only by reversing the current polarity. The designed all-pH-CDWE can maintain a continuous round-trip water electrolysis for over 800 consecutive cycles with an electrolyte utilization ratio of nearly 100%. As compared to CWE, the all-pH-CDWE achieves energy efficiencies of 94% in acidic electrolytes and 97% in alkaline electrolytes at a current density of 5 mA cm-2. Further, the designed all-pH-CDWE can be scaled up to a capacity of 720 C in a high current of 1 A for each cycle with a stable HER average voltage of 0.99 V. This work provides a new strategy toward the mass production of H2 in a facilely rechargeable process with high efficiency, good robustness, and large-scale applications.
AB - In conventional water electrolysis (CWE), the H2 and O2 evolution reactions (HER/OER) are tightly coupled, making the generated H2 and O2 difficult to separate, thus resulting in complex separation technology and potential safety issues. Previous efforts on the design of decoupled water electrolysis mainly concentrated on multi-electrode or multi-cell configurations; however, these strategies have the limitation of involving complicated operations. Here, we propose and demonstrate a pH-universal, two-electrode capacitive decoupled water electrolyzer (referred to as all-pH-CDWE) in a single-cell configuration by utilizing a low-cost capacitive electrode and a bifunctional HER/OER electrode to separate H2 and O2 generation for decoupling water electrolysis. In the all-pH-CDWE, high-purity H2 and O2 generation alternately occur at the electrocatalytic gas electrode only by reversing the current polarity. The designed all-pH-CDWE can maintain a continuous round-trip water electrolysis for over 800 consecutive cycles with an electrolyte utilization ratio of nearly 100%. As compared to CWE, the all-pH-CDWE achieves energy efficiencies of 94% in acidic electrolytes and 97% in alkaline electrolytes at a current density of 5 mA cm-2. Further, the designed all-pH-CDWE can be scaled up to a capacity of 720 C in a high current of 1 A for each cycle with a stable HER average voltage of 0.99 V. This work provides a new strategy toward the mass production of H2 in a facilely rechargeable process with high efficiency, good robustness, and large-scale applications.
KW - H production
KW - decoupling water electrolysis
KW - electrocatalytic H
KW - mass production of H
KW - pH-universal
UR - http://www.scopus.com/inward/record.url?scp=85146892127&partnerID=8YFLogxK
U2 - 10.1021/jacsau.2c00624
DO - 10.1021/jacsau.2c00624
M3 - 文章
AN - SCOPUS:85146892127
SN - 2691-3704
VL - 3
SP - 488
EP - 497
JO - JACS Au
JF - JACS Au
IS - 2
ER -