TY - JOUR
T1 - Carboxylated carbon nanotubes with high electrocatalytic activity for oxygen evolution in acidic conditions
AU - Zhang, Xin
AU - Zhang, Wenqing
AU - Dai, Jianying
AU - Sun, Mingzi
AU - Zhao, Jun
AU - Ji, Lifei
AU - Chen, Lin
AU - Zeng, Fanlong
AU - Yang, Fengchun
AU - Huang, Bolong
AU - Dai, Liming
N1 - Funding Information:
We gratefully acknowledge support from the Hydrogeological Survey Project of Huangshui River (No. DD20190331). We are also grateful for the partial support by Australian Research Council (DP 190103881 and FL 190100126).
Publisher Copyright:
© 2021 The Authors. InfoMat published by UESTC and John Wiley & Sons Australia, Ltd.
PY - 2022/1
Y1 - 2022/1
N2 - Since most electrocatalysts for oxygen evolution reaction (OER), except for precious metal oxides RuO2 and IrO2, are unstable in harsh acidic solutions, it is highly desirable to develop high-performance OER electrocatalysts for acidic media, though it is still a big challenge. Herein, we report a simple strategy to produce carboxyl-enriched multiwalled carbon nanotubes (COOH-MWNTs) that exhibit stable and high electrocatalytic activities for OER in acidic solutions, showing an overpotential at a current density of 10 mA cm–2 and a Tafel slope as low as of 265 mV and 82 mV dec–1, respectively. As far as we are aware, these results represent the best OER performance for metal-free electrocatalysts, even comparable to those of RuO2 and IrO2. We have further revealed the catalytic mechanism, which involves one electron lose from the COOH-MWNTs catalyst at the beginning of the OER process to trigger H2O molecule oxidation by forming peralcohol, followed by the recapture of one electron from water molecule to oxidize water and to recover the initial state for the COOH-MWNTs catalyst. The unravel of this new OER mechanism is important as it provides new insights into the crucial role of organic functional groups in electrocatalytic processes. Also, the mechanistic understanding can be used to guide the design and development of novel metal-free catalysts for acidic OER electrocatalysis and beyond. (Figure presented.).
AB - Since most electrocatalysts for oxygen evolution reaction (OER), except for precious metal oxides RuO2 and IrO2, are unstable in harsh acidic solutions, it is highly desirable to develop high-performance OER electrocatalysts for acidic media, though it is still a big challenge. Herein, we report a simple strategy to produce carboxyl-enriched multiwalled carbon nanotubes (COOH-MWNTs) that exhibit stable and high electrocatalytic activities for OER in acidic solutions, showing an overpotential at a current density of 10 mA cm–2 and a Tafel slope as low as of 265 mV and 82 mV dec–1, respectively. As far as we are aware, these results represent the best OER performance for metal-free electrocatalysts, even comparable to those of RuO2 and IrO2. We have further revealed the catalytic mechanism, which involves one electron lose from the COOH-MWNTs catalyst at the beginning of the OER process to trigger H2O molecule oxidation by forming peralcohol, followed by the recapture of one electron from water molecule to oxidize water and to recover the initial state for the COOH-MWNTs catalyst. The unravel of this new OER mechanism is important as it provides new insights into the crucial role of organic functional groups in electrocatalytic processes. Also, the mechanistic understanding can be used to guide the design and development of novel metal-free catalysts for acidic OER electrocatalysis and beyond. (Figure presented.).
UR - http://www.scopus.com/inward/record.url?scp=85123494360&partnerID=8YFLogxK
U2 - 10.1002/inf2.12273
DO - 10.1002/inf2.12273
M3 - Journal article
AN - SCOPUS:85123494360
SN - 2567-3165
VL - 4
JO - InfoMat
JF - InfoMat
IS - 1
M1 - e12273
ER -