TY - JOUR
T1 - A Surfactant-Free and General Strategy for the Synthesis of Bimetallic Core-Shell Nanocrystals on Reduced Graphene Oxide through Targeted Photodeposition
AU - Liu, Yidan
AU - Ji, Yali
AU - Li, Qian
AU - Zhu, Yi
AU - Peng, Jianchao
AU - Jia, Rongrong
AU - Lai, Zhuangchai
AU - Shi, Liyi
AU - Fan, Fengtao
AU - Zheng, Gengfeng
AU - Huang, Lei
AU - Li, Can
N1 - Publisher Copyright:
© 2023 American Chemical Society
PY - 2023/7/27
Y1 - 2023/7/27
N2 - Tunable physicochemical properties of bimetallic core-shell heterostructured nanocrystals (HNCs) have shown enormous potential in electrocatalytic reactions. In many cases, HNCs are required to load on supports to inhibit catalyst aggregation. However, the introduction of supports during the process of growing core-shell HNCs makes the synthesis much more complicated and difficult to control precisely. Herein, we reported a universal photochemical synthetic strategy for the controlled synthesis of well-defined surfactant-free core-shell metal HNCs on a reduced graphene oxide (rGO) support, which was assisted by the fine control of photogenerated electrons directly transferring to the targeted metal seeds via rGO and the precisely tuned adsorption capacity of the added second metal precursors. The surface photovoltage microscopy (SPVM) platform proved that photogenerated electrons flowed through rGO to Pd particles under illumination. We have successfully synthesized 24 different core-shell metal HNCs, i.,e., MA@MB (MA = Pd, Au, and Pt; MB = Au, Ag, Pt, Pd, Ir, Ru, Rh, Ni and Cu), on the rGO supports. The as-prepared Pd@Cu core-shell HNCs showed outstanding performance in the electrocatalytic reduction of CO2 to CH4. This work could shed light on the controlled synthesis of more functional bimetallic nanostructured materials on diverse supports for various applications.
AB - Tunable physicochemical properties of bimetallic core-shell heterostructured nanocrystals (HNCs) have shown enormous potential in electrocatalytic reactions. In many cases, HNCs are required to load on supports to inhibit catalyst aggregation. However, the introduction of supports during the process of growing core-shell HNCs makes the synthesis much more complicated and difficult to control precisely. Herein, we reported a universal photochemical synthetic strategy for the controlled synthesis of well-defined surfactant-free core-shell metal HNCs on a reduced graphene oxide (rGO) support, which was assisted by the fine control of photogenerated electrons directly transferring to the targeted metal seeds via rGO and the precisely tuned adsorption capacity of the added second metal precursors. The surface photovoltage microscopy (SPVM) platform proved that photogenerated electrons flowed through rGO to Pd particles under illumination. We have successfully synthesized 24 different core-shell metal HNCs, i.,e., MA@MB (MA = Pd, Au, and Pt; MB = Au, Ag, Pt, Pd, Ir, Ru, Rh, Ni and Cu), on the rGO supports. The as-prepared Pd@Cu core-shell HNCs showed outstanding performance in the electrocatalytic reduction of CO2 to CH4. This work could shed light on the controlled synthesis of more functional bimetallic nanostructured materials on diverse supports for various applications.
KW - bimetallic core−shell heterostructure nanocrystals
KW - electrochemical CO reduction reaction
KW - electron transfer
KW - photodeposition
KW - reduced graphene oxide
UR - http://www.scopus.com/inward/record.url?scp=85167470751&partnerID=8YFLogxK
U2 - 10.1021/acsnano.3c04281
DO - 10.1021/acsnano.3c04281
M3 - Journal article
C2 - 37497875
AN - SCOPUS:85167470751
SN - 1936-0851
VL - 17
SP - 15085
EP - 15096
JO - ACS Nano
JF - ACS Nano
IS - 15
ER -