Jong Hyeok Park

Jong Hyeok Park


Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 December 2005 in Nano Letters
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Journal Article
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JPJong Hyeok Park
Jong Hyeok Park
SKSungwook Kim
Sungwook Kim
ABAllen J. Bard
Allen J. Bard

12 July 2012 in ACS Applied Materials & Interfaces
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Journal Article
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SSSelim Arif Sher Shah
Selim Arif Sher Shah
APA Reum Park
A Reum Park
KZKan Zhang
Kan Zhang
JPJong Hyeok Park
Jong Hyeok Park
PYPil Jin Yoo
Pil Jin Yoo

10 February 2017 in Nano Letters
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Journal Article
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JNJae Keun Nam
Jae Keun Nam
SCSung Uk Chai
Sung Uk Chai
WCWonhee Cha
Wonhee Cha
YCYung Ji Choi
Yung Ji Choi
WKWanjung Kim
Wanjung Kim
JPJong Hyeok Park
Jong Hyeok Park

2 September 2014 in Nature Communications
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XSXinjian Shi
Xinjian Shi
ICIl Yong Choi
Il Yong Choi
KZKan Zhang
Kan Zhang
JKJeong Kwon
Jeong Kwon
DKDong Yeong Kim
Dong Yeong Kim
JPJong Hyeok Park
Jong Hyeok Park
Tungsten trioxide/bismuth vanadate heterojunction is one of the best pairs for solar water splitting, but its photocurrent densities are insufficient. Here we investigate the advantages of using helical nanostructures in photoelectrochemical solar water splitting. A helical tungsten trioxide array is fabricated on a fluorine-doped tin oxide substrate, followed by subsequent coating with bismuth vanadate/catalyst. A maximum photocurrent density of ~5.35±0.15 mA cm−2 is achieved at 1.23 V versus the reversible hydrogen electrode, and related hydrogen and oxygen evolution is also observed from this heterojunction. Theoretical simulations and analyses are performed to verify the advantages of this helical structure. The combination of effective light scattering, improved charge separation and transportation, and an enlarged contact surface area with electrolytes due to the use of the bismuth vanadate-decorated tungsten trioxide helical nanostructures leads to the highest reported photocurrent density to date at 1.23 V versus the reversible hydrogen electrode, to the best of our knowledge.

1 May 2019 in Nature Communications
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KZKan Zhang
Kan Zhang
BJBingjun Jin
Bingjun Jin
CPCheolwoo Park
Cheolwoo Park
YCYoonjun Cho
Yoonjun Cho
XSXiufeng Song
Xiufeng Song
JPJong Hyeok Park
Jong Hyeok Park
As the development of oxygen evolution co-catalysts (OECs) is being actively undertaken, the tailored integration of those OECs with photoanodes is expected to be a plausible avenue for achieving highly efficient solar-assisted water splitting. Here, we demonstrate that a black phosphorene (BP) layer, inserted between the OEC and BiVO4 can improve the photoelectrochemical performance of pre-optimized OEC/BiVO4 (OEC: NiOOH, MnOx, and CoOOH) systems by 1.2∼1.6-fold, while the OEC overlayer, in turn, can suppress BP self-oxidation to achieve a high durability. A photocurrent density of 4.48 mA·cm−2 at 1.23 V vs reversible hydrogen electrode (RHE) is achieved by the NiOOH/BP/BiVO4 photoanode. It is found that the intrinsic p-type BP can boost hole extraction from BiVO4 and prolong holes trapping lifetime on BiVO4 surface. This work sheds light on the design of BP-based devices for application in solar to fuel conversion, and also suggests a promising nexus between semiconductor and electrocatalyst.

21 April 2011 in Angewandte Chemie International Edition
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DWDong Hwan Wang
Dong Hwan Wang
DKDo Youb Kim
Do Youb Kim
KCKyeong Woo Choi
Kyeong Woo Choi
JSJung Hwa Seo
Jung Hwa Seo
SISang Hyuk Im
Sang Hyuk Im
AHAlan J. Heeger
Alan J. Heeger